Erector Spinae Plane Block for Postoperative Pain in Percutaneous Nephrolithotomy Patients: a Retrospective Study

TC Erciyes University60 enrolled

Overview

To evaluate the ability of Erector spina Plane block decrease postoperative pain and analgesia requirements in patients undergoing Percutaneous Nephrolithotomy.

Erector spina Plane block was performed with guided ultrasound at T10 Transverse process level would lead to adequate postoperative analgesia ,in Percutaneous Nephrolithotomy surgeries.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Percutaneous Nephrolithotomy

Interventions

Erector Spinae Plane block ( Group I)PROCEDURE

ESP Block was performed preoperative to all patients in ESP block group. Patients in all groups were provided with intravenous patient- controlled analgesia device containing morphine for postoperative analgesia.

non- blocked Group (GROUP II)PROCEDURE

This group was received no intervetion. Patients in all groups were provided with intravenous patient- controlled analgesia device containing morphine for postoperative analgesia.

Eligibility

Sex: ALLMin age: 18 YearsMax age: 65 Years

Medical Language ↔ Plain English

Inclusion Criteria: * ASA I- ASA II Patients Exclusion Criteria: * history of allergy to the study medication * refusal to participate

Locations (1)

Sibel Seçkin Pehlivan

Kayseri, Talas, Turkey (Türkiye)

Outcomes

Primary Outcomes

opioid consumption

In the recovery room, all patients were given a patient- controlled analgesia device containing morphine 0.5 mg/ml, set to deliver a 1mg bolus dose of morphine with an 10 min lockout time and 10 mg 4 h limit.Total morphine consumption during the 24 hours postoperative period will recorded at 5 times intervals ( 2, 4, 6, 12, 24 hours).

Time frame: 24 hours after surgery

Verbal analog Pain Scores on rest and movement

A Research assistant, blinded to the group allocation, interviewed patients and collected data at 5 times intervals ( 2, 4, 6, 12, 24, hours) in the 24 hours postoperatively. Patients were asked to rate their pain using verbal analog scale, where 0= no pain and 10= worst pain possible.

Time frame: 24 hours after surgery

Secondary Outcomes

Demographic data

Age, BMI, ASA, Duration of surgery was recorded.

Time frame: 24 hours after surgery

incidences of adverse effects (like nausea and vomiting)

incidences of nausea and vomiting during the 24 hours postoperative period was recorded recorded at 5 times intervals ( 2, 4, 6, 12, 24 hours).

Time frame: 24 hours after surgery

Data from ClinicalTrials.gov

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