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Nonstress testing at ≤ 32.0 weeks' gestation: a randomized trial comparing different assessment criteria.
Cousins, Larry M; Poeltler, Debra M; Faron, Sue; Catanzarite, Val; Daneshmand, Sean; Casele, Holly.
Afiliación
  • Cousins LM; Maternal Fetal Medicine Division, San Diego Perinatal Center and Children's Specialists of San Diego, San Diego, CA 92123, USA. Larry.Cousins@sharp.com
Am J Obstet Gynecol ; 207(4): 311.e1-7, 2012 Oct.
Article en En | MEDLINE | ID: mdl-23021694
ABSTRACT

OBJECTIVE:

Comparison of time and outcomes of National Institutes of Child Health and Human Development defined fetal heart rate acceleration criteria at ≤ 32 weeks (≥ 10 beats/min, ≥ 10 seconds) compared with standard criteria (≥ 15 beats/min, ≥ 15 seconds). STUDY

DESIGN:

Singleton high-risk pregnancies that were referred for nonstress testing at ≤ 32 weeks' gestation were randomly assigned to 15 × 15 or 10 × 10 criteria. Data included nonstress test information, maternal data, and outcomes.

RESULTS:

One hundred forty-three women were randomly assigned to 15 × 15 (n = 71) or 10 × 10 (n = 72). The groups were similar in maternal and pregnancy characteristics. Median time to reactive nonstress testing was shorter in the 10 × 10 group (37.3 minutes) than the 15 × 15 group (41.3 minutes; P = .04). There were no serious adverse events.

CONCLUSION:

The time to attain a reactive nonstress testing at ≤ 32 weeks' gestation was 4 minutes shorter when the 10 × 10 criteria were used. There were no adverse events related to use of 10 × 10 nonstress testing criteria.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Frecuencia Cardíaca Fetal / Cardiotocografía / Sufrimiento Fetal Tipo de estudio: Clinical_trials Límite: Adult / Female / Humans / Pregnancy Idioma: En Revista: Am J Obstet Gynecol Año: 2012 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Frecuencia Cardíaca Fetal / Cardiotocografía / Sufrimiento Fetal Tipo de estudio: Clinical_trials Límite: Adult / Female / Humans / Pregnancy Idioma: En Revista: Am J Obstet Gynecol Año: 2012 Tipo del documento: Article País de afiliación: Estados Unidos
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