Skip to main content An official website of the United States government Here's how you know Here's how you know Official websites use .gov A .gov website belongs to an official government organization in the United States. Secure .gov websites use HTTPS A lock ( Lock Locked padlock icon ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites. Search Log in Dashboard Publications Account settings Log out Search… Search NCBI Primary site navigation Search Logged in as: Dashboard Publications Account settings Log in Search PMC Full-Text Archive Search in PMC Journal List User Guide PERMALINK Copy As a library, NLM provides access to scientific literature. Inclusion in an NLM database does not imply endorsement of, or agreement with, the contents by NLM or the National Institutes of Health. Learn more: PMC Disclaimer | PMC Copyright Notice JMIR AI . 2026 Apr 13;5:e81028. doi: 10.2196/81028 Search in PMC Search in PubMed View in NLM Catalog Add to search Using Machine Learning to Improve Screening for Oropharyngeal Dysphagia in Hospitalized Versus Primary Care Adult Patients With COVID-19 Disease: Retrospective Observational Study Cristina Amadó Ruiz Cristina Amadó Ruiz , MSc 1 Gastrointestinal Physiology Laboratory, Department of Surgery, Hospital Universitari de Mataró, Consorci Sanitari del Maresme, Universitat Autònoma de Barcelona, C. Cirera s/n, Barcelona, 08304, Spain, 34 937417700 2 Artificial Intelligence Massive Screening—Medical SL (AIMS MEDICAL), Mataró, Spain Find articles by Cristina Amadó Ruiz 1, 2 , Alberto Martín Alberto Martín , PhD 1 Gastrointestinal Physiology Laboratory, Department of Surgery, Hospital Universitari de Mataró, Consorci Sanitari del Maresme, Universitat Autònoma de Barcelona, C. Cirera s/n, Barcelona, 08304, Spain, 34 937417700 3 Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Instituto de Salud Carlos III, Madrid, Spain Find articles by Alberto Martín 1, 3 , Jaume Miró Ramos Jaume Miró Ramos , MSc 1 Gastrointestinal Physiology Laboratory, Department of Surgery, Hospital Universitari de Mataró, Consorci Sanitari del Maresme, Universitat Autònoma de Barcelona, C. Cirera s/n, Barcelona, 08304, Spain, 34 937417700 2 Artificial Intelligence Massive Screening—Medical SL (AIMS MEDICAL), Mataró, Spain 4 Fundació Salut Consorci Sanitari del Maresme, Mataró, Spain Find articles by Jaume Miró Ramos 1, 2, 4 , Francisco Javier Ruz Torres Francisco Javier Ruz Torres , MSc 5 IT Department, Hospital de Mataró (Universitat Autònoma de Barcelona), Maresme Health Consortium, Mataró, Spain Find articles by Francisco Javier Ruz Torres 5 , Antonio Ruiz Antonio Ruiz , MSc 5 IT Department, Hospital de Mataró (Universitat Autònoma de Barcelona), Maresme Health Consortium, Mataró, Spain Find articles by Antonio Ruiz 5 , Adil El Haji Adil El Haji , BSc 1 Gastrointestinal Physiology Laboratory, Department of Surgery, Hospital Universitari de Mataró, Consorci Sanitari del Maresme, Universitat Autònoma de Barcelona, C. Cirera s/n, Barcelona, 08304, Spain, 34 937417700 2 Artificial Intelligence Massive Screening—Medical SL (AIMS MEDICAL), Mataró, Spain Find articles by Adil El Haji 1, 2 , Pere Clavé Pere Clavé , PhD 1 Gastrointestinal Physiology Laboratory, Department of Surgery, Hospital Universitari de Mataró, Consorci Sanitari del Maresme, Universitat Autònoma de Barcelona, C. Cirera s/n, Barcelona, 08304, Spain, 34 937417700 3 Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Instituto de Salud Carlos III, Madrid, Spain Find articles by Pere Clavé 1, 3, ✉ , Omar Ortega Omar Ortega , PhD 1 Gastrointestinal Physiology Laboratory, Department of Surgery, Hospital Universitari de Mataró, Consorci Sanitari del Maresme, Universitat Autònoma de Barcelona, C. Cirera s/n, Barcelona, 08304, Spain, 34 937417700 3 Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Instituto de Salud Carlos III, Madrid, Spain Find articles by Omar Ortega 1, 3 Editor: Gang Luo Author information Article notes Copyright and License information 1 Gastrointestinal Physiology Laboratory, Department of Surgery, Hospital Universitari de Mataró, Consorci Sanitari del Maresme, Universitat Autònoma de Barcelona, C. Cirera s/n, Barcelona, 08304, Spain, 34 937417700 2 Artificial Intelligence Massive Screening—Medical SL (AIMS MEDICAL), Mataró, Spain 3 Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Instituto de Salud Carlos III, Madrid, Spain 4 Fundació Salut Consorci Sanitari del Maresme, Mataró, Spain 5 IT Department, Hospital de Mataró (Universitat Autònoma de Barcelona), Maresme Health Consortium, Mataró, Spain ✉ Pere Clavé, PhD, Gastrointestinal Physiology Laboratory, Department of Surgery, Hospital Universitari de Mataró, Consorci Sanitari del Maresme, Universitat Autònoma de Barcelona, C. Cirera s/n, Barcelona, 08304, Spain, 34 937417700; [email protected] Received 2025 Jul 21; Revised 2026 Jan 16; Accepted 2026 Jan 20; Collection date 2026. Copyright © Cristina Amadó Ruiz, Alberto Martín, Jaume Miró Ramos, Francisco Javier Ruz Torres, Antonio Ruiz, Adil El Haji, Pere Clavé, Omar Ortega. Originally published in JMIR AI (https://ai.jmir.org) This is an open-access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/ ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in JMIR AI, is properly cited. The complete bibliographic information, a link to the original publication on https://www.ai.jmir.org/ , as well as this copyright and license information must be included. PMC Copyright notice PMCID: PMC13075777 PMID: 41973941 Abstract Background Oropharyngeal dysphagia (OD) commonly occurs in patients with COVID-19 disease, posing diagnostic challenges due to isolation protocols. Objective This study aimed at evaluating Artificial Intelligence Massive Screening for Oropharyngeal Dysphagia (AIMS-OD), a machine learning software for real-time OD screening, comparing OD prevalence and clinical outcomes using OD ICD-10 ( International Statistical Classification of Diseases, Tenth Revision ) R13 codes (R13-OD) and high-risk AIMS-OD (H-AIMS-OD) scores (>0.5), in hospital and primary care patients with COVID-19 disease. It explored clinical characteristics, OD risk factors, and clinical outcomes. Methods This retrospective, observational study analyzed patients with SARS-CoV-2 aged 18 years and older in Catalonia from January 1 to August 31, 2020, including hospital and primary care data on clinical information, International Classification of Diseases, Tenth Revision ( ICD-10 ) codes, hospital stay, discharge destination, and mortality. AIMS-OD assessed OD risk, stratifying patients by age (aged 18‐69 years and 70 years and older). Results Among 257,541 patients with COVID-19 disease, 59.3% (152,721/257,541) were aged 18‐69 years and 40.7% (104,820/257,541) were aged 70 years and older. Hospital and primary care R13-OD prevalence was 3.5% and 4.3%, respectively; AIMS-OD showed 34.8% and 15.4%, with True prevalence at 16.7% and 7.4%. Patients aged 70 years and older had worse clinical outcomes and worse prognosis. Patients in R13-OD experienced significantly worse clinical outcomes than patients with H-AIMS-OD, who in turn fared worse than those with no R13-OD and with low AIMS-OD risk. Risk factors for patients with COVID-19 R13-OD included age, neuroleptic use, stroke, dementia, and delirium. Conclusions AIMS-OD screening revealed high prevalence and significant underdiagnosis in patients with COVID-19 disease across settings. Early detection and risk stratification using AIMS-OD could improve clinical decision-making, diagnosis, and management, particularly in older patients with comorbidities. Introduction COVID-19 pandemic originated in the city of Wuhan, China, in late 2019. It is a serious illness caused by SARS-CoV-2. The infection spread globally and was declared a pandemic by the World Health Organization on March 11, 2020 [ 1 ], and the first case in Catalonia, Spain, was reported on February 25, 2020. The COVID-19 pandemic had devastating effects worldwide, with high rates of severely ill patients and mortality [ 2 ]. The most common symptoms of the disease were fever, cough, difficulty breathing, fatigue, loss of taste or smell, sore throat, and diarrhea [ 3 ]. Mortality from the COVID-19 pandemic in older patients was very high during the initial waves of the pandemic. This vulnerability was linked to the biological wear and tear inherent to age, to the higher prevalence of comorbidities, and to the fact that up to 50% of older patients requiring hospitalization were malnourished [ 4 ]. Several factors associated with increased disease severity and poor prognosis in COVID-19 have been identified, including advanced age, oropharyngeal dysphagia (OD), malnutrition (MN), frailty, and impaired functionality [ 5 ], as well as chronic conditions such as type 2 diabetes mellitus, arterial hypertension, or obesity and diseases of the immune system [ 4 ]. The first wave of the pandemic in Spain occurred from the second half of March to the second half of June 2020. During that period, we found that of the 205 patients with COVID-19 disease admitted consecutively to the Hospital de Mataró, 51.7 % (106/205) had OD on admission and 43.8% (90/205) had OD on discharge [ 5 ]. OD is a symptom of a swallowing disorder that is characterized by the inability to safely and effectively move the alimentary bolus from the mouth to the esophagus [ 6 ]. This condition has been recognized as a geriatric syndrome [ 7 ], acknowledged by the World Health Organization [ 8 ], and classified in the ICD ( International Classification of Diseases ) with codes 787.2 ICD-9 ( International Classification of Diseases, Ninth Revision ), R13 ICD-10 ( International Statistical Classification of Diseases, Tenth Revision ), and MD93 ICD-11 ( International Classification of Diseases, 11th Revision ). OD is highly prevalent among different phenotypes of patients [ 6 , 9 ], including those with COVID-19 disease [ 5 , 10 ]. Moreover, OD is associated with severe complications, including MN, dehydration (DH), respiratory infections, aspiration pneumonia (AP), reduced quality of life, and increased mortality [ 8 , 11 ]. Recent prospective studies have further documented the high prevalence of OD in populations with COVID-19 disease using bedside screening methods. Zayed et al [ 12 ] reported that 45.4% of patients hospitalized with COVID-19 disease tested positive for OD using the Eating Assessment Tool and the Yale Swallowing Protocol, with risk factors including advanced age, dysphonia, ageusia, anosmia, intensive care unit (ICU) admission, and mechanical ventilation. In a subsequent study using instrumental assessment on patients with OD after COVID-19 disease, the same authors identified swallowing abnormalities using fiberoptic endoscopic evaluation of swallowing (FEES), including delayed activation of the swallowing reflex and altered laryngeal sensitivity, reinforcing the clinical relevance of systematic screening for OD in this population [ 13 ]. A swallow screening test is defined according to Swigert et al [ 14 ] as a minimally invasive evaluation procedure that quickly “determines the likelihood that dysphagia exists; whether the patient requires referral for further swallowing assessment; whether it is safe to feed the patient orally (for the purposes of nutrition, hydration, and administration of medication); whether the patient requires referral for nutritional or hydrational support.” It is essential for health care centers to implement a systematic screening process for OD in patients with COVID-19 disease to identify those who require clinical evaluation for accurate diagnosis and appropriate compensatory treatment to avoid respiratory and nutritional complications. The diagnostic algorithm for OD involves a 3-step approach: screening, clinical assessment, and instrumental evaluation. The screening incorporates a specific anamnesis and validated questionnaires to identify OD risk factors [ 15 ]. Failure in screening leads to reduced diagnosis rates, increasing clinical risks, and health care costs [ 15 , 16 ]. If a patient is positive, a subsequent clinical assessment has to be performed involving the evaluation of clinical signs of impaired efficacy and safety of swallow to be able to prescribe the first compensatory treatment for the patient. The Volume-Viscosity Swallow Test is a clinical method with high sensitivity (93.17%) and specificity (81.39%) for OD diagnosis that uses different volumes and viscosities to clinically assess deglutition [ 15 , 17 , 18 ]. Finally, the instrumental assessment uses gold standard techniques such as videofluoroscopy and FEES, enabling the objective evaluation of deglutition mechanisms and the understanding of the pathophysiology of OD, including aspiration mechanisms [ 19 , 20 ]. Nowadays, there are automatic screening tools that have been developed using artificial intelligence (AI). AI is a branch of computer science capable of analyzing complex medical data. Its potential to explore meaningful relationships within a dataset can be used in the diagnosis, treatment, and outcome prediction in many clinical scenarios [ 21 ]. Furthermore, machine learning (ML) algorithms used in AI have demonstrated their potential in offering solutions to intricate issues [ 22 ]. Recent work in the field of AI applied to health care emphasizes that, beyond predictive performance, AI-based tools intended for clinical use must address issues related to interpretability, transparency, and clinical usability. In this regard, the ability of AI systems to rely on clinically meaningful variables and to support, rather than replace, clinical reasoning has been identified as a key factor for successful implementation in real-world settings. Moreover, current evidence highlights the expanding role of AI in health care not only for individual risk assessment but also for large-scale screening, population-level risk stratification, and improvements in health system efficiency, provided that these tools can be effectively integrated into existing clinical workflows and electronic health records (EHRs). In this context, AI-based screening approaches may offer complementary value by enabling systematic and scalable identification of patients at risk in scenarios where conventional clinical assessment is limited or not routinely feasible [ 23 , 24 ]. Artificial Intelligence Massive Screening for Oropharyngeal Dysphagia (AIMS-OD) [ 15 ] is a ML-based screening tool that has been developed to measure the risk of OD in acute hospitals, rehabilitation centers, nursing homes, and primary care. Specifically, AIMS-OD uses a nonlinear model built with Random Forest to predict the risk of OD in patients. The tool uses nonidentifying data, such as age, gender, Barthel index, and ICD codes [ 15 ]. The aims of this study are to demonstrate the underdiagnosis of OD in patients with COVID-19 across both hospitalized and primary care settings; to compare the prevalence of OD in patients with COVID-19 disease according to ICD-10 coding (R13), group called R13-OD, or high-risk AIMS-OD scores (>0.5), group called H-AIMS-OD, in hospitalization patients and primary care settings; and to study the clinical characteristics, risk factors for OD, and clinical outcomes associated with 2 age groups: patients aged 18‐69 years and those aged 70 years. Methods Study Design A retrospective observational and comparative study was conducted in a cohort that included all SARS-CoV-2-positive patients in Catalonia during the first wave of the COVID-19 pandemic. Prevalence of OD identified by the primary care and hospital clinicians and codified by ICD codes was compared with that determined by AIMS-OD (risk >0.5). Ethical Considerations The study protocol was approved by the ethics committee of the Consorci Sanitari del Maresme (code: CEIm 43/20) and was conducted according to the principles and rules laid down in the Declaration of Helsinki and its amendments. Exemption of the informed consent form was granted by the institutional review board and followed the Guidance on the Management of Clinical Trials during the COVID-19 pandemic (European Commission, version 4; February 4, 2021). To ensure privacy and confidentiality, all data were anonymized prior to analysis and handled in accordance with the General Data Protection Regulation and applicable national regulations. No directly identifiable personal information was accessible to the research team. Participants did not receive any financial compensation for participation in this study. Study Population and Dataset The study population included all patients aged 18 years and older who tested positive for SARS-CoV-2 (reverse transcription polymerase chain reaction with GeneXpert Dx [Cepheid]) in Catalonia from a database that included all Catalan patients from January 1 to August 31, 2020, at 2 levels of care, primary and hospital care. The first confirmed positive SARS-CoV-2 patient was reported in our database on February 26, 2020. Patient data were provided by the Agència de Qualitat i Avaluació Sanitàries de Catalunya [ 25 ] , within the framework of the Analytical Program of Dades per a la Recerca i la Innovació en Salut (PADRIS) [ 26 ]. The PADRIS program allows access to the reuse and cross-referencing of health data generated by the Sistema Sanitari Integral d’Utilització Pública de Catalunya [ 27 ] to promote research in the health field. PADRIS emphasizes the use of anonymized and deidentified data, which is a positive aspect in terms of privacy protection [ 26 ]. The dataset was composed of 707,369 assistance records of the COVID-19 positive population, consisting of 257,541 patients who were admitted to hospital and/or treated in primary care centers. As illustrated in Figure 1 , for the entire datasets (hospital and primary care), individuals were stratified into 2 categories: those aged between 18 and 69 years, and those aged 70 years and older. This initial division yielded 6 main groups, each of which was subsequently subcategorized into three distinct subgroups: (1) R13-OD, (2) H-AIMS-OD (sensitivity 0.950, specificity 0.304) [ 15 ] and, (3) those with no R13-OD and with no high risk of AIMS-OD, a group called with no R13-OD and low AIMS-OD risk (L-AIMS-OD). The ICD-10 R13-OD diagnostic code was assigned during routine clinical practice by physicians based on clinical judgment and documentation, and these codes were present in the database of the study (retrospective data). The AIMS-OD risk categories (high risk or AIMS-OD risk of >0.5 vs low risk or AIMS-OD risk of <0.5) were generated retrospectively and automatically by the AIMS-OD algorithm using the anonymized health records data present in the study database. No speech-language pathologist, nurse, or physician manually classified patients into AIMS-OD risk groups for the purposes of this study. Figure 1. CONSORT (Consolidated Standards of Reporting Trials) flowchart showing the distribution of the whole study population into groups by setting and age range. H-AIMS-OD: high-risk Artificial Intelligence Massive Screening for Oropharyngeal Dysphagia; L-AIMS-OD: low Artificial Intelligence Massive Screening for Oropharyngeal Dysphagia; R13-OD: OD in patients with COVID-19 according to ICD-10 coding (R13). Open in a new tab Clinical Variables and Measures To establish a clinically consistent basis for comparison, the ICD-10 code R13 for OD was used as the reference standard. Table 1 shows a summary of the study variables. The anatomical therapeutic chemical codes of drugs related to OD and the ICD-10 codes during the previous 2 years and during the period from January 1 to August 31, 2020, were included. Table 1. Variables of interest extracted through database processing, storage, and treatment. Data type Description Variables, n Demographic data Sex and age 2 Diagnosis codes ICD -10 a codes 1215 Dysphagia Dysphagia (R13.0 to R13.19) 20 Clinical outcomes AP b (J69.0, J69.8), MN c (E45, E44, E43), DH d (E86), total mortality, 1-month mortality, 6-month mortality, and 1-year mortality 10 Administrative data Length of hospital stay, discharge to nursing home, Charlson, admission to ICU e and days in ICU 5 Anthropometric variables Weight and BMI 2 Dispensed medication Drugs related to OD f 20 Open in a new tab a ICD-10 : International Classification of Diseases, Tenth Revision . b AP: aspiration pneumonia. c MN: malnutrition. d DH: dehydration. e ICU: intensive care unit. f OD: oropharyngeal dysphagia. Data Processing Duplicated patients were removed from the database. Data manipulation methods were also used, such as the creation and deletion of aggregate variables, dummies, and variable collapse [ 28 ], to select the most relevant variables for our results. In order to obtain the study variables, new variables derived from existing data were generated to determine the discharge to nursing homes, the number of days of hospital stay, and the number of readmissions for each patient. These variables provided complementary information on patient clinical status and outcomes. For the variables age, weight, BMI, days of admission to the ICU and hospital stays, and number of admissions, the most recent record over time was selected as it is necessary to choose a single value for each variable. The processing of the database variables was performed with the programming languages R (R Project for Statistical Computing version 4.3.0; R Foundation for Statistical Computing) and Python (Python version 3.10.0; Python Software Foundation). ML Screening Software: AIMS-OD The risk estimation service is offered through an application programming interface (API), allowing any facility with EHRs to request their patients’ OD risk. AIMS-OD has an area under the receiver operating characteristic curve of 0.840, sensitivity 0.940, specificity 0.416, positive predictive value 0.834, negative predictive value 0.690, positive likelihood ratio 1.61, and negative likelihood ratio 0.146 [ 15 ]. The web service process involves the following steps: (1) First, the health care facility anonymizes the clinical data of its EHR and sends a query via Hypertext Transfer Protocol Secure using the JavaScript Object Notation format, which is an international standard. (2) The API receives the query and verifies the user’s authorization and whether it contains the required fields and security measures. (3) Finally, the API sends the query to our expert system (ES), which predicts the risk of OD. The risk is returned as a number between 0 and 1 to the consulting health care facility. The ES system uses a proprietary algorithm that uses nonlinear ML methods to perform OD risk prediction. Both the ES and the API have been developed using open source software and are highly scalable as the system includes several API-based microservices [ 15 ]. To develop our predictive model, we drew on a comprehensive database created based on the knowledge of health care experts, established literature, and our team’s extensive knowledge of OD in older people. This expert database covers more than 25,000 potential variables, directly or indirectly related to OD. These variables covered the presence or absence of pathologies documented in the patients’ EHR in the 24 months prior to admission [ 15 ]. Data Analysis and Statistical Methods The prevalence and risk of OD; the prevalence of AP, MN, and DH; length of stay; discharge to nursing home; ICU admission; and the total mortality rate were the main outcome study variables. Several analyses were carried out: an initial descriptive statistical analysis with the entire group of patients described in the study design section and illustrated in Figure 1 ; a subsequent comparative analysis between the 3 groups (patients with COVID-19 disease according to R13-OD, H-AIMS-OD, and L-AIMS-OD groups); a comparative analysis between the proportions of OD prevalence in the overall, hospital, and primary care groups; and the true prevalence of OD in different age groups. We then performed descriptive and comparative analysis with the hospital and primary care groups ( Figure 1 ), and finally bivariate and multivariate analysis for R13-OD and H-AIMS-OD. For the comparative analysis between proportions, the prevalence of OD in patients with an R13-OD, the prevalence of OD in H-AIMS-OD patients, and the true prevalence of OD in patients in different age ranges were studied with the test of proportions based on the normality test (z). The estimated and true prevalences of the overall, hospital, and primary care patients were studied ( Figure 1 ). When estimating disease prevalence using imperfect screening tools (ie, those with sensitivity and specificity less than 100%), the observed prevalence is subject to misclassification bias. To obtain an unbiased estimate of the “True prevalence,” a standard epidemiological correction method is applied, accounting for the known sensitivity and specificity of the screening tool [ 29 , 30 ]. In this study, AIMS-OD has a sensitivity of 94% and a specificity of 42%. True prevalence is the actual proportion of diseased persons in the study sample [ 31 ]. In our case, it is the true prevalence of positive patients taking into account the sensitivity and specificity of AIMS-OD. To estimate true prevalence of OD, the sensitivity (94%) and the specificity (42%) of AIMS-OD were taken into account by applying the following formula: True prevalence = Estimated AIMS − OD prevalence + [ ( 1 − sensitivity ) × ( Estimated AIMS − OD prevalence ) ] − [ ( 1 − specificity ) × ( Estimated AIMS − OD prevalence ) ] In this way, the true prevalence of OD patients is obtained, that is, without false positive diagnoses and with missing true positive diagnoses [ 30 ]. In the descriptive analyses, dichotomous data were presented in the results tables as relative and absolute frequencies, corresponding to analysis with chi-square test [ 32 ], due to the large size of the samples. Continuous data were presented in tables as mean and SD. The mortality variables do not include patients who died in the previous time period, that is, the patients who died in the monthly variable are those who died in the 30 days following discharge. The total mortality variable does not correspond to the sum of the mortality variables, since there are patients with a death date after 1 year. The comparison analysis between samples was performed using the 2-tailed t test (between-group comparisons) [ 33 ] and the nonparametric Mann-Whitney U test [ 34 ] was used for those variables that did not follow a normal distribution (comparison between 2 groups). To perform the 3-sample comparison analysis, the Kruskal-Wallis test [ 35 ] was used. A comparative analysis was also carried out between the variables of 2 groups, R13-OD patients versus H-AIMS-OD patients and the union of the 2 previous groups versus patients with no R13-OD and L-AIMS-OD. For those variables that did not follow a normal distribution, a comparative analysis was performed with the nonparametric Mann-Whitney U test (between-group comparisons). For the analysis of normality of variables, we used Shapiro’s normality test to evaluate the normality of a single variable within a group, and Levene’s test to evaluate the equality of variances between the 3 groups studied. In the bivariate analysis, Fisher exact test was used to assess the relationships between the different OD factors and elevated risk of AIMS-OD. For continuous factors, Student t test (normal distribution) and Mann-Whitney U test (nonnormal distribution) were used. Multivariate models were performed with the significantly associated factors ( P <.05) and clinically relevant factors for the different outcomes by numerical normalization of the data and logistic regression. Comparative plots of prevalences of R13-OD and H-AIMS-OD were created for each age range. The results were interpreted according to the P value obtained, the probability of occurrence of the outcome (odds ratio), the magnitude of the observed effect, and its clinical and biological plausibility. Statistical significance was accepted if P values were <.05. Statistical analysis was performed with the specific language R and Python. Results Demographics and Clinical Characteristics of the Overall Study Population A total of 257,541 patients with COVID-19 disease were studied, divided into 152,643 patients in the group aged 18‐69 years, and 104,898 patients in the group aged 70 years and older. Prevalence of AP, MN, and DH was higher in patients aged 70 years and older. Weight was lower but BMI was higher in patients aged 70 years and older than in the whole population or patients aged 18‐69 years. The main clinical characteristics of the sample by age groups are shown in Table 2 . Table 2. Clinical and descriptive conditions of the total samples for patients aged 18 years and older and for the 18‐69 years and 70 years and older subgroups. P values in italics indicate statistical differences, and the unitalicized P values nearly reach statistical significance. Characteristics Total (18 years and older; N=257,541) 18‐69 years (N=152,643) 70 years and older (N=104,898) P value Age (years), mean (SD) 62.0 (20.1) 48.3 (13.6) a , b 81.9 (7.4) a <.001 Sex (female), n (%) 146,474 (56.9) 88,525 (58.0) a , b 57,949 (55.2) a <.001 Length of stay (days), mean (SD) 10.5 (20.1) 10.3 (16.7) a , b 10.7 (22.4) a .04 Charlson, mean (SD) 1.5 (2.4) 0.9 (2.0) a 2.2 (2.7) a <.001 Aspiration pneumonia, n (%) 3666 (1.4) 827 (0.5) a , b 2839 (2.7) a <.001 Malnutrition, n (%) 3140 (1.2) 1165 (0.8) a , b 1975 (1.9) a <.001 Dehydration, n (%) 3391 (1.3) 715 (0.5) a , b 2676 (2.6) a <.001 Discharge to nursing home, n (%) 20,362 (7.9) 6060 (4.0) a , b 14,302 (13.6) a <.001 ICU c admissions, n (%) 10,431 (4.1) 6301 (4.1) d 4130 (3.9) .054 ICU days, mean (SD) 7.6 (15.2) 8.7 (13.4) a , b 6.0 (10.1) a <.001 Weight (kg), mean (SD) 76.8 (22.3) 76.9 (22.8) 75.4 (16.5) .02 BMI, mean (SD) 28.4 (10.7) 28.2 (10.5) e 30.1 (11.5) f .05 Total mortality, n (%) 9926 (3.9) 1204 (0.8) a , b 8722 (8.3) <.001 Mortality during hospital stay, n (%) 4892 (1.9) 840 (0.6) a , b 4052 (3.9) a <.001 One-month mortality, n (%) 4610 (1.8) 494 (0.3) a , b 4116 (3.9) a <.001 Six-month mortality, n (%) 1238 (0.5) 134 (0.1) a , b 1104 (1.1) a <.001 One-year mortality, n (%) 87 (0.03) 10 (0.007) a , b 77 (0.07) a <.001 Open in a new tab a P <.001 vs Total ≥18 years. b P <.001 vs ≥70 years. c ICU: intensive care unit. d P <.05 vs ≥70 years. e P <.01 vs ≥70 years. f P <.05 vs Total ≥18 years. Prevalence of OD in the Overall Study Population and in Hospitalization Versus Primary Care Population According to ICD Codes Versus AIMS-OD The overall prevalence of R13-OD for those aged 18 years and older was 4.6%; for those aged 18‐69 years, 2.4%; and for those aged 70 years and older, 7.7%. In contrast, AIMS-OD estimated a prevalence of 25.5% for those aged 18 years and older, of 20.8% for those aged 18‐69 years, and of 32.3% for those aged 70 years and older. Calculated true prevalences for the study groups were 12.2%, 10.0%, and 15.5%, respectively. As shown in Figure 2 , in the group of patients in R13-OD, prevalence of OD increased significantly from 11 to 100 years to reach an OD prevalence of 13.0%. In those at H-AIMS-OD, OD increased between the age range of 71‐80 and 81‐90 years to reach a prevalence of 33.0% and then decreased. In contrast, when true prevalence was taken into account, OD increased between 61‐70 and 81‐90 years to reach a prevalence of 15.8% and then decreased. Figure 2. Prevalence of total patients aged 18 years and older with oropharyngeal dysphagia (OD) by 10-year age ranges. The orange line shows the estimated prevalence of H-AIMS-OD, the green line shows the true prevalence of OD, and the blue line shows the prevalence of R13-OD for patients aged 18 years and older. The orange dashed line shows the comparison between the estimated prevalence of high risk of OD versus the true prevalence of OD in each age range. The green dashed line shows the comparison between the true prevalence of OD versus the R13-OD prevalence in each age range. The blue dashed line shows the comparison between the estimated prevalence of H-AIMS-OD versus R13-OD prevalence in each age range. These comparisons are represented with * P <.001. ICD-10 : International Statistical Classification of Diseases, Tenth Revision ; OD: oropharyngeal dysphagia. Open in a new tab The prevalence in each age range in patients in R13-OD versus patients in H-AIMS-OD was statistically significantly different. The same is true between the groups of patients in R13-OD versus the True prevalence according to AIMS-OD psychometrics, and between the groups of patients in H-AIMS-OD versus the True prevalence ( Figure 2 ). The mean prevalence of hospitalized patients in R13-OD was 3.5%; in H-AIMS-OD, 34.8%; and according to the calculated true prevalence, 16.7%. The prevalence in each age range in hospitalized patients in each of the 3 groups was significantly different ( Figure 3 ). Figure 3. Prevalence of hospitalized patients aged 18 years and older with oropharyngeal dysphagia (OD) by 10-year age ranges. The orange line shows the estimated prevalence of high risk of OD (AIMS-OD > 0.5), the green line shows the true prevalence of OD, and the blue line shows the prevalence of R13-OD for hospitalized patients aged 18 years and older. The orange dashed line shows the comparison between the estimated prevalence of H-AIMS-OD versus the true prevalence of OD in each age range. The green dashed line shows the comparison between the true prevalence of OD versus R13-OD prevalence in each age range. The blue dashed line shows the comparison between the estimated prevalence of H-AIMS-OD versus the R13-OD prevalence in each age range. These comparisons are represented with * P <.05, ** P <.001. ICD-10 : International Statistical Classification of Diseases, Tenth Revision ; OD: oropharyngeal dysphagia. Open in a new tab The mean prevalence of primary care in patients in the R13-OD group was 4.3%; in H-AIMS-OD, 15.4%; and according to the calculated true prevalence, 7.4%. The prevalence in each age range in primary care patients in each of the 3 groups was significantly different except in the 81‐90 years age group between the prevalence of patients in R13-OD versus patients in H-AIMS-OD ( Figure 4 ). Figure 4. Prevalence of primary care patients aged 18 years and older with oropharyngeal dysphagia (OD) by 10-year age ranges. The orange line shows the estimated prevalence of high risk of OD (AIMS-OD>0.5), the green line shows the true prevalence of OD, and the blue line shows the prevalence of R13-OD for hospitalized patients aged 18 years and older. The orange dashed line shows the comparison between the estimated prevalence of H-AIMS-OD versus the true prevalence of OD in each age range. The green dashed line shows the comparison between the true prevalence of OD versus R13-OD prevalence in each age range. The blue dashed line shows the comparison between the estimated prevalence of H-AIMS-OD versus R13-OD prevalence in each age range. These comparisons are represented with * P <.001. ICD-10 : International Statistical Classification of Diseases, Tenth Revision ; OD: oropharyngeal dysphagia. Open in a new tab Clinical Characteristics and Outcomes of the Patients in R13-OD Versus AIMS-OD Status Overall Study Population Patients in R13-OD in all 3 samples had higher rates of AP, MN, DH, hospital stay, and total mortality than those in H-AIMS-OD, and these, in turn, were higher than those with no R13-OD and L-AIMS-OD. In contrast, in patients aged 70 years and older, institutionalization was higher in H-AIMS-OD patients, and Charlson was also higher in H-AIMS-OD patients of the 3 patient groups. Of all groups, weight was lower in R13-OD patients. The main clinical characteristics according to age groups and R13-OD or AIMS-OD subgroups are shown in Table 3 . Table 3. Clinical conditions for patients aged 18 years and older, those between 18 and 69 years, and those aged 70 years and older according to OD a classification (R13-OD; H-AIMS-OD, and no R13-OD and L-AIMS-OD) b . Characteristics Total (18 years and older) 18‐69 years 70 years and older R13-OD H-AIMS-OD No R13-OD and L-AIMS-OD P value R13-OD H-AIMS-OD No R13-OD and L-AIMS-OD P value R13-OD H-AIMS-OD No R13-OD and L-AIMS-OD P value Participants, n/N (%) 11,744/257,541 (4.6) 65,576/257,541 (25.5) 183,739/257,541 (71.3) 3649/152,643 (2.4) 31,698/152,643 (20.8) 118,181/152,643 (77.4) 8095/104,898 (7.7) 33,878/104,898 (32.3) 65,558/104,898 (62.5) Age, mean (SD) 74.7 (17.7) 67.3 (18.3) 59.6 (20.3) <.001 c ; <.001 c 52.4 (12.7) 51.8 (12.9) 47.3 (13.6) .005 c ; <.001 c 84.8 (7.4) 81.9 (7.3) 82.0 (7.5) <.001 c ; <.001 c Sex (female), n (%) 6571 (56.0) 34,104 (52.0) 107,596 (58.6) <.001 c ; <.001 c 1879 (51.5) 16,522 (52.1) 70,505 (59.7) .50; <.001 c 4692 (58.0) 17,582 (51.9) 37,091 (56.6) <.001 c ; <.001 c Length of stay, mean (SD) 15.5 (19.7) 10.9 (25.7) 10.0 (15.0) <.001 c ; <.001 c 19.9 (27.3) 10.8 (17.7) 9.8 (15.7) <.001 c ; <.001 c 14.1 (16.5) 10.9 (29.7) 10.2 (14.4) <.001 c ; <.001 c Charlson, mean (SD) 1.7 (2.7) 2.1 (2.8) 1.2 (2.2) <.001 c ; <.001 c 0.9 (2.0) 1.4 (2.5) 0.8 (1.8) <.001 c ; <.001 c 2.2 (2.7) 2.7 (2.9) 2.0 (2.5) <.001 c ; <.001 c Aspiration pneumonia, n (%) 1255 (10.7) 1506 (2.3) 1455 (0.8) <.001 c ; <.001 c 213 (5.8) 307 (1.0) 395 (0.3) <.001 c ; <.001 c 1042 (12.9) 1199 (3.5) 1060 (1.6) <.001 c ; <.001 c Malnutrition, n (%) 491 (4.2) 1312 (2.0) 1564 (0.9) <.001 c ; <.001 c 133 (3.6) 434 (1.4) 659 (0.6) <.001 c ; <.001 c 358 (4.4) 878 (2.3) 905 (1.4) <.001 c ; <.001 c Dehydration, n (%) 441 (3.8) 1391 (2.1) 1751 (1.0) <.001 c ; <.001 c 50 (1.4) 268 (0.8) 422 (0.4) .001 c ; <.001 c 391 (4.8) 1123 (3.3) 1329 (2.0) <.001 c ; <.001 c Discharge to nursing home, n (%) 1762 (15.0) 8501 (13.0) (10,867 (5.9) <.001 c ; <.001 c 329 (9.0) 2251 (7.1) 3610 (3.1) <.001 c ; <.001 c 1433 (17.7) 6250 (18.4) 7257 (11.1) .12; <.001 c ICU d admissions, n (%) 433 (3.7) 4095 (6.2) 6101 (3.3) <.001 c ; <.001 c 234 (6.4) 2328 (7.3) 3839 (3.3) .04 c ; <.001 c 199 (2.5) 1767 (5.2) 2262 (3.5) <.001 c ; <.001 c ICU days, mean (SD) 12.6 (17.5) 7.8 (12.4) 7.3 (11.8) <.001 c ; .88 15.6 (18.9) 8.9 (13.5) 8.3 (13.0) <.001 c ; .13 9.2 (15.1) 6.3 (10.7) 5.7 (9.3) .13; .04 c Weight, mean (SD) 73.2 (15.9) 77.2 (17.6) 76.8 (22.7) <.001 c ; .05 74.7 (16.1) 78.7 (19.0) 76.9 (23.0) .003 c ; .03 c 68.7 (14.4) 76.0 (16.4) 75.7 (16.6) <.001 c ; .90 c BMI, mean (SD) 28.1 (14.4) 28.9 (9.1) 28.3 (10.8) .06; .07 27.3 (14.0) 28.1 (6.6) 28.2 (10.6) .87; .82 29.0 (15.1) 31.1 (10.6) 29.7 (10.8) .009 c ; .89 Total mortality, n (%) 1207 (8.7) 3617 (5.5) 5646 (3.1) <.001 c ; <.001 c 71 (1.9) 430 (1.4) 731 (0.6) .004 c ; <.001 c 956 (11.8) 3187 (9.4) 4915 (7.5) <.001 c ; <.001 c Mortality during hospital stay, n (%) 350 (3.0) 2139 (3.3) 2568 (1.4) .11; <.001 c 45 (1.2) 318 (1.0) 497 (0.4) .19; <.001 c 305 (3.8) 1821 (5.4) 2071 (3.2) <.001 c ; <.001 c One-month mortality, n (%) 333 (2.8) 863 (1.3) 1560 (0.8) <.001 c ; <.001 c 13 (0.4) 65 (0.2) 125 (0.1) .01 c ; <.001 c 320 (4.0) 798 (2.4) 1435 (2.2) <.001 c ; <.001 c Six-month mortality, n (%) 122 (1.0) 413 (0.6) 527 (0.3) <.001 c ; <.001 c 16 (0.2) 43 (0.1) 73 (0.06) .36; <.001 c 116 (1.4) 370 (1.1) 454 (0.7) <.001 c ; <.001 c One-year mortality, n (%) 9 (0.08) 30 (0.05) 42 (0.02) .14; <.001 c 0 (0.0) 2 (0.006) 5 (0.004) .60; .01 c 9 (0.1) 28 (0.08) 37 (0.06) .46; .05 Open in a new tab a OD: oropharyngeal dysphagia. b In each P value row, the first P value is the comparison between the group of R13-OD patients and the group of H-AIMS-OD patients. The second P value is the comparison between the union of the first groups (R13-OD and H-AIMS-OD) versus the group of patients with no R13-OD and L-AIMS-OD. c These values indicate statistical differences ( P values), and values in italics nearly reach statistical significance. d ICU: intensive care unit. Hospitalized Patients A total of 108,039 patients were admitted to hospital, of whom 44.3% (n=47,841) were aged between 18 and 69 years and 55.7% (n=60,198) were aged 70 years and older. Hospitalized patients aged 70 years and older had a mean age of 81.5 (SD 7.1) years ( P <.001); had a total mortality of 10.5% (6320/60,198; P <.001); prevalence of AP of 4.0% (2407/60,198; P <.001), MN of 3.1% (1866/60,198; P <.001), and DH of 3.8% (2287/60,198; P <.001); and mean weight of 76.9 (SD 16.7) kg ( P =.002). As shown in Table 4 , inpatient populations aged 18 years and older, 18‐69 years, and 70 years and older were analyzed, according to R13-OD, H-AIMS-OD, no R13-OD, and L-AIMS-OD. We found that the prevalence of OD in patients aged 18 years and older was 3.5% (3753/108,039) in R13-OD and 34.8% (37,618/108,039) in H-AIMS-OD with a true prevalence of 16.7% (18,042/108,039), with 63.0% (68,053/108,039) of patients in this age group with no R13-OD and L-AIMS-OD. Patients aged 18‐69 years had a prevalence of 2.0% (965/47,841) in R13-OD, 30.6% (14,645/47,841) in H-AIMS-OD, with a True prevalence of 14.7% (7032/47,841), with 68.0% (62,552/47,841) of patients in this age group with no R13-OD and L-AIMS-OD. Patients aged 70 years and older had a prevalence of OD of 4.6% (2788/60,198; R13-OD), and of 38.2% (22,973/60,198; H-AIMS-OD) with a True prevalence of 18.3% (11,016/60,198), with 59.0% (35,501/60,198) of patients in this age group with no R13-OD and L-AIMS-OD. Table 4. Clinical conditions of the hospitalization samples and comparison between R13-OD individuals, H-AIMS-OD, and those with no R13-OD and L-AIMS-OD a . Characteristics Hospitalized patients aged 18 years and older 18‐69 years 70 years and older R13-OD b H-AIMS-OD No R13-OD and L-AIMS-OD P value R13-OD H-AIMS-OD No R13-OD and L-AIMS-OD P value R13-OD H-AIMS-OD No R13-OD and L-AIMS-OD P value Participants, n/N (%) 3753/108,039 (3.5) 37,618/108,039 (34.8) 68,053/108,039 (63.0) 965/47,841 (2.0) 14,645/47,841 (30.6) 32,552/47,841 (68.0) 2788/60,198 (4.6) 22,973/60,198 (38.2) 35,501/60,198 (59.0) Age, mean (SD) 77.1 (15.2) 71.7 (15.2) 67.9 (17.0) <.001; <.001 55.7 (11.8) 56.1 (10.7) 53.3 (11.9) .70; <.001 84.5 (7.1) 81.7 (7.1) 81.3 (7.1) <.001; <.001 Sex (female), n (%) 1694 (45.1) 17,200 (45.7) 31,434 (46.2) .49; .09 307 (31.8) 6051 (41.3) 14,076 (43.2) <.001 ; <.001 1387 (49.7) 11,149 (48.5) 17,358 (48.9) .22; .39 Length of stay, mean (SD) 14.2 (17.2) 9.0 (24.9) 8.4 (12.7) <.001; <.001 18.5 (24.4) 8.9 (13.3) 8.4 (13.8) <.001; <.001 12.8 (13.5) 9.0 (30.0) 8.4 (11.5) <.001; <.001 Charlson, mean (SD) 3.2 (3.3) 3.0 (3.0) 3.0 (3.0) <.001; <.001 2.0 (3.1) 2.1 (3.0) 1.9 (2.9) .009; <.001 3.6 (3.3) 3.2 (3.0) 3.2 (3.0) <.001; .003 Aspiration pneumonia, n (%) 907 (24.2) 1149 (3.1) 1398 (2.1) <.001; <.001 162 (16.8) 241 (1.6) 377 (1.2) <.001; <.001 745 (26.7) 908 (4.0) 1021 (2.9) <.001; <.001 Malnutrition, n (%) 399 (10.6) 1116 (3.0) 1682 (2.5) <.001; <.001 108 (11.2) 380 (3.0) 706 (2.2) <.001; <.001 291 (10.4) 736 (3.2) 976 (2.7) <.001 ; . 001 Dehydration, n (%) 301 (8.0) 1115 (3.0) 1667 (2.4) <.001; <.001 40 (4.1) 222 (1.5) 415 (1.3) <.001; <.001 261 (9.4) 893 (3.9) 1252 (3.5) <.001; .023 Discharge to nursing home, n (%) 1297 (34.6) 7371 (19.6) 12,153 (17.9) <.001; <.001 282 (29.2) 1947 (13.3) 3927 (12.1) <.001; <.001 1015 (36.4) 5424 (23.6) 8226 (23.2) <.001 ; .22 ICU c admissions, n (%) 330 (8.8) 3536 (9.4) 6692 (9.8) .22; .008 185 (19.2) 2002 (13.7) 4176 (12.8) < .001; <.001 145 (5.2) 1534 (6.7) 2516 (7.1) .22; .06 ICU days, mean (SD) 14.6 (18.7) 7.9 (12.4) 7.2 (11.8) <.001; .01 17.7 (19.9) 9.0 (13.3) 8.2 (13.1) <.001; .02 10.7 (16.3) 6.5 (11.0) 5.6 (9.1) .01; .04 Weight, mean (SD) 77.1 (16.6) 77.3 (16.7) 80.7 (18.9) .70; <.001 79.8 (17.4) 83.4 (17.3) 81.0 (19.1) .14; .53 72.3 (14.2) 76.4 (16.5) 77.5 (16.9) .17; .26 BMI, mean (SD) 26.1 (8.9) 31.8 (10.6) 30.2 (11.8) .10; .34 24.5 (13.3) 31.8 (4.7) 30.2 (11.7) .29; .44 27.4 (2.8) 31.8 (11.4) 30.4 (12.4) .14; .48 Total mortality, n (%) 416 (11.1) 2847 (7.6) 4255 (6.3) <.001; <.001 52 (5.4) 369 (2.5) 661 (2.0) <.001; <.001 364 (13.1) 2478 (10.8) 3594 (10.1) <.001; <.001 Mortality during admission, n (%) 229 (6.1) 1906 (5.1) 2832 (4.2) <.001; .31 41 (4.2) 289 (2.0) 523 (1.6) .93; .77 188 (6.7) 1617 (7.0) 2309 (6.5) <.001; .54 One-month mortality, n (%) 102 (2.7) 555 (1.5) 851 (1.3) .02; .88 7 (0.7) 50 (0.3) 84 (0.3) .98; .69 95 (3.4) 505 (2.2) 767 (2.2) .01; .82 Six-month mortality, n (%) 80 (2.1) 361 (1.0) 532 (0.8) <.001; .19 4 (0.4) 28 (0.2) 47 (0.1) .98; .76 76 (2.7) 333 (1.4) 485 (1.4) < .001; .30 One-year mortality, n (%) 4 (0.1) 21 (0.1) 32 (0.05) .62; .94 0 (0.0) 2 (0.01) 4 (0.01) .59; .78 4 (0.14) 19 (0.08) 28 (0.08) .50; .89 Open in a new tab a In each P value row, the first P value is the group of R13-OD patients compared with the group of H-AIMS-OD patients. The second P value is the comparison between the union of the first groups (R13-OD and H-AIMS-OD) versus the group of patients with no R13-OD and L-AIMS-OD. Values in italics indicate statistical differences ( P values). b OD: oropharyngeal dysphagia. c ICU: intensive care unit. The main clinical characteristics of the hospitalized groups are shown in Table 4 . Primary Care Patients A total of 206,151 patients were visited in primary care, of whom 62.4% (n=128,714) were aged between 18 and 69 years and 37.6% (n=77,437) were aged 70 years and older. Primary care patients aged 70 years and older had a mean age of 82.2 (SD 7.5) years ( P <.001), a prevalence of total mortality of 7.3% (5,652/77,437; P <.001), a prevalence of AP of 0.8% (619/77,437; P <.001), MN of 0.1% (77/77,437; P <.001), and DH of 0.6% (464/77,437; P <.001), and mean weight was 74.8 (SD 16.5) kg ( P =.002). The 3 age groups in the primary care population were analyzed according to OD diagnosis. In patients aged 18 years and older, we found that the prevalence of OD in the R13-OD group was 4.3% (8863/206,151); in H-AIMS-OD patients, 15.4% (31,749/206,151); and True prevalence, 7.39% (15,234/206,151), with 81.0% (167,033/206,151) of patients from this age group with no R13-OD and L-AIMS-OD. Patients aged between 18 and 69 years had a prevalence of OD in the R13-OD group of 2.2% (2879/128,714); in the H-AIMS-OD group, 14.3% (18,411/128,714) and True prevalence, 6.9% (8881/128,714), with 83.8% (107,864/128,714) of patients from this age group with no R13-OD and L-AIMS-OD. Patients aged 70 years and older from the R13-OD group had a prevalence of OD of 7.7% (5984/77,437), H-AIMS-OD patients had an estimated prevalence of 17.2% (13,338/77,437), and True prevalence was 8.3% (6427/77,437), with 76.4% (59,169/77,437) of patients from this age group with no R13-OD and L-AIMS-OD. In the hospitalized population, the prevalence of OD, AP, MN, and DH was higher than in primary care, except for OD for those aged 70 years and older. The main clinical characteristics of the primary care groups are shown in Table 5 . Table 5. Clinical conditions of the primary care groups and comparison between R13-OD, H-AIMS-OD, and those with no R13-OD and L-AIMS-OD a . Characteristics Primary care patients aged 18 years and older 18‐69 years 70 years and older R13-OD b H-AIMS-OD NO R13-OD and L-AIMS-OD P value R13-OD H-AIMS-OD NO R13-OD and L-AIMS-OD P value R13-OD H-AIMS-OD NO R13-OD and L-AIMS-OD P value Participants, n/N (%) 8863/206,151 (4.3) 31,749/206,151 (15.4) 167,033/206,151 (81.0) 2879/128,714 (2.2) 18,411/128,714 (14.3) 107,864/128,714 (83.8) 5984/77,437 (7.7) 13,338/77,437 (17.2) 59,169/77,437 (76.4) Age (years), mean (SD) 74.1 (18.3) 62.8 (20.0) 59.3 (20.5) <.001; <.001 51.7 (12.7) 48.7 (13.4) 46.9 (13.7) <.001; <.001 84.9 (7.5) 82.2 (7.5) 81.9 (7.4) <.001; .56 Sex (female), n (%) 5270 (59.5) 18,644 (58.7) 99,914 (59.8) .21; <.001 1629 (56.6) 11,040 (60.0) 65,937 (61.1) <.001; <.001 3641 (60.8) 7604 (57.0) 33,977 (57.4) <.001; .12 Charlson, mean (SD) 0.4 (1.0) 0.6 (1.1) 0.6 (1.1) <.001; .007 0.3 (0.8) 0.5 (1.0) 0.5 (1.0) <.001; .07 0.5 (1.0) 0.9 (1.2) 0.9 (1.2) <.001; <.001 Aspiration pneumonia, n (%) 200 (2.3) 138 (0.4) 445 (0.3) <.001; <.001 31 (1.1) 33 (0.2) 94 (0.09) <.001; <.001 169 (2.8) 105 (0.8) 351 (0.6) < .001; .88 Malnutrition, n (%) 25 (0.3) 14 (0.04) 69 (0.04) <.001; <.001 6 (0.2) 1 (0.005) 8 (0.007) <.001; .002 19 (0.3) 13 (0.1) 61 (0.1) <.001; .54 Dehydration, n (%) 43 (0.5) 83 (0.3) 379 (0.2) <.001; .002 2 (0.07) 7 (0.04) 57 (0.05) .46; .53 41 (0.7) 76 (0.6) 322 (0.5) .34; .89 Weight, mean (SD) 72.3 (15.5) 77.5 (18.4) 76.4 (23.0) <.001; .49 73.8 (15.6) 77.8 (19.1) 76.6 (23.4) .01; .70 67.3 (14.2) 76.8 (16.7) 75.2 (16.5) <.001; .06 BMI, mean (SD) 28.7 (15.2) 27.6 (6.0) 28.1 (10.2) .69; .56 28.0 (14.4) 27.4 (6.7) 28.0 (10.4) .67; .89 29.4 (16.4) 28.3 (3.9) 28.9 (8.2) .23; .72 Total mortality, n (%) 701 (7.9) 1037 (3.3) 4627 (2.8) <.001; <.001 30 (1.0) 79 (0.4) 498 (0.5) <.001; .33 671 (11.2) 958 (7.2) 4129 (7.0) <.001; .65 One-month mortality, n (%) 350 (3.9) 607 (1.9) 2818 (1.7) <.001; <.001 17 (0.6) 52 (0.3) 334 (0.3) .38; .45 333 (5.6) 555 (4.2) 2484 (4.2) <.001; <.001 Six-month mortality, n (%) 37 (0.4) 67 (0.2) 295 (0.2) .30; .57 1 (0.03) 5 (0.03) 61 (0.06) .55; .04 36 (0.6) 62 (0.5) 234 (0.4) .36; .61 One-year mortality, n (%) 6 (0.07) 12 (0.04) 35 (0.02) .54; .27 0 (0.0) 1 (0.005) 5 (0.005) .55; .93 6 (0.1) 11 (0.08) 30 (0.05) .62; .22 Open in a new tab a In each P value row, the first P value is the group of R13-OD patients compared with the group of H-AIMS-OD patients. The second P value is the comparison between the union of the first groups (R13-OD and H-AIMS-OD) versus the group of patients with no R13-OD and L-AIMS-OD. Values in italics indicate statistical differences ( P values). b OD: oropharyngeal dysphagia. Risk Factors for OD From Bivariate and Multivariate Analysis Risk Factors for All Patients For the bivariate analysis, the risk factors in the total population for the ICD-10 R13 variable and risk >0.5 according to AIMS-OD, there is one that differs: in the results of the dependent variable risk of >0.5, the main risk factors were respiratory diseases such as chronic obstructive pulmonary disease. On the other hand, in the results of the multivariate analysis of the dependent variable ICD-10 R13, the main risk factors were age, the use of neuroleptics, and cerebral infarction, the same as for the dependent variable risk >0.5 according to AIMS-OD ( Tables6 7 ). Table 6. The main risk factors studied in the bivariate and multivariate analysis of the total hospitalized and primary care populations according to the dependent variable ICD-10 R13, with the P values and odds ratio a . Total patients Hospitalized patients Primary care patients Bivariate analysis Multivariate analysis Bivariate analysis Multivariate analysis Bivariate analysis Multivariate analysis P value OR b Variable P value OR Variable P value OR Variable P value OR Variable P value OR Variable P value OR Age >70 years <.0001 3.31 Age >70 years <.0001 1.74 Age >70 years <.0001 2.37 Age >70 years <.0001 1.62 Age >70 years <.0001 3.67 N/A c N/A N/A Trazodone <.0001 3.20 Trazodone .03 1.20 Trazodone <.0001 2.80 Trazodone <.0001 1.53 N/A N/A N/A N/A N/A N/A Cerebral infarction <.0001 2.55 Cerebral infarction <.0001 1.96 Delirium <.0001 3.75 Delirium <.0001 1.55 N/A N/A N/A N/A N/A N/A Institutionalization <.0001 2.20 Institutionalization <.0001 1.63 Institutionalization <.0001 2.41 Institutionalization <.0001 1.49 N/A N/A N/A N/A N/A N/A Citalopram .0001 2.04 Vitamin D deficiency <.0001 1.41 Dementia <.0001 4.00 Dementia <.0001 1.69 N/A N/A N/A N/A N/A N/A Acute renal failure <.0001 1.95 Acute renal failure <.0001 1.26 Acute renal failure <.0001 2.03 Acute renal failure <.0001 1.32 N/A N/A N/A N/A N/A N/A Sertraline <.0001 1.90 Deficiency of other B vitamins <.0001 1.27 Admissions <.0001 1.14 Type 2 diabetes mellitus with hyperglycemia .04 1.28 N/A N/A N/A N/A N/A N/A Hypertensive renal disease <.0001 1.77 Pneumonia caused by microorganisms <.0001 1.30 Alzheimer disease <.0001 3.76 Pneumonia caused by microorganisms <.0001 1.37 N/A N/A N/A N/A N/A N/A Depressive episode <.0001 1.44 Mirtazapine <.0001 2.29 Mirtazapine <.0001 2.05 Mirtazapine <.0001 1.33 N/A N/A N/A N/A N/A N/A Chronic kidney disease <.0001 1.39 Acute bronchitis <.0001 1.16 Stays <.0001 1.01 N/A N/A N/A N/A N/A N/A N/A N/A N/A COPD d <.0001 1.27 COPD .04 1.10 Charlson <.0001 1.05 N/A N/A N/A N/A N/A N/A N/A N/A N/A Open in a new tab a Values in italics indicate a significant association between the dependent variable and the factor. b OR: odds ratio. c N/A: not applicable. d COPD: chronic obstructive pulmonary disease. Table 7. The main risk factors studied in the bivariate and multivariate analysis of the total hospitalization and primary care populations according to the dependent variable risk >0.5, with the P values and odds ratios a . Total patients Hospitalized patients Primary care patients Bivariate analysis Multivariate analysis Bivariate analysis Multivariate analysis Bivariate analysis Multivariate analysis Variable P value OR b Variable P value OR Variable P value OR Variable P value OR Variable P value OR Variable P value OR COPD c <.0001 1.40 Age >70 years <.0001 1.30 Age >70 years <.0001 1.40 Age >70 years <.0001 1.17 Age >70 years <.0001 1.25 Age >70 years <.0001 1.16 COPD with exacerbation <.0001 1.19 Mirtazapine <.0001 1.30 Alzheimer disease <.0001 1.24 Chronic obstructive pulmonary disease .04 1.09 Mirtazapine <.0001 1.14 N/A d N/A N/A COPD with acute infection of the airways <.0001 1.17 Cerebral infarction <.0001 1.21 Dementia <.0001 1.19 N/A N/A N/A Chronic kidney disease <.0001 1.11 N/A N/A N/A Acute lower respiratory tract infection <.0001 1.17 Pneumonia caused by microorganisms <.0001 1.15 Delirium <.0001 1.17 N/A N/A N/A N/A N/A N/A N/A N/A N/A Pneumonia caused by microorganisms <.0001 1.15 Acute bronchitis <.0001 1.14 Chronic kidney disease <.0001 1.17 N/A N/A N/A N/A N/A N/A N/A N/A N/A Other types of pneumonia <.0001 1.15 N/A N/A N/A N/A N/A N/A N/A N/A N/A N/A N/A N/A N/A N/A N/A Open in a new tab a Values in italics indicate a significant association between the dependent variable and the factor. b OR: odds ratio. c COPD: Chronic obstructive pulmonary disease. d N/A: not applicable. Hospitalized Patients For the hospitalized population, for the bivariate analysis, there were more protective factors for the dependent variable ICD-10 R13 than for risk >0.5, such as heart disease, myocardial infarction, diabetes, and anxiety. The variables hospital stays and admissions were risk factors for the dependent variable ICD-10 R13, whereas for the dependent variable risk >0.5, the variables hospital stays, admissions, and ICU admission were protective factors ( Tables6 7 ). The most relevant differences in the protective factors were that in the factors of the dependent variable ICD-10 R13, hospital stays, admissions, and Charlson are risk factors, while in the factors of the dependent variable risk >0.5 according to AIMS-OD, they were clearly protective factors, together with admission to the ICU. Primary Care Patients For the primary care population, we observed that the main risk factors were age, the use of neuroleptics, and chronic kidney disease ( Tables6 7 ). The main risk factors for the total, hospitalized, and primary care populations with the dependent variable ICD-10 R13 are shown in Table 6 . The main risk factors for the same populations but with the dependent variable risk >0.5 according to AIMS-OD are shown in Table 7 . Discussion Principal Findings This study assessed 257,541 patients with COVID-19 disease during the first wave of the 2020 pandemic across Catalonia, representing 82.2% (257,541/313,310) of Catalan citizens diagnosed with COVID-19 disease then according to PADRIS database [ 36 ]. The overall prevalence of OD in R13-OD was 4.6% (11,744/257,541), in contrast to 12.2% based on the True AIMS-OD prevalence, both showing significant age-related differences. In hospitalized patients, R13-OD prevalence of OD was 3.5%, and the True AIMS-OD prevalence was 16.7%, also with significant age-related differences. Among primary care patients, R13-OD prevalence of OD was 4.3%, and the True AIMS-OD prevalence was 7.4%, with age-related differences except in the 81‐90 years age group. Taken together, our study suggests that the overall rate of OD underdiagnosis during the first wave of the pandemic in Catalonia was as high as 62.3%. Discrepancies between R13-OD–coded prevalence and actual prevalence are 7.6% in the general patient population, 13.2% in hospitalized patients, and 3.1% in primary care patients. In hospitalized patients, where the discrepancy is most pronounced, this underdiagnosis suggests that a significant number of cases are not being identified by conventional R13-OD coding. This finding is of concern, given the higher risk profile of hospitalized patients. These gaps suggest that relying solely on R13-OD coding may result in substantial underestimation of OD prevalence, which could affect patient outcomes and care strategies. Patients with R13-OD diagnosis from all age categories had higher rates of AP, MN, and DH; longer hospital stays; and higher total mortality than patients with H-AIMS-OD; in turn, in this group, these complications were also higher than those with no R13-OD and L-AIMS-OD. However, in patients aged 70 years and older, institutionalization was higher in H-AIMS-OD, and the Charlson score was also higher in these patients. Risk factors for R13-OD in the entire population included age, neuroleptic use, and cerebral infarction. Risk factors related to H-AIMS-OD were similar to those in R13-OD. For hospitalized patients, higher risks related to delirium and dementia were observed, and for primary care patients, the only related risk factor was age. Our entire patient population had a mean age of 62.0 (SD 20.1) years, 56.9% (146,474/257,541) were female, and had a Charlson score of 1.5 (SD 2.4). The mean age of the hospitalized patients in this study was 69.4 (SD 16.5) years. One of our previously published studies with a cohort of 605 patients hospitalized with COVID-19 disease during the first 3 waves of the pandemic also in Catalonia shows a similar mean average age of 69.2 (SD 17.3) years and a percentage of female sex of 49.9% (301/605) [ 37 ]. In several of our studies in patients with COVID-19 disease, mean average Charlson scores of 5.3 (SD 1.7) and 3.7 (SD 2.6) were reported, higher than those reported in our study [ 5 , 38 ]. This is because in our cohort, there are patients treated in primary care who are generally less severe than hospitalized patients. The prevalence of OD in R13-OD in the total and hospitalized population was lower than in several of our studies with patients hospitalized with COVID-19 disease that found a prevalence of OD of 47% (1108/2359), 51.7% (106/205), and 65.4% (166/254) during the first 3 waves of the pandemic [ 37-39 ]. The prevalence of H-AIMS-OD for the total population was 25.5% (65,576/257,541) and for those hospitalized, 34.8%, which were closer to the prevalence of OD reported in those studies. This further shows the high rate of underdiagnosis of OD in hospital and primary care settings during the COVID-19 pandemic. In our study, the rate of underdiagnosis of OD, according to the calculated true prevalence, was 41.9% in primary care and 79.0% in hospitalized patients. We also found that the prevalence of OD in R13-OD in primary care patients was higher than that in hospitalized patients. The cause of this could be that patients in primary care centers were older and included nursing home residents who had previously been diagnosed with OD, while hospitalized patients in the first wave of the pandemic were younger, and the diagnosis of OD was more complicated and frequently not performed due to lack of awareness of OD or health care saturation and risk of infection during the COVID-19 pandemic [ 5 , 37 , 38 ]. Patients with R13-OD had worse clinical outcomes and higher rates of complications than patients with H-AIMS-OD, and these patients had worse outcomes than patients with no R13-OD or L-AIMS-OD. The increased complications in the R13 group are probably due to higher severity of dysphagia and more obvious signs of swallowing impairment which alerted clinicians to their condition. Patients diagnosed with OD according to ICD-10 (R13-OD) probably represent the most clinically severe cases, since the coding of OD in routine clinical practice is usually motivated by clear symptoms, such as aspiration, severe complications, or advanced disease. This represents a recurring selection bias in underdiagnosed conditions such as OD or AP [ 40 ]. The gradient observed in the results (R13-OD>H-AIMS-OD>L-AIMS-OD) should be interpreted as reflecting different levels of severity along the dysphagia continuum. ICD-10 coding captures only a small, highly selected subgroup of severe cases, while AIMS-OD identifies a broader at-risk population, including patients who do not yet have obvious symptoms but who have a clinically significant risk profile. H-AIMS-OD patients experience clinical outcomes ranging between R13-OD and L-AIMS-OD patients, which is consistent with the role of screening tools: to detect risk earlier and more broadly than routine clinical diagnosis. A recent study using AIMS-OD to assess the prevalence of AP found similar patterns, in which the algorithm identified 84.77% of clinically diagnosed cases ( ICD-10 J69.0) and revealed 1891 additional cases undetected by clinical practice, representing a 62.6% increase in detection compared with standard approaches [ 40 ]. Patients with R13 had a mean stay of 15.5 (SD 19.7) days, similar to one of our studies with an overall hospital stay of 14.0 (SD 11.2 days) [ 38 ]. The prevalence of AP was 10.7%, lower than in another study with 16.3% [ 41 ]. That could also be due to the underdiagnosis of AP and the lack of standardized clinical criteria for its diagnosis [ 42 ]. In the case of MN, the prevalence was 4.2%, much lower than that reported in several of our studies, which were 50.6%, 45.5%, and 45.9% in patients hospitalized with COVID-19 disease [ 5 , 38 , 39 ]. The prevalence of DH was 3.8%, also lower than that reported in one of our studies with a prevalence of 19%‐100% [ 43 ]. Again, MN and DH are seldom evaluated in older patients, and this underdiagnosis was even more severe during the COVID-19 pandemic, clearly evidenced in this study. Of the R13-OD patients, 15.0% (1762/257,541) were institutionalized upon discharge, a lower percentage compared with 2 of our previous studies with 27.5% and 15.2% [ 5 , 37 ]. This could be due to different political management as, during the first wave, improvised discriminatory decisions were made regarding the admission and destination of discharge in these older patients [ 44 ]. The mortality rate for R13-OD was 8.7% (1207/257,541) in all patients and increased to 11.8% (956/104,898) in patients aged 70 years or older. Other studies have shown mortality prevalence similar to ours, of 11.4% during the first wave in Spain [ 45 ] and 11.0% in China [ 46 ]. On the other hand, patients with H-AIMS-OD had a higher prevalence of ICU admission than R13-OD patients in our study. Hospitalized patients in the 3 groups (R13-OD, H-AIMS-OD, and with no R13-OD and L-AIMS-OD) had a higher prevalence of complications associated with OD and higher total mortality than patients treated in primary care. This is because patients with the worst prognosis were hospitalized. Prevalences of complications in hospitalized patients were 24.2% for AP, higher than that reported in one of our studies (16.3%) [ 41 ]. A prevalence of 10.6% in MN was significantly lower than the prevalences reported in several studies (50.6%, 45.5%, and 45.9%) with patients with COVID-19 disease [ 5 , 37 , 47 ]. The prevalence of DH was 8.0%, which is lower than the prevalence reported in our previous studies (19%‐100%) [ 43 ]. We found that neuroleptic use, cerebral infarction, and being older than 70 years were independent risk factors for OD diagnosis according to both R13-OD and H-AIMS-OD in the overall population. These results are consistent with our previous publications on the pathophysiology of OD in older patients [ 9 , 30 , 48 ]. In another study [ 38 ], similar risk factors were shown, such as associated complications and the intake of drugs such as anticholinergics, muscle relaxants, and opioids. In the case of neuroleptic use, the study by Miarons et al [ 49 , 50 ] showed that both typical and atypical antipsychotics can be associated with OD. For hospitalized patients, the main risk factors for OD diagnosis according to ICD-10 were dementia, being aged 70 years and older, and delirium. These risk factors are consistent with the results obtained in one of our studies of 255 hospitalized patients with dementia, where the risk factors for OD were older age, poorer functioning, poorer nutritional status, and greater severity of dementia [ 51 ]. On the other hand, being aged 70 years and older and chronic obstructive pulmonary disease were risk factors for patients with H-AIMS-OD. In a systematic review on swallowing function and chronic respiratory diseases, results indicated that chronic respiratory diseases increase the prevalence of OD [ 52 ]. Other risk factors for OD according to R13-OD were hospital stay, hospital admissions, and comorbidities assessed with the Charlson index. In contrast, for OD with H-AIMS-OD, these previous factors, including ICU admission, became protective. This could be explained because, due to the excess demand during the pandemic, younger patients and those with fewer comorbidities were given priority to ICU admission (for critical patients) as they had a better chance of survival [ 5 , 38 , 47 ]. Importantly, our population-level findings derived from routine clinical data show strong external consistency with recent prospectively collected clinical cohorts. In this regard, the risk factors we have identified are in line with those reported in patients with COVID-19 disease. Zayed et al [ 12 ] observed that advanced age, longer duration of COVID-19 symptoms, presence of ageusia and anosmia, dysphonia, ICU admission, lower oxygen saturation, and use of mechanical ventilation were significantly associated with dysphagia in 500 hospitalized patients [ 12 ]. Their subsequent instrumental study, using FEES, confirmed the persistence of swallowing abnormalities in patients with post-COVID-19 disease, including a delayed swallowing reflex and altered laryngeal sensitivity [ 13 ]. The length of hospital stay, the number of admissions, and a high Charlson index emerged as relevant risk markers, particularly among older patients, reflecting their increased vulnerability and more severe clinical prognosis. In the H-AIMS-OD group, a broader age distribution was observed. In this context, variables that traditionally represent risk factors in older populations appear as protective factors for H-AIMS-OD, largely due to the management strategies applied during the COVID-19 pandemic [ 53 ], which prioritized younger patients in decisions regarding hospitalization, length of stay, and ICU admission. Consequently, these variables become statistically associated with younger age and are therefore perceived as protective in this subgroup. Finally, in primary care patients, the only risk variable found was being aged 70 years and older. Age has been previously determined in many studies as a risk factor for dysphagia [ 9 , 46 , 54-56 , undefined , undefined ]. In addition, aging is one of the main causes of the disease [ 56 ] and in the community (primary care level), OD has a high prevalence (27%) despite the lower complexity of patients in that setting [ 57 ]. The main result of our study is the underdiagnosis of OD in patients with COVID-19 disease, since we know that approximately only 20% (50/253) of patients with OD were correctly diagnosed. The clinical and instrumental diagnosis of OD during COVID-19 disease was hampered by the danger of contagion and overstretched health care workers, but AIMS-OD provides systematic and universal screening for OD during hospital admission, allowing the most appropriate diagnostic and therapeutic strategies to be selected for each patient. This is a big step forward and represents a marked improvement in health care: patients with OD who are hospitalized or discharged due to COVID-19 disease have the right to be diagnosed and treated for OD, their family and caregiver organizations gain a deeper understanding of OD, health care professionals can identify and effectively manage high-risk (AIMS-OD>0.5) patients, and health care providers improve their results and lower costs. Currently, there are 2 more services being developed, AIMS-AP for AP and AIMS-MN for MN. AIMS-AP is in the in vitro development phase and has a database of more than 5000 patients and good psychometrics to detect patients with AP. In parallel, awareness of OD and its complications should be increased in all health care settings through education and promotion of evidence-based clinical practice. Our findings are consistent with a number of studies that use large-scale population-based epidemiological methodologies to examine changes in disease prevalence before and during the COVID-19 pandemic. A recent ecological study analyzing more than 103.000 patients in South Korea showed that the incidence of Bell palsy decreased significantly during the nationwide vaccination and infection phases of the pandemic compared with the pre-COVID-19 baseline, highlighting how pandemic-related public health interventions may have influenced disease patterns [ 58 ]. Similarly, an analysis of national trends examining asthma prevalence using data from more than 206,000 participants found that while asthma prevalence increased in the prepandemic era, it decreased significantly during the pandemic period, suggesting that factors such as reduced air pollution, universal mask wearing, and social distancing may have contributed to these changes [ 59 ]. These studies, like ours, demonstrate the value of leveraging national health databases to identify underdiagnosed conditions and monitor changes in disease prevalence during public health crises. These studies highlight the potential of AI-based screening tools, such as AIMS-OD, not only to address current underdiagnosis but also to serve as scalable screening systems for emerging health conditions in future pandemics. Limitations This study has some limitations. First, AIMS-OD was not validated in patients with COVID-19 disease; however, this limitation reflects the extraordinary clinical context of the pandemic, during which instrumental and bedside swallowing assessments were often not feasible. Second, the database had some missing values and the absence of important variables for OD such as Barthel Index, among others, could have affected our ability to better estimate the risk with AIMS-OD of the patients studied and their risk factors. This has meant that the calculation of true prevalence was affected in the estimation of the reality of OD. This study shows a high prevalence of patients with COVID-19 disease at high risk of OD during the first wave of the pandemic in Catalonia and that most of them (53,832/65,576, 82.1%) were underdiagnosed and thus, R13-OD–detected patients were very few. In contrast, massive screening with AIMS-OD allowed us to identify a large group of patients with COVID-19 disease with a high risk of OD and associated complications and poor clinical outcomes aligned with those of R13-OD patients. We believe that systematic screening with AIMS-OD will aid clinical decision-making and improve the diagnosis of OD, still a neglected condition in several phenotypes of patients, and especially in the context of a pandemic. Risk factors for OD in the whole population included neuroleptic use, cerebral infarction, and age. Hospitalized patients had additional risk factors such as delirium and dementia. On the other hand, primary care patients had only 1 risk factor, age. Our findings further suggest that OD is a significant problem in patients with COVID-19 disease. Early identification of patients at risk of OD using tools such as the AIMS-OD will help improve the management and clinical outcomes of these patients. Conclusions Our findings further suggest that OD is a significant and underrecognized problem in patients with COVID-19 disease, especially in those of advanced age and with comorbidities. The high proportion of underdiagnosed cases observed in this study highlights the limitations of routine clinical detection during the pandemic. Systematic screening using tools such as AIMS-OD may facilitate earlier identification of patients at risk, support clinical decision-making, and improve the management and clinical outcomes of these patients. Acknowledgments The authors would like to thank the IT Department of the Consorci Sanitari del Maresme, led by Francesc Moya, for their support and collaboration during the study. The authors thank Mrs Jane Lewis for reviewing the English of the manuscript and Dr Neus Giménez for help in reviewing the results. Abbreviations AI artificial intelligence AIMS-OD Artificial Intelligence Massive Screening for Oropharyngeal Dysphagia AP aspiration pneumonia API application programming interface DH dehydration EHR electronic health record ES expert system FEES fiberoptic endoscopic evaluation of swallowing H-AIMS-OD high-risk AIMS-OD ICD International Classification of Diseases ICD-10 International Classification of Diseases, Tenth Revision ICD-11 International Classification of Diseases, 11th Revision ICD-9 International Classification of Diseases, Ninth Revision ICU intensive care unit L-AIMS-OD low AIMS-OD risk ML machine learning MN malnutrition OD oropharyngeal dysphagia PADRIS Program of Dades per a la Recerca i la Innovació en Salut Footnotes Funding: Financial support received from: (1) Acadèmia de Ciències Mèdiques de Catalunya i Balears, a subsidiary of Maresme; (2) from the Network Biomedical Research Center in the Area of Liver and Digestive Diseases (CIBERehd), Carlos III Health Institute; (3) the project that gives rise to these standards has received funding and support from the “la Caixa” Foundation, through the CaixaImpulse Grant (CI2000158); (4) the Specialization Project in Territorial Competitiveness (PECT) of Mataró-Maresme (PRE/161/2019) funded by the Generalitat of Catalonia within the framework of the Operational Program of the European Regional Development Funds of Catalonia 2014-2020 and the Strategic Plan for Research and Innovation in Health (PERIS), Generalitat de Catalunya; (5) the Agència de Gestió d'Ajuts Universitaris de Recerca (AGAUR), with help from Modality B Product 2021 for AIMS-OD; and (6) Transformative Project iNEXES CSC with code PT-092023-CSC promoted by CatSalut within the framework of SISCAT, funding with nonfinalist affected funds (FANF). The content of this publication reflects only the opinions of the authors. CatSalut is not responsible for the use that may be made of the information contained herein. Data Availability: The datasets generated and/or analyzed during the present study are not publicly available because they were provided by the Agència de Qualitat i Avaluació Sanitàries de Catalunya (AQuAS) [ 25 ], in the framework of the Programa Analític de Dades per a la Recerca i la Innovació en Salut (PADRIS) [ 26 ]. Authors’ Contributions: CAR, AM, OO, and PC participated in conceptualization. CAR, JMR, AEH, and PC contributed to methodology. CAR and JMR participated in formal analysis and investigation. CAR participated in writing—original draft preparation. CAR, AM, OO, and PC participated in writing—review and editing. AM participated in funding acquisition. FJRT, AR, and AEH contributed to resources. PC participated in supervision. Conflicts of Interest: PC is a cofounder of the startup AIMS Medical SL. All other authors declare no conflicts of interest. References 1. Pneumonia of unknown cause in China: disease outbreak news. World Health Organization. Jan 5, 2020. [26-04-2023]. https://www.who.int/csr/don/05-january-2020-pneumonia-of-unkown-cause-china/en/ URL. Accessed. 2. Dhakal BP, Sweitzer NK, Indik JH, Acharya D, William P. SARS-CoV-2 infection and cardiovascular disease: COVID-19 heart. Heart Lung Circ. 2020 Jul;29(7):973–987. doi: 10.1016/j.hlc.2020.05.101. doi. Medline. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 3. Kosari M, Noureddini M, Khamechi SP, et al. The effect of propolis plus Hyoscyamus niger L. methanolic extract on clinical symptoms in patients with acute respiratory syndrome suspected to COVID-19: a clinical trial. Phytother Res. 2021 Jul;35(7):4000–4006. doi: 10.1002/ptr.7116. doi. Medline. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 4. Carretero Gómez J, Mafé Nogueroles MC, Garrachón Vallo F, Escudero Álvarez E, Maciá Botejara E, Miramontes González JP. Inflammation, malnutrition, and SARS-CoV-2 infection: a disastrous combination. Revista Clínica Española (English Edition) 2020 Nov;220(8):511–517. doi: 10.1016/j.rceng.2020.07.006. doi. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 5. Martin-Martinez A, Ortega O, Viñas P, et al. COVID-19 is associated with oropharyngeal dysphagia and malnutrition in hospitalized patients during the spring 2020 wave of the pandemic. Clin Nutr. 2022 Dec;41(12):2996–3006. doi: 10.1016/j.clnu.2021.06.010. doi. Medline. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 6. Clavé P, Shaker R. Dysphagia: current reality and scope of the problem. Nat Rev Gastroenterol Hepatol. 2015 May;12(5):259–270. doi: 10.1038/nrgastro.2015.49. doi. Medline. [ DOI ] [ PubMed ] [ Google Scholar ] 7. Baijens LW, Clavé P, Cras P, et al. European Society for Swallowing Disorders - European Union Geriatric Medicine Society white paper: oropharyngeal dysphagia as a geriatric syndrome. Clin Interv Aging. 2016;11:1403–1428. doi: 10.2147/CIA.S107750. doi. Medline. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 8. International Statistical Classification of Diseases and Related Health Problems (ICD) World Health Organization. [26-04-2023]. https://www.who.int/standards/classifications/classification-of-diseases URL. Accessed. 9. Carrión S, Cabré M, Monteis R, et al. Oropharyngeal dysphagia is a prevalent risk factor for malnutrition in a cohort of older patients admitted with an acute disease to a general hospital. Clin Nutr. 2015 Jun;34(3):436–442. doi: 10.1016/j.clnu.2014.04.014. doi. Medline. [ DOI ] [ PubMed ] [ Google Scholar ] 10. Osbeck Sandblom H, Dotevall H, Svennerholm K, Tuomi L, Finizia C. Characterization of dysphagia and laryngeal findings in COVID-19 patients treated in the ICU-An observational clinical study. PLoS ONE. 2021;16(6):e0252347. doi: 10.1371/journal.pone.0252347. doi. Medline. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 11. Barroso J. Disfagia orofaríngea y broncoaspiración. Revista Española de Geriatría y Gerontología. 2009 Nov;44:22–28. doi: 10.1016/j.regg.2009.06.010. doi. [ DOI ] [ PubMed ] [ Google Scholar ] 12. Zayed AM, Afsah O, Elhadidy T, Abou-Elsaad T. Screening for oropharyngeal dysphagia in hospitalized COVID-19 patients: a prospective study. Eur Arch Otorhinolaryngol. 2023 May;280(5):2623–2631. doi: 10.1007/s00405-022-07810-z. doi. Medline. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 13. Zayed AM, Afsah O, Elhadidy T, Abou-Elsaad T. Swallowing evaluation in post-COVID-19 patients with oropharyngeal dysphagia. Dysphagia. 2025 Oct;40(5):1145–1155. doi: 10.1007/s00455-025-10810-w. doi. Medline. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 14. Swigert NB, Steele C, Riquelme LF. Dysphagia screening for patients with stroke: challenges in implementing a Joint Commission guideline. Leader. 2007 Mar;12(3):4–29. doi: 10.1044/leader.FTR1.12032007.4. doi. [ DOI ] [ Google Scholar ] 15. Martin-Martinez A, Miró J, Amadó C, et al. A systematic and universal artificial intelligence screening method for oropharyngeal dysphagia: improving diagnosis through risk management. Dysphagia. 2023 Aug;38(4):1224–1237. doi: 10.1007/s00455-022-10547-w. doi. Medline. [ DOI ] [ PubMed ] [ Google Scholar ] 16. Rofes L, Arreola V, Mukherjee R, Clavé P. Sensitivity and specificity of the Eating Assessment Tool and the Volume‐Viscosity Swallow Test for clinical evaluation of oropharyngeal dysphagia. Neurogastroenterology Motil. 2014 Sep;26(9):1256–1265. doi: 10.1111/nmo.12382. doi. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 17. Riera SA, Marin S, Serra-Prat M, et al. A systematic and a scoping review on the psychometrics and clinical utility of the Volume-Viscosity Swallow Test (V-VST) in the clinical screening and assessment of oropharyngeal dysphagia. Foods. 2021 Aug 16;10(8):1900. doi: 10.3390/foods10081900. doi. Medline. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 18. Clavé P, Arreola V, Romea M, Medina L, Palomera E, Serra-Prat M. Accuracy of the volume-viscosity swallow test for clinical screening of oropharyngeal dysphagia and aspiration. Clin Nutr. 2008 Dec;27(6):806–815. doi: 10.1016/j.clnu.2008.06.011. doi. Medline. [ DOI ] [ PubMed ] [ Google Scholar ] 19. Rosenbek JC, Robbins JA, Roecker EB, Coyle JL, Wood JL. A penetration-aspiration scale. Dysphagia. 1996;11(2):93–98. doi: 10.1007/BF00417897. doi. Medline. [ DOI ] [ PubMed ] [ Google Scholar ] 20. Langmore SE. Evaluation of oropharyngeal dysphagia: which diagnostic tool is superior? Curr Opin Otolaryngol Head Neck Surg. 2003 Dec;11(6):485–489. doi: 10.1097/00020840-200312000-00014. doi. [ DOI ] [ PubMed ] [ Google Scholar ] 21. Ramesh AN, Kambhampati C, Monson JRT, Drew PJ. Artificial intelligence in medicine. Ann R Coll Surg Engl. 2004 Sep;86(5):334–338. doi: 10.1308/147870804290. doi. Medline. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 22. Rebala G, Ravi A, Churiwala S, Rebala G, Ravi A, Churiwala S. An Introduction to Machine Learning. Springer; 2019. Machine learning definition and basics; pp. 1–17. doi. [ DOI ] [ Google Scholar ] 23. Abbas Q, Jeong W, Lee SW. Explainable AI in clinical decision support systems: a meta-analysis of methods, applications, and usability challenges. Healthcare (Basel) 2025;13(17):2154. doi: 10.3390/healthcare13172154. doi. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 24. Abbas SR, Seol H, Abbas Z, Lee SW. Exploring the role of artificial intelligence in smart healthcare: a capability and function-oriented review. Healthcare (Basel) 2025;13(14):1642. doi: 10.3390/healthcare13141642. doi. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 25. 2025 Report of the Agency for Health Quality and Assessment of Catalonia. Agency for Health Quality and Assessment of Catalonia (AQuAS) [26-04-2023]. http://aquas.gencat.cat/ca/inici URL. Accessed. 26. Data Analytics Programme for Health Research and Innovation. Agency for Health Quality and Assessment of Catalonia (AQuAS) [26-04-2023]. http://aquas.gencat.cat/ca/fem/intelligencia-analitica/padris URL. Accessed. 27. SISCAT: Comprehensive Public Health System of Catalonia. CatSalut. Catalan Health Service. [26-04-2023]. http://catsalut.gencat.cat/ca/coneix-catsalut/presentacio/model-sanitari-catala/siscat URL. Accessed. 28. User guide—pandas 214 documentation. Pydata.org. [26-04-2023]. https://pandas.pydata.org/docs/user_guide/index.html URL. Accessed. 29. Gupta N, Kishore J, Ray PC, Kohli C, Kumar N. Determination of prevalence of type 2 diabetes mellitus by screening tests using a mathematical formula in place of invasive blood tests. J Clin Diagn Res. 2016 Jan;10(1):LC05–9. doi: 10.7860/JCDR/2016/14812.7039. doi. Medline. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 30. Serra-Prat M, Hinojosa G, López D, et al. Prevalence of oropharyngeal dysphagia and impaired safety and efficacy of swallow in independently living older persons. J Am Geriatr Soc. 2011 Jan;59(1):186–187. doi: 10.1111/j.1532-5415.2010.03227.x. doi. Medline. [ DOI ] [ PubMed ] [ Google Scholar ] 31. Habibzadeh F, Habibzadeh P, Yadollahie M. The apparent prevalence, the true prevalence. Biochem Med (Zagreb) 2022 Jun 15;32(2):020101. doi: 10.11613/BM.2022.020101. doi. Medline. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 32. Tallarida RJ, Murray RB. Manual of Pharmacologic Calculations: With Computer Programs. Springer-Verlag; 1987. [26-04-2023]. Chi-square test; pp. 140–142. https://link.springer.com/book/10.1007/978-1-4612-4974-0 URL. Accessed. [ Google Scholar ] 33. Kim TK. T test as a parametric statistic. Korean J Anesthesiol. 2015 Dec;68(6):540–546. doi: 10.4097/kjae.2015.68.6.540. doi. Medline. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 34. McKnight PE, Najab J. In: The Corsini Encyclopedia of Psychology. Weiner IB, Craighead WE, editors. Wiley; 2010. Mann‐Whitney u test; pp. 1–1. doi. [ DOI ] [ Google Scholar ] 35. Ostertagová E, Ostertag O, Kováč J. Methodology and application of the Kruskal-Wallis Test. AMM. 2014;611:115–120. doi: 10.4028/www.scientific.net/AMM.611.115. doi. [ DOI ] [ Google Scholar ] 36. Open Government of Catalonia. The Generalitat. [26-04-2023]. https://web.gencat.cat/ca/generalitat/dades-indicadors/dades-obertes URL. Accessed. 37. Viñas P, Martín-Martínez A, Alarcón C, et al. A comparative study between the three waves of the pandemic on the prevalence of oropharyngeal dysphagia and malnutrition among hospitalized patients with COVID-19. Nutrients. 2022 Sep 16;14(18):3826. doi: 10.3390/nu14183826. doi. Medline. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 38. Martín-Martínez A, Viñas P, Carrillo I, Martos J, Clavé P, Ortega O. The impact of frailty, oropharyngeal dysphagia and malnutrition on mortality in older patients hospitalized for Covid-19. Aging Dis. 2024 Apr 1;15(2):927–938. doi: 10.14336/AD.2023.0425-2. doi. Medline. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 39. Cabré M, Serra-Prat M, Force L, Almirall J, Palomera E, Clavé P. Oropharyngeal dysphagia is a risk factor for readmission for pneumonia in the very elderly persons: observational prospective study. J Gerontol A Biol Sci Med Sci. 2014 Mar;69(3):330–337. doi: 10.1093/gerona/glt099. doi. Medline. [ DOI ] [ PubMed ] [ Google Scholar ] 40. Martín-Martínez A, Sitges-Milà C, Miró J, et al. Assessing the prevalence and the underdiagnosis of aspiration pneumonia among older hospitalized patients with community-acquired pneumonia using an artificial intelligence algorithm. Pneumonia (Nathan) 2025 Sep 25;17(1):23. doi: 10.1186/s41479-025-00175-x. doi. Medline. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 41. Aoyagi Y, Ohashi M, Funahashi R, Otaka Y, Saitoh E. Oropharyngeal dysphagia and aspiration pneumonia following coronavirus disease 2019: a case report. Dysphagia. 2020 Aug;35(4):545–548. doi: 10.1007/s00455-020-10140-z. doi. Medline. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 42. Yoshimatsu Y, Melgaard D, Westergren A, Skrubbeltrang C, Smithard DG. The diagnosis of aspiration pneumonia in older persons: a systematic review. Eur Geriatr Med. 2022 Oct;13(5):1071–1080. doi: 10.1007/s41999-022-00689-3. doi. Medline. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 43. Viñas P, Bolivar-Prados M, Tomsen N, et al. The hydration status of adult patients with oropharyngeal dysphagia and the effect of thickened fluid therapy on fluid intake and hydration: results of two parallel systematic and scoping reviews. Nutrients. 2022 Jun 16;14(12):2497. doi: 10.3390/nu14122497. doi. Medline. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 44. Ruano JM, Díaz-Tendero A. COVID-19 and the structural vulnerabilities in the Spanish health and long-term care systems. Eur Polit Sci. 2023 Sep;22(3):395–405. doi: 10.1057/s41304-022-00381-x. doi. [ DOI ] [ Google Scholar ] 45. Matta S, Chopra KK, Arora VK. Morbidity and mortality trends of Covid 19 in top 10 countries. Indian J Tuberc. 2020 Dec;67(4S):S167–S172. doi: 10.1016/j.ijtb.2020.09.031. doi. Medline. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 46. Chen N, Zhou M, Dong X, et al. Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study. Lancet. 2020 Feb 15;395(10223):507–513. doi: 10.1016/S0140-6736(20)30211-7. doi. Medline. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 47. COVID-19. Semicyuc. [26-04-2023]. https://semicyuc.org/covid-19 URL. Accessed. 48. Cabre M, Serra-Prat M, Palomera E, Almirall J, Pallares R, Clavé P. Prevalence and prognostic implications of dysphagia in elderly patients with pneumonia. Age Ageing. 2010 Jan;39(1):39–45. doi: 10.1093/ageing/afp100. doi. Medline. [ DOI ] [ PubMed ] [ Google Scholar ] 49. Miarons Font M, Rofes Salsench L. Antipsychotic medication and oropharyngeal dysphagia: systematic review. Eur J Gastroenterol Hepatol. 2017;29(12):1332–1339. doi: 10.1097/MEG.0000000000000983. doi. [ DOI ] [ PubMed ] [ Google Scholar ] 50. Miarons M, Clavé P, Wijngaard R, et al. Pathophysiology of oropharyngeal dysphagia assessed by videofluoroscopy in patients with dementia taking antipsychotics. J Am Med Dir Assoc. 2018 Sep;19(9):812. doi: 10.1016/j.jamda.2018.04.016. doi. Medline. [ DOI ] [ PubMed ] [ Google Scholar ] 51. Espinosa-Val MC, Martín-Martínez A, Graupera M, et al. Prevalence, risk factors, and complications of oropharyngeal dysphagia in older patients with dementia. Nutrients. 2020 Mar 24;12(3):863. doi: 10.3390/nu12030863. doi. Medline. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 52. Ghannouchi I, Speyer R, Doma K, Cordier R, Verin E. Swallowing function and chronic respiratory diseases: systematic review. Respir Med. 2016 Aug;117:54–64. doi: 10.1016/j.rmed.2016.05.024. doi. [ DOI ] [ PubMed ] [ Google Scholar ] 53. Gómez‐Belda AB, Fernández‐Garcés M, Mateo‐Sanchis E, et al. COVID ‐19 in older adults: what are the differences with younger patients? Geriatrics Gerontology Int. 2021 Jan;21(1):60–65. doi: 10.1111/ggi.14102. doi. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 54. Martos Pérez F, Luque del Pino J, Jiménez García N, et al. Comorbidity and prognostic factors on admission in a COVID-19 cohort of a general hospital. Revista Clínica Española (English Edition) 2021 Nov;221(9):529–535. doi: 10.1016/j.rceng.2020.05.010. doi. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 55. Bedock D, Bel Lassen P, Mathian A, et al. Prevalence and severity of malnutrition in hospitalized COVID-19 patients. Clin Nutr ESPEN. 2020 Dec;40:214–219. doi: 10.1016/j.clnesp.2020.09.018. doi. Medline. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 56. Almirall J, Cabré M, Clavé P. Stepping Stones to Living Well with Dysphagia. Vol. 72. Karger; 2012. Complications of oropharyngeal dysphagia: aspiration pneumonia; pp. 67–76. Vol. doi. [ DOI ] [ PubMed ] [ Google Scholar ] 57. Serra-Prat M, Palomera M, Gomez C, et al. Oropharyngeal dysphagia as a risk factor for malnutrition and lower respiratory tract infection in independently living older persons: a population-based prospective study. Age Ageing. 2012 May 1;41(3):376–381. doi: 10.1093/ageing/afs006. doi. [ DOI ] [ PubMed ] [ Google Scholar ] 58. Lee S, Lee NK, Lee SW, Kim YJ. Changes in the nationwide incidence of Bell’s palsy in the general population before and after the COVID-19 pandemic: an ecological study. J Med Virol. 2025 Jun;97(6):e70431. doi: 10.1002/jmv.70431. doi. Medline. [ DOI ] [ PMC free article ] [ PubMed ] [ Google Scholar ] 59. Park J, Nguyen A, Kattih M, et al. National trends in asthma prevalence in South Korea before and during the COVID ‐19 pandemic, 1998–2021. Clin Experimental Allergy. 2023 Dec;53(12):1291–1294. doi: 10.1111/cea.14394. doi. [ DOI ] [ PubMed ] [ Google Scholar ] Articles from JMIR AI are provided here courtesy of JMIR Publications Inc. ACTIONS View on publisher site PDF (537.3 KB) Cite Collections Permalink PERMALINK Copy RESOURCES Similar articles Cited by other articles Links to NCBI Databases Cite Copy Download .nbib .nbib Format: AMA APA MLA NLM Add to Collections Create a new collection Add to an existing collection Name your collection * Choose a collection Unable to load your collection due to an error Please try again Add Cancel Follow NCBI NCBI on X (formerly known as Twitter) NCBI on Facebook NCBI on LinkedIn NCBI on GitHub NCBI RSS feed Connect with NLM NLM on X (formerly known as Twitter) NLM on Facebook NLM on YouTube National Library of Medicine 8600 Rockville Pike Bethesda, MD 20894 Web Policies FOIA HHS Vulnerability Disclosure Help Accessibility Careers NLM NIH HHS USA.gov Back to Top