Literature DB >> 26224322

Nonsteroidal anti-inflammatory drugs for dysmenorrhoea.

Jane Marjoribanks1, Reuben Olugbenga Ayeleke, Cindy Farquhar, Michelle Proctor.   

Abstract

BACKGROUND: Dysmenorrhoea is a common gynaecological problem consisting of painful cramps accompanying menstruation, which in the absence of any underlying abnormality is known as primary dysmenorrhoea. Research has shown that women with dysmenorrhoea have high levels of prostaglandins, hormones known to cause cramping abdominal pain. Nonsteroidal anti-inflammatory drugs (NSAIDs) are drugs that act by blocking prostaglandin production. They inhibit the action of cyclooxygenase (COX), an enzyme responsible for the formation of prostaglandins. The COX enzyme exists in two forms, COX-1 and COX-2. Traditional NSAIDs are considered 'non-selective' because they inhibit both COX-1 and COX-2 enzymes. More selective NSAIDs that solely target COX-2 enzymes (COX-2-specific inhibitors) were launched in 1999 with the aim of reducing side effects commonly reported in association with NSAIDs, such as indigestion, headaches and drowsiness.
OBJECTIVES: To determine the effectiveness and safety of NSAIDs in the treatment of primary dysmenorrhoea. SEARCH
METHODS: We searched the following databases in January 2015: Cochrane Menstrual Disorders and Subfertility Group Specialised Register, Cochrane Central Register of Controlled Trials (CENTRAL, November 2014 issue), MEDLINE, EMBASE and Web of Science. We also searched clinical trials registers (ClinicalTrials.gov and ICTRP). We checked the abstracts of major scientific meetings and the reference lists of relevant articles. SELECTION CRITERIA: All randomised controlled trial (RCT) comparisons of NSAIDs versus placebo, other NSAIDs or paracetamol, when used to treat primary dysmenorrhoea. DATA COLLECTION AND ANALYSIS: Two review authors independently selected the studies, assessed their risk of bias and extracted data, calculating odds ratios (ORs) for dichotomous outcomes and mean differences for continuous outcomes, with 95% confidence intervals (CIs). We used inverse variance methods to combine data. We assessed the overall quality of the evidence using GRADE methods. MAIN
RESULTS: We included 80 randomised controlled trials (5820 women). They compared 20 different NSAIDs (18 non-selective and two COX-2-specific) versus placebo, paracetamol or each other. NSAIDs versus placeboAmong women with primary dysmenorrhoea, NSAIDs were more effective for pain relief than placebo (OR 4.37, 95% CI 3.76 to 5.09; 35 RCTs, I(2) = 53%, low quality evidence). This suggests that if 18% of women taking placebo achieve moderate or excellent pain relief, between 45% and 53% taking NSAIDs will do so.However, NSAIDs were associated with more adverse effects (overall adverse effects: OR 1.29, 95% CI 1.11 to 1.51, 25 RCTs, I(2) = 0%, low quality evidence; gastrointestinal adverse effects: OR 1.58, 95% CI 1.12 to 2.23, 14 RCTs, I(2) = 30%; neurological adverse effects: OR 2.74, 95% CI 1.66 to 4.53, seven RCTs, I(2) = 0%, low quality evidence). The evidence suggests that if 10% of women taking placebo experience side effects, between 11% and 14% of women taking NSAIDs will do so. NSAIDs versus other NSAIDsWhen NSAIDs were compared with each other there was little evidence of the superiority of any individual NSAID for either pain relief or safety. However, the available evidence had little power to detect such differences, as most individual comparisons were based on very few small trials. Non-selective NSAIDs versus COX-2-specific selectorsOnly two of the included studies utilised COX-2-specific inhibitors (etoricoxib and celecoxib). There was no evidence that COX-2-specific inhibitors were more effective or tolerable for the treatment of dysmenorrhoea than traditional NSAIDs; however data were very scanty. NSAIDs versus paracetamolNSAIDs appeared to be more effective for pain relief than paracetamol (OR 1.89, 95% CI 1.05 to 3.43, three RCTs, I(2) = 0%, low quality evidence). There was no evidence of a difference with regard to adverse effects, though data were very scanty.Most of the studies were commercially funded (59%); a further 31% failed to state their source of funding. AUTHORS'
CONCLUSIONS: NSAIDs appear to be a very effective treatment for dysmenorrhoea, though women using them need to be aware of the substantial risk of adverse effects. There is insufficient evidence to determine which (if any) individual NSAID is the safest and most effective for the treatment of dysmenorrhoea. We rated the quality of the evidence as low for most comparisons, mainly due to poor reporting of study methods.

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Year:  2015        PMID: 26224322      PMCID: PMC6953236          DOI: 10.1002/14651858.CD001751.pub3

Source DB:  PubMed          Journal:  Cochrane Database Syst Rev        ISSN: 1361-6137


  183 in total

1.  Effect of acetylsalicylic acid, paracetamol, and placebo on pain and blood loss in dysmenorrhoeic women.

Authors:  T Janbu; P Løkken; B I Nesheim
Journal:  Eur J Clin Pharmacol       Date:  1978-12-18       Impact factor: 2.953

2.  Efficacy of indomethacin suppository in primary dysmenorrhoea.

Authors:  N S al-Waili; Z D Khalaf
Journal:  Indian J Med Res       Date:  1990-08       Impact factor: 2.375

3.  A crossover comparison of bromfenac sodium, naproxen sodium, and placebo for relief of pain from primary dysmenorrhea.

Authors:  D R Mehlisch; R I Fulmer
Journal:  J Womens Health       Date:  1997-02       Impact factor: 2.681

4.  Endogenous prostaglandins in dysmenorrhea and the effect of prostaglandin synthetase inhibitors (PGSI) on uterine contractility.

Authors:  V Lundström; K Gréen; K Svanborg
Journal:  Acta Obstet Gynecol Scand Suppl       Date:  1979

5.  Efficacy of fenoprofen in the treatment of primary dysmenorrhea.

Authors:  R Osathanondh; B V Caldwell; A F Kaul; B J Sokoloff; R M White; J M Scavone; R A Burt; F Naftolin
Journal:  J Reprod Med       Date:  1985-12       Impact factor: 0.142

6.  Objective changes in intrauterine pressure during placebo treatment of dysmenorrhea.

Authors:  R P Smith
Journal:  Pain       Date:  1987-04       Impact factor: 6.961

7.  Ibuprofen is a useful treatment for primary dysmenorrhoea.

Authors:  I S Fraser; G McCarron
Journal:  Aust N Z J Obstet Gynaecol       Date:  1987-08       Impact factor: 2.100

8.  A double-blind cross-over study comparing flurbiprofen with naproxen-sodium for the treatment of primary dysmenorrhea.

Authors:  B Andersch; I Milsom
Journal:  Acta Obstet Gynecol Scand       Date:  1989       Impact factor: 3.636

9.  Naproxen in the treatment of OC-resistant primary dysmenorrhea. A double-blind cross-over study.

Authors:  J Jacobson; V Lundström; B Nilsson
Journal:  Acta Obstet Gynecol Scand Suppl       Date:  1983

Review 10.  Surgical interruption of pelvic nerve pathways for primary and secondary dysmenorrhoea.

Authors:  M L Proctor; P M Latthe; C M Farquhar; K S Khan; N P Johnson
Journal:  Cochrane Database Syst Rev       Date:  2005-10-19
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Authors:  Saima Rafique; Alan H Decherney
Journal:  Clin Obstet Gynecol       Date:  2017-09       Impact factor: 2.190

Review 3.  Pharmacological Management of Chronic Pelvic Pain in Women.

Authors:  Erin T Carey; Sara R Till; Sawsan As-Sanie
Journal:  Drugs       Date:  2017-03       Impact factor: 9.546

Review 4.  Current and Emerging Therapeutics for the Management of Endometriosis.

Authors:  Simone Ferrero; Fabio Barra; Umberto Leone Roberti Maggiore
Journal:  Drugs       Date:  2018-07       Impact factor: 9.546

Review 5.  Nonsteroidal anti-inflammatory drugs for pain in women with endometriosis.

Authors:  Julie Brown; Tineke J Crawford; Claire Allen; Sally Hopewell; Andrew Prentice
Journal:  Cochrane Database Syst Rev       Date:  2017-01-23

6.  Diagnosis and Treatment of Endometriosis. Guideline of the DGGG, SGGG and OEGGG (S2k Level, AWMF Registry Number 015/045, August 2020).

Authors:  Stefanie Burghaus; Sebastian D Schäfer; Matthias W Beckmann; Iris Brandes; Christian Brünahl; Radek Chvatal; Jan Drahoňovský; Wojciech Dudek; Andreas D Ebert; Christine Fahlbusch; Tanja Fehm; Peter Martin Fehr; Carolin C Hack; Winfried Häuser; Katharina Hancke; Volker Heinecke; Lars-Christian Horn; Christian Houbois; Christine Klapp; Heike Kramer; Harald Krentel; Jan Langrehr; Heike Matuschewski; Ines Mayer; Sylvia Mechsner; Andreas Müller; Armelle Müller; Michael Müller; Peter Oppelt; Thomas Papathemelis; Stefan P Renner; Dietmar Schmidt; Andreas Schüring; Karl-Werner Schweppe; Beata Seeber; Friederike Siedentopf; Horia Sirbu; Daniela Soeffge; Kerstin Weidner; Isabella Zraik; Uwe Andreas Ulrich
Journal:  Geburtshilfe Frauenheilkd       Date:  2021-04-14       Impact factor: 2.915

7.  The Role of Cyclooxygenase Enzymes in the Effects of Losartan and Lisinopril on the Contractions of Rat Thoracic Aorta.

Authors:  Fikriye Yasemin Ozatik; Bilgin Kaygisiz; Kevser Erol
Journal:  Eurasian J Med       Date:  2017-02

Review 8.  Co-occurrence of pain syndromes.

Authors:  Giannapia Affaitati; Raffaele Costantini; Claudio Tana; Francesco Cipollone; Maria Adele Giamberardino
Journal:  J Neural Transm (Vienna)       Date:  2019-11-29       Impact factor: 3.575

Review 9.  Nonsteroidal antiinflammatory drug resistance in dysmenorrhea: epidemiology, causes, and treatment.

Authors:  Folabomi A Oladosu; Frank F Tu; Kevin M Hellman
Journal:  Am J Obstet Gynecol       Date:  2017-09-06       Impact factor: 8.661

Review 10.  Non-prescription (OTC) oral analgesics for acute pain - an overview of Cochrane reviews.

Authors:  R Andrew Moore; Philip J Wiffen; Sheena Derry; Terry Maguire; Yvonne M Roy; Laila Tyrrell
Journal:  Cochrane Database Syst Rev       Date:  2015-11-04
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