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Time- and dose-dependent correlations between patient-controlled epidural analgesia and intrapartum maternal fever.
Zhao, Bai-Song; Li, Bing; Wang, Qing-Ning; Jia, Jun-Xiang; Song, Xing-Rong.
Afiliação
  • Zhao BS; Department of Anesthesiology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No. 9 Jinsui Road, Tianhe District, Guangzhou, 510623, Guangdong, China.
  • Li B; Department of Anesthesiology, Women and Children's Hospital, School of Medicine, Xiamen University, Xiamen, 361000, Fujian, China.
  • Wang QN; Department of Anesthesiology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No. 9 Jinsui Road, Tianhe District, Guangzhou, 510623, Guangdong, China.
  • Jia JX; Department of Anesthesiology, Women and Children's Hospital, School of Medicine, Xiamen University, Xiamen, 361000, Fujian, China. ybmzjjx@126.com.
  • Song XR; Department of Anesthesiology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No. 9 Jinsui Road, Tianhe District, Guangzhou, 510623, Guangdong, China. songxingrong510623@163.com.
BMC Anesthesiol ; 21(1): 31, 2021 01 29.
Article em En | MEDLINE | ID: mdl-33514322
ABSTRACT

BACKGROUND:

To investigate the relationship between intrapartum maternal fever and the duration and dosage of patient-controlled epidural analgesia (PCEA).

METHODS:

This observational study included 159 pregnant women who voluntarily accepted PCEA. During labor, patients with body temperature ≥ 38 °C were classified into the Fever group, (n = 42), and those with body temperature < 38 °C were classified into the No-fever group (n = 117). The outcome measures included the duration of PCEA, number of PCEA, and total PCEA amount. Body temperature and parturient variables, including interpartum fever status and the duration of any fever were monitored.

RESULTS:

The total PCEA duration and total PCEA amount in the Fever group were significantly higher than the corresponding values in the No-fever group (both, p < 0.05). The duration of fever was weakly correlated with the duration of PCEA (R2 = 0.08) and the total PCEA amount (R2 = 0.05) (both, p < 0.05). The total and effective PCEA were higher in the Fever group than in the No-fever group (both, p < 0.05). The total PCEA duration and total PCEA amount were positively correlated with the incidence of fever (both, p < 0.05). The diagnostic cutoff value for fever was 383 min, with a sensitivity of 78.6% and specificity of 57.3%. The mean temperature-time curves showed that parturients who developed fever had a steeper rise in temperature.

CONCLUSIONS:

This study showed that there were weak time- and dose-dependent correlations between PCEA and maternal fever during delivery. A total PCEA duration exceeding 6.3 h was associated with an increase in the duration of maternal intrapartum fever.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Trabalho de Parto / Analgesia Epidural / Analgesia Obstétrica / Analgesia Controlada pelo Paciente / Febre Tipo de estudo: Observational_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Revista: BMC Anesthesiol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Trabalho de Parto / Analgesia Epidural / Analgesia Obstétrica / Analgesia Controlada pelo Paciente / Febre Tipo de estudo: Observational_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Revista: BMC Anesthesiol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China