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1.
J Clin Pharmacol ; 64(1): 111-117, 2024 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-37566902

RESUMEN

In this study, we examined the impact of dexmedetomidine (DEX) on the effectiveness of epidural analgesia and labor outcomes. We administered different doses of DEX combined with 0.1% ropivacaine for epidural analgesia to evaluate the clinical effects and safety. To assess the effects of different concentrations of DEX in parturient women receiving epidural analgesia, we conducted a randomized double-blind trial. We selected 400 parturient women and randomly assigned them to 4 groups, with 100 parturient women in each group: S0.1 (0.1 µg/mL DEX), S0.2 (0.2 µg/mL DEX), S0.3 (0.3 µg/mL DEX), and a control group (0.3 µg/mL sufentanil). Post-analgesia, we recorded the Bromage score, duration of labor, method of delivery, bleeding, neonatal Apgar score, adverse reactions, and maternal satisfaction. The number of patients with a Bromage score of ≥2 and the incidence of bradycardia were higher in the S0.3 group compared with the other 3 groups (P < .05), whereas the high satisfaction rate was lower in the S0.3 group (P < .05). Moreover, we found that the number of times that additional patient-controlled analgesia was administered was higher in the S0.1 group compared with the remaining 3 groups (P < .05). The control group exhibited a higher incidence of pruritus than the other 3 groups (P < .05). In conclusion, when administering spinal anesthesia for the relief of labor pain, epidural analgesia with 0.1% ropivacaine combined with 0.2 µg/mL DEX provides relatively ideal analgesic effects, higher maternal satisfaction, and reduces the incidence of pruritus, compared with the combination of 0.1% ropivacaine and 0.3 µg/mL sufentanil.


Asunto(s)
Analgesia Epidural , Dexmedetomidina , Embarazo , Recién Nacido , Humanos , Femenino , Ropivacaína , Sufentanilo/efectos adversos , Dexmedetomidina/efectos adversos , Anestésicos Locales , Analgésicos Opioides , Analgésicos , Analgesia Epidural/efectos adversos , Analgesia Epidural/métodos , Adyuvantes Inmunológicos , Satisfacción Personal , Prurito/inducido químicamente , Método Doble Ciego , Amidas/efectos adversos
2.
PLoS One ; 10(9): e0137267, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26340002

RESUMEN

OBJECTIVE: Combined spinal-epidural analgesia (CSEA) is sometimes used for difficult births, but whether it contributes to postpartum pelvic muscle disorder is unclear. This randomized controlled trial examined whether CSEA given during labor affects the electrophysiological index of postpartum pelvic floor muscle function. METHODS: A consecutive sample of primiparous women who delivered vaginally at term were randomly assigned to a CSEA group (n = 143) and control group (n = 142) between June 2013 and June 2014. All were assessed 6-8 weeks later for electrophysiological function of pelvic floor muscle. RESULTS: The two groups were similar in the degree of muscle strength, muscle fatigue, and pelvic dynamic pressure of pelvic floor muscle. The CSEA and control groups showed similar proportions of women with normal muscle strength (score ≥4) in type I pelvic fibers (23.1% vs. 14.1%, P = 0.051) and type II pelvic fibers (28.0% vs. 24.6%, P = 0.524). The groups also contained similar proportions of women who showed no fatigue in type I fibers (54.5% vs. 48.6%, P = 0.315) or type II fibers (88.8% vs. 87.3%, P = 0.699). Similarly low proportions of women in the CSEA group and control group showed normal pelvic dynamic pressure (11.2% vs. 7.7%, P = 0.321). However, women in the CSEA group spent significantly less time in labor than those in the control group (7.25 vs. 9.52 h, P <0.001). CONCLUSIONS: CSEA did not affect the risk of postpartum pelvic muscle disorder in this cohort of primiparous women who gave birth vaginally. A significant shorter duration of labour was observed in the CSEA-group. TRIAL REGISTRATION: ClinicalTrials.gov NCT02334150.


Asunto(s)
Analgesia Epidural/métodos , Analgesia Obstétrica/métodos , Fatiga Muscular , Diafragma Pélvico/fisiología , Adulto , Analgésicos Opioides , Estudios de Casos y Controles , Electrofisiología , Femenino , Humanos , Trabajo de Parto , Fibras Musculares Esqueléticas/fisiología , Fuerza Muscular/fisiología , Paridad , Periodo Posparto , Embarazo , Sufentanilo
3.
Hepatobiliary Pancreat Dis Int ; 10(5): 516-20, 2011 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-21947726

RESUMEN

BACKGROUND: Although low central venous pressure (CVP) has been used to minimize blood loss during hepatectomy, the impact of variations of CVP on the rate of blood loss and on the perfusion of end-organs has not been evaluated. This animal study aimed to evaluate the hemodynamics and oxygen transport changes during hepatic resection at different CVP levels. METHODS: Forty-eight anesthetized Bama miniature pigs were divided into 8 groups with CVP during hepatic resection controlled at 0 to <1, 1 to <2, 2 to <3, 3 to <4, 4 to <5, 5 to <6, 6 to <7, and 7 to <8 cmH2O. Intergroup comparisons were made for hemodynamic parameters, oxygen transport dynamics, and the rate of blood loss. RESULTS: The rate of blood loss and the hepatic venous pressure during hepatic resection were almost linearly related to the CVP. A significant drop in the mean arterial pressure, cardiac output, and cardiac index occurred between CVP ≥2 and <2 cmH2O. Oxygen delivery (DO2), oxygen consumption (VO2) and oxygen extraction ratio (ERO2) remained relatively constant between CVPs of 2 to <8 cmH2O. There was a significant drop in DO2 when the CVP was <2 cmH2O. There was also a significant drop in VO2 and ExO2 when the CVP was <1 cmH2O. CONCLUSION: The optimal CVP for hepatic resection is 2 to 3 cmH2O.


Asunto(s)
Pérdida de Sangre Quirúrgica/prevención & control , Presión Venosa Central , Hemodinámica , Hepatectomía/métodos , Oxígeno/sangre , Animales , Encéfalo/metabolismo , Femenino , Hepatectomía/efectos adversos , Modelos Animales , Consumo de Oxígeno , Porcinos , Porcinos Enanos , Factores de Tiempo
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