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1.
Obstet Gynecol ; 139(3): 368-372, 2022 03 01.
Artículo en Inglés | MEDLINE | ID: mdl-35115451

RESUMEN

OBJECTIVE: To describe outcomes associated with monoclonal antibody use in pregnant persons with mild-to-moderate coronavirus disease 2019 (COVID-19). METHODS: We present a retrospective case series of pregnant patients who received anti-severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) monoclonal antibody infusions at a single center from April 1, 2021, through October 16, 2021. Pregnant patients who had a positive SARS-CoV-2 polymerase chain reaction (PCR) test result and mild-to-moderate COVID-19 symptoms were eligible for monoclonal antibody infusion. Exclusion criteria for administration included need for supplemental oxygen, hospitalization due to COVID-19, and positive SARS-CoV-2 PCR test result more than 7 days before screening. All patients received either bamlanivimab plus etesevimab or casirivimab plus imdevimab based on availability and dosing instructions of the product and emerging resistance patterns in the community. RESULTS: During the study period, monoclonal antibody infusions were administered to 450 individuals at our institution, of whom 15 were pregnant. Of the 15 pregnant persons receiving monoclonal antibody, six (40%) had full-vaccination status at the time of infusion. Two individuals (13%, CI 0-31%) experienced systemic reactions during the infusion, both resulting in temporary changes in the fetal heart rate tracing that recovered with maternal and intrauterine resuscitative efforts. One patient delivered after infusion for worsening maternal and fetal status; the remainder of the patients did not require admission for COVID-19. CONCLUSION: In this case series, pregnant persons who received anti-SARS-CoV-2 monoclonal antibody infusions had generally favorable outcomes.


Asunto(s)
Anticuerpos Monoclonales Humanizados/efectos adversos , Anticuerpos Monoclonales/efectos adversos , Anticuerpos Neutralizantes/efectos adversos , Tratamiento Farmacológico de COVID-19 , Complicaciones Infecciosas del Embarazo/tratamiento farmacológico , Combinación de Medicamentos , Femenino , Corazón Fetal/efectos de los fármacos , Humanos , Sobretratamiento , Embarazo , Estudios Retrospectivos
2.
Nurs Womens Health ; 17(2): 98-107, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23594322

RESUMEN

Because women hospitalized in obstetric units are typically young and healthy, they might be overlooked when health care providers assess for risk for falls. Recent literature has identified pregnant and postpartum women as being prone to falls, with hospitalization compounding their risk. A review of current practices among perinatal units for assessing risk for falls revealed that existing fall risk tools, which were created for geriatric and/or medical surgical patients, are used. Without any focused prevention efforts, hospitalized obstetric patients are vulnerable to a preventable event. The Obstetric Fall Risk Assessment System™ is intended to improve safety among hospitalized women on obstetric units, using an assessment tool and scoring system to determine fall risk.


Asunto(s)
Accidentes por Caídas/prevención & control , Evaluación en Enfermería/métodos , Enfermería Obstétrica , Administración de la Seguridad/métodos , Enfermería Basada en la Evidencia , Femenino , Humanos , Investigación en Evaluación de Enfermería , Investigación Metodológica en Enfermería , Servicio de Ginecología y Obstetricia en Hospital , Embarazo , Estudios Retrospectivos , Medición de Riesgo/métodos
3.
Am J Infect Control ; 40(9): 820-5, 2012 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-22418608

RESUMEN

BACKGROUND: We implemented evidence-based interventions to reduce risk of surgical site infection (SSI) following low transverse cesarean section (LTCS). METHODS: An observational study was conducted to determine LTCS SSI rates and the impact of infection control interventions at an academic teaching hospital during the period October 2005 to December 2008, including the use of 2% chlorhexidine gluconate (CHG) for surgical skin preparation before LTCS and no-rinse CHG cloths for preoperative skin cleansing. We compared overall and risk strata specific SSI rates and standardized incidence ratios during 4 study periods and estimated cost savings. RESULTS: Of 1,844 LTCSs performed, 99 patients were identified with SSI. SSI rates per 100 LTCS declined from 6.27 at baseline and 10.84 during the outbreak period to 5.92 in intervention 1 period and 2.29 in intervention 2 period. Overall, a 63.5% reduction in SSI rate from baseline was achieved by ensuring compliance with SSI prevention guidelines and improving skin antisepsis (P = .003). In intervention 2 period, the standardized incidence ratio was 0.99 compared with 2.64 at baseline and 4.50 during the outbreak period. CONCLUSION: A multidisciplinary approach including evidence-based SSI prevention practices, effective infection prevention products, and staff and patient engagement substantially reduced infection risk and improved patient safety following LTCS.


Asunto(s)
Cesárea/efectos adversos , Cesárea/métodos , Control de Infecciones/métodos , Infección de la Herida Quirúrgica/epidemiología , Infección de la Herida Quirúrgica/prevención & control , Clorhexidina/administración & dosificación , Clorhexidina/análogos & derivados , Desinfectantes/administración & dosificación , Desinfección/métodos , Hospitales Universitarios , Humanos , Incidencia , Cuidados Preoperatorios/métodos
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