Postop Pain in the MICS Patients Versus Sternotomy Patients

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

179 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-06-01

Study Completion Date

2018-01-30

Brief Summary

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To adequately assess postoperative pain in the coronary artery bypass surgical population a multicentered retrospective chart review was carried out; the study utilized a nonexperimental comparative descriptive study design. The retrospective review was conducted over a six-month time frame, consisting of June 2017 through November 2017, at two hospitals within the same organization. The data collection process began in late December of 2017 and January of 2018. The assessment of postop pain was performed by using a standard 11-point numeric pain rating scale on post extubation day one and the day of discharge.

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Detailed Description

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Conditions

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Pain, Postoperative Surgery

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Minimally Invasive Cardiac Bypass patients

Coronary bypass surgery

Intervention Type PROCEDURE

Reviewed postoperative coronary bypass patients and compared postoperative pain levels

Traditional Sternotomy Cardiac Bypass patients

Coronary bypass surgery

Intervention Type PROCEDURE

Reviewed postoperative coronary bypass patients and compared postoperative pain levels

Interventions

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Coronary bypass surgery

Reviewed postoperative coronary bypass patients and compared postoperative pain levels

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patients who had an isolated coronary artery bypass surgery at Charlotte Medical Center (CMC) and CMC-Pineville
* Minimally invasive cardiac surgery
* Traditional sternotomy cardiac surgery

Exclusion Criteria

* Documented history of any chronic pain syndromes requiring active treatment
* The "relative" recent requirement of narcotic analgesic use for pain relief prior to operation
* Any CABG operation that inadvertently resulted in an operative surgical complication
* Patient cases that resulted in a readmission within 30 days from surgery.

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes