Background: Acute pain in the postoperative phase affects around 80% of patients, with nearly 86 percent experiencing moderate to severe pain [1]. To reduce postoperative pain and improve results, enhanced recovery after surgery (ERAS) proposes a multimodal analgesic regimen [2]. The multimodal analgesic regimen prioritises the decrease of opioid analgesia reliance, and pain is handled at different levels using different mechanisms of action, thereby treating pain and reducing complications associated with any specific medicine. Various methods (regional anaesthesia, nerve blocks, local infiltration) and medications, including non-opiate nonsteroidal anti-inflammatory drugs, paracetamol, Cyclooxygenase2 inhibitors, NMDA receptor antagonists, gabapentins, pregabalins, and alpha 2 receptor agonists, and opioids, are incorporated into the treatment regimen as needed. After 12-24 hours of administration, the transdermal fentanyl patch provides steady-state plasma levels, and the plasma levels remain stable for the remaining 72 hours, providing effective analgesia [3].
The primary goal of
this study was to evaluate pain treatment in the postoperative period using a
transdermal fentanyl patch in opioid-naive patients, and the secondary goal was
to evaluate any associated side effects.
Material and
Methods: A total of 44 patients were randomly assigned to one of two groups.
The groups were labelled as FP (Fentanyl patch) and P (Paracetamol patch) (
Placebo). The Patch was applied 10-12 hours before surgery, and the patient was
monitored for pain by NRS for 72 hours after surgery (Numeric Rating Scale).
All of the patients were regularly given Paracetamol and Diclofenac Sodium.
Tramadol was given as a rescue analgesic if the NRS scale was more than 5. The
data was analysed using the Windows stat version 9.2 of Indostat services.
Results: There was
a statistically significant difference in Tramadol intake over 72 hours between
patients in the FP group (19.44mg) and the P group (72.22mg). The FP group also
had significantly lower Numerical Rating scale scores of 8, 16, 24, 32, 40, 48,
56, 64, and 72 hours. The FP group had the greatest difference in pain score at
24 hours. Sedation, pruritus, respiratory depression, nausea, and vomiting
scores did not differ between the two groups.
Author(S) Details
S. Kalyani Surya Dhana Lakshmi
Department of Anaesthesiology, AIIMS Bibinagar Hyderabad, Telangana, India.
C. N. Chandrasekhar
Department of Anaesthesiology, AIIMS Bibinagar Hyderabad, Telangana, India.
View Book:- https://stm.bookpi.org/NHMMR-V2/article/view/6129
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