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蔗糖用于接受疼痛性操作的新生儿镇痛。

Sucrose for analgesia in newborn infants undergoing painful procedures.

作者信息

Stevens B, Ohlsson A

机构信息

Paediatrics, Mount Sinai Hospital, 600 University Avenue, Toronto, Ontario, Canada.

出版信息

Cochrane Database Syst Rev. 2000(2):CD001069. doi: 10.1002/14651858.CD001069.

Abstract

BACKGROUND

Management of pain for neonates is less than optimal. The administration of sucrose with and without non-nutritive sucking (pacifiers) has been the most frequently studied non-pharmacological intervention for relief of procedural pain in neonates.

OBJECTIVES

To determine the efficacy, effect of dose, and safety of sucrose for relieving procedural pain as assessed by physiologic and/or behavioural indicators.

SEARCH STRATEGY

Standard methods as per the Neonatal Collaborative Review Group. A MEDLINE search was carried out for relevant randomized controlled trials (RCTs) published from January 1966 - November 1, 1997; EMBASE from 1993-1997; Reference Update search on November 11, 1997 and search of the Cochrane Library Issue 4 on November 11, 1997. Key words and (MeSH) terms included, infant/newborn, pain, analgesia and sucrose. Personal files, bibliographies, the most recent relevant neonatal and pain journals and conference proceedings were searched manually. Unpublished studies were not included. Language restrictions were not imposed.

SELECTION CRITERIA

RCTs in which term and/or preterm neonates undergoing heel lance, venepuncture or intramuscular injection (immunization) received sucrose or water/placebo or no intervention.

DATA COLLECTION AND ANALYSIS

Trial quality was assessed according to the methods of the Neonatal Collaborative Review Group. Quality measures included; blinding of randomization, blinding of intervention, completeness of follow up and blinding of outcome measurement. Data were abstracted and independently checked for accuracy by the two investigators. The inconsistency in outcome measures and differences in the statistical reporting of results made meta-analysis impossible. We were not able to identify two studies in which the same physiologic and/or behavioral outcomes following a noxious stimulus (heel-lance, venepuncture, intramuscular injection) were measured and reported in an identical fashion using means and standard deviations (or standard errors). The results are therefore reported for each accepted study separately.

MAIN RESULTS

Fifteen studies were identified for possible inclusion in this systematic review. Five studies were excluded; three RCTs were excluded as in these trials the number of infants randomized to treatment vs. placebo groups were not reported; one study was not an RCT, and in one RCT the neonates did not undergo a painful procedure. Ten RCTs were included in this review. Sucrose in a wide range of dosages was generally found to decrease univariate physiologic (heart rate) and behavioural (the mean percent time crying, total cry duration, duration of first cry, and facial action) pain indicators and multivariate [Premature Infant Pain Profile (PIPP)] pain outcomes in neonates undergoing heelstick or venepuncture. An optimal dose of sucrose to reduce pain associated with procedures in preterm and term neonates could not be identified through this systematic review.

REVIEWER'S CONCLUSIONS: Sucrose reduces physiologic and/or behavioral indicators of stress/pain in neonates following procedural pain stimuli (heel lance, venepuncture, immunization). There was inconsistency in the dose of sucrose that was effective and an optimal dose to be used in preterm and/or term infants could not be identified. Considerations for future research are to describe the painful procedure and intervention in detail, to use appropriate sample size to show a statistically significant reduction in pain, to use a multidimensional conceptualization of pain, to select outcome measures that are reliable and valid pain indicators and to account for the variation in the infant's response and context in which the pain is experienced. The use of repeated administrations of sucrose in neonates needs to be investigated. Use of sucrose in neonates that are very low birth weight, unstable and/or ventilated also needs to be addressed. (ABSTRACT TRUNCATED)

摘要

背景

新生儿疼痛管理尚不尽如人意。给予蔗糖并配合或不配合非营养性吸吮(安抚奶嘴)是针对缓解新生儿程序性疼痛研究最为频繁的非药物干预措施。

目的

通过生理和/或行为指标评估,确定蔗糖缓解程序性疼痛的疗效、剂量效应及安全性。

检索策略

采用新生儿协作审查组的标准方法。对1966年1月至1997年11月1日发表的相关随机对照试验(RCT)进行MEDLINE检索;检索1993 - 1997年的EMBASE;1997年11月11日进行参考文献更新检索,并于1997年11月11日检索考克兰图书馆第4期。关键词及(医学主题词)包括婴儿/新生儿、疼痛、镇痛和蔗糖。手动检索个人档案、参考文献目录、最新相关的新生儿和疼痛期刊以及会议论文集。未纳入未发表的研究。未设语言限制。

选择标准

纳入足月儿和/或早产儿接受足跟采血、静脉穿刺或肌肉注射(免疫接种)并接受蔗糖或水/安慰剂或未接受干预的随机对照试验。

数据收集与分析

根据新生儿协作审查组的方法评估试验质量。质量指标包括随机分组的盲法、干预措施的盲法、随访的完整性以及结果测量的盲法。数据由两名研究人员提取并独立核对准确性。由于结果测量的不一致以及结果统计报告的差异,无法进行荟萃分析。我们未能找到两项以相同方式使用均值和标准差(或标准误)测量并报告有害刺激(足跟采血、静脉穿刺、肌肉注射)后相同生理和/或行为结果的研究。因此,分别报告每项纳入研究的结果。

主要结果

确定了15项可能纳入本系统评价的研究。排除5项研究;排除3项随机对照试验,因为这些试验未报告随机分配至治疗组与安慰剂组的婴儿数量;1项研究不是随机对照试验,且1项随机对照试验中的新生儿未接受疼痛操作。本评价纳入10项随机对照试验。一般发现,各种剂量的蔗糖均可降低接受足跟采血或静脉穿刺的新生儿的单变量生理(心率)和行为(平均哭闹时间百分比、总哭闹持续时间、首次哭闹持续时间及面部动作)疼痛指标以及多变量[早产儿疼痛量表(PIPP)]疼痛结果。通过本系统评价无法确定降低早产儿和足月儿与操作相关疼痛的最佳蔗糖剂量。

综述作者结论

蔗糖可减轻新生儿在程序性疼痛刺激(足跟采血、静脉穿刺、免疫接种)后应激/疼痛的生理和/或行为指标。有效蔗糖剂量存在不一致性,无法确定用于早产儿和/或足月儿的最佳剂量。未来研究的考虑因素包括详细描述疼痛操作和干预措施、使用适当样本量以显示疼痛有统计学意义的显著减轻、采用疼痛的多维概念化、选择可靠且有效的疼痛指标作为结果测量,并考虑婴儿反应的差异以及疼痛发生的背景。需要研究在新生儿中重复给予蔗糖的情况。还需探讨在极低出生体重、不稳定和/或接受通气的新生儿中使用蔗糖的情况。(摘要截选)

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