Percutaneous Nephrolithotomy
Conditions
Keywords
Erector spinae block, percutaneous, nephrolithotomy, stone, ultrasound
Brief summary
To evaluate the ability of Erector spina Plane block decrease postoperative pain and analgesia requirements in patients undergoing Percutaneous Nephrolithotomy.
Detailed description
Erector spina Plane block was performed with guided ultrasound at T10 Transverse process level would lead to adequate postoperative analgesia ,in Percutaneous Nephrolithotomy surgeries.
Interventions
PROCEDUREnon- blocked Group (GROUP II)
This group was received no intervetion. Patients in all groups were provided with intravenous patient- controlled analgesia device containing morphine for postoperative analgesia.
PROCEDUREErector Spinae Plane block ( Group I)
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.
Sponsors
TC Erciyes University
Study design
Observational model
COHORT
Time perspective
RETROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
* ASA I- ASA II Patients
Exclusion criteria
* history of allergy to the study medication * refusal to participate
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| opioid consumption | 24 hours after surgery | 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). |
| Verbal analog Pain Scores on rest and movement | 24 hours after surgery | 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. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Demographic data | 24 hours after surgery | Age, BMI, ASA, Duration of surgery was recorded. |
| incidences of adverse effects (like nausea and vomiting) | 24 hours after surgery | incidences of nausea and vomiting during the 24 hours postoperative period was recorded recorded at 5 times intervals ( 2, 4, 6, 12, 24 hours). |
Countries
Turkey (Türkiye)
Outcome results
None listed