The Effect of Pressure Wound Care Package on the Development of Operating Room Pressure Wound in Orthopedic Surgery

NCT ID: NCT05852236

Last Updated: 2023-05-10

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 190 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-07-01
• Study Completion Date: 2022-04-30

Brief Summary

SUMMARY In a non-randomised (quasi-experimental) clinical study, it was aimed to determine the effect of the care package applied in the early postoperative period on operating theatre pressure sores, pain, fear of falling and comfort in patients undergoing orthopaedic surgery. In the study, the care bundle for pressure injuries was prepared in accordance with the clinical guidelines and was applied to the patients in the study group. This study was conducted in the orthopaedics and traumatology clinic of a public hospital in the Southeastern Anatolia Region of Turkey.

Detailed Description

Medhod:Patients in the control group underwent routine practice of the clinic and this group was observed for 199 days. The care bundle for pressure injuries developed within the scope of the research was not applied. In the study group, in addition to routine clinical practice, the care bundle for pressure injuries developed for this study was applied for 105 days. Since the pressure ulcer originating from the operating room was seen until the 48th-72nd hour, the evaluations and interventions within the scope of the study were performed for three days, considering the operation day as the zeroth day for the control and study groups. A total of 190 patients, 122 in the control group and 68 in the study group, were included in the study.

The care bundle consisted of "skin care, positioning, early mobilization, nutrition, and fluid intake" interventions. In the study, first, the data of the control group and then the data of the study group were collected.

Data Collection Tools: The Patient Descriptive Information Form consists of sociodemographic data. The 3S OR Pressure Injury Risk Assessment Scale was used to identify patients at risk of developing OR pressure ulcers. Visual Analogue Scale was used to evaluate pain perception. The Visual Analog Scale was used to determine the fear of falling. General Comfort Questionnaire-Short Form was used to determine the comfort level. The National Pressure Ulcer Advisory Panel (NPUAP) 2016 Pressure Injury Staging System was used to assess and stage pressure ulcer development. Pressure Injury Areas and Stages Follow-up Registration Form; The form in which the pressure ulcer development status is recorded.

Conditions

Pressure Injury; Orthopedic Surgery

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: FACTORIAL
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: NONE

Study Groups

Control Group

The standard care of the clinic was applied to the control group.

Group Type: EXPERIMENTAL

Assigned Interventions

Intervention Type: OTHER

Pressure ulcer care package application.

Study Group

The pressure ulcer care package developed for this study was applied to the study group.

Group Type: EXPERIMENTAL

Assigned Interventions

Intervention Type: OTHER

Pressure ulcer care package application.

Interventions

Assigned Interventions

Pressure ulcer care package application.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

18 years of age or older

• Orthopaedics and traumatology department
• Those who have undergone general or spinal anaesthesia
• No history of surgery in the last month
• Without any communication problems
• 3S Patients with a score of 18 and above on the Operating Theatre Pressure Wound Risk Assessment Scale
• Patients admitted to the emergency clinic, whose trauma-related surgery is planned within 24 hours from the emergency clinic
• Admission to the orthopaedics and traumatology clinic within maximum 24 hours from the day of surgery planned as elective surgery
• Patients who volunteered to participate in the study were included.

Exclusion Criteria

• I'm the one whose surgery was cancelled
• Those who have undergone local or regional anaesthesia
• Patients referred to the intensive care unit after surgery
• Patients who wanted to leave the study after volunteering were excluded from the study.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Sehitkamil Devlet Hastanesi

OTHER

Sponsor Role: lead

Responsible Party

Hatice Eğilmez

Nurse, RN

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Ayla YAVA, PhD

Role: STUDY_DIRECTOR

Prefessor

Locations

Şehitkamil Devlet Hastanesi

Gaziantep, , Turkey (Türkiye)

Countries

Turkey (Türkiye)

Other Identifiers

ŞehitkamilDH275002727

Identifier Type: -

Identifier Source: org_study_id