Cochrane Database of Systematic Reviews 2007
DOI: 10.1002/14651858.cd004959.pub3
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Opioids for chronic low-back pain

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Cited by 125 publications
(56 citation statements)
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“…Women become amenorrheic or develop anovulatory menstrual cycles and reported reduced libido soon after initiating treatment with sustained-action opioid analgesics [103]. Hormone supplementation with testosterone in males and estrogen and progestin in females improves libido [47,98,105]. Infertility is a major negative health consequence of low levels of GnRH, FSH and LH in women.…”
Section: Opioid Endocrinopathy -Effects Of Suppression Of Hypothalamomentioning
confidence: 99%
See 1 more Smart Citation
“…Women become amenorrheic or develop anovulatory menstrual cycles and reported reduced libido soon after initiating treatment with sustained-action opioid analgesics [103]. Hormone supplementation with testosterone in males and estrogen and progestin in females improves libido [47,98,105]. Infertility is a major negative health consequence of low levels of GnRH, FSH and LH in women.…”
Section: Opioid Endocrinopathy -Effects Of Suppression Of Hypothalamomentioning
confidence: 99%
“…Some of the reviews reanalyzed pooled data from multiple RCTs and showed opioids have limited efficacy in reducing pain (TABLE 3). Two Cochrane reviews found non-significant pain reduction with opioids in chronic low back pain (LBP) patients [32,47]. Opioids decreased pain in osteoarthritis (OA) of hip or knee joint, but the overall benefit was small, corresponding to a difference in pain scores of 0.9 cm on a 10 cm visual analog scale (VAS) or 15% pain reduction [48].…”
mentioning
confidence: 99%
“…14 In addition to NSAIDs and opioids, other therapies used for the treatment of CLBP include antidepressants, paracetamol (acetaminophen), muscle relaxants and steroids. 15 Although NSAIDs and opioids are the most widely used of these treatments, there is still a lack of sufficient evidence regarding their effectiveness in managing CLBP 3,14,16,17 or in improving daily functioning, 3,14,16 -21 whilst concerns regarding their long-term safety and tolerability still exist. 17,19,22,23 The aim of the two randomized, parallelgroup studies reported here was to compare the analgesic efficacy, tolerability and safety of celecoxib, a cyclo-oxygenase-2 (COX-2) selective NSAID, and tramadol hydrochloride (HCl), a 'weak' opioid with relatively low addiction potential, in patients with CLBP.…”
Section: Celecoxib Versus Tramadol In Clbp Patientsmentioning
confidence: 99%
“…The analgesic efficacy of celecoxib has been shown to be similar to that of non-selective NSAIDs, 41 -44 while recent systematic reviews have concluded that opioids may be effective in reducing pain and improving functionality in subjects with chronic pain. 17,19,21 As previously discussed, safety is also a key consideration when assessing analgesic therapies; the welldocumented GI and CV risks associated with both non-selective and COX-2 selective NSAIDs 29 and the abuse potential of stronger opioids, such as oxycodone and morphine 45 should be considered before deciding on the most appropriate treatment.…”
Section: Celecoxib Versus Tramadol In Clbp Patientsmentioning
confidence: 99%
“…These treatments range from educational programs [8] to behavioural cognitive therapy [9], medication [10], electrophysical agents [11], manual therapy [12-14] (e.g. joint mobilisation/manipulation, myofascial release), general exercises [15] and specific spinal stabilisation exercises [16], among others [7].…”
Section: Introductionmentioning
confidence: 99%