Ketamine as an adjuvant to opioids for cancer pain

被引:37
作者
Bell, Rae F. [1 ,2 ]
Eccleston, Christopher [3 ]
Kalso, Eija A. [4 ]
机构
[1] Haukeland Hosp, Ctr Pain Management & Palliat Care, N-5021 Bergen, Norway
[2] Haukeland Hosp, Reg Ctr Excellence Palliat Care, N-5021 Bergen, Norway
[3] Univ Bath, Cochrane Pain Palliat & Support Care Review Grp, Ctr Pain Res, Bath BA2 7AY, Avon, England
[4] Univ Helsinki, Cent Hosp, Dept Anaesthesia & Intens Care Med, Helsinki, Finland
来源
COCHRANE DATABASE OF SYSTEMATIC REVIEWS | 2012年 / 11期
关键词
Analgesics [adverse effects; therapeutic use; Chemotherapy; Adjuvant; Hallucinations [chemically induced; Ketamine [adverse effects; Morphine [adverse effects; Neoplasms [complications; Pain [drug therapy; etiology; Palliative Care; Randomized Controlled Trials as Topic; Adult; Humans; INTRATHECAL KETAMINE; SUBCUTANEOUS KETAMINE; MORPHINE-TOLERANCE; PALLIATIVE CARE; NEUROPATHIC PAIN; ORAL KETAMINE; DOSE KETAMINE; DOUBLE-BLIND; INFUSION; MANAGEMENT;
D O I
10.1002/14651858.CD003351.pub2
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Background This is an update of the original review published in Issue 1, 2003. Ketamine is a commonly used anaesthetic agent, and in subanaesthetic doses is also given as an adjuvant to opioids for the treatment of cancer pain, particularly when opioids alone prove to be ineffective. Ketamine is known to have psychotomimetic (including hallucinogenic), urological and hepatic adverse effects. Objectives To determine the effectiveness and adverse effects of ketamine as an adjuvant to opioids in the treatment of cancer pain. Search methods Studies were originally identified from MEDLINE (1966 to 2002), EMBASE (1980 to 2002), CancerLit (1966 to 2002), The Cochrane Library (Issue 1, 2001); by handsearching reference lists from review articles, trials, and chapters from standard textbooks on pain and palliative care. The manufacturer of ketamine (Pfizer Parke-Davis) provided search results from their in-house database, PARDLARS. An improved and updated search of the following was performed in May 2012: CENTRAL, MEDLINE & OVID MEDLINE R, EMBASE. Selection criteria Randomized controlled trials (RCTs) of adult patients with cancer and pain being treated with an opioid, and receiving either ketamine (any dose and any route of administration) or placebo or an active control. Studies having a group size of at least 10 participants who completed the trial. Data collection and analysis Two independent review authors identified four RCTs for possible inclusion in the review, and 32 case studies/case series reports. Quality and validity assessment was performed by three independent review authors, and two RCTs were excluded because of inappropriate study design. Patient-reported pain intensity and pain relief was assessed using visual analogue scales (VAS), verbal rating scales or other validated scales, and adverse effects data were collated. For the update three RCTs were identified for possible inclusion in the review. Main results Three new studies were identified by the updated search. All three were excluded from the review. Two studies were eligible for inclusion in the original review and both concluded that ketamine improves the effectiveness of morphine in the treatment of cancer pain. However, pooling of the data was not appropriate because of the small total number of participants (30), and the presence of clinical heterogeneity. Some patients experienced hallucinations on both ketamine plus morphine and morphine alone and were treated successfully with diazepam. No other serious adverse effects were reported. Authors' conclusions Since the last version of this review three new studies were identified but excluded from the review. Current evidence is insufficient to assess the benefits and harms of ketamine as an adjuvant to opioids for the relief of cancer pain. More RCTs are needed.
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页数:25
相关论文
共 50 条
[1]
Ketamine for chronic noncancer pain: concerns regarding toxicity [J].
Bell, Rae F. .
CURRENT OPINION IN SUPPORTIVE AND PALLIATIVE CARE, 2012, 6 (02) :183-187
[2]
Low-dose subcutaneous ketamine infusion and morphine tolerance [J].
Bell, RF .
PAIN, 1999, 83 (01) :101-103
[3]
British Medical Association and Royal Pharmaceutical Society of Great Britain, 2012, BRIT NATL FORMULARY, V63
[4]
HOW STUDY DESIGN AFFECTS OUTCOMES IN COMPARISONS OF THERAPY .1. MEDICAL [J].
COLDITZ, GA ;
MILLER, JN ;
MOSTELLER, F .
STATISTICS IN MEDICINE, 1989, 8 (04) :441-454
[5]
Currow DC, 2011, EUR J CANCER, V47, pS152
[6]
DICKENSON AH, 1994, CANCER SURV, V21, P5
[8]
Targeting the N-methyl-D-aspartate receptor for chronic pain management:: Preclinical animal studies, recent clinical experience and future research directions [J].
Fisher, K ;
Coderre, TJ ;
Hagen, NA .
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2000, 20 (05) :358-373
[9]
Fukuida E, 1981, IRYO, V35, P584
[10]
Garry AC, 1996, PAIN CLINIC, V9, P335