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新生儿重症监护病房中的药物输注相容性。

Compatibility of drug infusions in the NICU.

机构信息

Institute of Clinical Medicine, University of Oslo, Norway.

出版信息

Arch Dis Child. 2010 Sep;95(9):745-8. doi: 10.1136/adc.2009.174268. Epub 2010 Jun 22.

DOI:10.1136/adc.2009.174268
PMID:20570841
Abstract

OBJECTIVES

The majority of drugs used in sick newborns receiving intensive care are unlicensed and off-label, exposing infants to greater risk of adverse drug reactions (ADRs). Our aim was to study the compatibility of co-infusions for a selected group of drugs and nutrition solutions as part of our quality assurance programme in the neonatal intensive care unit.

METHODS

The authors reviewed drug studies in the literature. Documented compatibility or the lack thereof was the main end point for the 1042 co-infusions investigated. The results of searches were reviewed against predetermined criteria for co-infusion of 13 intensive care drugs with 66 other drugs and two nutrition solutions and albumin.

RESULTS

33/820 (4%) co-infusions were documented as compatible without any restrictions. 212/820 (26%) drug co-infusions were compatible, but 196 of the 212 (93%) had restrictions on infusion fluid, concentration or contact time. 608/820 (74%) drug co-infusions in neonates have either been shown to be incompatible or have not been tested. Among those not tested, 163/486 (34%) entailed major differences in pH level which could cause co-infusion instability.

CONCLUSION

There is a lack of data on compatibility for the majority of drugs used for co-infusions in neonates. Caregivers therefore need to pay special attention to infusion lines when drugs are co-administered. Our results suggest that further studies on drug compatibility are needed to reduce possible ADRs and toxicity, and avoid precipitation and occlusion of infusion lines in critically ill neonates.

摘要

目的

在接受重症监护的患病新生儿中,大多数使用的药物都未经许可和超适应证使用,这使婴儿面临更大的药物不良反应风险。我们的目的是研究选定药物和营养溶液的混合输注的相容性,作为新生儿重症监护病房质量保证计划的一部分。

方法

作者查阅了文献中的药物研究。1042 次共输注的主要终点是记录的相容性或缺乏相容性。对搜索结果进行了审查,以对照预定标准进行审查,这些标准规定了 13 种重症监护药物与 66 种其他药物以及两种营养溶液和白蛋白的共输注。

结果

33/820(4%)的共输注被记录为无任何限制的相容。212/820(26%)的药物共输注是相容的,但其中 196/212(93%)对输注液、浓度或接触时间有限制。608/820(74%)新生儿的药物共输注要么显示不相容,要么尚未经过测试。在未经过测试的药物中,163/486(34%)涉及 pH 值的重大差异,这可能导致共输注不稳定。

结论

大多数用于新生儿共输注的药物的相容性数据不足。因此,护理人员在药物同时给药时需要特别注意输注管路。我们的结果表明,需要进一步研究药物相容性,以降低潜在的药物不良反应和毒性,并避免在危重病新生儿中出现输注管路沉淀和阻塞。

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