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Research

JAMA Cardiology | Original Investigation

Maternal and Fetal Outcomes of Admission for Delivery


in Women With Congenital Heart Disease
Robert M. Hayward, MD; Elyse Foster, MD; Zian H. Tseng, MD, MAS

Invited Commentary
BACKGROUND Women with congenital heart disease (CHD) may be at increased risk for Supplemental content
adverse events during pregnancy and delivery.

OBJECTIVE To compare delivery outcomes between women with and without CHD.

DESIGN, SETTING, AND PARTICIPANTS This retrospective study of inpatient delivery


admissions in the Healthcare Cost and Utilization Projects California State Inpatient Database
compared maternal and fetal outcomes between women with and without CHD by using
multivariate logistic regression. Female patients with codes for delivery from the International
Classification of Diseases, Ninth Revision, from January 1, 2005, through December 31, 2011,
were included. The association of CHD with readmission was assessed to 7 years after
delivery. Cardiovascular morbidity and mortality were hypothesized to be higher among
women with CHD. Data were analyzed from April 4, 2014, through January 23, 2017.

EXPOSURES Noncomplex and complex CHD.

MAIN OUTCOMES AND MEASURES Maternal outcomes included in-hospital arrhythmias,


eclampsia or preeclampsia, congestive heart failure (CHF), length of stay, preterm labor,
anemia complicating pregnancy, placental abnormalities, infection during labor, maternal
readmission at 1 year, and in-hospital mortality. Fetal outcomes included growth restriction,
distress, and death.

RESULTS Among 3 642 041 identified delivery admissions, 3189 women had noncomplex
CHD (mean [SD] age, 28.6 [7.6] years) and 262 had complex CHD (mean [SD] age, 26.5 [6.8]
years). Women with CHD were more likely to undergo cesarean delivery (1357 [39.3%] vs
1 164 509 women without CHD [32.0%]; P < .001). Incident CHF, atrial arrhythmias,
ventricular arrhythmias, and maternal mortality were uncommon during hospitalization, with
each occurring in fewer than 10 women with noncomplex or complex CHD (<0.5% each).
After multivariate adjustment, noncomplex CHD (odds ratio [OR], 9.7; 95% CI, 4.7-20.0) and
complex CHD (OR, 56.6; 95% CI, 17.6-182.5) were associated with greater odds of incident
CHF. Similar odds were found for atrial arrhythmias in noncomplex (OR, 8.2; 95% CI,
3.0-22.7) and complex (OR, 31.8; 95% CI, 4.3-236.3) CHD, for fetal growth restriction in
noncomplex (OR, 1.6; 95% CI, 1.3-2.0) and complex (OR, 3.5; 95% CI, 2.1-6.1) CHD, and for
hospital readmission in both CHD groups combined (OR, 3.6; 95% CI, 3.3-4.0). Complex CHD
was associated with greater adjusted odds of serious ventricular arrhythmias (OR, 31.8; Author Affiliations: Section of
Cardiac Electrophysiology, Division of
95% CI, 4.3-236.3) and maternal in-hospital mortality (OR, 79.1; 95% CI, 23.9-261.8). Cardiology, Department of Medicine,
University of California, San Francisco
CONCLUSIONS AND RELEVANCE In this study of hospital admissions for delivery in California, (Hayward, Tseng); now with Division
of Cardiovascular Medicine,
CHD was associated with incident CHF, atrial arrhythmias, and fetal growth restriction and
Department of Medicine, University
complex CHD was associated with ventricular arrhythmias and maternal in-hospital mortality, of Massachusetts Memorial Medical
although these outcomes were rare, even in women with complex CHD. These findings may Center, Worcester (Hayward);
guide monitoring decisions and risk assessment for pregnant women with CHD at the time of Division of Cardiology, Department of
Medicine, University of California,
delivery.
San Francisco (Foster).
Corresponding Author: Zian H.
Tseng, MD, MAS, Section of Cardiac
Electrophysiology, University
of California, San Francisco,
500 Parnassus Ave, Box 1354,
JAMA Cardiol. doi:10.1001/jamacardio.2017.0283 San Francisco, CA 94143
Published online April 12, 2017. (zhtseng@medicine.ucsf.edu).

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Research Original Investigation Maternal and Fetal Outcomes of Admission for Delivery in CHD

L
abor, delivery, and the postpartum period are a time of
increased arrhythmia and heart failure incidences, even Key Points
in patients without cardiovascular disease. Possible
Question How do the risks and outcomes for labor and delivery
explanations include altered hemodynamics with myocar- compare in women with and without congenital heart disease?
dial irritability owing to increases in intravascular volume, hy-
Findings In this study capturing nearly every delivery admission in
pokalemia, autonomic changes, and hormonal influences on California during a 7-year period, congenital heart disease was
adrenergic receptor number and behavior.1-3 Maternal arrhyth- associated with incident heart failure, atrial arrhythmias, fetal
mias increase during labor and delivery, possibly owing to vol- growth restriction, and readmission; complex congenital heart
ume shifts and hypertension.4 In women with arrhythmias be- disease was also associated with ventricular arrhythmias and
fore pregnancy, recurrence during pregnancy is common and maternal in-hospital mortality, although these outcomes were
rare, even in women with congenital heart disease.
is associated with an increased risk for fetal complications.5
Despite these risks, a small series including women with im- Meaning This study highlights some of the peripartum and
plantable cardioverter defibrillators followed up during sub- postpartum risks for women with CHD, findings that may guide
monitoring decisions and risk assessment for pregnant women
sequent pregnancies has revealed no increase in implantable
with CHD at the time of delivery.
cardioverter defibrillator shocks.6,7 Likewise, congestive heart
failure (CHF) is more common during and after pregnancy in
women without a history of cardiovascular disease.8 other CHD defects were classified as noncomplex.22-24 Pa-
Owing to improvements in the treatment of congenital heart tients with complex and noncomplex CHD diagnoses were
disease (CHD), most patients with CHD now survive to adult- assigned to the complex CHD group.
hood, and more than 1 million adults are living with CHD in the Maternal cardiovascular outcomes included in-hospital
United States.9,10 As patients with CHD live longer, arrhyth- atrial arrhythmias (including atrial fibrillation, atrial flutter, or
mias are an increasing cause of morbidity and mortality.11,12 In paroxysmal supraventricular tachycardia), serious ventricu-
addition, more women with CHD are becoming pregnant, and lar arrhythmias (including paroxysmal ventricular tachycar-
these patients are at increased risk for arrhythmias and CHF.13,14 dia, ventricular fibrillation, ventricular flutter, cardiac arrest,
We sought to evaluate contemporary maternal and fetal and sudden death due to an unknown cause during the puer-
outcomes in women with and without CHD during admis- perium), eclampsia or preeclampsia, and CHF (eTable 3 in the
sions for delivery in California. We used the Health Care Cost Supplement). Other maternal outcomes included length of stay
and Utilization Project (HCUP), a group of databases that and in-hospital mortality. Maternal and fetal outcomes, de-
have already been used to study CHD hospitalizations and fined by others previously,25 included preterm labor, anemia
procedures,15-19 to evaluate cardiac and other complications complicating pregnancy, placental abnormalities (previa,
of labor and delivery for women with and without CHD from abruptio, or accreta), infection during labor, fetal growth re-
2005 through 2011. striction, fetal distress, and fetal death.
Outcomes after discharge included readmission to the hos-
pital (after excluding admissions for subsequent delivery) for
CHF, atrial arrhythmias, and serious ventricular arrhythmias
Methods at 1 year. Women with a primary residence outside California
Admissions for female patients with a diagnosis code from the were excluded from this analysis. Because these outcomes were
International Classification of Diseases, Ninth Revision (ICD-9), uncommon and because we found no significant differences
a procedure code from the International Classification of Dis- between the complex and noncomplex CHD groups, both were
eases, Ninth Revision, Clinical Modification, or a diagnosis re- analyzed as a single group for the 1-year follow-up.
lated group code for delivery20,21 from January 1, 2005, through Medical comorbidities were classified based on ICD-9 di-
December 31, 2011, were identified from HCUPs California State agnosis codes for coronary artery disease, CHF, cerebrovas-
Inpatient Database. If an ICD-9 code for cesarean delivery was cular disease, chronic kidney disease, hypertension, diabe-
not present and the delivery type was not specified, delivery tes, and depression (eTable 4 in the Supplement).19,25 Patients
was categorized as vaginal. The details of the ICD-9 codes used were identified as having the comorbidity of interest if the di-
are listed in eTable 1 in the Supplement. Identifying patient in- agnosis code was recorded for any health care encounter from
formation was anonymized before analysis, and certification January 1, 2005, to the admission date for delivery. Thus, these
to use these deidentified HCUP data was obtained from the comorbidities included comorbidities diagnosed before preg-
Committee on Human Research at the University of Califor- nancy and those diagnosed during pregnancy but before the
nia, San Francisco. admission for delivery.
Diagnoses of CHD were determined by ICD-9 or Current
Procedural Terminology codes used by others previously Statistical Analysis
(eTable 2 in the Supplement).17,22-24 If a CHD diagnosis code Data were analyzed from April 4, 2014, through January 23,
was present for any encounter during the study period, the pa- 2017. Continuous variables are presented as mean (SD); cat-
tient was assigned that diagnosis for all visits. Complex CHD egorical variables, as percentages. Continuous variables that
included endocardial cushion defects, hypoplastic left heart were not normally distributed are presented as median (inter-
syndrome, tetralogy of Fallot, transposition of the great arter- quartile range [IQR]). We compared outcomes using multivar-
ies, truncus arteriousus, and univentricular heart defects. All iate logistic regression with the following covariates: age, race,

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Maternal and Fetal Outcomes of Admission for Delivery in CHD Original Investigation Research

Table 1. Baseline Characteristics of Women Admitted for Deliveriesa

Patient Group, No. (%)


No CHD Noncomplex CHD Complex CHD
Characteristic (n = 3 638 590) (n = 3189) (n = 262) P Valueb
Age, mean (SD), y 28.3 (6.6) 28.6 (7.6) 26.5 (6.8) <.001
Race or ethnicity
Asian or Pacific Islander 380 592 (10.8) 293 (9.3) 25 (9.6)
Black 187 794 (5.4) 218 (6.9) 13 (5.0)
Hispanic 1 765 517 (50.3) 1314 (41.7) 100 (38.5)
<.001
Native American 5428 (0.2) 13 (0.4) 0
White 1 058 119 (30.1) 1173 (37.2) 107 (41.2)
Other 114 822 (3.3) 140 (4.4) 15 (5.8)
Cesarean delivery 1 164 509 (32.0) 1236 (38.8) 121 (46.2) <.001
Multiple birth 55 745 (1.5) 63 (1.9) <10c .20 Abbreviations: AF, atrial fibrillation;
CHF 4517 (0.1) 111 (3.5) 19 (7.3) <.001 AFL, atrial flutter; CHD, congenital
Hypertension 37 930 (1.0) 202 (6.3) 14 (5.3) <.001 heart disease; CHF, congestive heart
failure; SCA, sudden cardiac arrest;
Diabetes 37 270 (1.0) 118 (3.7) 16 (6.1) <.001 SVT, supraventricular tachycardia;
Depression 35 728 (1.0) 82 (2.6) <10c <.001 VF, ventricular fibrillation;
History of AF, AFL, or SVT 1796 (0.05) 41 (1.3) <10c <.001 VT, ventricular tachycardia.
a
History of VT, VF, or SCA 744 (0.02) <10c <10c <.001 Owing to missing data, totals may
not equal column heads.
Hospital delivery volume quartile b
Calculated using Pearson 2 test.
Lowest 1323 (0.04) 10 (0.3) 0 c
Health Care Cost and Utilization
Second 242 539 (6.7) 182 (5.7) 13 (5.0) Project policy prohibits reporting
<.001
Third 1 003 283 (27.6) 874 (27.4) 81 (30.9) cell frequencies of less than 10, but
each frequency was more common
Highest 2 391 445 (65.7) 2123 (66.6) 168 (64.1)
than for women without CHD.

cesarean delivery, multiple birth, maternal history of CHF, hy- in the Supplement). The remaining 3 638 590 women with-
pertension, coronary artery disease, chronic kidney disease, dia- out CHD (mean [SD] age, 28.3 [6.6] years) comprised the com-
betes, and cerebrovascular disease. We assessed the association parison group. A history of CHF was more common in women
of CHD with readmission to the hospital for reasons other than with CHD (19 [7.3%] with complex CHD, 111 [3.5%] with non-
subsequent delivery by using survival analysis, with failure de- complex CHD, and 4517 [0.1%] without CHD; P < .001). A his-
fined as readmission to the hospital to 7 years after delivery. tory of arrhythmias was rare in all groups but somewhat more
Women without a readmission were administratively censored common in women with CHD.
on December 31, 2011. The association of CHD with the hazard
of readmission was evaluated with Cox proportional hazards In-Hospital Maternal and Fetal Outcomes
modeling. Beginning with an a priori set of predictors, backward Women with CHD were more likely to undergo cesarean de-
selection was used to remove covariates with P < .1 in adjusted livery (121 [46.2%] with complex CHD, 1236 [38.8%] with non-
analyses. Two-tailed P < .05 was considered to be statistically complex CHD, and 1 164 509 [32.0%] without CHD; P < .001).
significant. Owing to HCUP publication requirements,26 cell sizes For tetralogy of Fallot, 56 of 102 women with CHD (54.9%) un-
of less than 10 are not reported, although the exact number is derwent cesarean delivery (eTable 5 in the Supplement).
used in the analyses. Statistical analyses were performed using Median length of stay was longer for women with CHD com-
STATA/SE software (version 13.1; StataCorp). pared with women without CHD (3 [IQR, 2-4] vs 2 [IQR, 2-3]
days; P < .001). In addition, 29 women with complex CHD (11.1%)
and 191 women with noncomplex CHD (6.0%) were admitted
for longer than 7 days, compared with only 49 089 women with-
Results out CHD (1.3%). After multivariate adjustment, CHD was asso-
Of a total of 27 907 535 inpatient hospitalizations in Califor- ciated with greater odds of admissions longer than 1 week
nia from January 1, 2005, through December 31, 2011, we iden- (Table 2). Preeclampsia or eclampsia was observed in 19 women
tified 3 642 041 admissions for women with a delivery diag- with complex CHD (7.3%), 182 women with noncomplex CHD
nosis. After including codes for multiple births, we identified (5.7%), and 122 539 women without CHD (3.4%). After multi-
3 702 838 live births accounting for 98.4% of all live births in variate adjustment, noncomplex CHD was significantly asso-
California during the 7-year period.27 ciated with increased odds of preeclampsia or eclampsia (OR,
Among these admissions for delivery, we identified 3189 1.3; 95% CI, 1.1-1.5; P = .003); the association for complex CHD
women with noncomplex CHD (mean [SD] age, 28.6 [7.6] years) was not significant (OR, 1.5; 95% CI, 0.9-2.4; P = .12).
and 262 women with complex CHD (mean [SD] age, 26.5 [6.8] Incident CHF, atrial arrhythmias, serious ventricular ar-
years) (Table 1) with a variety of congenital defects (eTable 5 rhythmias, and maternal mortality were uncommon during

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Research Original Investigation Maternal and Fetal Outcomes of Admission for Delivery in CHD

Table 2. Maternal and Fetal In-Hospital Outcomes

Patient Group, No. (%) Noncomplex vs No CHD Complex vs No CHD


No CHD Noncomplex CHD Complex CHD AOR
Outcome (n = 3 638 583) (n = 3189) (n = 262) (95% CI) P Valuea AOR (95% CI) P Valuea
Maternal
LOS, median (IQR), d 2 (2-3) 3 (2-4) 3 (2-4)
LOS>7 d 49 089 (1.3) 191 (6.0) 29 (11.1) 2.8 (2.3-3.3) <.001 6.7 (4.4-10.1) <.001
Preeclampsia or eclampsia 122 539 (3.4) 182 (5.7) 19 (7.3) 1.3 (1.1-1.5) .003 1.5 (0.9-2.4) .12
Preterm labor 235 834 (6.5) 356 (11.2) 49 (18.7) 1.6 (1.4-1.8) <.001 3.0 (2.2-4.1) <.001
Anemia complicating 296 207 (8.1) 446 (14.0) 39 (14.9) 1.5 (1.4-1.7) <.001 1.6 (1.1-2.3) .007
pregnancy
Placental abnormalities 75 043 (2.1) 85 (2.7) <10b 1.2 (0.95-1.5) .14 1.6 (0.8-3.0) .20
Infection during labor 143 333 (3.9) 151 (4.7) 16 (6.1) 1.2 (1.01-1.4) .04 1.5 (0.9-2.5) .13
Incident CHF 508 (0.01) <10b <10b 9.7 (4.7-20.0) <.001 56.6 (17.6-182.5) <.001
Incident AF, AFL, or SVT 253 (0.01) <10b <10b 8.2 (3.0-22.7) <.001 31.8 (4.3-236.3) .001
b
Incident VT, VF, or SCA 744 (0.02) <10 <10b 1.9 (0.7-5.1) .23 35.3 (13.4-93.5) <.001
In-hospital mortality 1143 (0.03) <10b (0.2) <10b 1.7 (0.8-4.0) .19 79.1 (23.9-261.8) <.001
Fetal/neonatal
Growth restriction 48 765 (1.3) 76 (2.4) 14 (5.3) 1.6 (1.3-2.0) <.001 3.5 (2.1-6.1) <.001
Distress 526 343 (14.5) 490 (15.4) 49 (18.7) 1.1 (1.0-1.2) .34 1.3 (0.9-1.7) .15
Death 13 017 (0.36) 22 (0.69) 0 1.7 (1.09-2.64) .02
Abbreviations: AF, atrial fibrillation; AFL, atrial flutter; AOR, adjusted odds ratio; CHD, congenital heart disease; CHF, congestive heart failure; IQR, interquartile
range; LOS, length of stay; SCA, sudden cardiac arrest; SVT, supraventricular tachycardia; VF, ventricular fibrillation; VT, ventricular tachycardia.
a
Calculated using multivariate logistic regression.
b
Although Health Care Cost and Utilization Project policy prohibits reporting cell frequencies less than 10, actual numbers were known to investigators and used for
analyses.

Fetal growth restriction was reported in 14 women with


Table 3. Maternal Outcomes at 1 Yeara
complex CHD (5.3%), 76 women with noncomplex CHD (2.4%),
No CHD CHD CHD vs No CHD,
Outcome (n = 2 807 672) (n = 3106)b AOR (95% CI) and 48 765 women without CHD (1.3%). After multivariate ad-
Any readmission 119 441 (4.3) 544 (17.5) 3.6 (3.3-4.0) justment, noncomplex CHD (OR, 1.6; 95% CI, 1.3-2.0; P < .001)
Readmission for CHF 689 (0.02) 19 (0.6) 6.7 (4.0-11.1) and complex CHD (OR, 3.5; 95% CI, 2.1-6.1; P < .001) were as-
Readmission for atrial 736 (0.03) 32 (1.0) 10.9 (7.0-17.1) sociated with greater odds of fetal growth restriction. Fetal
arrhythmiasc death occurred in no deliveries for women with complex CHD,
Readmission for serious 543 (0.02) 15 (0.5) 6.2 (3.5-11.2) 22 deliveries for women with noncomplex CHD (0.7%), and
ventricular arrhythmias
13 017 deliveries for women without CHD (0.4%). After mul-
Abbreviations: AOR, adjusted odds ratio; CHD, congenital heart disease;
tivariate adjustment, noncomplex CHD was associated with
CHF, congestive heart failure.
a greater odds of fetal death compared with women without CHD
Excludes admissions for subsequent delivery and women with a primary
residence outside California. (OR, 1.7; 95% CI, 1.1-2.6; P = .02).
b
Noncomplex CHD and complex CHD were pooled owing to small numbers of
outcomes and the fact that the 2 groups were not significantly different. Maternal Outcomes After Hospital Discharge
Groups were compared with 2 tests, and all differences were statistically When women were followed up after discharge, 30 155 women
significant (P < .001). without CHD (1.1%) and 166 women with CHD (5.6%) were re-
c
Includes atrial fibrillation, atrial flutter, or paroxysmal supraventricular admitted to the hospital within 30 days (P < .001); the read-
tachycardia.
mission rate exclusive of subsequent deliveries remained
higher for women with CHD at 1 year (OR, 3.6; 95% CI, 3.3-
hospitalization, each occurring in fewer than 0.5% of women 4.0; P < .001) (Table 3) and to 7 years after discharge (2 = 3941,
with CHD (Table 2). After multivariate adjustment, noncom- P < .001, log-rank test for comparing complex CHD, noncom-
plex CHD (OR, 9.7; 95% CI, 4.7-20.0; P < .001) and complex CHD plex CHD, and no CHD) (Figure 1). At 1 year, readmissions for
(OR, 56.6; 95% CI, 17.6-182.5; P < .001) were associated with CHF (OR, 6.7; 95% CI, 4.0-11.1; P < .001), atrial arrhythmias (OR,
greater odds of CHF. Similar associations for noncomplex CHD 10.9; 95% CI, 7.0-17.1; P < .001), and serious ventricular ar-
(OR, 8.2; 95% CI, 3.0-22.7; P < .001) and complex CHD (OR, 31.8; rhythmias (OR, 6.2; 95% CI, 3.5-11.2; P < .001) were more com-
95% CI, 4.3-236.3; P = .001) were found for atrial arrhyth- mon for women with CHD than for those without (Table 3). For
mias. After multivariate adjustment, only complex CHD was readmissions within 1 year of delivery, the 10 most common
associated with greater odds of serious ventricular arrhyth- diagnoses were noncardiac for women without CHD, whereas
mias (OR, 35.3; 95% CI, 13.4-93.5; P < .001) or maternal in- for women with CHD, 3 of the top 10 were cardiac (CHF, ostium
hospital mortality (OR, 79.1; 95% CI, 23.9-261.8; P < .001) secundum, atrial septal defect, and chest pain). After multi-
(Table 2). variate analysis, noncomplex CHD (hazard ratio, 3.88; 95% CI,

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Maternal and Fetal Outcomes of Admission for Delivery in CHD Original Investigation Research

3.66-4.12) and complex CHD (hazard ratio, 4.51; 95% CI, 3.70- than 98% of all live births, women with CHD were more likely
5.49) had the largest association with increasing the hazard of to have a history of CHF, undergo cesarean delivery, and have
readmission (Figure 2). longer lengths of stay. Incident maternal CHF, arrhythmias, and
mortality were uncommon for all groups of women, but the
odds of these outcomes were substantially greater for women
Discussion with complex CHD. The adjusted odds of CHF, atrial arrhyth-
In this study of more than 3.6 million admissions for delivery mias, and maternal death were also increased for women with
in California during a 7-year period that accounted for more noncomplex CHD. At 1 year, readmissions for CHF, atrial ar-
rhythmias, and serious ventricular arrhythmias were more
Figure 1. Cumulative Proportion of Women Readmitted After Delivery
common for women with CHD. After multivariate analysis, CHD
1.0 had a greater associaton with increasing the hazard of read-
P <.001
mission than did diabetes, chronic kidney disease, or hyper-
0.8 tension. Despite these associations, the absolute risks for ad-
verse cardiovascular outcomes among women with CHD were
Proportion Readmitted

0.6
still low. The risks for incident CHF, supraventricular arrhyth-
Complex CHD mias, serious ventricular arrhythmias, and maternal in-
Noncomplex CHD hospital mortality were less than 0.5% among women with
0.4
CHD. The magnitude of the increases in relative risk among
women with CHD appears to be high in part owing to com-
0.2
parisons against the rare levels of these complications in the
No CHD general population.
0
0 500 1000 1500 2000
Women with CHD more often underwent cesarean deliv-
Time After Delivery, d ery, but the underlying reasons for this difference are unclear.
Cesarean delivery is more commonly used in mothers who have
Includes admissions other than for subsequent delivery. P values comparing delivered by cesarean delivery previously and in cases of breech
equality of survivor functions for complex, noncomplex, and no congenital
presentation, dystocia, and fetal distress.28-30 Women with CHD
heart disease (CHD) were calculated using log-rank test (2 = 3941; P < .01).
were not more likely to have codes for fetal distress; therefore,

Figure 2. Multivariate Analysis for Hospital Readmission

Covariate HR (95% CI) P Value


No CHD 1 [Reference] NA
Complex CHD 4.51 (3.70-5.49) <.001
Noncomplex CHD 3.88 (3.66-4.12) <.001
Age, y
<18 1.34 (1.32-1.36) <.001
18-29 1 [Reference] NA
30-39 0.80 (0.79-0.80) <.001
40 1.25 (1.23-1.27) <.001
Race
White 1 [Reference] NA
Black 1.63 (1.61-1.65) <.001
Hispanic 1.16 (1.15-1.17) <.001
Asian or Pacific Islander 0.68 (0.67-0.69) <.001
Native American 2.24 (2.10-2.39) <.001
Other 1.40 (1.37-1.43) <.001
Cesarean delivery 1.17 (1.16-1.17) <.001
Multiple birth 1.03 (1.00-1.06) .03
Hospital delivery volume
Lowest quartile 1.04 (1.02-1.05) <.001
Second quartile 1.01 (0.99-1.02) .30
Third quartile 0.98 (0.97-0.99) <.001
Highest quartile 1 [Reference] NA
Comorbidities
CHF 1.66 (1.57-1.76) <.001
Hypertension 2.63 (1.57-2.69) <.001
Coronary artery disease 1.58 (1.49-1.68) <.001
Cerebrovascular disease 1.56 (1.45-1.68) <.001
Chronic kidney disease 2.71 (2.57-2.86) <.001 Includes admissions other than for
Diabetes 2.38 (2.32-2.44) <.001 subsequent delivery. CHD indicates
congenital heart disease;
0 1 2 3 4 5 6 CHF, congestive heart failure;
HR (95% CI) HR, hazard ratio; and NA, not
applicable.

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Research Original Investigation Maternal and Fetal Outcomes of Admission for Delivery in CHD

increased use of cesarean delivery does not seem to be attrib- riages and terminations for medical reasons are more com-
utable to fetal instability. Cesarean deliveries may have been mon in women with CHD,13,38 but this study did not capture
more likely to be planned owing to physician and/or patient pref- any outcomes before the time of delivery.
erence because of the belief that the procedure has less effect This study also found a higher risk for maternal readmis-
on maternal physiology, although at present no definitive data sion among mothers with CHD at 30 days and 1 and 7 years.
on this issue exist. We found a higher rate of cesarean delivery Although we examined the cause of readmission at 1 year, we
among women with CHD (46.2% for complex CHD and 38.8% did not do so at 7 years, and the higher readmission rates across
for noncomplex CHD) than did other studies. In a multicenter long-term follow-up may be attributable to the natural his-
cohort of mothers with CHD from more than a decade ago, Siu tory of CHD and not to complications of pregnancy.
and colleagues31 found that 27% of births were by cesarean de-
livery and 96% of these were for obstetric indications (com- Limitations
pared with maternal cardiac status indication in only 4%). Despite the large number of women with CHD captured in the
We also found significantly greater odds of preeclampsia or study, this study has several limitations. First, ICD-9 codes have
eclampsia in women with noncomplex CHD and increased odds imperfect sensitivity and specificity,40 and CHD may have been
in women with complex CHD. Reduced placental perfusion may undercoded. However, undercoding is unlikely to bias the re-
cause preeclampsia,32 which could be more common in wom- sults, because even a small number of women with CHD mis-
en with CHD. Studies have shown that compared with the gen- classified as not having CHD would not have a sizable effect on
eral population and women with repaired defects, women with summary estimates of more than 3.6 million women. Second,
an unrepaired atrial septal defect or ventricular septal defect have the administrative nature of the database does not allow the
an increased risk for preeclampsia.33,34 In addition, even in wom- medical records of mothers and neonates to be linked to deter-
en with CHD, preeclampsia or eclampsia is uncommon and only mine the long-term health outcomes of these infants. Third, this
occurred in 7.3% of women in our complex CHD group. analysis captured only women who chose to become pregnant
Compared with the studies by Karamlou and colleagues35 and carried pregnancies to term. We did not evaluate women
and Thompson and colleagues,36 our study captured nearly ev- who chose not to become pregnant or who did not carry preg-
ery birth in California, as opposed to a representative sample nancies to term, which may account for approximately 20% of
of the United States obtained from the HCUP Nationwide In- pregnancies among women with CHD.13 Fourth, the number of
patient Sample. All 3 studies found higher rates of cesarean de- women with CHD who delivered at low-volume centers was
livery and cardiac complications among women with CHD. Be- small, and multivariate analysis did not demonstrate an asso-
cause of differences between the databases, the present study ciation of hospital delivery volume with outcomes for women
was also able to ascertain serious complications requiring re- with CHD. Fifth, the inpatient nature of this database did not
admission after discharge. allow us to capture intensity or quality of care before and after
Cardiac complications were less commonly observed in this delivery. In a recent study of cardiovascular deaths related to
study than in the study by Siu and colleagues,31 who reported pregnancy in California, health care professional factors were
a primary cardiac event in 13% of completed pregnancies. How- found to play a role in most cardiovascular deaths.41 Finally, for
ever, more than half of these events occurred in the prepar- the follow-up analysis, only women who were readmitted to a
tum period, which was not evaluated in the present study. One California hospital were captured; therefore, women who moved
review13 found cardiac events in 1.9%, CHF in 4.8%, and ar- or died outside the hospital were not captured.
rhythmias in 4.5% of deliveries in women with CHD. A Dutch
national study of CHD37 identified cardiovascular events at 1
year in 6.4% of pregnancies, and 9 of 11 events were new-
onset arrhythmias. In our contemporary statewide study of
Conclusions
nearly every delivery to mothers with CHD, arrhythmias oc- In this study of nearly all women admitted to California hos-
curred in approximately 1% of women. pitals for delivery during a 7-year period, women with CHD
Prior studies of women with CHD have found that their off- were more likely to undergo cesarean delivery and have a lon-
spring are at increased risk for premature birth, being small for ger length of stay. Incident maternal CHF, arrhythmias, and
gestational age, and neonatal mortality.13,38,39 We found greater mortality were uncommon in all groups of women, but CHD
odds of fetal growth restriction for women with CHD and was significantly associated with incident CHF, atrial arrhyth-
greater odds of fetal death for women with noncomplex CHD. mias, fetal growth restriction, and hospital readmission. Com-
Patients with complex disease are at particular risk for intra- plex CHD was a significant predictor of ventricular arrhyth-
uterine growth restriction, and monitoring for such compli- mias and maternal in-hospital mortality. These results may
cations requires vigilance by obstetricians. Owing to coding re- guide monitoring decisions and risk assessment for pregnant
strictions, we could not examine prematurity as an end point women with CHD at the time of delivery. Given the higher rate
or as a mediator of the association between maternal CHD and of cardiac and obstetrical complications, pregnant women with
neonatal mortality. Prior studies have also shown that miscar- CHD should be treated in a center with expertise in adult CHD.

ARTICLE INFORMATION Published Online: April 12, 2017. Author Contributions: Drs Hayward and Tseng had
Accepted for Publication: January 25, 2017. doi:10.1001/jamacardio.2017.0283 full access to all the data in the study and take

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Maternal and Fetal Outcomes of Admission for Delivery in CHD Original Investigation Research

responsibility for the integrity of the data and the 10. Warnes CA, Liberthson R, Danielson GK, et al. Nationwide HCUP databases. 2005-2011.
accuracy of the data analysis. Task Force 1: the changing profile of congenital https://www.hcup-us.ahrq.gov/databases.jsp.
Study concept and design: All authors. heart disease in adult life. J Am Coll Cardiol. 2001;37 Modified November 11, 2016. Accessed August 26,
Acquisition, analysis, or interpretation of data: (5):1170-1175. 2015.
Hayward. 11. Oechslin EN, Harrison DA, Connelly MS, Webb 27. State of California, Department of Public
Drafting of the manuscript: Hayward, Tseng. GD, Siu SC. Mode of death in adults with congenital Health. Live Births, California Counties, 2002-2011.
Critical revision of the manuscript for important heart disease. Am J Cardiol. 2000;86(10):1111-1116. http://www.cdph.ca.gov/data/statistics/Documents
intellectual content: Hayward, Foster. /VSC-2011-0218.pdf. Accessed July 31, 2015.
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Conflict of Interest Disclosures: All authors have Heart J. 2009;158(5):874-879. United States. Am J Obstet Gynecol. 2010;203(4):
completed and submitted the ICMJE Form for 326.e-326.e10.
Disclosure of Potential Conflicts of Interest. 13. Drenthen W, Pieper PG, Roos-Hesselink JW,
Dr Hayward reports receiving educational travel et al; ZAHARA Investigators. Outcome of pregnancy 29. Taffel SM, Placek PJ, Liss T. Trends in the United
grants from Medtronic and Boston Scientific. in women with congenital heart disease: a literature States cesarean section rate and reasons for the
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honoraria from Biotronik. No other disclosures were Investigators. Predictors of pregnancy Changes in indications for cesarean delivery: United
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by 5R01 HL102090 from the National Heart, Lung, 15. Gurvitz MZ, Inkelas M, Lee M, Stout K, Escarce 31. Siu SC, Sermer M, Colman JM, et al; Cardiac
and Blood Institute, National Institutes of Health J, Chang RK. Changes in hospitalization patterns Disease in Pregnancy (CARPREG) Investigators.
(Dr Tseng). among patients with congenital heart disease Prospective multicenter study of pregnancy
Role of the Funder/Sponsor: The sponsor had no during the transition from adolescence to outcomes in women with heart disease. Circulation.
role in the design and conduct of the study; adulthood. J Am Coll Cardiol. 2007;49(8):875-882. 2001;104(5):515-521.
collection, management, analysis, or interpretation 16. Opotowsky AR, Siddiqi OK, Webb GD. Trends in 32. Roberts JM, Gammill HS. Preeclampsia: recent
of the data; preparation, review, or approval of the hospitalizations for adults with congenital heart insights. Hypertension. 2005;46(6):1243-1249.
manuscript; or decision to submit the manuscript disease in the U.S. J Am Coll Cardiol. 2009;54(5): 33. Yap SC, Drenthen W, Meijboom FJ, et al;
for publication. 460-467. ZAHARA investigators. Comparison of pregnancy
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