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Postoperative Nausea, Vomiting and Pain After Bariatric Surgery - a National Registry Study (BAROSPOR)

27 de agosto de 2026 actualizado por: Jakob Walldén, Umeå University

Pain and Nausea in the Post-Anaesthesia Care Unit After Bariatric Surgery: A Registry Study Linking the Swedish Perioperative Register (SPOR) and the Scandinavian Obesity Surgery Registry (SOReg)

Around 4,000-5,000 bariatric (weight-loss) operations are performed in Sweden every year. Nausea, vomiting and pain are common immediately after these operations, cause considerable suffering and increase the intensity and length of hospital care. Bariatric surgery is one of the procedures with the highest risk of postoperative nausea and vomiting (PONV): about one third of patients experience PONV already in the recovery unit, and registry data indicate that around 40% report severe pain at the same stage.

This study links two national quality registries - the Swedish Perioperative Register (SPOR) and the Scandinavian Obesity Surgery Registry (SOReg) - to describe how often adult patients experience nausea, vomiting and pain in the post-anaesthesia care unit after primary bariatric surgery, and to identify patient, anaesthetic and surgical factors associated with these outcomes. The study tests whether total intravenous anaesthesia, the addition of a regional nerve block, and preoperative health-related quality of life are associated with PONV and pain, and whether early PONV or pain is associated with complications, unplanned hospital care or reoperation up to one year after surgery. The results are intended to show how well current evidence on preventing PONV and pain is applied in everyday practice and where care can be improved.

Descripción general del estudio

Descripción detallada

BACKGROUND Bariatric surgery is common in Sweden with 4,000-5,000 procedures per year. Data on each operation are recorded in the Swedish Perioperative Register (SPOR), covering more than 90% of all surgical procedures in Sweden with automatic data transfer from hospital IT systems, and in the Scandinavian Obesity Surgery Registry (SOReg), with a coverage of approximately 98% of bariatric surgery. Postoperative nausea and vomiting (PONV) and pain are frequent after bariatric surgery. Evidence-based guidelines exist, but 25-40% of surgical patients still experience PONV, and up to 50% may experience severe postoperative pain. Risk factors are validated at a general level but not specifically for bariatric surgery.

OBJECTIVES

  1. To describe the risk of early PONV and pain in the post-anaesthesia care unit (PACU) after primary bariatric surgery.
  2. To identify factors associated with early PONV and pain.
  3. To test the hypotheses that total intravenous anaesthesia (compared with inhalational anaesthesia) and the addition of a regional block are associated with lower risk of PONV or pain in the PACU; that poorer preoperative health-related quality of life (RAND-36) is associated with higher risk of PONV, pain and severe pain; and that PONV or pain in the PACU is associated with higher risk of postoperative complications up to one year after surgery. Separate hypothesis tests are performed for PONV and pain.

DESIGN Exploratory observational cohort study based on registry data. Patients aged 18 years or older with a primary bariatric procedure registered in SOReg during 2018-2027 are identified. Records are linked to SPOR by Uppsala Clinical Research Center (UCR) using personal identity number and date of surgery (+/- 3 days). If several SPOR records fall within the interval, each is included as a separate row with an index variable linking to the SOReg operation. Each individual is assigned a unique serial number and the dataset delivered to the research group contains pseudonymised data only. Data extractions are made at most once per year from 2025; the first analyses cover 2018-2023.

VARIABLES From SOReg: preoperative data (patient characteristics, comorbidity, laboratory values, preoperative work-up, RAND-36), operative data (procedure type, technique, intraoperative complications) and postoperative follow-up up to one year (complications, hospital care, reoperation). From SPOR: patient characteristics, process data, operative data (diagnosis, procedure, anaesthesia type, times, deviations), postoperative data (pain, nausea/vomiting, deviations, level of care) and date of death.

STATISTICAL ANALYSIS Descriptive statistics with univariable and multivariable analysis of associations. Candidate variables include sex, age, comorbidity, preoperative pain, anaesthesia type, procedure type, surgical technique and length of stay. The expected sample is approximately 70% of all bariatric operations in Sweden, about 3,000 patients per year; the main reason for exclusion is expected to be missing PACU registration of pain and/or nausea at some hospitals. As the study includes more than half of the target population, no formal power calculation is performed.

DATA PROTECTION Only pseudonymised data are handled. Data are stored at Umeå University with access restricted to the study researchers, in accordance with current legislation.

Tipo de estudio

De observación

Inscripción (Estimado)

30000

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

  • Nombre: Jakob Walldén, MD, PhD
  • Número de teléfono: +46 60 14 52 55
  • Correo electrónico: jakob.wallden@umu.se

Ubicaciones de estudio

      • Sundsvall, Suecia, 851 86
        • Reclutamiento
        • Sundsvall Hospital, Department of Anaesthesia and Intensive Care
      • Umeå, Suecia, 901 87
        • Reclutamiento
        • Umeå University, Department of Diagnostics and Intervention
        • Sub-Investigador:
          • Antonio Moraitis, MD
        • Contacto:
          • Jakob Walldén, MD, PhD
          • Número de teléfono: +46 60 14 52 55
          • Correo electrónico: jakob.wallden@umu.se
        • Investigador principal:
          • Jakob Walldén, MD, PhD
        • Sub-Investigador:
          • Magnus Hultin, MD, PhD
        • Sub-Investigador:
          • Yucel Cengiz, MD, PhD

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Método de muestreo

Muestra no probabilística

Población de estudio

All adult patients registered in the Scandinavian Obesity Surgery Registry (SOReg) with a primary bariatric procedure during 2018-2027 and a matching operation record in the Swedish Perioperative Register (SPOR).

Descripción

Inclusion Criteria:

  • Age 18 years or older
  • Primary bariatric surgery registered in SOReg during 2018-2027

Exclusion Criteria:

  • Revision bariatric surgery
  • If more than one bariatric operation is registered for the same patient, only the primary operation is included

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

Cohortes e Intervenciones

Grupo / Cohorte
Adults undergoing primary bariatric surgery in Sweden 2018-2027
Patients aged 18 years or older with a primary bariatric procedure registered in the Scandinavian Obesity Surgery Registry (SOReg) 2018-2027 and a matching operation record in the Swedish Perioperative Register (SPOR).

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Incidence of postoperative nausea and/or vomiting in the post-anaesthesia care unit
Periodo de tiempo: During the stay in the post-anaesthesia care unit (approximately 0-4 hours after surgery)
Number of operations with registered nausea and/or vomiting in the PACU divided by the total number of operations. Source: SPOR variable "Illamående postoperativt" (postoperative nausea).
During the stay in the post-anaesthesia care unit (approximately 0-4 hours after surgery)
Pain intensity in the post-anaesthesia care unit, numerical rating scale (NRS) 0-10
Periodo de tiempo: During the stay in the post-anaesthesia care unit (approximately 0-4 hours after surgery)
Median NRS score (0 = no pain, 10 = worst imaginable pain). Source: SPOR variables "Smärta inom 1 tim efter ankomst UVA" (pain within 1 hour of PACU arrival) and "Smärta postoperativt, högsta" (highest postoperative pain).
During the stay in the post-anaesthesia care unit (approximately 0-4 hours after surgery)
Incidence of severe pain in the post-anaesthesia care unit
Periodo de tiempo: During the stay in the post-anaesthesia care unit (approximately 0-4 hours after surgery)
Number of operations with NRS >= 7 divided by the total number of operations.
During the stay in the post-anaesthesia care unit (approximately 0-4 hours after surgery)

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Proportion of patients with postoperative complications, unplanned hospital care or reoperation - 6 weeks
Periodo de tiempo: Up to 6 weeks after surgery
Complications (including Clavien-Dindo grade), unplanned hospital care and reoperation as registered in SOReg at the 6-week follow-up.
Up to 6 weeks after surgery
Proportion of patients with postoperative complications, unplanned hospital care or reoperation - 1 year
Periodo de tiempo: Up to 1 year after surgery
Complications (including Clavien-Dindo grade), unplanned hospital care and reoperation as registered in SOReg at the 1-year follow-up.
Up to 1 year after surgery

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Investigadores

  • Investigador principal: Jakob Walldén, MD, PhD, Umeå University

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

1 de octubre de 2025

Finalización primaria (Estimado)

31 de diciembre de 2027

Finalización del estudio (Estimado)

1 de diciembre de 2028

Fechas de registro del estudio

Enviado por primera vez

27 de agosto de 2026

Primero enviado que cumplió con los criterios de control de calidad

27 de agosto de 2026

Publicado por primera vez (Actual)

1 de septiembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

1 de septiembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

27 de agosto de 2026

Última verificación

1 de agosto de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • BAROSPOR-2025-01
  • 2025 (Subvención/contrato del NIH de EE. UU.: Faculty of Social Sciences Scientific Grant at the University of Gdańsk)
  • 2025-00877-01 (Otro identificador: Swedish Ethical Review Authority (Etikprovningsmyndigheten))

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

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