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Episiotomy Wound Care, Episiotomy Wound Healing and Pain Perception

Not Applicable
Completed
Conditions
Pain
Episiotomy Wound
Wound Healing
Training, Toilet
Interventions
Other: Episiotomy Wound Care and Genital Hygiene Training
Registration Number
NCT05358236
Lead Sponsor
Aydin Adnan Menderes University
Brief Summary

The World Health Organization (WHO) and professional societies recommend restricted episiotomy instead of routine episiotomy. However, since the 1990s, there has been evidence of the risks of the procedure, and although routine use has no benefit, it is still widely used. In this study, investigators aimed to determine the effect of episiotomy on the wound healing process and pain perception by providing episiotomy wound healing and genital hygiene training with training material created to raise awareness about wound care after episiotomy and to eliminate factors that delay the healing of episiotomy wound.

Detailed Description

This study aimed to determine the effect of episiotomy wound care and genital hygiene training on episiotomy wound healing and pain perception.

Methods: In this study, investigators used a randomized controlled trial approach.

It was carried out in the postpartum service of the medical faculty hospital. 128 participants who underlap vaginal postpartum episiotomy were randomly assigned to the experimental and control group. The women who gave birth in the experimental group were given episiotomy wound care and genital hygiene training. The routine postpartum care was given to the participants who gave birth in the control group. The data were collected using the personal information form, the episiotomy area evaluation scale (REEDA score), and the Visual Analog Scale (VAS).

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Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
128
Inclusion Criteria
  • 18 years of age and older
  • primiparous
  • givingbirth vaginally on due date (37-42 gestational weeks)
  • who have a healthy newborn,
  • who have a mediolateral episiotomy,
  • who do not have communication problems
  • who can understand and speak Turkish were included in the research.
Exclusion Criteria
  • Givingbirth by cesarean section
  • Having third and fourth-degree perineal tears,
  • Having a history of diseases that prevent wound healing,
  • Using certain drugs (eg, glucocorticoids, anticoagulants, chemotherapy, immunosuppressant, and radiotherapy),
  • Having chronic systemic diseases (heart, kidney and lung diseases, coagulation disorder, immunodeficiency, connective tissue disorders, and diabetes),
  • Having history of genital warts, symptomatic vaginitis,
  • Having history of perineal reconstructive surgery, any postpartum complication (hemorrhage, puerperal infection, mastitis, thromboembolic disease or postpartum psychiatric disorder)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
training + written and illustrated training brochureEpisiotomy Wound Care and Genital Hygiene TrainingPostpartum first day was given wound care and genital hygiene training (one hour). At the end of the training, the mothers were given a written and illustrated training brochure.
Primary Outcome Measures
NameTimeMethod
Episiotomy Area Evaluation before interventionpostpartum 1sth day (after birth first 24 hours)

Assessed using the Episiotomy Area Evaluation Scale (REEDA SCORE) before intervention. This scale covers five factors indicating perineal wound healing: (1) Redness, (2) Edema, (3) Ecchymosis, (4) Discharge, and (5) Approximation. A total REEDA score is obtained by evaluating each category of these five recovery factors. The scale is evaluated by giving 0, 1, 2, and 3 points to each evaluation. The lowest score is 0 and the highest score is 15.

Personal information form before interventionpostpartum 1sth day (after birth first 24 hours)

Assessed using personal information. This instrument contains questions on women's sociodemographic and postpartum.

Episiotomy pain Evaluation before interventionpostpartum 1sth day (after birth first 24 hours)

The Visual Analogue Scale (VAS) scale, which would be applied to evaluate episiotomy pain in the postpartum period, was used to convert some values that cannot be measured numerically, and two-end definitions of the parameter to be evaluated are written at both ends of a 100 mm line. The participant was asked to indicate where his or her condition is suitable on this line by drawing a line or by placing a dot or pointing. "No pain" is written on one end and "very severe pain" on the opposite end; the participant was asked to mark the pain condition on this line.was used to convert some values that could not be measured numerically, and two-end definitions of the parameter to be evaluated are written at both ends of a 100 mm line.

Secondary Outcome Measures
NameTimeMethod
Episiotomy Area Evaluation after interventionPostpartum 15th day

Assessed using the Episiotomy Area Evaluation Scale (REEDA SCORE) before intervention. This scale covers five factors indicating perineal wound healing: (1) Redness, (2) Edema, (3) Ecchymosis, (4) Discharge, and (5) Approximation. A total REEDA score is obtained by evaluating each category of these five recovery factors. The scale is evaluated by giving 0, 1, 2, and 3 points to each evaluation. The lowest score is 0 and the highest score is 15.

Episiotomy pain Evaluation after interventionPostpartum 15th day

The Visual Analogue Scale (VAS) scale, which would be applied to evaluate episiotomy pain in the postpartum period, was used to convert some values that cannot be measured numerically, and two-end definitions of the parameter to be evaluated are written at both ends of a 100 mm line. The participant was asked to indicate where his or her condition is suitable on this line by drawing a line or by placing a dot or pointing. "No pain" is written on one end and "very severe pain" on the opposite end; the participant was asked to mark the pain condition on this line.was used to convert some values that could not be measured numerically, and two-end definitions of the parameter to be evaluated are written at both ends of a 100 mm line.

Trial Locations

Locations (1)

Gonca Buran

🇹🇷

Bursa, Turkey

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