首页> 外文期刊>Pain medicine : >Combination of intrathecal opioids with bupivacaine attenuates opioid dose escalation in chronic noncancer pain patients.
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Combination of intrathecal opioids with bupivacaine attenuates opioid dose escalation in chronic noncancer pain patients.

机译:鞘内注射阿片类药物与布比卡因的组合可减轻慢性非癌性疼痛患者的阿片类药物剂量升高。

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OBJECTIVE: The purpose of this study was to examine the effect of intrathecal (IT) coadministration of bupivacaine with opioids during the initial phase of opioid titration and up to 1 year after implantation of an IT drug delivery system (IDDS). DESIGN: The study was designed as a retrospective study. OUTCOMES ANALYZED: The outcomes analyzed for this study were pain relief, oral opioid consumption, IT opioid, and bupivacaine dosage. METHODS AND PATIENT POPULATION: The patient population for this study were consecutively implanted patients over a period of 6 years in a tertiary single center with multiple practitioners. In this retrospective study, 126 consecutive noncancer intractable pain patients were implanted with IDDS and initiated with an IT opioid (O) as a single medication or an IT opioid and bupivacaine (O + B). Pain intensity, amount of oral opioids, dose, rate, and concentration of IT opioids and bupivacaine, and number and type of IT medication used were recorded at preimplant, implant, and at 3, 6, and 12 months postimplant. INTERVENTION: The intervention used for the study was the IT delivery device implant. RESULTS: Significant reduction in pain intensity was observed in both groups at 12 months postimplant (O group: baseline 7.42 +/- 2.1 to 5.85 +/- 2.8 [n = 72, P < 0.001]; O + B group 7.35 +/- 2 to 5.03 +/- 2.4 (n = 54; P < 0.001]). The combination of opioids with bupivacaine from the start of IT infusion treatment resulted in a reduced progression of opioid dose escalation in comparison to patients started with opioids (O group). The rate of increase of IT opioids in the O group at 12 months was 535 +/- 180%, whereas in the O + B, the dose increase was significantly lower at 185 +/- 85% (P < 0.004). In both groups, there was a statistically significant decrease in oral opioid consumption compared with preimplant doses. CONCLUSION: Concomitant initial coadministration of IT bupivacaine with opioids blunts the rate of IT opioid dose escalation during the first year after implant of an IDDS. More studies are necessary to thoroughly examine IT opioid dose escalation and the effects of addition of bupivacaine to IT opioids. Blunting IT opioid dose escalation may be a beneficial long-term effect of IT bupivacaine.
机译:目的:本研究的目的是检查在阿片类药物滴定的初始阶段以及植入IT药物递送系统(IDDS)后长达1年的鞘内(IT)联合布比卡因和阿片类药物的作用。设计:该研究被设计为回顾性研究。分析的结果:本研究分析的结果是缓解疼痛,口服阿片类药物,IT阿片类药物和布比卡因剂量。方法和患者人群:本研究的患者人群是在三级单一中心由多名从业者连续植入的患者,历时6年。在这项回顾性研究中,将126名连续的非癌性难治性疼痛患者植入IDDS,并以IT阿片类药物(O)作为单一药物或IT阿片类药物和布比卡因(O + B)进行治疗。在植入前,植入后以及植入后3、6和12个月记录疼痛强度,口服阿片类药物的量,IT阿片类药物和布比卡因的剂量,比率和浓度以及IT药物的使用数量和类型。干预:用于研究的干预措施是IT输送设备植入。结果:两组在植入后12个月的疼痛强度均明显降低(O组:基线7.42 +/- 2.1至5.85 +/- 2.8 [n = 72,P <0.001]; O + B组为7.35 +/- 2至5.03 +/- 2.4(n = 54; P <0.001]。与开始使用阿片类药物的患者相比,从IT输注治疗开始起,阿片类药物与布比卡因的组合导致阿片类药物剂量递增的进展减少(O组)。O组在12个月时IT阿片类药物的增加率为535 +/- 180%,而在O + B中,剂量增加显着降低至185 +/- 85%(P <0.004)。结论:IT布比卡因与阿片类药物同时并用最初的共同用药使IDDS植入后第一年IT阿片类药物剂量的上升速度变慢,两组之间的口服阿片类药物的消费量在统计学上均有显着降低。彻底检查IT阿片类药物剂量递增和阿迪的作用所必需的布比卡因对IT阿片类药物的治疗。钝化IT阿片类药物剂量增加可能是IT布比卡因的长期有益效果。

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