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Labor therapeutics and BMI as risk factors for postpartum preeclampsia: A case-control study.
Skurnik, Geraldine; Hurwitz, Shelley; McElrath, Thomas F; Tsen, Lawrence C; Duey, Stacey; Saxena, Aditi R; Karumanchi, Ananth; Rich-Edwards, Janet W; Seely, Ellen W.
Afiliación
  • Skurnik G; Division of Endocrine, Diabetes, and Hypertension, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States. Electronic address: gskurnik@partners.org.
  • Hurwitz S; Division of Endocrine, Diabetes, and Hypertension, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States.
  • McElrath TF; Division of Maternal and Fetal Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States.
  • Tsen LC; Department of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States.
  • Duey S; Research Patient Data Registry/Biobank Portal, Brigham and Women's Hospital, Boston, MA, United States.
  • Saxena AR; Division of Endocrine, Diabetes, and Hypertension, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States.
  • Karumanchi A; Division of Nephrology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, United States.
  • Rich-Edwards JW; Connors Center for Women's Health and Gender Biology, Brigham and Women's Hospital, Harvard Medical School, and Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, United States.
  • Seely EW; Division of Endocrine, Diabetes, and Hypertension, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States.
Pregnancy Hypertens ; 10: 177-181, 2017 Oct.
Article en En | MEDLINE | ID: mdl-29153674
ABSTRACT

OBJECTIVES:

This study aims at identifying associations between therapeutics used during labor and the occurrence of postpartum preeclampsia (PPPE), a poorly understood entity. STUDY DESIGN AND MAIN OUTCOME

MEASURES:

This is a case-control study of women who received an ICD-9 code for PPPE (cases) during the years 2009-2011, compared to women with a normotensive term pregnancy, delivery and postpartum period until discharge (controls), matched on age (±1year) and delivery date (±3months). Cases were defined as women having a normotensive term pregnancy, delivery and initial postpartum period (48h post-delivery) but developing hypertension between 48h and 6weeks postpartum. Single variable and multiple variable models were used to determine significant risk factors.

RESULTS:

Forty-three women with PPPE were compared to 86 controls. Use of vasopressors and oxytocin did not differ between cases and controls, but rate of fluids administered during labor (OR=1.68 per 100cc/h; 95% CI 1.09-2.59, p=0.02) and an elevated pre-pregnancy/first trimester BMI (OR=1.18 per kg/m2, 95% CI 1.07-1.3, p=0.001) were identified as significant risk factors in multivariate analysis.

CONCLUSIONS:

We identified two potentially modifiable risk factors for PPPE; further studies are needed to better define the role of these two variables in the development of PPPE.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Preeclampsia / Trastornos Puerperales Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Pregnancy País/Región como asunto: America do norte Idioma: En Revista: Pregnancy Hypertens Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Preeclampsia / Trastornos Puerperales Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Pregnancy País/Región como asunto: America do norte Idioma: En Revista: Pregnancy Hypertens Año: 2017 Tipo del documento: Article