![]() |
![]() |
| Ann Geriatr Med Res > Epub ahead of print |
The authors thank Fuyuko Ogawa at the Library of the National Institute of Public Health for her help with the literature search, as well as all collaborators from the Japanese Working Group on Sarcopenic Dysphagia for their clinical work, data collection, and data registration.
During the preparation of this work, the authors used ChatGPT (Chat-4o, by OpenAI, San Francisco, CA, USA) and Claude (Claude3.5 Opus, Anthropic, San Francisco, CA, USA) to enhance readability and proofread the English text. After using these services, the authors reviewed and edited the content as required and take full responsibility for the content of the publication.
FUNDING
This study was supported by the Japan Society for the Promotion of Science, KAKENHI (Grant No. 19H03979).
AUTHOR CONTRIBUTIONS
Conceptualization, ST, HW; Data acquisition, collaborators from the Japanese Working Group on Sarcopenic Dysphagia; Data analysis and interpretation, ST, TM, HW; Funding acquisition, HW; Writing-original draft preparation, ST, TM; Writing-review and editing, ST, TM, HW, AS, SN, RM.
Values are presented as number (%) or median (interquartile range).
BMI, body mass index; CCI, Charlson Comorbidity Index; FILS, Food Intake LEVEL Scale.
Conditions leading dysphagia were included esophageal cancer (10th revision of the International Statistical Classification of Diseases and Related Health Problems [ICD-10] codes: C15x), laryngeal cancer (C32x), pharyngeal cancer (C14x), stroke (I630, I631–I636, I638, I639, I600–I611, I613–I616, I619, I629, and G459), Alzheimer’s disease (G20), head injury (S00x–S19x), Parkinson disease (G20x), and pneumonia (J15x, J18x, and J690).
Values are presented as median (interquartile range) or number (%).
FILS, Food Intake LEVEL Scale; FIM, Functional Independence Measure; N/A, not applicable.
We conducted a repeated two-way ANOVA (times×cachexia). Also, we applied Fisher exact test for discharge destinations at follow-up period (category variable; to home, transfer to other hospitals/care facilities, and continued hospitalization).
FILS, Food Intake LEVEL Scale; FIM, Functional Independence Measure; MICE, multivariate imputation by chained equation; CI, confidential interval; N/A, not applicable.
We applied a generalized linear regression model to evaluate whether cachexia associated with total FIM and FILS at discharge. Model 1 was crude; model 2 included age+sex+FIM at baseline+FILS at baseline; model 3 included CCI in addition to model; model 4 included enteral feeding in addition to model 3.
MICE, multivariate imputation by chained equation, OR; odds ratio; CI, Confidential interval; N/A, not applicable.
We applied a multivariate logistic regression analysis to evaluate whether cachexia associated with discharge destinations. Model 1 was crude; model 2 included age+sex+FIM (Functional Independence Measure) at baseline+FILS (Food Intake LEVEL Scale) at baseline; model 3 included Charlson Comorbidity Index in addition to model 2; model 4 included enteral feeding in addition to model 3. In addition, we applied a multivariate logistic model to evaluate whether cachexia associated with discharge outcome at follow-up using multivariate model adjusted by age, sex, FIM at baseline, and FILS at baseline.

![]() |
![]() |