DeFrancesco Christopher J, Shah Divya K, Rogers Benjamin H, Shah Apurva S
Division of Orthopaedics, Children's Hospital of Philadelphia.
Department of Obstetrics and Gynecology, University of Pennsylvania, Philadelphia, PA.
J Pediatr Orthop. 2019 Feb;39(2):e134-e140. doi: 10.1097/BPO.0000000000001089.
The epidemiology of brachial plexus birth palsy (BPBP) in the United States may be changing over time due to population-level changes in obstetric care.
The Kids' Inpatient Database from 1997 to 2012 was analyzed. Annual estimates of BPBP incidence and disease determinant distribution were calculated for the general population and the study population with BPBP. Long-term trends were analyzed. A multivariate logistic regression model was used to quantify the risk associated with each determinant.
The database yielded a combined total of 5,564,628 sample births extrapolated to 23,385,597 population births. The population incidence of BPBP dropped 47.1% over the 16-year study period, from 1.7 to 0.9 cases per 1000 live births (P<0.001). Female, black, and Hispanic subgroups had moderately increased risks of BPBP. Among children with BPBP, 55.0% had no identifiable risk factor. Shoulder dystocia was the strongest risk factor for BPBP in the regression model [odds ratio (OR), 113.2; P<0.001], although the risk of sustaining a BPBP in the setting of shoulder dystocia decreased from 10.7% in 1997 to 8.3% in 2012 (P=0.006). Birth hypoxia was independently associated with BPBP (OR, 3.1; P<0.001). Cesarean delivery (OR, 0.16; P<0.001) and multiple gestation birth (OR, 0.45; P<0.001) were associated with lower incidence of BPBP. Notably, the rate of cesarean delivery increased by 62.8% during the study period, from 20.9% in 1997 to 34.0% in 2012 (P<0.001).
Over a 16-year period, the incidence of BPBP fell dramatically, paralleled by a significant increase in the rate of cesarean delivery. Systemic changes in obstetric practice may have contributed to these trends. As more than half of BPBP cases have no identifiable risk factor, prospective investigation of established risk factors and characterization of new disease determinants are needed to more reliably identify infants at greatest risk. Racial and geographic inequalities in disease burden should be investigated to identify interventional targets.
Level III-case series.
由于产科护理在人群层面的变化,美国臂丛神经产瘫(BPBP)的流行病学可能会随时间而改变。
对1997年至2012年的儿童住院数据库进行分析。计算了一般人群以及患有BPBP的研究人群中BPBP发病率和疾病决定因素分布的年度估计值。分析了长期趋势。使用多变量逻辑回归模型来量化与每个决定因素相关的风险。
该数据库得出总计5564628例样本出生数,推算至23385597例人口出生数。在16年的研究期内,BPBP的人群发病率下降了47.1%,从每1000例活产1.7例降至0.9例(P<0.001)。女性、黑人及西班牙裔亚组患BPBP的风险适度增加。在患有BPBP的儿童中,55.0%没有可识别的风险因素。肩难产是回归模型中BPBP最强的风险因素[比值比(OR)为113.2;P<0.001],尽管在肩难产情况下发生BPBP的风险从1997年的10.7%降至2012年的8.3%(P=0.006)。出生时缺氧与BPBP独立相关(OR为3.1;P<0.001)。剖宫产(OR为0.16;P<0.001)和多胎妊娠分娩(OR为0.45;P<0.001)与BPBP较低的发病率相关。值得注意的是,在研究期间剖宫产率增加了62.8%,从1997年的20.9%增至2012年的34.0%(P<0.001)。
在16年期间,BPBP的发病率大幅下降,同时剖宫产率显著上升。产科实践的系统性变化可能促成了这些趋势。由于超过一半的BPBP病例没有可识别的风险因素,需要对既定风险因素进行前瞻性调查并确定新的疾病决定因素,以便更可靠地识别风险最高的婴儿。应调查疾病负担方面的种族和地理不平等情况,以确定干预目标。
三级病例系列。