Congenital diaphragmatic hernia: associated anomalies and antenatal diagnosis - Outcome-related variables at two Detroit hospitals

被引:44
作者
Bedoyan, JK
Blackwell, SC
Treadwell, MC
Johnson, A
Klein, MD
机构
[1] Wayne State Univ, Childrens Hosp Michigan, Sch Med, Dept Pediat Surg, Detroit, MI 48201 USA
[2] Wayne State Univ, Hutzel Hosp, Sch Med, Dept Obstet & Gynecol, Detroit, MI USA
关键词
congenital diaphragmatic hernia; associated anomalies; antenatal diagnosis; prognostic factors; extracorporeal membrane oxygenation;
D O I
10.1007/s00383-004-1138-2
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
This retrospective study reviews the medical records of 77 fetuses and babies with congenital diaphragmatic hernia (CDH) referred to two hospitals in Detroit from 1986 through 2000. The aims were to examine the effects on outcome of multiple variables, especially the type of CDH, associated anomalies, and ultrasound prognostic parameters. Ultrasound measurements of head (HC), chest (CC), and abdominal circumferences (AC) were obtained from videotapes. ANOVA and chi-square analysis were used to determine statistical significance between groups and proportions. Eighty-nine percent (65/73) of pregnancies resulted in live births, and 54% (35/65) of patients survived past 30 days. Liveborn patients with low APGAR scores were less likely to survive. Forty-three percent (30/70) had major associated anomalies, with cardiac anomalies constituting about 52% (33/64) of the major associated anomalies. Seventy percent of patients with isolated CDH survived versus 36% of patients with both CDH and cardiac anomalies. Sixty-seven percent (8/12) of fetuses antenatally diagnosed before 25 weeks of gestation survived past 30 days of birth. The survival rate of right-sided CDH with liver herniation was 80% (8/10), compared with 29% (4/14) for left-sided CDH with liver herniation ( p =0.088). There was a significant linear relationship ( r =0.603, p =0.029) between CC/AC and CC/HC among patients with CDH; survivors had higher CC/AC and CC/HC values than nonsurvivors. These results support the utility of CC/AC and CC/HC measurements and the presence of liver herniation as important prognostic factors that can be used in antenatal counseling and in planning clinical trials.
引用
收藏
页码:170 / 176
页数:7
相关论文
共 23 条
[1]  
Adzick N. Scott, 1997, P48
[2]   DIAPHRAGMATIC-HERNIA IN THE FETUS - PRENATAL-DIAGNOSIS AND OUTCOME IN 94 CASES [J].
ADZICK, NS ;
HARRISON, MR ;
GLICK, PL ;
NAKAYAMA, DK ;
MANNING, FA ;
DELORIMIER, AA .
JOURNAL OF PEDIATRIC SURGERY, 1985, 20 (04) :357-361
[3]   Current surgical management of congenital diaphragmatic hernia: A report from the congenital diaphragmatic hernia study group [J].
Clark, RH ;
Hardin, WD ;
Hirschl, RB ;
Jaksic, T ;
Lally, KP ;
Langham, MR ;
Wilson, JM .
JOURNAL OF PEDIATRIC SURGERY, 1998, 33 (07) :1004-1007
[4]   Congenital diaphragmatic herniation: antenatal detection and outcome [J].
Dillon, E ;
Renwick, M ;
Wright, C .
BRITISH JOURNAL OF RADIOLOGY, 2000, 73 (868) :360-365
[5]   Congenital diaphragmatic hernia: retrospective study of 123 cases [J].
Dubois, A ;
Storme, L ;
Jaillard, S ;
Truffert, P ;
Riou, Y ;
Rakza, T ;
Pierrat, V ;
Gottrand, F ;
Pruvot, FR ;
Leclerc, F ;
Lequien, P .
ARCHIVES DE PEDIATRIE, 2000, 7 (02) :132-142
[6]  
Flake A W, 1996, Semin Pediatr Surg, V5, P266
[7]  
GORDON JD, 2001, OBSTET GYNECOLOGY IN
[8]  
Greenholz S K, 1996, Semin Pediatr Surg, V5, P216
[9]   Correction of congenital diaphragmatic hernia in utero .7. A prospective trial [J].
Harrison, MR ;
Adzick, NS ;
Bullard, KM ;
Farrell, JA ;
Howell, LJ ;
Rosen, MA ;
Sola, A ;
Goldberg, JD ;
Filly, RA .
JOURNAL OF PEDIATRIC SURGERY, 1997, 32 (11) :1637-1642
[10]   Correction of congenital diaphragmatic hernia in utero IX: Fetuses with poor prognosis (liver herniation and low lung-to-head ratio) can be saved by fetoscopic temporary tracheal occlusion [J].
Harrison, MR ;
Mychaliska, GB ;
Albanese, CT ;
Jennings, RW ;
Farrell, JA ;
Hawgood, S ;
Sandberg, P ;
Levine, AH ;
Lobo, E ;
Filly, RA .
JOURNAL OF PEDIATRIC SURGERY, 1998, 33 (07) :1017-1022