Abdominal Hysterectomy Clinical Trial
Official title:
Phase IV Study of Postoperative Pain Management
The investigators hypothesis is that patient controlled local anesthetics administered intraabdominally are more efficacious compared to continuous infusion in reducing postoperative pain and morphine consumption.
Open abdominal hysterectomy is a common procedure performed for many benign and malignant
gynaecological diseases and is associated with moderate to severe pain. Traditional methods
for postoperative pain management include patient controlled intravenous analgesia (PCA)
using morphine, epidural analgesia and spinal analgesia with opiates but recently, even
local aesthetic (LA) has been used intra-abdominally and into the abdominal wall. Although
epidural analgesia may be considered by some to be gold standard for pain relief following
abdominal surgery, a recent publication and past experience over several years may question
the use of invasive techniques for lower abdominal surgery. Thus, there is a trend towards
movement from central blocks towards other non-invasive methods for pain relief.
PCA with morphine is now commonly used for management of pain following major surgery and
compared to central blocks, has advantages in being relatively safe, easy to use and
associated with a high degree of patient satisfaction. However, the large doses of morphine
necessary to ensure adequate postoperative analgesia means that side effects such as
postoperative nausea and vomiting (PONV), tiredness, pruritus, headache and constipation may
be a major problem in this group of patients. Therefore, alternative techniques to reduce
morphine requirements are increasingly being used. These include the use of paracetamol,
non-steroidal anti-inflammatory drugs (NSAID) and recently local anaesthetics (LA). The
latter have been found to result in morphine sparing by 30 - 40 % and even a reduction in
postoperative nausea (PON). LA infused intraperitoneally is safe and effective and a recent
study showed that using 12.5 mg/h levobupivacaine could attain adequate analgesia. Thus,
efficacy of LA has been established as well as the dose. However, the method of
administration of LA intraperitoneally remains unclear.
This study is designed with the primary aim of studying whether morphine consumption can be
reduced postoperatively using the patient-controlled administration system for
intraperitoneal LA compared to a continuous infusion, and whether this translates into
improved recovery parameters or reduced side effects and improved patient satisfaction.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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