Ann Rehabil Med Search

CLOSE


Ann Rehabil Med > Volume 47(5); 2023 > Article
Kakehi, Isono, Wakabayashi, Shioya, Ninomiya, Aoyama, Murai, Sato, Takemura, Mori, Masumura, and Suzuki: Sarcopenic Dysphagia and Simplified Rehabilitation Nutrition Care Process: An Update

Abstract

Sarcopenic dysphagia is characterized by weakness of swallowing-related muscles associated with whole-body sarcopenia. As the number of patients with sarcopenia increases with the aging of the world, the number of patients with sarcopenic dysphagia is also increasing. The prevalence of sarcopenic dysphagia is high in the institutionalized older people and in patients hospitalized for pneumonia with dysphagia in acute care hospitals. Prevention, early detection and intervention of sarcopenic dysphagia with rehabilitation nutrition are essential. The diagnosis of sarcopenic dysphagia is based on skeletal and swallowing muscle strength and muscle mass. A reliable and validated diagnostic algorithm for sarcopenic dysphagia is used. Sarcopenic dysphagia is associated with malnutrition, which leads to mortality and Activities of Daily Living (ADL) decline. The rehabilitation nutrition approach improves swallowing function, nutrition status, and ADL. A combination of aggressive nutrition therapy to improve nutrition status, dysphagia rehabilitation, physical therapy, and other interventions can be effective for sarcopenic dysphagia. The rehabilitation nutrition care process is used to assess and problem solve the patient’s pathology, sarcopenia, and nutrition status. The simplified rehabilitation nutrition care process consists of a nutrition cycle and a rehabilitation cycle, each with five steps: assessment, diagnosis, goal setting, intervention, and monitoring. Nutrition professionals and teams implement the nutrition cycle. Rehabilitation professionals and teams implement the rehabilitation cycle. Both cycles should be done simultaneously. The nutrition diagnosis of undernutrition, overnutrition/obesity, sarcopenia, and goal setting of rehabilitation and body weight are implemented collaboratively.

INTRODUCTION

Sarcopenia, defined as loss of muscle strength, muscle mass, and physical function, is increasing with the aging population [1]. According to the World Health Organization report, the percentage of the world population aged 65 and over is projected to increase from 5% in 1950 to 10% in 2022 and 16% by 2050 [2]. Aging is associated with a wide range of aging phenomena. Handgrip strength increases with age, peaking in the 30s and 40s, then declines thereafter [3,4]. Muscle mass increases with age, then maintains or decreases after the 40s and 50s [3,5,6]. The number of comorbidities increases with age in older people [7], and they suffer from polypharmacy. Polypharmacy is a risk factor for sarcopenia [8]. Sarcopenia is associated with adverse outcomes of falls, fractures, mortality, decreased Activities of Daily Living (ADL), dysphagia, dyspnea, and decreased quality of life [9-11]. Therefore, treatment and prevention of sarcopenia are essential.
Poor swallowing muscle mass and strength and swallowing function worsen outcomes such as malnutrition, aspiration pneumonia, prolonged hospitalization, and survival in older people [12]. Many muscles are involved in swallowing, such as the tongue, geniohyoid, mylohyoid, digastric, stylohyoid, and temporal muscles. Unlike skeletal muscles, the geniohyoid muscle is a striated muscle, and its histological characteristics make it difficult for swallowing muscles to atrophy [13]. However, the geniohyoid muscle volume and cross-sectional area of the tongue decrease with age [14,15]. The prevalence of dysphagia in older people is approximately 20%–35%, although it varies by countries and regions [16,17]. The prevalence increases further in the presence of dementia and cerebrovascular diseases. Community-dwelling older people may be at risk for malnutrition and poor swallowing function [18], and hospitalized and institutionalized adults are at increased risk for malnutrition due to poor swallowing function [19]. Many patients hospitalized for community-acquired pneumonia may have dysphagia [20]. As many as 75% of aspiration pneumonia patients over the age of 65 have dysphagia, and dysphagia increases hospital stay by 3.5 days and mortality by 1.7 times [21]. The association of swallowing muscles and swallowing function/severity assessment with frailty and sarcopenia has been reported [22,23].
Sarcopenic dysphagia is due to whole-body sarcopenia and low muscle mass and strength related to swallowing [13]. Decreased limb and trunk skeletal muscle mass involved in postural retention leads to decreased swallowing muscle mass [14,23]. In a study of the effects of food abstinence in older hospitalized patients, 77% had sarcopenia and 26% had dysphagia after two months [24]. This development of dysphagia was related to the effects of bed rest and no oral intake during hospitalization. Effective intervention with rehabilitation nutrition can lead to the prevention of sarcopenic dysphagia [25,26].
Rehabilitation nutrition is defined as that (1) a holistic assessment using the International Classification of Functioning, Disability and Health and evaluation of the cause of malnutrition, sarcopenia, and excess or deficient nutritional intake, (2) diagnosis and goal setting through rehabilitation nutrition, (3) to improve the nutrition status, sarcopenia, frailty and disability to practice nutritional management from rehabilitation and rehabilitation from nutrition to maximize their function and quality of life [27].
Evidence on rehabilitation nutrition was gradually accumulating, and the 2020 Clinical Practice Guidelines for Rehabilitation Nutrition weakly recommend enhanced nutrition therapy in cerebrovascular disease, hip fracture, cancer, and acute illness [28]. The Japanese Association of Rehabilitation Nutrition have been reported 7 position papers, including “Goal setting for nutrition and body weight in rehabilitation nutrition” [29], “Nutritional, physical therapy for specific diseases” [30] and “Respiratory sarcopenia: a position paper by four professional organizations” [31].
With medical advances in today’s aging population, the number of people with sarcopenia and frailty are expected to increase. The challenge is how to increase healthy life expectancy. Sarcopenia, dysphagia and oral frailty affect quality of life [32-34]. Early identification of patients with sarcopenic dysphagia and effective prevention and treatment strategies are important. This review describes the diagnosis, prevalence, epidemiology, treatment and prevention, and rehabilitation nutrition of sarcopenic dysphagia and the simplified rehabilitation nutrition care process.

SARCOPENIC DYSPHAGIA

Diagnostic criteria and screening

Diagnostic criteria for sarcopenic dysphagia are based on loss of skeletal and swallowing-related muscle mass and strength [35]. According to Wakabayashi [36], Diagnostic criteria for sarcopenic dysphagia is as follows: (1) Presence of dysphagia. (2) Presence of whole-body sarcopenia. (3) Results of imaging studies are consistent with loss of swallowing muscle mass. (4) Causes of dysphagia other than sarcopenia are excluded. Ultrasound, computed tomography, and magnetic resonance imaging can evaluate swallowing-related muscle mass [37-39]. In particular, ultrasound evaluation of the geniohyoid muscle shows good reliability and validity [40,41].
The diagnostic flowchart of sarcopenic dysphagia does not include an assessment of swallowing-related muscle mass [42]. Patients 65 years of age and older with no cognitive decline are evaluated and diagnosed for physical function, muscle mass, swallowing function, underlying disease, and strength of swallowing-related muscle (Fig. 1). Physical function and total body muscle mass are determined using the diagnostic criteria of the European Working Group on Sarcopenia in Older People 2 [10] or the Asian Working Group for Sarcopenia (AWGS) 2019 [43]. The cut-off values for hand grip strength are determined by male≤28 kg, female≤18 kg, or gait speed<1.0 m/sec in the AWGS 2019 diagnostic criteria. Assessment of swallowing function includes the revised Modified Water Swallowing Test, Water Swallowing Test, Food Test, Video Endoscopic Examination of Swallowing, and Video Fluoroscopic Examination of Swallowing. Muscle strength of the swallowing-related muscle is assessed by tongue pressure [44-52]. A diagnosis of probable sarcopenic dysphagia is made if there is muscle weakness in tongue pressure (<20 kPa). If there is no weakness in tongue pressure or if tongue pressure is difficult to measure, a diagnosis of possible sarcopenic dysphagia is made.
Screening for sarcopenic dysphagia includes handgrip strength, calf circumference, or body mass index. The cut-off values were 19.7 kg for handgrip strength in males and 29.5 cm for calf circumference in females [53]. The body mass index cut-off value was 20.1 kg/m2 in older dysphagia patients [54]. Early assessment of swallowing function may prevent sarcopenic dysphagia. Therefore, early screening and using the diagnostic flowchart is recommended [13].

Prevalence

Sarcopenic dysphagia has a high prevalence among institutionalized older people and patients hospitalized for pneumonia with dysphagia in acute care hospitals. Of 100 sarcopenic seniors aged 65 years and older in nursing homes, 45% had sarcopenic dysphagia [55]. In an acute general hospital, 32% of patients undergoing swallowing rehabilitation had sarcopenic dysphagia [56]. Among patients hospitalized for pneumonia with dysphagia, 81% had sarcopenic dysphagia [57]. Patients with lower skeletal muscle mass and grip strength at baseline <8 kg had a higher incidence of dysphagia at discharge in postoperative hip fracture inpatients [58]. Dysphagia is common in patients with older age, poor performance status, gait disturbance, low body weight, malnutrition, and poorer food intake [59]. Sarcopenic dysphagia in community-dwelling older people is underreported and its prevalence is unknown.

Prognosis

Patients with sarcopenic dysphagia have poor improvement in swallowing function and are prone to malnutrition [60]. In addition, patients with malnutrition have significantly weaker swallowing-related muscles, which can easily lead to a vicious cycle of further deterioration of swallowing function compared to patients with normal nutrition status [61]. Patients with sarcopenic dysphagia have less improvement in swallowing function than patients with non-sarcopenic dysphagia [60]. From a nutritional standpoint, sarcopenic dysphagia is associated with poor improvement in swallowing function because they tend to be malnourished. On the other hand, swallowing function improves better with swallow muscle strengthening interventions in patients with sarcopenic dysphagia compared to patients without sarcopenic dysphagia [62]. From a physiological perspective, targeting the swallowing muscles directly seems effective in improving swallowing function because they do not suffer from damage caused by diseases such as stroke and neck cancer.
Sarcopenic dysphagia is associated with increased mortality and poor ADL improvement in older people. Malnutrition is associated with muscle weakness, wasting, physical frailty, and complications during hospitalization, and impedes improvement in ADL and increases mortality [61,63]. Mortality is 1.4 times higher among older people with sarcopenic dysphagia than among those without dysphagia in care facilities [62]. The risk of death is higher, especially when they are affected by weight loss and malnutrition [64]. Patients with sarcopenic dysphagia tend to have low ADL independence and poor improvement compared to patients with non-sarcopenic dysphagia [60]. Moreover, ADL improvement is significantly lower in malnourished patients compared those with normal nuti status.
High levels of inflammation are associated with poor improvement in swallowing function, and C-reactive protein (CRP) may be a prognostic predictor of swallowing function in patients with sarcopenic dysphagia [64]. Mori et al. [64] defined patients with CRP of ≥5.0 mg/L as the high-inflammation group and reported poor improvement in swallowing function in the high-inflammation group compared to the low-inflammation group. Adding the result of CRP levels to the initial assessment of swallowing function could predict the more accurate prognosis.

Treatment and prevention

The combination of aggressive nutrition therapy and rehabilitation can effectively treat sarcopenic dysphagia [13,25]. Aggressive nutrition therapy is nutritional care management that sets goals for total daily energy intake according to daily energy expenditure and daily energy accumulation [35]. Older patients require more than 250 kcal/day of daily energy accumulation to gain 1 kg of body weight per month [65]. A mean provided energy intake of ≥30 kcal/ideal body weight (kg)/day improved swallowing function in older patients with dysphagia, and ADL improved significantly in the patient undergoing rehabilitation in the acute care hospital [66]. Treatment of sarcopenic dysphagia could improve muscle strength and function throughout the body, including the swallowing muscles, by combining aggressive nutrition therapy, dysphagia rehabilitation, and physical interventions such as physical therapy [66-68].
Hospitalized patients need to evaluate and monitored to minimize sarcopenic dysphagia. Hospital-associated sarcopenia and acute sarcopenia are classified into iatrogenic and non-iatrogenic [69]. While prevention of non-iatrogenic sarcopenia is difficult, prevention of iatrogenic sarcopenia caused by the medical activities of health care professionals including doctors, nurses, and others is possible. The combination of rehabilitation, appropriate nutritional management, and medication review from admission may prevent sarcopenia during hospitalization [69].
Early detection and intervention are necessary because older people with presbyphagia are at risk for sarcopenic dysphagia. Presbyphagia is characterized by the fragility of the swallowing mechanism due to age-related changes [70-75]. Presbyphagia in older people could develop into sarcopenic dysphagia because of their disease, activity level, and nutrition status when hospitalized for diseases [36]. Monitoring nutrition status and swallowing function in older people by questionnaire such as the 10-item Eating Assessment Tool and clinical examination may be effective in preventing sarcopenic dysphagia during hospitalization [76-81].

REHABILITATION NUTRITION

Rehabilitation nutrition care process

The rehabilitation nutrition care process is a systematic problem-solving method used to assess the nutrition status, sarcopenia, and nutritional intake of people with disabilities and frail older people [82]. The rehabilitation nutrition care process consists of five steps [83]: (1) rehabilitation nutrition assessment and diagnostic reasoning, (2) rehabilitation nutrition diagnosis, (3) rehabilitation nutrition goal setting, (4) rehabilitation nutrition intervention, and (5) rehabilitation nutrition monitoring. Collaboration between rehabilitation and nutrition helps set appropriate goals and develop appropriate rehabilitation and nutrition care management [26].
The simplified rehabilitation nutrition care process consists of a nutrition cycle and a rehabilitation cycle, each with five steps. Nutrition professionals and teams implement the nutrition cycle (Fig. 2). Rehabilitation professionals and teams implement the rehabilitation cycle. Goal setting is based on diagnostic reasoning about the presence and cause of malnutrition and sarcopenia. In addition, rehabilitation and nutrition professionals should work together to achieve rehabilitation and nutrition goals. The nutrition diagnosis of undernutrition, overnutrition/obesity, sarcopenia, and goal setting of body weight and rehabilitation should be implemented collaboratively. Both cycles should be done simultaneously. The physiatrists can conduct both cycles simultaneously.

Diagnostic reasoning in rehabilitation nutrition

Diagnostic reasoning is the thought process that leads to a diagnosis based on symptoms, laboratory findings, and test results [84]. Diagnostic reasoning is a fundamental skill for healthcare professionals, because the correct diagnosis of a condition leads to the appropriate treatment. Inadequate diagnostic reasoning about nutrition status and sarcopenia would cause an inappropriate rehabilitation nutrition. Therefore, proper diagnostic reasoning is required to provide effective rehabilitation nutrition.
The thought process in diagnostic reasoning consists of non-analytic (intuitive) and analytic reasoning and requires taking advantage of them properly. Non-analytic reasoning is a diagnostic method that quickly understands and recognizes disease patterns based on experience. Intuitive, automatic, and fast are the main attributes of this method, and experienced medical professionals often use it appropriately [85]. However, it is susceptible to bias and carries the risk of misdiagnosis. Analytic reasoning is a logical diagnostic method that is time-consuming and requires more resources than the other [86]. Analytic reasoning is often used by novices with limited clinical experience. Balancing both methods without showing bias toward one or the other is important for proper diagnosis.
Among the various nutritional problems, diagnostic reasoning in rehabilitation nutrition is critical in three of them [84]: causes of anorexia, weight loss, and sarcopenia. The causes of anorexia, weight loss, and sarcopenia are not necessarily a single cause, but rather multiple causes. Therefore, analytical reasoning is recommended in these conditions to infer these causes.

Goal setting in rehabilitation nutrition

Goal setting in rehabilitation nutrition is based on SMART, an effective goal setting method to improve goal attainment [87]. This method recommends incorporating five elements: Specific, Measurable, Achievable, Relevant, and Time-Bound [87]. For example, gaining 2 kg of body weight in one month and being able to walk independently indoors with a walking cane in two weeks are considered SMART goals. Goal setting based on SMART affects the rate of goal attainment. In a study of patients with stage 3–4 chronic kidney disease, food intake was higher in the SMART goal-setting group than in the non-SMART goal-setting group [88]. Setting weight goals makes rehabilitation nutrition interventions more appropriate, whether to gain weight in underweight patients or to lose weight in overweight patients. In obese patients undergoing cardiac rehabilitation, setting a weight loss goal results in greater weight loss than not setting a goal [89].

Aggressive nutrition therapy

Aggressive nutrition therapy is a nutritional management method for malnutrition [35]. Aggressive nutritional therapy must be combined with active exercise and rehabilitation to increase muscle mass and strength. The target energy intake in this method is defined as the sum of the total energy expenditure and the daily energy accumulation used to gain or lose body weight intentionally. The energy requirements for weight gain in patients with malnutrition and sarcopenia depend on a variety of patient factors, including sex, age, nutrition status, functional status, changes in body composition, contents of exercise, systemic inflammation, and comorbidities.
The energy requirements are set by adding the amount of daily energy accumulation in patients with malnutrition. Older underweight post-stroke patients in convalescent rehabilitation ward require about 9,600 kcal intake to gain 1 kg of body weight [90]. On the other hand, the amount of energy intake is set lower than their actual activity to lose weight in patients with obesity.
The indication and timing of aggressive nutrition therapy depends on the etiology and severity of malnutrition. The efficacy of therapy, side effects, and comorbidities are monitored during the therapy [35]. Aggressive nutritional therapy is planned and implemented based on the four etiologies of the Global Leadership Initiative on Malnutrition criteria (Table 1) [91]. Nutritional intake should be adjusted according to the activity level to prevent malnutrition and maintain physical function and muscle strength in patients with diabetes mellitus. Energy intake and protein are calculated based on kilograms of ideal body weight. Specifically, ≥25–35 kcal/kg of energy intake is recommended according to the level of physical activity, and ≥1.0 g/kg of protein is required per day [66]. Monitoring is necessary during aggressive nutrition therapy because side effects such as hyperglycemia, dyslipidemia, elevated blood urea nitrogen, liver dysfunction, and electrolyte abnormalities may occur. The frequency of monitoring should be weekly rather than monthly for patients in convalescent rehabilitation wards [35]. Determination of whether to continue or modify aggressive nutrition therapy based on monitoring of function, body weight, fat mass, and muscle mass.

Nutritional physical therapy

Nutritional physical therapy was defined by the Nutrition and Swallowing Physical Therapy Committee of the Japanese Physical Therapy Association in September 2017. Nutritional physical therapy is the practice of setting goals based on an understanding of malnutrition, sarcopenia, and excess or deficient nutritional intake to maximize an individual’s function, activity, participation, and quality of life. Therefore, physical therapists should share nutrition and physical therapy assessments with registered dietitians and other multidisciplinary professionals to determine nutritional care management and physical therapy that takes into account activity level, muscle tone, and involuntary movements [30].
Nutritional physical therapy overlaps with rehabilitation nutrition, and the two concepts share goals, assessment, and intervention strategies. The practice of these two concepts requires both perspectives [30]: physical therapy that considers nutrition status and nutritional care management that maximizes the effectiveness of physical therapy. Exercise therapy consists of flexibility exercises, resistance training, and aerobic training. Flexibility exercises are prescribed for patients with any nutritional condition. Patients with nutritional deficiencies should receive low-intensity exercise to maintain physical function. In contrast, patients with adequate nutrition should receive moderate or higher intensity exercise to improve physical function. Exercise load settings are determined using subjective exercise intensity (Borg scale) and other factors, and exercise frequency, intensity, and duration are adjusted. Exercise and nutrition therapy are effective, however few reports exist on the effectiveness of nutritional physiotherapy [30]. In addition, systematic clinical practice based on a bi-directional nutrition and physical therapy perspective is limited. Further clinical practice and studies of nutritional physical therapy are needed.

CONCLUSION

Sarcopenic dysphagia reduces swallowing function, ADL and life prognosis. The triad of rehabilitation, nutrition, and oral management may be useful for patients with dysphagia [92]. The triad of rehabilitation, nutrition and oral management requires a multimodal approach based on collaboration among different professions, institutions, and communities. Prevention of whole-body sarcopenia is the priority for sarcopenic dysphagia, and early diagnosis and treatment of sarcopenic dysphagia are essential. However, the use of tools diagnose sarcopenic dysphagia is inconsistent and heterogeneous, and validation against objective measures of swallowing dysfunction is limited [93]. A review of diagnostic criteria and the development of clinical practice guidelines for sarcopenic dysphagia are needed. The development of evidence on the simplified rehabilitation nutrition care process is required.

CONFLICTS OF INTEREST

No potential conflict of interest relevant to this article was reported.

FUNDING INFORMATION

None.

AUTHOR CONTRIBUTION

Conceptualization: Wakabayashi H. Methodology: Wakabayashi H, Kakehi S. Formal analysis: all authors. Project administration: Wakabayashi H. Kakehi S. Visualization: Wakabayashi H, Ninomiya J, Shioya M. Writing – original draft: all authors. Writing – review and editing: Wakabayashi H, Kakehi S, Isono E. Approval of final manuscript: all authors.

Fig. 1.
Diagnostic flowchart of sarcopenic dysphagia. HS, hand grip strength; GS, gait speed; DXA, dual-energy X-ray absorptiometry; BIA, bioelectrical impedance analysis.
arm-23101f1.jpg
Fig. 2.
Simplified rehabilitation nutrition care process.
arm-23101f2.jpg
Table 1.
Indication/timing/contraindication of aggressive nutrition therapy
No. Indication Timing Contraindication
1 Cancer Pre cachexia Refractory cachexia
Chronic obstructive pulmonary disease Cachexia
Congestive heart failure
Chronic kidney disease
2 Anorexia nervosa Short bowel syndrome Severe dementia
Short bowel syndrome Mild to moderate dementia Bedridden
Stroke
Amyotrophic lateral sclerosis
Dementia
3 Major infection Mildly invasive disease and transition to the anabolic phase Acute disease or injuries with severe inflammation
Burns
Trauma
Closed head injury
4 Starvation No symptoms or risks for refeeding syndrome

REFERENCES

1. Kitamura A, Seino S, Abe T, Nofuji Y, Yokoyama Y, Amano H, et al. Sarcopenia: prevalence, associated factors, and the risk of mortality and disability in Japanese older adults. J Cachexia Sarcopenia Muscle 2021;12:30-8.
crossref pmid pmc pdf
2. United Nations. World population prospects 2022: summary of results [Internet]. United Nations; 2022 [cited 2023 Jun 12]. Available from: https://www.un.org/development/desa/pd/content/World-Population-Prospects-2022.

3. Wen Z, Gu J, Chen R, Wang Q, Ding N, Meng L, et al. Handgrip strength and muscle quality: results from the national health and nutrition examination survey database. J Clin Med 2023;12:3184.
crossref pmid pmc
4. Dodds RM, Syddall HE, Cooper R, Kuh D, Cooper C, Sayer AA. Global variation in grip strength: a systematic review and meta-analysis of normative data. Age Ageing 2016;45:209-16.
crossref pmid pmc
5. Yamada M, Moriguch Y, Mitani T, Aoyama T, Arai H. Age-dependent changes in skeletal muscle mass and visceral fat area in Japanese adults from 40 to 79 years-of-age. Geriatr Gerontol Int 2014;14 Suppl 1:8-14.
crossref pmid
6. Keller K, Engelhardt M. Strength and muscle mass loss with aging process. Age and strength loss. Muscles Ligaments Tendons J 2014;3:346-50.
crossref pmid pmc
7. Ho IS, Azcoaga-Lorenzo A, Akbari A, Davies J, Hodgins P, Khunti K, et al. Variation in the estimated prevalence of multimorbidity: systematic review and meta-analysis of 193 international studies. BMJ Open 2022;12:e057017.
crossref pmid pmc
8. Prokopidis K, Giannos P, Reginster JY, Bruyere O, Petrovic M, Cherubini A, et al. Sarcopenia is associated with a greater risk of polypharmacy and number of medications: a systematic review and meta-analysis. J Cachexia Sarcopenia Muscle 2023;14:671-83.
crossref pmid pmc pdf
9. Cruz-Jentoft AJ, Sayer AA. Sarcopenia. Lancet 2019;393:2636-46. Erratum in: Lancet 2019;393:2590.
crossref pmid
10. Cruz-Jentoft AJ, Bahat G, Bauer J, Boirie Y, Bruyère O, Cederholm T, et al. Sarcopenia: revised European consensus on definition and diagnosis. Age Ageing 2019;48:16-31. Erratum in: Age Ageing 2019;48:601.
crossref pmid pmc pdf
11. Nagano A, Wakabayashi H, Maeda K, Kokura Y, Miyazaki S, Mori T, et al. Respiratory sarcopenia and sarcopenic respiratory disability: concepts, diagnosis, and treatment. J Nutr Health Aging 2021;25:507-15.
crossref pmid pmc pdf
12. Thiyagalingam S, Kulinski AE, Thorsteinsdottir B, Shindelar KL, Takahashi PY. Dysphagia in older adults. Mayo Clin Proc 2021;96:488-97.
crossref pmid
13. Fujishima I, Fujiu-Kurachi M, Arai H, Hyodo M, Kagaya H, Maeda K, et al. Sarcopenia and dysphagia: position paper by four professional organizations. Geriatr Gerontol Int 2019;19:91-7.
crossref pmid pdf
14. Yamaguchi K, Nakagawa K, Yoshimi K, Ariya C, Nakane A, Ishii M, et al. Association between characteristics of swallowing-related muscles and trunk muscle mass. Sci Rep 2023;13:7814.
crossref pmid pmc pdf
15. Nakao Y, Uchiyama Y, Honda K, Yamashita T, Saito S, Domen K. Age-related composition changes in swallowing-related muscles: a Dixon MRI study. Aging Clin Exp Res 2021;33:3205-13.
crossref pmid pdf
16. Rech RS, de Goulart BNG, Dos Santos KW, Marcolino MAZ, Hilgert JB. Frequency and associated factors for swallowing impairment in community-dwelling older persons: a systematic review and meta-analysis. Aging Clin Exp Res 2022;34:2945-61.
crossref pmid pdf
17. Rajati F, Ahmadi N, Naghibzadeh ZA, Kazeminia M. The global prevalence of oropharyngeal dysphagia in different populations: a systematic review and meta-analysis. J Transl Med 2022;20:175.
crossref pmid pmc pdf
18. Tagliaferri S, Lauretani F, Pelá G, Meschi T, Maggio M. The risk of dysphagia is associated with malnutrition and poor functional outcomes in a large population of outpatient older individuals. Clin Nutr 2019;38:2684-9.
crossref pmid
19. Blanař V, Hödl M, Lohrmann C, Amir Y, Eglseer D. Dysphagia and factors associated with malnutrition risk: a 5-year multicentre study. J Adv Nurs 2019;75:3566-76.
crossref pmid pdf
20. Almirall J, Rofes L, Serra-Prat M, Icart R, Palomera E, Arreola V, et al. Oropharyngeal dysphagia is a risk factor for community-acquired pneumonia in the elderly. Eur Respir J 2013;41:923-8.
crossref pmid
21. Patel DA, Krishnaswami S, Steger E, Conover E, Vaezi MF, Ciucci MR, et al. Economic and survival burden of dysphagia among inpatients in the United States. Dis Esophagus 2018;31:1-7.
crossref pmid pmc
22. Yang RY, Yang AY, Chen YC, Lee SD, Lee SH, Chen JW. Association between dysphagia and frailty in older adults: a systematic review and meta-analysis. Nutrients 2022;14:1812.
crossref pmid pmc
23. Sakai K, Nakayama E, Yoneoka D, Sakata N, Iijima K, Tanaka T, et al. Association of oral function and dysphagia with frailty and sarcopenia in community-dwelling older adults: a systematic review and meta-analysis. Cells 2022;11:2199.
crossref pmid pmc
24. Maeda K, Takaki M, Akagi J. Decreased skeletal muscle mass and risk factors of sarcopenic dysphagia: a prospective observational cohort study. J Gerontol A Biol Sci Med Sci 2017;72:1290-4.
crossref pmid
25. Wakabayashi H, Kishima M, Itoda M, Fujishima I, Kunieda K, Ohno T, et al. Diagnosis and treatment of sarcopenic dysphagia: a scoping review. Dysphagia 2021;36:523-31.
crossref pmid pdf
26. Nagano A, Nishioka S, Wakabayashi H. Rehabilitation nutrition for iatrogenic sarcopenia and sarcopenic dysphagia. J Nutr Health Aging 2019;23:256-65.
crossref pmid pdf
27. Wakabayashi H. Rehabilitation nutrition in general and family medicine. J Gen Fam Med 2017;18:153-4.
crossref pmid pmc pdf
28. Nishioka S, Aragane H, Suzuki N, Yoshimura Y, Fujiwara D, Mori T, et al. Clinical practice guidelines for rehabilitation nutrition in cerebrovascular disease, hip fracture, cancer, and acute illness: 2020 update. Clin Nutr ESPEN 2021;43:90-103.
crossref pmid
29. Wakabayashi H, Yoshimura Y, Maeda K, Fujiwara D, Nishioka S, Nagano A. Goal setting for nutrition and body weight in rehabilitation nutrition: position paper by the Japanese Association of Rehabilitation Nutrition (secondary publication). J Gen Fam Med 2021;23:77-86.
crossref pmid pmc pdf
30. Inoue T, Iida Y, Takahashi K, Shirado K, Nagano F, Miyazaki S, et al. Nutrition and physical therapy: a position paper by the physical therapist section of the Japanese Association of Rehabilitation Nutrition (secondary publication). JMA J 2022;5:243-51.
crossref pmid pmc
31. Sato S, Miyazaki S, Tamaki A, Yoshimura Y, Arai H, Fujiwara D, et al. Respiratory sarcopenia: a position paper by four professional organizations. Geriatr Gerontol Int 2023;23:5-15.
crossref pmid pdf
32. Morisaki N. Relationship between swallowing functions and health-related quality of life among community-dwelling dependent older individuals. Jpn J Nurs Sci 2017;14:353-63.
crossref pmid pdf
33. Khanagar SB, Al-Ehaideb A, Shivanna MM, Ul Haq I, Al Kheraif AA, Naik S, et al. Age-related oral changes and their impact on oral health-related quality of life among frail elderly population: a review. J Contemp Dent Pract 2020;21:1298-303.
crossref pmid
34. Veronese N, Koyanagi A, Cereda E, Maggi S, Barbagallo M, Dominguez LJ, et al. Sarcopenia reduces quality of life in the long-term: longitudinal analyses from the English longitudinal study of ageing. Eur Geriatr Med 2022;13:633-9.
crossref pmid pmc pdf
35. Nakahara S, Takasaki M, Abe S, Kakitani C, Nishioka S, Wakabayashi H, et al. Aggressive nutrition therapy in malnutrition and sarcopenia. Nutrition 2021;84:111109.
crossref pmid
36. Wakabayashi H. Presbyphagia and sarcopenic dysphagia: association between aging, sarcopenia, and deglutition disorders. J Frailty Aging 2014;3:97-103.
crossref pmid
37. Kokura Y, Nishioka S, Maeda K, Wakabayashi H. Ultrasound utilized by registered dietitians for body composition measurement, nutritional assessment, and nutritional management. Clin Nutr ESPEN 2023;57:173-80.
crossref pmid
38. Inamoto Y, González-Fernández M, Saitoh E. 3D-CT evaluation of swallowing: metrics of the swallowing response using swallowing CT. Dysphagia 2022;37:237-49.
crossref pmid pdf
39. Nakao Y, Yamashita T, Honda K, Katsuura T, Hama Y, Nakamura Y, et al. Association among age-related tongue muscle abnormality, tongue pressure, and presbyphagia: a 3D MRI study. Dysphagia 2021;36:483-91.
crossref pmid pdf
40. Ogawa N, Mori T, Fujishima I, Wakabayashi H, Itoda M, Kunieda K, et al. Ultrasonography to measure swallowing muscle mass and quality in older patients with sarcopenic dysphagia. J Am Med Dir Assoc 2018;19:516-22.
crossref pmid
41. Allen JE, Clunie GM, Winiker K. Ultrasound: an emerging modality for the dysphagia assessment toolkit? Curr Opin Otolaryngol Head Neck Surg 2021;29:213-8.
crossref pmid pmc
42. Mori T, Fujishima I, Wakabayashi H, Oshima F, Itoda M, Kunieda K, et al. Development, reliability, and validity of a diagnostic algorithm for sarcopenic dysphagia. JCSM Clin Rep 2017;2:1-10.
crossref
43. Chen LK, Woo J, Assantachai P, Auyeung TW, Chou MY, Iijima K, et al. Asian Working Group for Sarcopenia: 2019 consensus update on sarcopenia diagnosis and treatment. J Am Med Dir Assoc 2020;21:300-7.e2.
crossref pmid
44. Mori T, Wakabayashi H, Ogawa N, Fujishima I, Oshima F, Itoda M, et al. The mass of geniohyoid muscle is associated with maximum tongue pressure and tongue area in patients with sarcopenic dysphagia. J Nutr Health Aging 2021;25:356-60.
crossref pmid pdf
45. Machida N, Tohara H, Hara K, Kumakura A, Wakasugi Y, Nakane A, et al. Effects of aging and sarcopenia on tongue pressure and jaw-opening force. Geriatr Gerontol Int 2017;17:295-301.
crossref pmid pdf
46. Murakami T, Kamide N, Ando M, Hata W, Sakamoto M. Association between tongue pressure and skeletal muscle mass and muscle function in community-dwelling older people without sarcopenia. Eur Geriatr Med 2022;13:649-53.
crossref pmid pdf
47. Shimizu A, Maeda K, Wakabayashi H, Nishioka S, Ohno T, Nomoto A, et al. Sarcopenic dysphagia with low tongue pressure is associated with worsening of swallowing, nutritional status, and activities of daily living. J Nutr Health Aging 2021;25:883-8.
crossref pmid pdf
48. Shimizu A, Fujishima I, Maeda K, Wakabayashi H, Nishioka S, Ohno T, et al. Effect of low tongue pressure on nutritional status and improvement of swallowing function in sarcopenic dysphagia. Nutrition 2021;90:111295.
crossref pmid
49. Chang KV, Wu WT, Chen LR, Wang HI, Wang TG, Han DS. Suboptimal tongue pressure is associated with risk of malnutrition in community-dwelling older individuals. Nutrients 2021;13:1821.
crossref pmid pmc
50. Kunieda K, Fujishima I, Wakabayashi H, Ohno T, Shigematsu T, Itoda M, et al. Relationship between tongue pressure and pharyngeal function assessed using high-resolution manometry in older dysphagia patients with sarcopenia: a pilot study. Dysphagia 2021;36:33-40.
crossref pmid pdf
51. Kaji A, Hashimoto Y, Kobayashi Y, Sakai R, Okamura T, Miki A, et al. Sarcopenia is associated with tongue pressure in older patients with type 2 diabetes: a cross-sectional study of the KAMOGAWA-DM cohort study. Geriatr Gerontol Int 2019;19:153-8.
crossref pmid pdf
52. Maeda K, Akagi J. Decreased tongue pressure is associated with sarcopenia and sarcopenic dysphagia in the elderly. Dysphagia 2015;30:80-7. Erratum in: Dysphagia 2015;30:88.
crossref pmid pdf
53. Kishimoto H, Wakabayashi H, Nishioka S, Momosaki R. Discriminative evaluation of sarcopenic dysphagia using handgrip strength or calf circumference in patients with dysphagia using the area under the receiver operating characteristic curve. J Clin Med 2022;12:118.
crossref pmid pmc
54. Togashi S, Wakabayashi H, Ohinata H, Nishioka S, Kokura Y, Momosaki R. Sensitivity and specificity of body mass index for sarcopenic dysphagia diagnosis among patients with dysphagia: a multi-center cross-sectional study. Nutrients 2022;14:4494.
crossref pmid pmc
55. Moncayo-Hernández BA, Herrera-Guerrero JA, Vinazco S, Ocampo-Chaparro JM, Reyes-Ortiz CA. Sarcopenic dysphagia in institutionalised older adults. Endocrinol Diabetes Nutr (Engl Ed) 2021;68:602-11.
crossref pmid
56. Wakabayashi H, Takahashi R, Murakami T. The prevalence and prognosis of sarcopenic dysphagia in patients who require dysphagia rehabilitation. J Nutr Health Aging 2019;23:84-8.
crossref pmid pdf
57. Miyauchi N, Nakamura M, Nakamura I, Momosaki R. Effect of early versus delayed mobilization by physical therapists on oral intake in patients with sarcopenic dysphagia after pneumonia. Eur Geriatr Med 2019;10:603-7.
crossref pmid pdf
58. Nagano A, Maeda K, Shimizu A, Nagami S, Takigawa N, Ueshima J, et al. Association of sarcopenic dysphagia with underlying sarcopenia following hip fracture surgery in older women. Nutrients 2020;12:1365.
crossref pmid pmc
59. Maeda K, Ishida Y, Nonogaki T, Shimizu A, Yamanaka Y, Matsuyama R, et al. Development and predictors of sarcopenic dysphagia during hospitalization of older adults. Nutrients 2019;12:70.
crossref pmid pmc
60. Nagai T, Wakabayashi H, Nishioka S, Momosaki R. Functional prognosis in patients with sarcopenic dysphagia: an observational cohort study from the Japanese sarcopenic dysphagia database. Geriatr Gerontol Int 2022;22:839-45.
crossref pmid pdf
61. Abe S, Kokura Y, Maeda K, Nishioka S, Momosaki R, Matsuoka H, et al. Effects of undernutrition on swallowing function and activities of daily living in hospitalized patients: data from the Japanese Sarcopenic Dysphagia Database. Nutrients 2023;15:1291.
crossref pmid pmc
62. Campo-Rivera N, Ocampo-Chaparro JM, Carvajal-Ortiz R, Reyes-Ortiz CA. Sarcopenic dysphagia is associated with mortality in institutionalized older adults. J Am Med Dir Assoc 2022;23:1720.e11-7.
crossref pmid
63. Nishioka S, Wakabayashi H. Interaction between malnutrition and physical disability in older adults: is there a malnutrition-disability cycle? Nutr Rev 2023;81:191-205.
crossref pmid pdf
64. Mori T, Wakabayashi H, Kishima M, Itoda M, Fujishima I, Kunieda K, et al. Association between inflammation and functional outcome in patients with sarcopenic dysphagia. J Nutr Health Aging 2022;26:400-6.
crossref pmid pdf
65. Nishioka S, Nakahara S, Takasaki M, Shiohama N, Kokura Y, Suzuki T, et al. The concept of aggressive nutrition therapy and clinical indication: a position paper. Clin Nutr ESPEN 2022;52:322-30.
crossref pmid
66. Shimizu A, Fujishima I, Maeda K, Wakabayashi H, Nishioka S, Ohno T, et al. Nutritional management enhances the recovery of swallowing ability in older patients with sarcopenic dysphagia. Nutrients 2021;13:596.
crossref pmid pmc
67. Kagaya H, Inamoto Y. Possible rehabilitation procedures to treat sarcopenic dysphagia. Nutrients 2022;14:778.
crossref pmid pmc
68. Nagano A, Maeda K, Koike M, Murotani K, Ueshima J, Shimizu A, et al. Effects of physical rehabilitation and nutritional intake management on improvement in tongue strength in sarcopenic patients. Nutrients 2020;12:3104.
crossref pmid pmc
69. Wakabayashi H. Hospital-associated sarcopenia, acute sarcopenia, and iatrogenic sarcopenia: prevention of sarcopenia during hospitalization. J Gen Fam Med 2023;24:146-7.
crossref pmid pmc
70. Feng HY, Zhang PP, Wang XW. Presbyphagia: dysphagia in the elderly. World J Clin Cases 2023;11:2363-73.
crossref pmid pmc
71. Yiğman ZA, Umay E, Cankurtaran D, Güzel Ş. Swallowing difficulty in the older adults: presbyphagia or dysphagia with sarcopenia? Int J Rehabil Res 2021;44:336-42.
crossref pmid
72. Labeit B, Muhle P, von Itter J, Slavik J, Wollbrink A, Sporns P, et al. Clinical determinants and neural correlates of presbyphagia in community-dwelling older adults. Front Aging Neurosci 2022;14:912691.
crossref pmid pmc
73. Nienstedt JC, Müller F, Rösler A, Pflug C. Presbyphagia diagnostics using M-mode ultrasound: changes in the tongue movement pattern. Dysphagia 2020;35:696-701.
crossref pmid pdf
74. Namasivayam-MacDonald AM, Riquelme LF. Presbyphagia to dysphagia: multiple perspectives and strategies for quality care of older adults. Semin Speech Lang 2019;40:227-42.
crossref pmid
75. de Lima Alvarenga EH, Dall'Oglio GP, Murano EZ, Abrahão M. Continuum theory: presbyphagia to dysphagia? Functional assessment of swallowing in the elderly. Eur Arch Otorhinolaryngol 2018;275:443-9.
crossref pmid pdf
76. Schindler A, Mozzanica F, Monzani A, Ceriani E, Atac M, Jukic-Peladic N, et al. Reliability and validity of the Italian Eating Assessment Tool. Ann Otol Rhinol Laryngol 2013;122:717-24.
crossref pmid pdf
77. Cheney DM, Siddiqui MT, Litts JK, Kuhn MA, Belafsky PC. The ability of the 10-Item Eating Assessment Tool (EAT-10) to predict aspiration risk in persons with dysphagia. Ann Otol Rhinol Laryngol 2015;124:351-4.
crossref pmid pdf
78. Wakabayashi H, Matsushima M. Dysphagia assessed by the 10-Item Eating Assessment Tool is associated with nutritional status and activities of daily living in elderly individuals requiring long-term care. J Nutr Health Aging 2016;20:22-7.
crossref pmid pdf
79. Izaola O, Gómez Hoyos E, López JJ, Ortola A, Torres B, Primo D, et al. The 10-Item Eating Assessment Tool is associated with nutritional status, mortality and hospital stay in elderly individuals requiring hospitalization with acute diseases. Nutr Hosp 2018;35:827-32.
pmid
80. Igarashi K, Kikutani T, Tamura F. Survey of suspected dysphagia prevalence in home-dwelling older people using the 10-Item Eating Assessment Tool (EAT-10). PLoS One 2019;14:e0211040.
crossref pmid pmc
81. Ko D, Oh J, Joo S, Park JY, Cho MS. Dietary habits, food product selection attributes, nutritional status, and depression in middle-aged and older adults with dysphagia. Nutrients 2022;14:4045.
crossref pmid pmc
82. Mizuno S, Wakabayashi H, Wada F. Rehabilitation nutrition for individuals with frailty, disability, sarcopenic dysphagia, or sarcopenic respiratory disability. Curr Opin Clin Nutr Metab Care 2022;25:29-36.
crossref pmid pmc
83. Wakabayashi H. Positive psychology and rehabilitation nutrition. J Gen Fam Med 2022;23:293-94.
crossref pmid pmc pdf
84. Wakabayashi H, Maeda K, Momosaki R, Kokura Y, Yoshimura Y, Fujiwara D, et al. Diagnostic reasoning in rehabilitation nutrition: position paper by the Japanese Association of Rehabilitation Nutrition (secondary publication). J Gen Fam Med 2022;23:205-16.
crossref pmid pmc pdf
85. Brush JE Jr, Sherbino J, Norman GR. How expert clinicians intuitively recognize a medical diagnosis. Am J Med 2017;130:629-34.
crossref pmid
86. Corazza GR, Lenti MV, Howdle PD. Diagnostic reasoning in internal medicine: a practical reappraisal. Intern Emerg Med 2021;16:273-9.
crossref pmid pmc pdf
87. Bovend'Eerdt TJ, Botell RE, Wade DT. Writing SMART rehabilitation goals and achieving goal attainment scaling: a practical guide. Clin Rehabil 2009;23:352-61. Erratum in: Clin Rehabil 2010;24:382.
crossref pmid pdf
88. Chan CH, Conley M, Reeves MM, Campbell KL, Kelly JT. Evaluating the impact of goal setting on improving diet quality in chronic kidney disease. Front Nutr 2021;8:627753.
crossref pmid pmc
89. Barrett KV, Savage PD, Ades PA. Effects of behavioral weight loss and weight loss goal setting in cardiac rehabilitation. J Cardiopulm Rehabil Prev 2020;40:383-7.
crossref pmid pmc
90. Yoshimura Y, Wakabayashi H, Momosaki R, Nagano F, Bise T, Shimazu S, et al. Stored energy increases body weight and skeletal muscle mass in older, underweight patients after stroke. Nutrients 2021;13:3274.
crossref pmid pmc
91. Cederholm T, Jensen GL, Correia MITD, Gonzalez MC, Fukushima R, Higashiguchi T, et al. GLIM criteria for the diagnosis of malnutrition - a consensus report from the global clinical nutrition community. J Cachexia Sarcopenia Muscle 2019;10:207-17.
crossref pmid pmc pdf
92. Wakabayashi H, Kakehi S, Kishima M, Itoda M, Nishioka S, Momosaki R. Impact of registered dietitian and dental hygienist involvement on functional outcomes in patients with dysphagia: triad of rehabilitation, nutrition, and oral management. Eur Geriatr Med 2023. doi: 10.1007/s41999-023-00833-7 [Epub ahead of print].
crossref pdf
93. Abu-Ghanem S, Graf A, Govind J. Diagnosis of sarcopenic dysphagia in the elderly: critical review and future perspectives. Dysphagia 2022;37:1093-102.
crossref pmid pdf


ABOUT
ARTICLE TYPES

Browse all articles >

BROWSE ARTICLES
AUTHOR INFORMATION
Terms of Use   |   Privacy Polity
Editorial Office
Department of Rehabilitation Medicine, Seoul National University Hospital
101 Daehak-ro, Jongno-gu, Seoul, Korea
Tel: +82-10-8678-2671    Fax: +82-2-6072-5244    E-mail: edit@e-arm.org; edit.karm@gmail.com
Business Registration: 110-82-07460                

Copyright © 2024 by Korean Academy of Rehabilitation Medicine.

Developed in M2PI

Close layer