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减压病的再加压及辅助治疗

Recompression and adjunctive therapy for decompression illness.

作者信息

Bennett M H, Lehm J P, Mitchell S J, Wasiak J

机构信息

Prince of Wales Hospital, Diving and Hyperbaric Medicine, Barker Street, Randwick, NSW, Australia, 2031.

出版信息

Cochrane Database Syst Rev. 2007 Apr 18(2):CD005277. doi: 10.1002/14651858.CD005277.pub2.

Abstract

BACKGROUND

Decompression illness (DCI) is due to bubble formation in the blood or tissues following the breathing of compressed gas. Clinically, DCI may range from a trivial illness to loss of consciousness, death or paralysis. Recompression is the universally accepted standard for the treatment of DCI. When recompression is delayed, a number of strategies have been suggested in order to improve the outcome.

OBJECTIVES

To examine the effectiveness and safety of both recompression and adjunctive therapies in the treatment of DCI.

SEARCH STRATEGY

We searched CENTRAL (The Cochrane Library 2005, Issue 2); MEDLINE (1966 to August 2005); CINAHL (1982 to August 2005); EMBASE (1980 to August 2005); the Database of Randomised Controlled Trials in Hyperbaric Medicine (August 2005), and hand-searched journals and texts.

SELECTION CRITERIA

We included randomized controlled trials that compared the effect of any recompression schedule or adjunctive therapy with a standard recompression schedule. We applied no language restrictions.

DATA COLLECTION AND ANALYSIS

Three authors extracted the data independently. We assessed each trial for internal validity and resolved differences by discussion. Data was entered into RevMan 4.2.

MAIN RESULTS

Two randomized controlled trials satisfied the inclusion criteria. Pooling of data was not possible. In one study there was no evidence of improved effectiveness with the addition of a non-steroidal anti-inflammatory drug (tenoxicam) to routine recompression therapy (at six weeks: relative risk (RR) 1.04, 95% confidence interval (CI) 0.90 to 1.20, P = 0.58) but there was a reduction in the number of compressions required when tenoxicam was added (P = 0.01, 95% CI 0 to 1). In the other study, the odds of multiple recompressions was lower with a helium and oxygen (heliox) table compared to an oxygen treatment table (RR 0.56, 95% CI 0.31 to 1.00, P = 0.05).

AUTHORS' CONCLUSIONS: Recompression therapy is standard for the treatment of DCI, but there is no randomized controlled trial evidence. Both the addition of an NSAID or the use of heliox may reduce the number of recompressions required, but neither improves the odds of recovery. The application of either of these strategies may be justified. The modest number of patients studied demands a cautious interpretation. Benefits may be largely economic and an economic analysis should be undertaken. There is a case for large randomized trials of high methodological rigour in order to define any benefit from the use of different breathing gases and pressure profiles during recompression therapy.

摘要

背景

减压病(DCI)是由于呼吸压缩气体后血液或组织中形成气泡所致。临床上,减压病的症状可轻可重,从轻微疾病到意识丧失、死亡或瘫痪不等。再加压治疗是治疗减压病普遍认可的标准方法。当再加压治疗延迟时,人们提出了多种策略以改善治疗效果。

目的

研究再加压治疗和辅助治疗在减压病治疗中的有效性和安全性。

检索策略

我们检索了Cochrane系统评价数据库(2005年第2期)、MEDLINE(1966年至2005年8月)、CINAHL(1982年至2005年8月)、EMBASE(1980年至2005年8月)、高压医学随机对照试验数据库(2005年8月),并对手检期刊和文献进行了检索。

选择标准

我们纳入了比较任何再加压方案或辅助治疗与标准再加压方案效果的随机对照试验。我们未设语言限制。

数据收集与分析

三位作者独立提取数据。我们评估了每项试验的内部效度,并通过讨论解决分歧。数据录入RevMan 4.2软件。

主要结果

两项随机对照试验符合纳入标准。无法进行数据合并。在一项研究中,常规再加压治疗添加非甾体类抗炎药(替诺昔康)后,没有证据表明有效性有所提高(六周时:相对危险度(RR)为1.04,95%置信区间(CI)为0.90至1.20,P = 0.58),但添加替诺昔康后所需的再加压次数减少(P = 0.01,95%CI为0至1)。在另一项研究中,与氧气治疗方案相比,氦氧混合气(heliox)方案进行多次再加压的几率更低(RR为0.56,95%CI为0.31至1.00,P = 0.05)。

作者结论

再加压治疗是减压病治疗的标准方法,但尚无随机对照试验证据。添加非甾体类抗炎药或使用氦氧混合气均可减少所需的再加压次数,但均不能提高康复几率。应用这些策略中的任何一种都可能是合理的。所研究的患者数量较少,需要谨慎解读。益处可能主要体现在经济方面,应进行经济分析。有必要开展方法学严谨的大型随机试验,以确定再加压治疗期间使用不同呼吸气体和压力模式的任何益处。

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