Effect of Implementing Evidence Based Practices on Prevention of Associated Nasal Pressure Injuries Among Preterm Neonates With Non-Invasive Respiratory Support

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age30-37
SponsorKafrelsheikh University

About this trial

This study aims to evaluate the effect of implementing evidence based practices on prevention of associated nasal pressure injuries among preterm neonates with non invasive respiratory support

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Preterm neonates receiving NIRS

whose gestational ages ranges between 30 and 37 weeks, and both genders

Disqualifiers

all preterm neonates not receiving NIRS,

have prior nasal trauma caused by tracheal intubation

or Infants exhibiting evidence of nasal damage during the NIRS procedure,

have upper respiratory abnormalities.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Non Invasive Respiratory Support bundle

    Procedure/Surgery

    premature neonates who will receive evidence-based guidelines for prevention of nasal pressure injuries associated with non invasive respiratory support till weaning

Treatment groups

30 Participants
are divided into 2 treatment groups
Group A: Control GroupNo intervention 0 interventions
Group B: Bundle groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

change from the baseline nasal skin integrity on Nasal injury classification tool

: it is adopted from (Fischer et al., 2010) based on the standardized classification of the decubitus lesions from the US National Pressure Ulcer Advisory Panel (NPUAP) (Black et al., 2007; The National Pressure Ulcer Advisory Panel, 1989). This tool will be employed to describe and track the progression and severity of nasal injuries caused by NIRS in neonates by assessing nasal region (the nasal tip, nasal septum, nostril, and nose shape change) for erythema, ulceration, and necrosis, in order to ensure proper and early treatment

Time frame
Researchers will assess the nasal skin of preterm infants every 3-6 hours from the first day of providing NIRS till 14 days to determine the nasal damage score in both groups.
2

change from the baseline pain score on Premature Infant Pain Profile (PIPP)

It will be adopted from (Stevens et al., 1996). The Premature Infant Pain Profile (PIPP) is a biobehavioral observational technique used to quantify acute and procedure pain in premature infants. It assesses seven indicators: gestational age, behavioral state, increased heart rate, decreased oxygen saturation, forehead bulging, eye squeezing, and nasolabial furrows. Each indicator is scored on a four-point Likert scale, from 0 to 3. The total PIPP score, which is the sum of points for all seven indications, varies between 0 to 21. Higher scores imply more painful conduct. A number of 0-6 indicates no pain, 7-12 indicates mild to moderate pain, and a score more than 12 indicates severe pain.

Time frame
- Researchers will evaluate pain scores for preterm infants in both groups every 3-4 hours from the first day of providing NIRS till 14 days

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.