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Cardiovascular Events During Pregnancy: Implications for Adverse Pregnancy Outcomes in Individuals With Autoimmune and Rheumatic Diseases.
Dhital, Rashmi; Baer, Rebecca J; Bandoli, Gretchen; Chambers, Christina.
Affiliation
  • Dhital R; R. Dhital, MD, Department of Medicine, Division of Rheumatology, Autoimmunity and Inflammation, School of Medicine, University of California San Diego, La Jolla, California, now with Department of Medicine, Division of Rheumatology & Immunology, Vanderbilt University Medical Center, Nashville, T
  • Baer RJ; R.J. Baer, MPH, Department of Pediatrics, Division of Environmental Science and Health, School of Medicine, University of California San Diego, La Jolla, and the California Preterm Birth Initiative, University of California San Francisco, San Francisco, California.
  • Bandoli G; G. Bandoli, PhD, Department of Pediatrics, Division of Environmental Science and Health, School of Medicine, and Herbert Wertheim School of Public Health and Human Longevity Science, University of California San Diego, La Jolla, California, USA.
  • Chambers C; C. Chambers, PhD, MPH, Department of Pediatrics, Division of Environmental Science and Health, School of Medicine, and Herbert Wertheim School of Public Health and Human Longevity Science, University of California San Diego, La Jolla, California, USA.
J Rheumatol ; 2024 Aug 01.
Article in En | MEDLINE | ID: mdl-38879185
ABSTRACT

OBJECTIVE:

This study examined maternal cardiovascular (CV) events relative to adverse pregnancy outcomes among individuals with autoimmune rheumatic diseases (ARDs), primary antiphospholipid syndrome (APS), and those with neither.

METHODS:

Using a California population-based birth cohort (2005-2020), we identified those with CV events (CVEs), ARDs, and APS through International Classification of Diseases, 9th and 10th revisions, Clinical Modification codes in maternal discharge records. Selected adverse pregnancy outcomes identified from birth certificates were preterm birth (PTB; < 37 weeks' gestation), small-for-gestational-age infants (SGA; birth weight < 10th percentile for age and sex), and a composite of either outcome. Adjusted risk ratios (aRRs) for adverse outcomes and their 95% CIs were calculated.

RESULTS:

CVEs occurred more frequently in individuals with ARDs (265 of 19,340 [1.4%]) and primary APS (428 of 7758 [5.5%]) than those without (17,130 of 7,004,334 [0.3%]). The presence vs absence of CVEs was associated with a greater incidence of adverse outcomes in ARD (53.2% vs 26.6%), APS (30.6% vs 20.7%), and non-ARD/APS pregnancies (28.2% vs 15.2%). CVEs were associated with increased risks of SGA in all groups (aRRs 1.2-1.5) and PTB in ARD (aRR 1.6, 95% CI 1.3-2.0) and non-ARD/APS (aRR 1.7, 95% CI 1.7-1.8) pregnancies.

CONCLUSION:

CVEs were associated with modestly increased risks (20-70%) for PTB, SGA, or both across the groups. Notably, > 50% of ARD pregnancies with CVEs experienced adverse pregnancy outcomes. Given that ARD and APS pregnancies have higher (although still low) rates of CVEs and have higher baseline risks of adverse pregnancy outcomes than the general population, the additional burden conferred by CVEs is clinically important.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Rheumatol Year: 2024 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Rheumatol Year: 2024 Type: Article