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Article |

Are Screening Echocardiograms Warranted for Neonates With Meningomyelocele? FREE

Saskia Ritter, MD; Lloyd Y. Tani, MD; Robert E. Shaddy, MD; L. LuAnn Minich, MD
[+] Author Affiliations

From Primary Children's Medical Center and University of Utah, Salt Lake City.


Arch Pediatr Adolesc Med. 1999;153(12):1264-1266. doi:10.1001/archpedi.153.12.1264.
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Published online

Objective  To evaluate the incidence and types of congenital heart defects associated with meningomyelocele.

Design  All neonates who underwent meningomyelocele repair and had a perioperative echocardiogram from July 1990 to October 1998 were studied. Medical records were reviewed for age, weight, clinical cardiac examination results, meningomyelocele location, and associated noncardiac defects. Heart defects were identified from reviewing echocardiographic reports and videotapes.

Results  At meningomyelocele surgery, the 105 patients (53 female; 52 male) ranged in age from 1 to 20 days and in weight from 0.6 to 4.1 kg. Congenital heart disease was detected in 39 patients (37%). A secundum atrial septal defect was the most common defect (24%). A ventricular septal defect was found in 10 patients, 2 patients had anomalous pulmonary venous return, and 1 each had tetralogy of Fallot, bicuspid aortic valve, coarctation, and hypoplastic left heart syndrome. A patent ductus arteriosus and patent foramen ovale were not considered abnormal in these neonates. The cardiac examination was abnormal in only 5 of the 39 patients with heart defects (sensitivity = 13%). The presence of associated noncardiac defects (in addition to meningomyelocele) and location of the meningomyelocele (cervicothoracic vs lumbar) did not affect the incidence of heart disease. Of the patients with heart defects, girls were more frequently affected (25 of 39 vs 14 of 39, P<.05).

Conclusions  Congenital heart defects are common in neonates, especially girls, with meningomyelocele and are unrelated to meningomyelocele location or associated noncardiac defects. Because the clinical examination is insensitive for detecting heart defects in this group, screening echocardiograms are warranted. This information has important implications for ventriculoatrial shunting, urinary tract instrumentation (antibiotic prophylaxis), and neurosurgical procedures (venous air embolism).

Figures in this Article

MENINGOMYELOCELE is the most severe form of dysraphism involving the vertebral column. Although its exact etiology is unknown, a multifactorial origin seems likely.1

Previous studies report that a high number of live-born infants with a meningomyelocele have at least 1 major malformation involving the central nervous, skeletal, cutaneous, or genitourinary system.1,2 The few previous investigations of associated cardiovascular malformations have suggested an increased incidence of conotruncal defects (Kousseff syndrome) and ventricular septal defects.37

The purpose of this study was to determine the incidence and types of congenital heart defects occurring in patients with meningomyelocele.

Neonates diagnosed with meningomyelocele between July 1990 and October 1998 were identified by searching the hospital computer database. All neonates undergoing meningomyelocele repair (open meningomyelocele) within the first month of life were included. Because it is part of the perioperative protocol for meningomyelocele repair at our institution, all patients had a perioperative complete 2-dimensional and Doppler echocardiogram.

The patient records were reviewed for demographic data, meningomyelocele location, and associated noncardiac defects. Heart defects were identified by reviewing echocardiographic reports and videotapes. Only the primary cardiac diagnosis was recorded for each patient. A true secundum atrial septal defect was diagnosed when all the following were present: (1) a defect in the atrial septum larger than 4 mm without a tissue flap to cover the opening, (2) t-artifact at each edge, and (3) a low-velocity shunt (<1.5 m/s) across the defect. A patent foramen ovale and patent ductus arteriosus were considered to be normal for this age group.

All data are expressed as mean ± SD. Nonparametric data were compared using the χ2 or Fisher exact tests. Statistical significance was inferred at P<.05.

The study was approved by the institutional review board at Primary Children's Medical Center, Salt Lake City, Utah.

Of the 130 patients diagnosed with meningomyelocele during the study period, 105 satisfied the inclusion criteria. The characteristics of the study group are summarized in Table 1. At the time of surgery, they ranged in age from 1 to 20 days and in weight from 0.6 to 4.1 kg. There was no significant difference in the number of boys and girls. Most patients had a meningomyelocele in the lumbar area. Additional noncardiac defects were present in 85%, including 65 patients with hydrocephalus, 36 with urinary tract involvement (neurogenic bladder, hydronephrosis, vesicoureteral reflux), 26 with skeletal abnormalities (club feet, scoliosis, hip dysplasia), 3 with intestinal abnormalities (cloacal dystrophy, rectal agenesis, rectal prolapse), and 2 with an identifiable clinical syndrome (DiGeorge, Cornelia de Lange).

The echocardiogram was abnormal in 39 patients (37%). Abnormalities included a secundum atrial septal defect in 25 (24%), ventricular septal defect in 10 (10%), and anomalous pulmonary venous return in 2 (2%). Tetralogy of Fallot, bicuspid aortic valve, coarctation, and hypoplastic left heart syndrome each occurred in 1 patient. Although a patent ductus arteriosus was found in 50 patients and a patent foramen ovale in 32, they were considered to be normal at this age and those patients were not included in the group with cardiac defects.

There were no significant differences in the incidence of heart defects between the groups with and without noncardiac defects (Figure 1). Similarly, the incidence of heart defects was not significantly different between the group of neonates with lumbar and the group with cervicothoracic meningomyeloceles (Figure 2). Heart defects were significantly more common (25 of 39) in girls (Figure 3).

Place holder to copy figure label and caption
Figure 1.

Relationship of heart defects to patients with and without associated noncardiac defects.

Graphic Jump Location
Place holder to copy figure label and caption
Figure 2.

Relationship of heart defects to the location of the meningomyelocele.

Graphic Jump Location
Place holder to copy figure label and caption
Figure 3.

Relationship of heart defects to the sex of the patient. Asterisk indicates P<.05.

Graphic Jump Location

Only 5 of the 39 patients with echocardiographic evidence of congenital cardiac defects had abnormal cardiac examination results (performed by the neonatologist, pediatrician, or neurosurgeon), for a sensitivity of 13%.

Meningomyeloceles occur at the end of week 4 of development if the neural tube fails to close spontaneously. If overproduction of spinal fluid occurs at this stage of development, the neural tube distends and fluid can infiltrate the surrounding mesoderm, destroying neural crest cells.8,9 The neural crest cells play an important role in forming mesodermal organs such as the heart, urinary tract, and skeleton; thus, their destruction may prevent normal development of both the spinal cord and the heart.10 In addition, both the heart and central nervous system rely on homocysteine for their normal development.11

Previous studies have demonstrated a 5% to 10% incidence of congenital heart defects in patients with neural tube defects. These studies differ from ours, however, because they included all neural tube defects rather than just open meningomyeloceles.4,6 The incidence of congenital heart defects in our study was 37% of patients with an open meningomyelocele (considerably higher than the 1% risk given for the general population), with atrial septal defects being the most common abnormality. We also found that newborn girls with meningomyelocele are more frequently affected. This may be explained by the higher incidence of atrial septal defects in the general female population as well.12 Because the location of the meningomyelocele and the presence or absence of additional noncardiac defects were similar between those with and without heart defects, they cannot be used to predict patients at higher risk. In addition, because most of the defects are clinically silent at this age, early diagnosis can be made only by echocardiographic screening.

The identification of even minor heart defects has several important implications for this group of patients. First, spinal fluid is often overproduced in patients with a meningomyelocele, resulting in hydrocephalus after repair.1 If the hydrocephalus requires treatment with a ventriculoatrial shunt, it is important to be aware of the presence of cardiac defects when determining the potential for paradoxical emboli. Second, prophylaxis for endocarditis is very important for patients with meningomyelocele who have associated renal defects and may have more frequent episodes of bacteremia from frequent manipulations of the genitourinary tract or from urinary tract infections.1,13 Third, the possibility of venous air embolism exists whenever the craniofacial operative field is above the heart and is a well-described complication of neurosurgical procedures.14,15 If an intracardiac connection between the right and left sides of the heart is present, systemic embolization may occur.

This study is limited by being retrospective, but we were able to obtain complete data from the clinical records. Although it may be difficult to differentiate between a secundum atrial septal defect and a patent foramen ovale, every attempt was made to include only true secundum atrial septal defects by adhering to strict criteria and reviewing all videotapes independent of the report. If there was a question, the defect was considered a patent foramen ovale.

Thus, congenital heart defects are common in neonates with meningomyelocele, especially in female patients. Because neither meningomyelocele location nor the presence of associated noncardiac defects can be used to predict patients at risk for heart defects, and the clinical examination is insensitive for detecting heart defects in this group, screening echocardiograms are warranted. This information has important implications for patients who may require a ventriculoatrial shunt, those at risk for endocarditis from urinary tract instrumentation, and those at risk for venous air embolism with certain neurosurgical procedures.

Accepted for publication April 30, 1999.

Presented at the annual meeting of the American Society of Echocardiography, Washington, DC, June 16, 1999.

Editor's Note: In this age of cost-conscious care, it's nice to have a study like this that points out the value of performing a relatively expensive diagnostic test in certain newborns.—Catherine D. DeAngelis, MD

Reprints: L. LuAnn Minich, MD, Primary Children's Medical Center, 100 N Medical Dr, Salt Lake City, UT 84113.

Wolraich  MLHesz  N Meningomyelocele: assessment and management. Pediatrician. 1988;1521- 28
Schey  WL Vertebral malformations and associated somatovisceral abnormalities. Clin Radiol. 1976;27341- 353
Link to Article
Jacobs  RAHohn  A Cardiovascular pathology in myelomeningocele care. Eur J Pediatr Surg. 1992;242
Link to Article
Nickel  REPillers  DAMerkens  M  et al.  Velo-cardio-facial syndrome and DiGeorge sequence with meningomyelocele and deletions of the 22q11 region. Am J Med Genet. 1994;52445- 449
Link to Article
Kasznica  JCarlson  ACoppedge  D Ectrodactyly, retrognathism, abnormal ears, highly arched palate, spina bifida, congenital heart defect, single umbilical artery. Am J Med Genet. 1991;40414- 416
Link to Article
Van Went  JJVan Went  GFDelleman  JWBecker  AG Spina bifida and so-called asplenia syndrome occurring separately in sibs. Teratology. 1977;15195- 198
Link to Article
Toriello  HVSharda  JKBeaumont  EJ Autosomal recessive syndrome of sacral and conotruncal developmental field defects (Kousseff syndrome). Am J Med Genet. 1985;22357- 360
Link to Article
Gardner  WJ Overdistension of the neural tube causes congenital heart disease. Med Hypotheses. 1981;7411- 420
Link to Article
Gardner  WJBreuer  AC Anomalies of heart, spleen, kidneys, gut, and limbs may result from an overdistended neural tube: a hypothesis. Pediatrics. 1980;65508- 514
Creazzo  TLGodt  RELeatherbury  LConway  SJKirby  ML Role of cardiac neural crest cells in cardiovascular development. Annu Rev Physiol. 1998;60267- 286
Link to Article
Rosenquist  THRatashak  SASelhub  J Homocysteine induces congenital defects of the heart and neural tube: effect of folic acid. Proc Natl Acad Sci U S A. 1996;9315227- 15232
Link to Article
Park  MK Left-to-right shunt lesions. Park  MKed.Pediatric Cardiology for Practitioners St Louis, Mo Mosby–Year Book1996;131
Cass  ASLuxemberg  MJohnson  CFGleich  P Incidence of urinary tract complications with myelomeningocele. Urology. 1985;25374- 378
Link to Article
Harris  MMStratford  MARowe  RWSanders  SPWinston  KRRockoff  MA Venous air embolism and cardiac arrest during craniotomy in a supine infant. Anesthesiology. 1986;65547- 550
Link to Article
Harris  MMYemen  TADavidson  A  et al.  Venous air embolism during craniectomy in supine infants. Anesthesiology. 1987;67816- 819
Link to Article

Figures

Place holder to copy figure label and caption
Figure 1.

Relationship of heart defects to patients with and without associated noncardiac defects.

Graphic Jump Location
Place holder to copy figure label and caption
Figure 2.

Relationship of heart defects to the location of the meningomyelocele.

Graphic Jump Location
Place holder to copy figure label and caption
Figure 3.

Relationship of heart defects to the sex of the patient. Asterisk indicates P<.05.

Graphic Jump Location

Tables

References

Wolraich  MLHesz  N Meningomyelocele: assessment and management. Pediatrician. 1988;1521- 28
Schey  WL Vertebral malformations and associated somatovisceral abnormalities. Clin Radiol. 1976;27341- 353
Link to Article
Jacobs  RAHohn  A Cardiovascular pathology in myelomeningocele care. Eur J Pediatr Surg. 1992;242
Link to Article
Nickel  REPillers  DAMerkens  M  et al.  Velo-cardio-facial syndrome and DiGeorge sequence with meningomyelocele and deletions of the 22q11 region. Am J Med Genet. 1994;52445- 449
Link to Article
Kasznica  JCarlson  ACoppedge  D Ectrodactyly, retrognathism, abnormal ears, highly arched palate, spina bifida, congenital heart defect, single umbilical artery. Am J Med Genet. 1991;40414- 416
Link to Article
Van Went  JJVan Went  GFDelleman  JWBecker  AG Spina bifida and so-called asplenia syndrome occurring separately in sibs. Teratology. 1977;15195- 198
Link to Article
Toriello  HVSharda  JKBeaumont  EJ Autosomal recessive syndrome of sacral and conotruncal developmental field defects (Kousseff syndrome). Am J Med Genet. 1985;22357- 360
Link to Article
Gardner  WJ Overdistension of the neural tube causes congenital heart disease. Med Hypotheses. 1981;7411- 420
Link to Article
Gardner  WJBreuer  AC Anomalies of heart, spleen, kidneys, gut, and limbs may result from an overdistended neural tube: a hypothesis. Pediatrics. 1980;65508- 514
Creazzo  TLGodt  RELeatherbury  LConway  SJKirby  ML Role of cardiac neural crest cells in cardiovascular development. Annu Rev Physiol. 1998;60267- 286
Link to Article
Rosenquist  THRatashak  SASelhub  J Homocysteine induces congenital defects of the heart and neural tube: effect of folic acid. Proc Natl Acad Sci U S A. 1996;9315227- 15232
Link to Article
Park  MK Left-to-right shunt lesions. Park  MKed.Pediatric Cardiology for Practitioners St Louis, Mo Mosby–Year Book1996;131
Cass  ASLuxemberg  MJohnson  CFGleich  P Incidence of urinary tract complications with myelomeningocele. Urology. 1985;25374- 378
Link to Article
Harris  MMStratford  MARowe  RWSanders  SPWinston  KRRockoff  MA Venous air embolism and cardiac arrest during craniotomy in a supine infant. Anesthesiology. 1986;65547- 550
Link to Article
Harris  MMYemen  TADavidson  A  et al.  Venous air embolism during craniectomy in supine infants. Anesthesiology. 1987;67816- 819
Link to Article

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