Insight into Clinical Assessment and Management of Sarcopenia
Ganesh Sankarrajan,
PT.DPT.OCS.GCS
Board-Certified Clinical Specialist
Bio
Texas Medical Center
Objectives
Why Sarcopenia demands clinical attention
Forty‐nine participants (17.0%) were identified as having sarcopenia.
The sarcopenia group had higher
Slow-progressing
PUBLIC HEALTH ISSUE
Prior to hospital admissions
https://www.cdc.gov/pcd/issues/2020/20_0167.htm
https://www.cdc.gov/falls/index.html
Types of Sarcopenia
Primary Sarcopenia
Secondary sarcopenia
Compound Sarcopenia
SO – Sarcopenic Obesity
Sarcopenia – frailty axis
Traditional MUSCLE MASS body composition measurements
Sarcopenia is defined as a gradual loss of muscle mass, strength and function.
EWGSOP
ESPEN-SIG
AWGS
FNIH
IWGS
Objective outcome measures
JAMAR GS
SPPB
Subjective measure
Recall Pathology to design an outcome measure
RECALL SPPB
Frailty in liver disease patients and has cutoffs for robust, prefrail, and frail categories. The LFI score for robust is defined as <3.2, prefrail is defined as LFI between 3.2 and 4.4, and frail is defined as LFI ≥4.5. The LFI had excellent reliability with ICC of 0.93 (95% confidence interval, 0.91-0.95). LFI also has external validity in non-cirrhotic populations as well and is highly reproducible among different raters. And an LFI cut-off of >4.62 discriminated best between patients with and without elevated risk for re-hospitalization within 30 days.
LFI = (–0.330 × sex-adjusted grip strength) + (–2.529 × number of chair stands per second) + (–0.040 × balance time) + 6
The classifications of frailty were determined by using previously established cutoffs of the LFI with robust defined as LFI <3.2, prefrail defined as LFI between 3.2 and 4.4, and frail defined as LFI ≥4.5
Objectives
The primary objective of this study is an attempt to identify sarcopenia in chronic liver disease patients using SARC-F questionnaire and to find out its internal consistency and diagnostic validity in relation to LFI.
The secondary objective is to identify which among the 5 functional tasks has highest sensitivity and specificity with reference to objective measures used in the study.
Using regression analysis find out whether the accepted cut off score of ≥ 4 in SARC-F questionnaire is applicable to patients with CLD
How scoring can impact a change in clinical practice.
Study Design
Description of the design of the study -Cross-Sectional single-center study design
Expected duration of study and subject participation -6 months to 8 months, A total of 10-15 min for administration of SARC-F questionnaire and to perform basic testing with outcomes measures.
Study Population
The study population and inclusion criteria- Patients with Chronic Liver Disease (CLD) from the outpatient transplant center and from the hospital being treated for chronic liver disease will be included in this study. The study will include CLD patients who has underwent TIPS, liver transplant in the part or on wait-list for liver transplant also will be included.
Exclusion Criteria - The study will exclude subjects if they have cognitive disorders or hepatic encephalopathy, with inability to fill the SARC-F questionnaire. The study will also exclude subjects with orthopedic disorders due to inability to complete the 4MWT and Short Physical Performance battery.
Describe the recruitment strategy – Since its a cross sectional design, subjects with Chronic Liver disease, incl Alcoholic cirrhosis and NASH will be recruited based on their verbal consent to fill up the SARC-F questionnaire and followed up by objective tests which include as grip strength, 4MWT and SPPB.
Study Procedures
Total amount of time required of each subject to participate in the project – 1
10 -15 Min for each subject in the cross -sectional study design
Type of information the PI will gather, along with the means for collecting and recording it -
MRN, Age, Sex, Education level, BMI, Type of CLD with regard to cirrhosis type, co-morbidness, MELD score, Transplant status, SARC-F questionnaire with 5 elements, Grip strength, Short Physical Performance Battery, Gait speed, Stairs
Therapeutic Interventions
Exercise (at 30% of peak work-load) significantly increased arterial pressure and cardiac output and decreased systemic vascular resistance. This was associated with a significant increase in HVPG (from 16.7 +/- 1.5 to 19.2 +/- 1.6 mm Hg; P < 0.01) and a significant reduction in hepatic blood flow (from 1291 +/- 216 to 1034 +/- 152 mL-min-1; P < 0.05). All of these changes were intensified at 50% of target workload.
Conclusions: The present study shows that moderate exercise increases portal pressure and may therefore increase the risk of variceal bleeding in patients with esophageal varices. These findings suggest that cirrhotic patients with portal hypertension should be advised of potential risks during exercise.
Nutritional education