Anesthesia Methods on Percutaneous Kyphoplasty

B

Bursa Yüksek İhtisas Education and Research Hospital

Status

Completed

Conditions

Vertebral Fracture

Treatments

Procedure: Analgesic consumption

Study type

Observational

Funder types

Other

Identifiers

NCT05526794
2021-KAEK-25 2021/12-09

Details and patient eligibility

About

The aim of this research is to examine the effects of the anesthesia method and preoperative characteristics on postoperative results and complications in patients who underwent percutaneous kyphoplasty (PKP). Method: Patients were split into three groups according to anesthesia methods: (1) General Anesthesia (Sedation), (2) Central Block (Spinal and Epidural Anesthesia), (3) Peripheral Block [Erector Spina Plane Block (ESPB), and Paravertebral Block (PVB)]. Patients' pain values, hemodynamic parameters, additional need for sedation, and perioperative and postoperative complications were recorded prospectively together with Visual Pain Scales (VAS).

Full description

Demographic characteristics (body mass index [BMI], gender, age, ASA use, pain values [VAS] before surgery, analgesic use habits, anesthesia technique chosen by anesthesiologist blind to the study, perioperative hemodynamic parameters, additional opioid during surgery, parol? or anesthetic need, perioperative complications [patients who willingly stopped the procedure during the intervention, moaning, hypotension, hypertension, bradycardia, respiratory depression, desaturation and need for mask ventilation] were taken from the records of the individuals with the treatment of PKP between 01/22-07/22 after the approval of the SBÜ Bursa Yüksek İhtisas EAH Ethics Committee (2021-KAEK-25 2021/12-09) and the patient's consent. In addition, the first mobilization time, additional analgesic need, total amount of analgesic used in 24 hours, discharge time, VAS values at 2, 6,12, and 18 hours, complications (nausea, vomiting, pain, delirium, respiratory insufficiency, infection, deep vein thrombosis, pulmonary embolus, need for re-operation, need for intensive care or mechanic ventilator) were also recorded.

Enrollment

66 patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18-100 ages kyphoplasty surgery patients
  • written consent form received

Exclusion criteria

  • The patient's unwillingness to participate in the study
  • inability to communicate with the patient
  • the patient does not speak Turkish,
  • previous CVO, presence of cognitive impairment

Trial design

66 participants in 3 patient groups

Group 1
Description:
General anesthesia or sedation
Treatment:
Procedure: Analgesic consumption
Group 2
Description:
Central Block (Spinal and Epidural Anesthesia
Treatment:
Procedure: Analgesic consumption
Group 3
Description:
Peripheral Block [Erector Spina Plane Block (ESPB), and Paravertebral Block (PVB)
Treatment:
Procedure: Analgesic consumption

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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