Suscribirse

Enhanced recovery after elective craniotomy: A randomized controlled trial - 27/11/21

Doi : 10.1016/j.jclinane.2021.110575 
Lei Wang, MD a, Hongwei Cai, MD, PhD a, Yanjin Wang, MD, PhD b, Jian Liu, MD, PhD b, Tiange Chen, MD b, Jing Liu, MD a, Jiapeng Huang, MD, PhD c, Qulian Guo, MD, PhD a, Wangyuan Zou, MD, PhD a, d,
a Department of Anesthesiology, Xiangya Hospital, Central South University, Changsha, Hunan, China 
b Department of Neurosurgery, Xiangya Hospital, Central South University, Changsha, Hunan, China 
c Department of Anesthesiology & Perioperative Medicine, University of Louisville, Louisville, KY, United States of America 
d National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, China 

Corresponding author at: Department of Anesthesiology, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, Hunan 410008, China. E-mail addresses: wangyuanzou@csu.edu.cn (W. Zou).Department of AnesthesiologyXiangya HospitalCentral South UniversityChangshaHunanChina

Abstract

Study objectives

Enhanced recovery after surgery (ERAS) protocols have been proven to improve outcomes but have not been widely used in neurosurgery. The purpose of this study was to design a multidisciplinary enhanced recovery after elective craniotomy protocol and to evaluate its clinical efficacy and safety after implementation.

Design

A prospective randomized controlled trial.

Setting

The setting is at an operating room, a post-anesthesia care unit, and a hospital ward.

Patients

This randomized controlled trial (RCT) prospectively analyzed 151 patients who underwent elective craniotomy between January 2019 and June 2020.

Interventions

The neurosurgical ERAS group was cared for with evidence-based systematic optimization approaches, while the control group received routine care.

Measurements

The primary outcomes were the postoperative length of stay (LOS) and hospitalization costs. The secondary outcomes included 30-day readmission rates, postoperative complications, postoperative pain scores, length of intensive care unit (ICU) stay, duration of the drainage tube, time to oral intake, time to ambulation, and postoperative functional recovery status.

Main results

After ERAS protocol implementation, the median postoperative LOS (4 days to 3 days, difference [95% confidence interval, CI], 2 [1, 2], P < 0.0001) and hospitalization costs (6266 USD to 5880 USD, difference [95% CI], 427.0 [234.8 to 633.6], P < 0.0001) decreased. Compared to routine perioperative care, the ERAS protocol reduced the incidence of postoperative nausea and vomiting (PONV) (28.0% to 9.2%, adjusted odds ratio [OR] 0.3, 95% CI 0.1–0.7, P = 0.003), shortened urinary catheter removal time by 24 h (64.0% to 83.0%, adjusted OR 2.9, 95% CI 1.3–6.5, P = 0.031), improved ambulation on postoperative day 1 (POD 1) (30.7% to 75.0%, adjusted OR 7.5, 95% CI 3.6–15.8, P < 0.0001), shortened the time to oral intake (15 h to 13 h, difference [95% CI], 3 [1, 2, 3, 4], P < 0.001), and improved perioperative pain management.

Conclusions

Implementation of an enhanced recovery after elective craniotomy protocol had significant benefits over conventional perioperative management. It was associated with a significant reduction in postoperative length of stay, medical cost, and postoperative complications.

El texto completo de este artículo está disponible en PDF.

Highlights

Implementation of the ERAS protocol in patients undergoing elective craniotomy reduce postoperative length of stay and hospitalization costs.
The application of multimodal analgesic approaches reduce moderate and severe postoperative pain, and shorten the pain duration in craniotomy.
Patients who received the ERAS protocol achieved a low incidence of PONV and early postoperative functional recovery.
Our study complements the gap in clinical research on the application of the ERAS protocol in neurosurgical anesthesia.

El texto completo de este artículo está disponible en PDF.

Keywords : Enhanced recovery after surgery, Neurosurgical anesthesia, Perioperative care, Postoperative length of stay, Outcomes


Esquema


© 2021  Elsevier Inc. Reservados todos los derechos.
Añadir a mi biblioteca Eliminar de mi biblioteca Imprimir
Exportación

    Exportación citas

  • Fichero

  • Contenido

Vol 76

Artículo 110575- février 2022 Regresar al número
Artículo precedente Artículo precedente
  • Development and assessment of an efficient pediatric affect and cooperation scale
  • Kristin M. Kennedy, Ellen Wang, Samuel T. Rodriguez, Jimmy Qian, Michael Khoury, Madison N. Kist, Christian Jackson, Romy Yun, Thomas J. Caruso
| Artículo siguiente Artículo siguiente
  • Exploratory study of VVZ-149, a novel analgesic molecule, in the affective component of acute postoperative pain after laparoscopic colorectal surgery
  • Srdjan S. Nedeljkovic, Inkyung Song, Xiaodong Bao, Jose L. Zeballos, Darin J. Correll, Yi Zhang, Johanna S. Ledley, Ashish Bhandari, Xiang Bai, Sang Rim Lee, Sunyoung Cho

Bienvenido a EM-consulte, la referencia de los profesionales de la salud.
El acceso al texto completo de este artículo requiere una suscripción.

¿Ya suscrito a @@106933@@ revista ?

@@150455@@ Voir plus

Mi cuenta


Declaración CNIL

EM-CONSULTE.COM se declara a la CNIL, la declaración N º 1286925.

En virtud de la Ley N º 78-17 del 6 de enero de 1978, relativa a las computadoras, archivos y libertades, usted tiene el derecho de oposición (art.26 de la ley), el acceso (art.34 a 38 Ley), y correcta (artículo 36 de la ley) los datos que le conciernen. Por lo tanto, usted puede pedir que se corrija, complementado, clarificado, actualizado o suprimido información sobre usted que son inexactos, incompletos, engañosos, obsoletos o cuya recogida o de conservación o uso está prohibido.
La información personal sobre los visitantes de nuestro sitio, incluyendo su identidad, son confidenciales.
El jefe del sitio en el honor se compromete a respetar la confidencialidad de los requisitos legales aplicables en Francia y no de revelar dicha información a terceros.


Todo el contenido en este sitio: Copyright © 2026 Elsevier, sus licenciantes y colaboradores. Se reservan todos los derechos, incluidos los de minería de texto y datos, entrenamiento de IA y tecnologías similares. Para todo el contenido de acceso abierto, se aplican los términos de licencia de Creative Commons.