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Risk of placental abruption in relation to maternal depressive, anxiety and stress symptoms

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Background Little is known about the influence of psychiatric factors on the etiology of placental abruption (PA), an obstetrical condition that complicates 1–2% of pregnancies. We examined the risk of PA in relation to maternal psychiatric symptoms during pregnancy. Methods This case–control study...

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Detalles Bibliográficos
Autores: de Paz, Nicole C., Sanchez, Sixto E., Huaman, Luis E., Diez Chang, Guillermo, Pacora, Percy N., Garcia, Pedro J., Ananth, Cande V., Qiu, Chungfang, Williams, Michelle A.
Formato: artículo
Fecha de Publicación:2011
Institución:Universidad de San Martín de Porres
Repositorio:USMP-Institucional
Lenguaje:inglés
OAI Identifier:oai:repositorio.usmp.edu.pe:20.500.12727/6357
Enlace del recurso:https://hdl.handle.net/20.500.12727/6357
Nivel de acceso:acceso abierto
Materia:Desprendimiento prematuro de la placenta
Epidemiología
Embarazo
Depresión
Ansiedad
Factores de riesgo
https://purl.org/pe-repo/ocde/ford#3.02.00
Descripción
Sumario:Background Little is known about the influence of psychiatric factors on the etiology of placental abruption (PA), an obstetrical condition that complicates 1–2% of pregnancies. We examined the risk of PA in relation to maternal psychiatric symptoms during pregnancy. Methods This case–control study included 373 PA cases and 368 controls delivered at five medical centers in Lima, Peru. Depressive, anxiety and stress symptoms were assessed using the Patient Health Questionnaire (PHQ-9) and the Depression Anxiety Stress Scales (DASS-21). Multivariable logistic regression models were fit to calculate odds ratios (aOR) and 95% confidence intervals (CI) adjusted for confounders. Results Depressive symptoms of increasing severity (using the DASS depression subscale) was associated with PA (p for trend = 0.02). Compared with women with no depressive symptoms, the aOR (95%CI) for PA associated with each level of severity of depression symptoms based on the DASS assessment were as follows: mild 1.84 (0.91–3.74); moderate 1.25 (0.67–2.33); and severe 4.68 (0.98–22.4). The corresponding ORs for mild, moderate, and moderately severe depressive symptoms based on the PHQ assessment were 1.10 (0.79–1.54), 3.31 (1.45–7.57), and 5.01 (1.06–23.6), respectively. A positive gradient was observed for the odds of PA with severity of anxiety (p for trend = 0.002) and stress symptoms (p for trend = 0.002). Limitations These cross-sectionally collected data may be subject to recall bias. Conclusions Maternal psychiatric disorders may be associated with an increased occurrence of AP. Larger studies that allow for more precise evaluations of maternal psychiatric health in relation to PA risk are warranted.
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