Pain control infusion pumps: a prospective randomized evaluation in bilateral total knee arthroplasty.

Abstract:

:We prospectively monitored pain scores on 24 patients who underwent bilateral total knee arthroplasty (TKA). Patients were blinded to receiving either a functional or placebo pain control infusion pumps. After 3 days, pump volume was recorded, and patients were asked to identify which knee they believed received the functional pain control infusion pump. Fourteen patients (58%) correctly identified their knee with the functional pain control infusion pump. Pump volumes ranged from 70 to 310 mL, with an average flow rate of 4.3 mL/hour. Positive identification rates were similar to rates routinely generated from standard placebo symptom treatment pain trials (0%-60%). Our data suggest that the placebo effect plays at least a partial role in pain control infusion pump effectiveness, and that pain control infusion pump use for TKA unpredictably contributes to postoperative pain management. [corrected]

journal_name

Orthopedics

journal_title

Orthopedics

authors

Argintar E,Armstrong B,Zawadsky M,Evans B,Romness D

doi

10.3928/01477447-20110124-18

subject

Has Abstract

pub_date

2011-03-01 00:00:00

pages

188

issue

3

eissn

0147-7447

issn

1938-2367

journal_volume

34

pub_type

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