Comparison of efficacy of diclofenac and tramadol in relieving pain in patients of acute pancreatitis: A randomized parallel group double blind active controlled pilot study.


Journal

European journal of pain (London, England)
ISSN: 1532-2149
Titre abrégé: Eur J Pain
Pays: England
ID NLM: 9801774

Informations de publication

Date de publication:
03 2020
Historique:
received: 18 07 2019
revised: 22 11 2019
accepted: 25 11 2019
pubmed: 30 11 2019
medline: 21 11 2020
entrez: 30 11 2019
Statut: ppublish

Résumé

Opioids and non steroidal anti inflammatory drugs (NSAIDs) are commonly used for pain relief in acute pancreatitis (AP). Opioids carry risk of sphincter of oddi constriction. Although diclofenac prevents post endoscopic retrograde cholangio-pancreatography (ERCP) pancreatitis, few reports of diclofenac associated AP are also present. Although, both tramadol and diclofenac are commonly used for pain relief in AP, no study has evaluated their comparative efficacy and safety. Forty-six eligible participants were randomized to either diclofenac or tramadol. Primary objectives of our study were improvement in pain intensity on visual analogue scale (VAS pain score after 1 hr of drug administration) and number of patients requiring supplementary analgesia. The secondary objectives were total number of times of supplementary analgesia requirement, time to significant decrease (33%) in VAS pain score from baseline, number of painful days (VAS pain score >5), VAS pain score on 7th day, side effects, all cause death and complications of pancreatitis between the two groups. Although 46 patients were randomized, the final analysis included 41 participants. Five patients were withdrawn from the study (intubation = 3, altered sensorium = 2). No significant difference was seen in terms of VAS score after 1 hr of drug administration, number of patients requiring supplementary analgesic and number of painful days. However, time taken to significant reduction of pain was lower in the diclofenac group (p = .028). Both the agents were comparable in terms of safety. Although complications were less in the diclofenac group, the difference was not statistically significant. Both diclofenac and tramadol are equally effective in controlling pain in AP with similar safety profile. There are no studies that have compared the safety and efficacy of two commonly used analgesics for pain relief in patients with AP. We found that both diclofenac and tramadol are equally effective in decreasing the pain associated with AP. There is also no significant difference in the incidence of side effects between both the groups. Hence both diclofenac and tramadol can be used safely and effectively for pain control in AP. The trial was registered with clinical trials registry India (Number- CTRI/2018/05/014309).

Sections du résumé

BACKGROUND
Opioids and non steroidal anti inflammatory drugs (NSAIDs) are commonly used for pain relief in acute pancreatitis (AP). Opioids carry risk of sphincter of oddi constriction. Although diclofenac prevents post endoscopic retrograde cholangio-pancreatography (ERCP) pancreatitis, few reports of diclofenac associated AP are also present. Although, both tramadol and diclofenac are commonly used for pain relief in AP, no study has evaluated their comparative efficacy and safety.
MATERIALS AND METHODS
Forty-six eligible participants were randomized to either diclofenac or tramadol. Primary objectives of our study were improvement in pain intensity on visual analogue scale (VAS pain score after 1 hr of drug administration) and number of patients requiring supplementary analgesia. The secondary objectives were total number of times of supplementary analgesia requirement, time to significant decrease (33%) in VAS pain score from baseline, number of painful days (VAS pain score >5), VAS pain score on 7th day, side effects, all cause death and complications of pancreatitis between the two groups.
RESULTS
Although 46 patients were randomized, the final analysis included 41 participants. Five patients were withdrawn from the study (intubation = 3, altered sensorium = 2). No significant difference was seen in terms of VAS score after 1 hr of drug administration, number of patients requiring supplementary analgesic and number of painful days. However, time taken to significant reduction of pain was lower in the diclofenac group (p = .028). Both the agents were comparable in terms of safety. Although complications were less in the diclofenac group, the difference was not statistically significant.
CONCLUSION
Both diclofenac and tramadol are equally effective in controlling pain in AP with similar safety profile.
SIGNIFICANCE
There are no studies that have compared the safety and efficacy of two commonly used analgesics for pain relief in patients with AP. We found that both diclofenac and tramadol are equally effective in decreasing the pain associated with AP. There is also no significant difference in the incidence of side effects between both the groups. Hence both diclofenac and tramadol can be used safely and effectively for pain control in AP.
TRIAL REGISTRATION
The trial was registered with clinical trials registry India (Number- CTRI/2018/05/014309).

Identifiants

pubmed: 31782864
doi: 10.1002/ejp.1515
doi:

Substances chimiques

Anti-Inflammatory Agents, Non-Steroidal 0
Diclofenac 144O8QL0L1
Tramadol 39J1LGJ30J

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

639-648

Informations de copyright

© 2019 European Pain Federation - EFIC®.

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Auteurs

Nadipalli S Kumar (NS)

Department of Gastroenterology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Gaurav Muktesh (G)

Department of Gastroenterology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Tanvir Samra (T)

Department of Anaesthesiology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Phulen Sarma (P)

Department of Pharmacology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Jayanta Samanta (J)

Department of Gastroenterology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Saroj K Sinha (SK)

Department of Gastroenterology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Narendra Dhaka (N)

Department of Gastroenterology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Thakur D Yadav (TD)

Department of Surgery, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Vikas Gupta (V)

Department of Surgery, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Rakesh Kochhar (R)

Department of Gastroenterology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

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