ASA or CFS for ICU Prediction in Geriatric Hip Fracture

Comparative Analysis of ASA Score and Clinical Frailty Scale in Predicting Postoperative Intensive Care Requirements in Geriatric Hip Fracture Surgery

The aim of this retrospective study is to compare the efficacy of the American Society of Anesthesiologists (ASA) physical status classification and the Clinical Frailty Scale (CFS) in predicting postoperative intensive care unit (ICU) requirements in geriatric patients undergoing hip fracture surgery. The investigators will analyze medical records of patients aged 65 and older. The study will evaluate whether the CFS provides better predictive value for ICU admission compared to the traditional ASA score in this specific surgical population.

Study Overview

Detailed Description

Study Title Comparative analysis of American Society of Anesthesiologists (ASA) physical status classification and Clinical Frailty Scale (CFS) in predicting postoperative intensive care unit (ICU) admission in geriatric hip fracture surgery Introduction With the rapid increase in the elderly population worldwide, geriatric hip fracture cases have become one of the most critical health issues in anesthesia and surgical practice. This patient group is characterized not only by surgical trauma but also by reduced physiological reserve, multiple chronic diseases, and high frailty levels. Major complications following hip fracture surgery extend hospital stays, increase healthcare costs, and lead to high mortality rates. Therefore, predicting which patients will require intensive care unit (ICU) support in the preoperative period is vital for both patient safety and efficient hospital resource management.

The American Society of Anesthesiologists (ASA) physical status classification, widely used in traditional anesthesia practice, successfully defines a patient's systemic disease burden but does not fully reflect the biological resistance and functional capacity of an elderly individual against surgical stress. It is reported in the literature that patients with the same ASA score can have significantly different clinical outcomes; even with similar chronic disease burdens, patients defined as "frail" face worse postoperative results. The Clinical Frailty Scale (CFS), developed by Kenneth Rockwood, measures "biological aging" based on a patient's mobility level and independence in activities of daily living, revealing the "reserve depletion" that traditional scoring systems overlook.

The primary rationale for this study is to directly compare the success of the ASA score and the CFS in predicting the need for postoperative ICU admission in a geriatric hip fracture population. While both scores are known to have predictive value, their superiority over each other and their combined use in clinical decision-making remain controversial in acute trauma groups like hip fractures. This research will provide a scientific basis for anesthesiologists to use more sensitive tools in preoperative risk assessment and to develop appropriate triage strategies for patients in the "hidden risk" group (low ASA but high CFS scores).

Materials and Methods This study is a retrospective cohort study examining the data of patients aged 65 and older who underwent surgery for a hip fracture (femur neck, intertrochanteric, or subtrochanteric fracture) between November 2023 and December 2025. Approval was obtained from the relevant ethics committee, and the data of 243 patients with complete operative records were evaluated. Cases transferred to another center before surgery, those with inaccessible surgical data, or those followed conservatively were excluded. Demographic information such as age and gender, as well as comorbidities (hypertension, diabetes, coronary artery disease, dementia), preoperative laboratory values (hemoglobin, albumin, creatinine), and echocardiography findings, were obtained through the hospital information management system.

Among the parameters used for risk assessment, ASA scores were recorded directly from preoperative anesthesia forms. Clinical Frailty Scale (CFS) scores were retrospectively calculated based on the Rockwood scale by scoring functional data such as mobility levels, domestic independence, and history of assistive device use found in nursing follow-up notes. Intraoperative variables, including anesthesia technique (general or spinal), surgical duration, and the requirement for vasoactive drugs, were also included. The primary endpoint of the study is the requirement for postoperative ICU admission, while secondary endpoints include total ICU stay, development of delirium in the first 48 hours, myocardial injury after non-cardiac surgery (MINS), acute kidney injury (AKI), and in-hospital mortality.

Inclusion and Exclusion Criteria

Inclusion Criteria

Age: Patients aged 65 years and older.

Diagnosis: Acute traumatic hip fracture (femoral neck, intertrochanteric, or subtrochanteric).

Surgical Intervention: Patients scheduled for and undergoing surgery (arthroplasty, osteosynthesis, etc.) for a hip fracture.

Data Integrity: Complete records of preoperative ASA score, laboratory findings, and postoperative follow-up notes.

Functional Information: Sufficient clinical notes to allow for retrospective CFS scoring.

Exclusion Criteria

Pathological and Periprosthetic Fractures: Fractures due to bone metastasis/tumors or fractures occurring around an existing prosthesis.

Multi-trauma: Presence of other major organ injuries or additional extremity fractures.

Conservative Follow-up: Patients not undergoing surgery due to medical contraindications or preference.

Missing Data: Patients with incomplete records or those transferred to another center immediately post-op.

Study Type

Observational

Enrollment (Estimated)

200

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Ankara, Turkey (Türkiye), 06630
        • Abdurrahman yurtarslan onkoloji eğitim ve araştırma hastanesi

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

Study Population

The study population consists of approximately 243 geriatric patients aged 65 years and older who underwent surgery for acute traumatic hip fracture (femoral neck, intertrochanteric, or subtrochanteric) at the Department of Anesthesiology and Reanimation, University of Health Sciences, Dr. Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital, between November 2023 and December 2025. The population includes patients with complete preoperative anesthesia records, ASA physical status scores, and sufficient clinical documentation for retrospective Clinical Frailty Scale (CFS) scoring

Description

Inclusion Criteria:Age: Patients aged 65 years and older.

Diagnosis: Patients diagnosed with acute traumatic hip fracture, including femoral neck, intertrochanteric, or subtrochanteric fractures.

Surgical Intervention: Patients who have undergone or are scheduled for surgical treatment (e.g., arthroplasty, internal fixation/osteosynthesis) for hip fracture.

Data Integrity: Availability of complete electronic health records, including preoperative anesthesia evaluation forms and ASA physical status scores.

Functional Assessment: Presence of sufficient clinical and nursing documentation to retrospectively determine the Clinical Frailty Scale (CFS) score based on preoperative functional status.

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Exclusion Criteria:Pathological and Periprosthetic Fractures: Fractures resulting from bone metastases or those occurring around an existing prosthesis.

Multiple Trauma: Patients with concomitant major organ injuries or additional limb fractures that could impact clinical outcomes.

Conservative Management: Patients who did not undergo surgical intervention and were managed non-surgically.

Incomplete Data: Cases with missing ASA scores, laboratory results, or postoperative clinical follow-up data in the hospital records.

Insufficient Functional Documentation: Patients whose clinical or nursing notes are inadequate for retrospective determination of the Clinical Frailty Scale (CFS) score.

Patient Transfer: Patients transferred to another healthcare facility preoperatively or in the immediate postoperative period, leading to incomplete data follow-up.

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Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Geriatric Hip Fracture Cohort
This cohort includes retrospective data from approximately 200 patients aged 65 and older who underwent surgery for hip fractures (femoral neck, intertrochanteric, or subtrochanteric) between November 2023 and November 2025. The study evaluates the requirement for Intensive Care Unit (ICU) admission following routine surgical and anesthesia (general or spinal) interventions. The primary focus is to comparatively analyze the predictive value of preoperative ASA physical status classification and Clinical Frailty Scale (CFS) scores on patients' postoperative ICU needs and clinical outcomes
Since this is a retrospective record review, no new intervention is administered. The intervention name represents the standard surgical (arthroplasty or osteosynthesis) and anesthetic (general or spinal) management received by patients for hip fractures according to institutional protocols. The study analyzes the relationship between these routine clinical processes and preoperative ASA and CFS scores

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Postoperative Intensive Care Unit (ICU) Admission Requirement
Time Frame: Within 24 hours postoperatively
Assessment of whether the patient required immediate postoperative admission to the intensive care unit due to clinical necessity, physiological instability, or the need for advanced monitoring.
Within 24 hours postoperatively

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Length of Stay in the Intensive Care Unit and Total Hospital Stay
Time Frame: From the day of surgery until hospital discharge, up to 1 year
Calculation of the total duration of stay in the intensive care unit (recorded in days) and the total hospital stay from the date of surgery until hospital discharge.
From the day of surgery until hospital discharge, up to 1 year
Postoperative Delirium
Time Frame: Up to 48 hours postoperatively
Assessment of clinical signs of delirium (such as acute confusion, disorientation, or agitation) as documented in medical and nursing follow-up notes.
Up to 48 hours postoperatively
Major Postoperative Complications
Time Frame: From the end of surgery until hospital discharge, up to 30 days
Frequency of major adverse events based on laboratory results and clinical findings, specifically including myocardial injury after non-cardiac surgery (MINS) and acute kidney injury (AKI).
From the end of surgery until hospital discharge, up to 30 days
In-hospital Mortality
Time Frame: From the day of surgery until hospital discharge, up to 30 days
Assessment of the all-cause mortality rate occurring during the patient's hospital stay following the surgical procedure.
From the day of surgery until hospital discharge, up to 30 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 30, 2026

Primary Completion (Estimated)

July 1, 2026

Study Completion (Estimated)

August 1, 2026

Study Registration Dates

First Submitted

April 1, 2026

First Submitted That Met QC Criteria

April 8, 2026

First Posted (Actual)

April 13, 2026

Study Record Updates

Last Update Posted (Actual)

May 28, 2026

Last Update Submitted That Met QC Criteria

May 24, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

The datasets generated during the current study are not publicly available due to institutional regulations and the sensitive nature of patient medical records but are available from the corresponding author on reasonable request

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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