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Pressure Ulcer Prevention in Ventilated Patients Using Two Repositioning Regimens (PUPPAS)

Primary Purpose

Pressure Ulcers

Status
Completed
Phase
Phase 3
Locations
Spain
Study Type
Interventional
Intervention
repositioning
Sponsored by
University Hospital Virgen de las Nieves
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Pressure Ulcers focused on measuring Pressure ulcers, Repositioning, Prevention, Mechanical Ventilation, Critical care

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients admitted to the medical-surgical ICU, requiring more than 24 hours of mechanical ventilation.
  • Patients on alternating-pressure air mattresses.
  • Patients or their legal representative able to provide written informed consent to participate in the study
  • Patients whose weight are within the limits accepted by the mattresses (45-140 Kg)
  • Over 18 years

Exclusion Criteria:

  • Patients with pressure ulcer at ICU admission.
  • Pregnant patients
  • Patients in which informed consent is not obtained in the first 48 hours of mechanical ventilation

Sites / Locations

  • Hospital Universitario Virgen de las Nieves

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Turning every 4 hours

Turning every 2 hours

Arm Description

The four-hours repositioning group patients were turned every four hours following the next sequence: left side, back with a 30º elevation of the head end and the foot end of the bed, right side using the 30º tilt, back.

The two-hours repositioning group patients, were turned every two hours following the next sequence: left side, back with a 30º elevation of the head end and the foot end of the bed, right side using the 30º tilt, back.

Outcomes

Primary Outcome Measures

Incidence of Pressure Ulcer (PU) Grade ≥ II
Pressure ulcers were categorized according to the EPUAP-classification system. A grade I PU is non-blanchable erythema, a grade II is an abrasion or blister, a grade III is a superficial ulcer and a grade IV is a deep ulcer

Secondary Outcome Measures

ICU Mortality
ICU mortality (number of death in ICU)
Workload of Nurses
Time actually spent to manual repositioning by nurses team, in minutes/day
Length of Mechanical Ventilation (MV)
Time from initiation to withdrawal of mechanical ventilation. Days

Full Information

First Posted
February 18, 2009
Last Updated
March 9, 2013
Sponsor
University Hospital Virgen de las Nieves
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1. Study Identification

Unique Protocol Identification Number
NCT00847665
Brief Title
Pressure Ulcer Prevention in Ventilated Patients Using Two Repositioning Regimens
Acronym
PUPPAS
Official Title
Comparison of Two Turning Regimens (2 Versus Every 4 Hours) in the Prevention of Pressure Ulcers in Patients on Mechanical Ventilation That Use Alternating-pressure Air Mattresses.
Study Type
Interventional

2. Study Status

Record Verification Date
March 2013
Overall Recruitment Status
Completed
Study Start Date
February 2009 (undefined)
Primary Completion Date
May 2011 (Actual)
Study Completion Date
May 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital Virgen de las Nieves

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to compare a 2-hour versus every 4-hour turning regimen on the incidence of grade > II pressure ulcers (PU) in patients in ICU on mechanical ventilation ≥ 24h that use alternating-pressure air mattresses (APAMs).
Detailed Description
Pressure ulcers (PUs) pose a major healthcare challenge and are associated with an increased risk of infection and sepsis, longer hospital stay, and higher hospitalization costs. Their reported incidence in critical care patients varies widely from 1% to 56%. Therefore it is important to take appropriate preventive measures, which can often be successful and less costly than the treatment of established ulcers. Among these measures are the use of pressure-reducing surfaces and repositioning strategies in a protocolized way. Though there is general agreement that critical care patients, including those under mechanical ventilation must use pressure-reducing surfaces, there is no enough evidence in the literature about what is the best repositioning schedule when new, high technology mattresses are used. The use of this new technology has lead to propose that repositioning can be less frequent. In the only clinical trial where this subject (time interval turning) has been addressed (Vanderwee et al, Journal of Advanced Nursing), it is concluded that a turning regimen every 4 hours is equally effective than a 2-hour turning, using this kind of mattresses. Nonetheless this study is not made in critically ill patients, that have more risk factors for developing PUs, the reason we don´t share this findings and recommendations cannot be generalized. The study hypothesis is that in patients using APAMs, a turning regimen every 2 hour compared to a 4-hour is most effective in the prevention of PUs and could be equally safe. The objective of this study is to investigate the effect of postural turnings every 2 hours compared to every 4 hours on the incidence of grade > II pressure ulcers (PU) in patients in ICU on mechanical ventilation (MV) ≥ 24h that use alternating-pressure air mattresses (APAMs) The study is an open label, randomized, controlled clinical trial. The main variable is the incidence of Pus grade ≥ II. As secondary variables measures of efficacy and safety of patients will be registered. The study will take place in a 26 bed medical-surgical ICU with APAMs. Randomization will be done between 24h-48h from the beginning of MV. The final analysis will be by intention to treat.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pressure Ulcers
Keywords
Pressure ulcers, Repositioning, Prevention, Mechanical Ventilation, Critical care

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
330 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Turning every 4 hours
Arm Type
Active Comparator
Arm Description
The four-hours repositioning group patients were turned every four hours following the next sequence: left side, back with a 30º elevation of the head end and the foot end of the bed, right side using the 30º tilt, back.
Arm Title
Turning every 2 hours
Arm Type
Experimental
Arm Description
The two-hours repositioning group patients, were turned every two hours following the next sequence: left side, back with a 30º elevation of the head end and the foot end of the bed, right side using the 30º tilt, back.
Intervention Type
Other
Intervention Name(s)
repositioning
Intervention Description
Turning every 4 or 2 hours
Primary Outcome Measure Information:
Title
Incidence of Pressure Ulcer (PU) Grade ≥ II
Description
Pressure ulcers were categorized according to the EPUAP-classification system. A grade I PU is non-blanchable erythema, a grade II is an abrasion or blister, a grade III is a superficial ulcer and a grade IV is a deep ulcer
Time Frame
Intensive Care Unit (ICU) length of stay (days)
Secondary Outcome Measure Information:
Title
ICU Mortality
Description
ICU mortality (number of death in ICU)
Time Frame
ICU length of stay (an average of 28 days)
Title
Workload of Nurses
Description
Time actually spent to manual repositioning by nurses team, in minutes/day
Time Frame
icu length of stay
Title
Length of Mechanical Ventilation (MV)
Description
Time from initiation to withdrawal of mechanical ventilation. Days
Time Frame
ICU length of stay

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients admitted to the medical-surgical ICU, requiring more than 24 hours of mechanical ventilation. Patients on alternating-pressure air mattresses. Patients or their legal representative able to provide written informed consent to participate in the study Patients whose weight are within the limits accepted by the mattresses (45-140 Kg) Over 18 years Exclusion Criteria: Patients with pressure ulcer at ICU admission. Pregnant patients Patients in which informed consent is not obtained in the first 48 hours of mechanical ventilation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francisco Manzano, MD,PhD
Organizational Affiliation
University Hospital Virgen de las Nieves
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Universitario Virgen de las Nieves
City
Granada
ZIP/Postal Code
18014
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
17184374
Citation
Vanderwee K, Grypdonck MH, De Bacquer D, Defloor T. Effectiveness of turning with unequal time intervals on the incidence of pressure ulcer lesions. J Adv Nurs. 2007 Jan;57(1):59-68. doi: 10.1111/j.1365-2648.2006.04060.x.
Results Reference
background
PubMed Identifier
15582638
Citation
Defloor T, De Bacquer D, Grypdonck MH. The effect of various combinations of turning and pressure reducing devices on the incidence of pressure ulcers. Int J Nurs Stud. 2005 Jan;42(1):37-46. doi: 10.1016/j.ijnurstu.2004.05.013.
Results Reference
background
PubMed Identifier
19018196
Citation
Krapfl LA, Gray M. Does regular repositioning prevent pressure ulcers? J Wound Ostomy Continence Nurs. 2008 Nov-Dec;35(6):571-7. doi: 10.1097/01.WON.0000341469.33567.61. Erratum In: J Wound Ostomy Continence Nurs. 2009 Jan-Feb;36(1):34.
Results Reference
background

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Pressure Ulcer Prevention in Ventilated Patients Using Two Repositioning Regimens

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