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6589

ASSOCIATION OF SURGICAL OUTCOMES AND EPIDURAL ANALGESIA EFFICACY, A SCORING ANALYSIS OF SUCCESS, PARTIAL SUCCESS, AND FAILURE

Part of Topic

Scientific Abstracts > Regional Anesthesia

INTRO

Postoperative epidural analgesia (EA) is among the most frequently performed procedures in daily anesthetic practice.

Traditionally, the evaluation of epidural analgesia effectiveness is categorized dichotomously as either successful or failed.

However, clinical experiences highlight significant variability in what constitutes a failure, emphasizing the complexity of

such evaluations.

Identifying partial or complete failures of epidural analgesia in the postoperative phase should incorporate clinically

relevant criteria, expert consensus, and implications for patient outcomes. Notably, institutional variations in defining and

assessing epidural analgesia failure introduce complexities in standardizing definitions and interpreting outcomes across

different centers. Moreover, local hospital culture and clinical practices significantly influence the recognition and

categorization of EA outcomes.

• This report presents a single-center review from Massachusetts General Hospital (MGH), outlining an expert-

informed and literature-supported grading system for evaluating epidural analgesia effectiveness. Based on expert

opinions and a comprehensive literature review, the authors developed a grading system to categorize epidural

analgesia outcomes across a spectrum ranging from complete failure through partial success to full success. ( Table

1) We hypothesize that partially successful epidural analgesia—where pain persists despite ongoing epidural use—

may result in delayed hospital discharge and increased hospitalization costs, representing primary outcomes of

interest—total morphine usage and out-of-bed time or hypotension between groups were our 2ndary outcomes.

 

METHODS

•Data Collection: Retrospective chart review (IRB #2023P003125) at a tertiary hospital, including patients receiving

thoracic or lumbar EA between January 1, 2022, and September 1, 2024.

Inclusion Criteria: Adult patients (≥18 years) who received thoracic or lumbar epidural catheters for postoperative

analgesia between May 2017 and September 2024.

Exclusion Criteria: Pregnancy, other regional analgesia techniques, multiple surgeries in one admission, opioid use

disorder, cardiac surgery, pos-op intubation, or history of spine pathology.

•Outcome Classification: Developed a novel scoring system categorizing EA outcomes into success (score = 0), partial

success (score = 1-2), and failure (score >2), based on the following factors :

•Statistical Analysis:

• Internal consistency measured using Cronbach’s alpha and McDonald’s omega.

• Linear regression assessed the impact of EA outcomes on hospital length of stay (HLOS).

• Cost analysis and opioid consumption comparisons were performed between groups by Non-parametric Kruskal-

Wallis test.

RESULTS

•Patient Distribution: Among 1,425 patients, 329 ( 23%) were classified as Successful, 718 as Partially Successful( 50%),

and 378 (27%) as Failure. Demographic and key outcomes are reflected in Table 2

•Reliability Metrics:

• Cronbach’s alpha = 0.45

• McDonald’s omega = 0.52

•Hospital Outcomes:

• The Failure group had a significantly longer HLOS compared to the Successful group (β = 1.02, p < 0.05) and the

Partially Successful group (β = 0.8, p < 0.05).

• No significant HLOS difference between Successful and Partially Successful groups (β = 0.24, p = 0.26).

•Costs and Opioid Consumption:

• The Failure group incurred higher hospitalization costs and greater morphine equivalent consumption than the

other groups.

• No significant differences in out-of-bed time or hypotension between groups.

 

DISCUSSION

This study is the first to introduce a structured, point-based scoring system that classifies

epidural analgesia (EA) outcomes into success, partial success, and failure. The findings

reveal that EA failure is significantly associated with longer hospital length of stay (LOS),

higher opioid consumption, and increased costs. Patients in the failure group had a mean

LOS of 7.87 days, significantly longer than the partially successful (6.86 days) and successful

(6.43 days) groups. Opioid use followed a stepwise increase, with the failure group

consuming nearly double the morphine equivalents of the partial success group and five

times that of the success group. The scoring system showed moderate internal consistency

(Cronbach’s alpha = 0.45, McDonald’s omega = 0.52), indicating the need for further

Non-Cognitive Predictors of Student Success:

refinement while capturing key clinical dimensions of EA performance.

A Predictive Validity Comparison Between Domestic and International Students

Despite the clear impact of EA failure on LOS and opioid use, no significant differences were

observed in time to ambulation or hypotension rates, suggesting that suboptimal EA does

not necessarily impair early mobilization or hemodynamic stability. The strong association

between EA failure and increased resource utilization underscores the importance of early

failure detection and intervention. Future efforts should refine this scoring system to

improve predictive accuracy and integrate it into clinical practice, ensuring timely

adjustments in analgesic management and optimizing patient outcomes.

Our study’s findings are well-supported by existing literature. McLeod et al. reported

epidural failure rates of approximately 20%, with 13% due to technical failure, reinforcing

the need for a precise scoring system to classify outcomes. Groen et al.’s meta-analysis

showed that epidural failures increase complications, length of stay, and opioid

consumption, consistent with our results. Aloia et al. and Desai et al. also confirmed that

successful epidurals reduce opioid use. However, Halabi et al. and Kone et al. noted that

epidurals may prolong hospital stays and increase costs in some settings, supporting the

need for a systematic approach to identify and manage epidural failure.

The criteria utilized within our grading system demonstrated strong internal consistency.

This ongoing study has now expanded to include approximately 4,000 patients. The

subsequent phase involves assessing both the internal and external validity of our grading

system, followed by a comprehensive final analysis.

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