Long-Term Functional Outcomes at 1-Year After Hospital Discharge in Critically Ill Neonates With Congenital Diaphragmatic Hernia

被引:3
|
作者
O'Hara, Jill E. [1 ,2 ]
Buchmiller, Terry L. [1 ,4 ]
Bechard, Lori J. [1 ,2 ]
Akhondi-Asl, Alireza [1 ,2 ]
Visner, Gary [1 ,5 ]
Sheils, Catherine [1 ,5 ]
Becker, Ronald [1 ,6 ]
Studley, Mollie [7 ]
Lemire, Lindsay [4 ]
Mullen, Mary P. [1 ,8 ]
Vitali, Sally [1 ,2 ]
Mehta, Nilesh M. [1 ,2 ,3 ]
Dickie, Belinda [1 ,2 ,4 ]
Zalieckas, Jill M. [1 ,2 ,3 ,4 ]
Albert, Ben D. [1 ,2 ,3 ]
机构
[1] Harvard Med Sch, Boston, MA 02115 USA
[2] Boston Childrens Hosp, Perioperat & Crit Care Ctr Outcomes Res & Evaluat, Dept Anesthesiol, Boston, MA 02115 USA
[3] Boston Childrens Hosp, Dept Anesthesiol Crit Care & Pain Med, Div Crit Care Med, Boston, MA 02115 USA
[4] Boston Childrens Hosp, Dept Surg, Boston, MA USA
[5] Boston Childrens Hosp, Div Pulm Med, Boston, MA USA
[6] Boston Childrens Hosp, Dept Pediat, Div Dev Med, Boston, MA USA
[7] Boston Childrens Hosp, Div Gastroenterol Hepatol & Nutr, Boston, MA USA
[8] Boston Childrens Hosp, Dept Cardiol, Boston, MA USA
关键词
congenital diaphragmatic hernia; Functional Status Scale; nutrition; outcomes; pediatric intensive care; EXTRACORPOREAL LIFE-SUPPORT; PEDIATRIC INTENSIVE-CARE; LIVER HERNIATION; STATUS SCALE; MORBIDITY; MORTALITY; SURVIVORS; PREDICTION; DISEASE;
D O I
10.1097/PCC.0000000000003249
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
OBJECTIVES:Congenital diaphragmatic hernia (CDH) is a birth defect associated with long-term morbidity. Our objective was to examine longitudinal change in Functional Status Scale (FSS) after hospital discharge in CDH survivors. DESIGN:Single-center retrospective cohort study. SETTING:Center for comprehensive CDH management at a quaternary, free-standing children's hospital. PATIENTS:Infants with Bochdalek CDH were admitted to the ICU between January 2009 and December 2019 and survived until hospital discharge. INTERVENTIONS:None. MEASUREMENTS AND MAIN RESULTS:One hundred forty-two infants (58% male, mean birth weight 3.08 kg, 80% left-sided defects) met inclusion criteria. Relevant clinical data were extracted from the medical record to calculate FSS (primary outcome) at hospital discharge and three subsequent outpatient follow-up time points. The median (interquartile range [IQR]) FSS score at hospital discharge was 8.0 (7.0-9.0); 39 patients (27.5%) had at least moderate impairment (FSS & GE; 9). Median (IQR) FSS at 0- to 6-month (n = 141), 6- to 12-month (n = 141), and over 12-month (n = 140) follow-up visits were 7.0 (7.0-8.0), 7.0 (6.0-8.0), and 6.0 (6.0-7.0), respectively. Twenty-one patients (15%) had at least moderate impairment at over 12-month follow-up; median composite FSS scores in the over 12-month time point decreased by 2.0 points from hospital discharge. Median feeding domain scores improved by 1.0 (1.0-2.0), whereas other domain scores remained without impairment. Multivariable analysis demonstrated right-sided, C- or D-size defects, extracorporeal membrane oxygenation use, cardiopulmonary resuscitation, and chromosomal anomalies were associated with impairment. CONCLUSIONS:The majority of CDH survivors at our center had mild functional status impairment (FSS & LE; 8) at discharge and 1-year follow-up; however, nearly 15% of patients had moderate impairment during this time period. The feeding domain had the highest level of functional impairment. We observed unchanged or improving functional status longitudinally over 1-year follow-up after hospital discharge. Longitudinal outcomes will guide interdisciplinary management strategies in CDH survivors.
引用
收藏
页码:E372 / E381
页数:10
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