Calle et al. (2014)
15
|
ColombiaPrado Clinic and CES University, Medellin |
Laparoscopic |
Patients with ASA surgical risk classification types 1 and 2; had no contraindications for administration of local anesthetics, NSAIDs, or acetaminophen; had an adequate level of understanding, i.e., being able to communicate by telephone and understand a numerical scale. |
Change in the standard anesthetic technique, hospitalization following hysterectomy, previous medical history of allergy to local anesthetics, and not being able to be reached by telephone |
Pain scale scores (VAS) at 24, 48, and 72 hours after surgery, opioid requirement after surgery |
Placebo |
100 / 97Sequence was generated using computer-generated randomization list in blocks, which were placed in sealed envelopes |
Triple blind: Patient, surgeon, and data analyst |
Bupivacaine 0.25%(96) |
I, II |
Laparoscopic-guided |
De Oliveira et al. (2011)
13
|
United States of AmericaNorthwestern University, Chicago |
Laparoscopic |
Healthy women undergoing laparoscopic hysterectomy |
Patients with previous history of allergy to local anesthetics, long-term use of opioid analgesics or corticosteroids, and pregnancy |
Quality of Recovery (QoR-40) at 24h; pain numeric scale score at 30 minutes, 60 minutes, and 24 hours; time to opioid requirement and cumulative opioid consumption at 24 hours, and number of postoperative antiemetics |
Placebo |
22 / 23Individuals were randomized into three groups using a computer-generated table of random numbers, and group assignments were sealed in sequentially numbered envelopes |
Double blind: patients, anesthesia care providers |
Ropivacaine 0.5%100 |
I, II |
Ultrasound |
Ghisi et al. (2016)
16
|
ItalyInstituti Ospitalieri Cremona |
Laparoscopic |
Patients between 18 and 70 years old, undergoing elective total laparoscopic hysterectomy |
Chronic opioid therapy in the previous 3 months before surgery, conversion to open surgical technique, BMI > 30 kg/m2 or < 18 kg/m2, postoperative recovery in intensive care unit, chronic therapy with antidepressants, known diagnosis of epilepsy or therapy with antiepileptic drugs, bilirubin level > 3.0 mg/dL, aspartate aminotransferase and/or alanine aminotransferase > 250 IU, creatinine level >1.4 mg/dL, pregnancy or lactation, known allergy to any drug used in the study, local infection at the block site, and drug or alcohol addiction. |
Postoperative pain at rest and during movement using NRS of 0 to 10, at 2, 4, 6, and 24 hours. Morphine requirement 24 hours, incidence of postoperative nausea and vomiting (PONV) using the Apfel score |
No block |
22 / 22Patients were randomized into two groups using computer-generated sequence of numbers placed in sealed envelopes |
Single blind: observer (data collection) |
Levobupivacaine 0.375%(75) |
I - III |
Ultrasound |
Guardabassi et al. (2017)
18
|
ArgentinaHospital Italiano de Buenos Aires |
Laparoscopic |
Patients between 18 and 70 years old; BMI < 35 kg/m2; undergoing total laparoscopic hysterectomy |
Previous medical history of allergy to local anesthetics; psychiatric disorders or dementia, abdominal wall infection; chronic use of analgesics, chronic pain syndrome; diagnosed peripheral neuropathy; known allergy to analgesics or corticoids. |
Pain NRS: non-randomized study scores at 60 minutes, 2, 8, and 24 hours after surgery; opioid consumption during the first 24 postoperative hours; adverse effects on quality of sleep of the first night after surgery; episodes of nausea and vomit; Ramsay sedation scale |
No block |
20 / 20Non-probability sampling of consecutive case series.Random assignment using sealed envelopes |
Single-blind: Data analysts |
Ropivacaíne 0.5%(75) |
I, II |
Ultrasound |
Bava et al. (2016)
17
|
ChinaDepartment of Anesthesiology and Operation, Hospital of People's Liberation Army. Xi'an |
Laparoscopic and LAVH |
Women scheduled for elective laparoscopic hysterectomy with benign lesions |
Patients with preoperative use of analgesics were excluded due to potential impact on postoperative analgesia requirement; BMI > 30 kg/m2; coagulopathy; contraindication for peripheral nerve block; any drug allergy |
Pain, with NRS: 30 and 60 minutes, 4, 8, 12, and 24 hoursPONV, Ramsay sedation scaleSatisfaction scores |
No block |
35 / 36Computer-generated randomization list in blocks, placed in sealed envelopes |
Double-blind: blinded to patients and data analysts, but not to members of the surgical and anesthesia care teams |
Ropivacaine 0.375%(112.5) |
— |
Ultrasound |
Kane et al. (2012)
14
|
United States of AmericaMetrohealth Medical Center, Case Western Reserve University, Cleveland |
Laparoscopic and single-port |
All women undergoing laparoscopic hysterectomy by a single surgeon between April and September 2011 were approached to participate in this study. |
Patients on chronic pain narcotic medications, or if they had allergy to local anesthetic. |
Numeric visual analog scales for pain and opioid requirement at 2 and 24 hours after surgery; quality of recovery (QoR-40 survey) at postoperative day 1 |
No block |
28 / 29Computer-based block randomization |
Single-blind: blinded to data analysts |
Ropivacaine 0.5% with epinephrine(100) |
— |
Ultrasound |