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Impact of Hand Grip Strength on Length of Hospital Stay After Cardiac Surgery Among Elderly Patients

Recruiting
Conditions
Sarcopenia
Frailty
Interventions
Diagnostic Test: Hand grip strength measurement
Registration Number
NCT05546671
Lead Sponsor
Kartal Kosuyolu High Speciality Training and Research Hospital
Brief Summary

Hand grip strength has been shown to be a predictor of adverse cardiovascular outcomes in the elderly population. This study aims to investigate whether measurement of hand grip strength could be used as a predictor of prolonged hospital stay after cardiac surgery in elderly patients.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
240
Inclusion Criteria
  • Age ≥70 years
  • Undergoing isolated coronary artery bypass grafting or isolated valve surgery or combined coronary and valve procedures
  • Being oriented and cooperative enough to understand and comply with the instruction of gripping the hand dynamometer
Exclusion Criteria
  • Age <70 years
  • Emergent status
  • Hemodynamic instability
  • Inability to cooperate due to neurocognitive disorder
  • Loss of upper extremity motor function of any degree (such as due to previous stroke)
  • History of upper extremity amputation of any level

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Weak grippersHand grip strength measurement-
Strong grippersHand grip strength measurement-
Primary Outcome Measures
NameTimeMethod
Prolonged hospital stay14 days

Prolonged hospital stay is defined as postoperative hospital stay for ≥14 days.

Secondary Outcome Measures
NameTimeMethod
Prolonged intensive care unit stay48 hours

Prolonged intensive care unit stay is defined as postoperative intensive care unit stay for \>48 hours. This includes sum of all time spent in intensive care unit including unplanned returns.

Prolonged mechanical ventilation12 hours

Prolonged mechanical ventilation is defined as mechanical ventilation of \>12 hours. This includes re-intubations and non-invasive mechanical ventilation.

Trial Locations

Locations (1)

Kosuyolu High Specialization Education and Research Hospital

🇹🇷

Istanbul, Turkey

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