Health Condition 1: M968- Other intraoperative and postprocedural complications and disorders of musculoskeletal system, not elsewhere classified
Conditions
Interventions
Intervention1: NIL: NIL
Intervention2: nil: nil
Control Intervention1: nil: nil
Sponsors
Bharati Hospital and Research Centre
Eligibility
Inclusion criteria
Inclusion criteria: 1.patients of the age above 65 of either sex 2.ASA I / II / III patients 3.patients undergoing elective lower limb Orthopedic surgeries under central neuraxial blockade
Exclusion criteria
Exclusion criteria: 1)Patients who are not willing to take part in the study. 2)Patients with pathological defects such as paralysis, arthritis, and trauma that obviously impair grip strength will be excluded 3)Patients who are unable to comprehend the commands or use the dynamometer freely 4)Patients with coagulopathy, spinal deformities and other contraindications to central neuraxial blockade 5)Patients posted for emergency Orthopedic surgeries.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| PRIMARY OBJECTIVE -To assess the Handgrip Strength in the Preoperative period -To assess Intra Operative and Post-Operative outcomes like blood loss, Inotrope requirement, post operative ICU stay and length of hospital stay. -To Compare the Grades of Hand Grip Strength with the Intra and Post Operative Outcomes. Timepoint: the patient will be assessed in the preoperative period, intraoperative period and the immediate postoperative period. | — |
Secondary
| Measure | Time frame |
|---|---|
| SECONDARY OBJECTIVE To Correlate Handgrip Strength with other Frailty Measurements(investigations) like- - CRP - Serum Albumin - Revised Cardiac Risk Index (RCRI) Timepoint: BASELINE | — |
Countries
India
Contacts
Public ContactDr Athira CN
Bharati Vidyapeeth (DTU) University, Pune
Outcome results
None listed