Analgesic management of uncomplicated acute sickle-cell pain crisis in pediatrics: a systematic review and meta-analysis.
Analgesic management of uncomplicated acute sickle-cell pain crisis in pediatrics: a systematic review and meta-analysis.
复制标题
对儿科中简单的急性镰状细胞疼痛危机的镇痛治疗:系统评价和荟萃分析。
DOI:
10.1016/j.jped.2019.05.004
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发表时间:
2020-03
影响因子:
3.3
通讯作者:
Zhao, Dongchi
中科院分区:
文献类型:
--
作者:
Saramba, Manou Irmina;Shakya, Sandeep;Zhao, Dongchi
To capture evidence of the efficacy and safety of pharmacological analgesia for uncomplicated acute sickle-cell pain in pediatric patients compared to placebo. Searches for key evidence were performed from March 1 to 31, 2018, for randomized controlled trials of pharmacological analgesia compared to placebo for uncomplicated acute sickle-cell pain in a pediatric sample. The authors searched ten scientific databases including, among others, PubMed, MEDLINE, Embase, and Clinicaltrials.gov for this systematic review and meta-analysis. Four trials (n = 227) were selected by the inclusion criteria (intranasal fentanyl, intravenous magnesium, arginine, and inhaled nitric oxide). The quality of evidence ranged from low to moderate for each outcome. Meta-analysis of changes in the ladder of pain score (p = 0.72), length-of-stay in hospital (p = 0.65), and amount of narcotics used during the study (p = 0.10) showed non-statistically significant differences and a lack of amelioration provided by pharmaceutical analgesics in treatment group. The adverse events reported that more participants in the intervention arm underwent pain, with statistically significant differences at the drug delivery site in studies using intranasal fentanyl and intravenous magnesium (p = 0.03). Pharmacological analgesia appears to be uncertain in improving the intensity and providing relief of acute pain crisis in pediatric patients with sickle-cell anemia. With respect to clinical advantage, no decisive deduction about the clinical efficacy may be made regarding these medications in acute sickle-cell pain management in the pediatric age group.
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影响因子:
2.6
作者:
Adegoke, Samuel Ademola;Shehu, Umar Abdullahi;Oyelami, Oyeku Akibu
通讯作者:
Oyelami, Oyeku Akibu
影响因子:
12.8
作者:
Archer N;Galacteros F;Brugnara C
通讯作者:
Brugnara C
影响因子:
20.3
作者:
Brousseau, David C.;Scott, J. Paul;Panepinto, Julie A.
通讯作者:
Panepinto, Julie A.
影响因子:
120.7
作者:
Brousseau, David C.;Owens, Pamela L.;Steiner, Claudia A.
通讯作者:
Steiner, Claudia A.
DOI:
10.1177/1740774513475850
发表时间:
2013-04
期刊:
Clinical trials (London, England)
影响因子:
--
作者:
Dampier CD;Smith WR;Wager CG;Kim HY;Bell MC;Miller ST;Weiner DL;Minniti CP;Krishnamurti L;Ataga KI;Eckman JR;Hsu LL;McClish D;McKinlay SM;Molokie R;Osunkwo I;Smith-Whitley K;Telen MJ;Sickle Cell Disease Clinical Research Network (SCDCRN)
通讯作者:
Sickle Cell Disease Clinical Research Network (SCDCRN)