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Monitoring Physiologic Data in the Development of Pressure Ulcers

Primary Purpose

Pressure Ulcer, Signs and Symptoms

Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Patch
Sponsored by
Johns Hopkins University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Pressure Ulcer focused on measuring Pressure ulcer, Monitoring, Pressure, Physiologic feedback

Eligibility Criteria

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

Inclusion Criteria:

  • Patients undergoing an operation that is scheduled to last more than 2 hours

Exclusion Criteria:

  • Existing sacral pressure ulcer, undergoing a cardiac procedure, or inability to provide informed consent.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Monitoring patch, no display

    Arm Description

    Participants in this condition will receive a padded bandage that monitors pressure over time. In this arm, healthcare providers will not be able to view the pressure data collected.

    Outcomes

    Primary Outcome Measures

    Interface pressure (mmHg) over time (minutes)
    The interface pressure trend on the sacrum throughout the duration of time a patient is on the operating table and how that is correlated with pressure ulcer development

    Secondary Outcome Measures

    Pressure ulcer development
    Skin will be checked immediately after the surgery and at 1 week using National Pressure Ulcer Advisory Panel (NPUAP) pressure ulcer staging system (grades I-IV).
    Effect of Braden Scale
    The relationship between interface pressure (mmHg), pressure ulcer development and Braden Scale Score (0-23).
    Effect of Body Weight (kg)
    The relationship between interface pressure (mmHg), pressure ulcer development and body weight (kilograms).
    Effect of Body Mass Index (kg/m^2)
    The relationship between interface pressure (mmHg), pressure ulcer development and body mass index (kg/m^2).
    Effect of Age (years)
    The relationship between interface pressure (mmHg), pressure ulcer development and age (years).
    Effect of American Society of Anesthesiologists Score (I-IV)
    The relationship between interface pressure (mmHg), pressure ulcer development and American Society of Anesthesiologists Score (I-VI).
    Number of Repositioning events
    The number of times a patient is repositioned (defined by a greater than 50% change in the interface pressure (mmHg)) throughout the duration of the surgery.

    Full Information

    First Posted
    February 16, 2016
    Last Updated
    October 31, 2019
    Sponsor
    Johns Hopkins University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02689817
    Brief Title
    Monitoring Physiologic Data in the Development of Pressure Ulcers
    Official Title
    Monitoring Physiologic Data in the Development of Pressure Ulcers
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2019
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    Study was withdrawn due to technical limitations to the device
    Study Start Date
    October 2019 (Anticipated)
    Primary Completion Date
    October 2019 (Anticipated)
    Study Completion Date
    January 2020 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Johns Hopkins University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Hospital-acquired pressure ulcers (HAPUs) are a well-established serious complication of hospitalization that have serious consequences on patient morbidity and mortality as well as the cost of care. At the core of the problem for patient-centered targeted prevention of HAPUs is the lack of knowledge surrounding the magnitude and duration of pressure necessary to cause pressure ulcers, and the lack of immediate feedback on whether these interventions do anything to substantially offload at risk areas. Previous studies have been inconsistent in their findings of an association between duration of time and HAPU occurrence. While retrospectively this has been investigated, there is currently no substantial prospective, randomized study. This study seeks to better understand the interface pressures between the patient and his or her support surface and how this relates to the development of pressure ulcers. The effect of patient characteristics and the relationship between total length of time on the operating table and pressure ulcer development will also be assessed. The findings from this study will significantly add to strengthening the body of evidence regarding pressure ulcer development, specifically the relationship between the magnitude of interface pressure between the patient and the support surface for what duration of time leads to the development of a pressure ulcer. The results will provide critical insight into the physiologic targets healthcare providers should use to develop better pressure ulcer prevention programs, which could ultimately lead to a reduction in the incidence of pressure ulcers.
    Detailed Description
    Hospital-acquired pressure ulcers (HAPUs) are a well-established serious complication of hospitalization that have serious consequences on patient morbidity and mortality as well as the cost of care. Following CMS's changes to hospital reimbursements and penalization for hospitals with the highest rate of hospital-acquired complications, numerous quality improvement initiatives have been implemented. An overall reduction in the reported incidence of HAPUs from approximately 7 to 4.5% was observed, largely attributed to these interventions. Though there had been a drop in incidence, the overall number of hospitalized patients who develop HAPUs remains large and more recently HAPU frequency in hospitals has not continued to decrease, despite educational pressure ulcer prevention programs and clinical practice guidelines. Due to the complications and costs associated with the development of a pressure ulcer, research has suggested that prevention is more effective than standard care. There are many current solutions for preventative interventions for HAPUs including leadership initiatives, data tracking, risk scales and many adjuvant pressure-offloading devices such as beds and mattress pads. Many of these devices have limited data supporting their effectiveness or are costly to implement in a purely prophylactic manner when current risk stratification methods fail to capture 60% of patients who go on to develop an ulcer. The vast majority of current preventative measures for pressure ulcers either seek to reduce the time a patient spends in one position or to reduce the magnitude of pressure that occurs on the high-risk areas for pressure ulcers. As such, manual repositioning (turning) is the most frequently used intervention as it is felt to be low-cost and part of standard care. Repositioning works by reducing or eliminating the interface pressure between the patient and the contact surface, but the standard recommendation on the 2 hour frequency were derived from animal studies and healthy volunteers. An expert consensus by Black et al. (2011) recommended the need for clinical decision-making based on the individual's needs and clinical situation when establishing a turning schedule, but there are very few objective tools that clinicians can use to make the decision. At the core of the problem for patient-centered targeted prevention of HAPUs is the lack of knowledge surrounding the magnitude and duration of pressure necessary to cause pressure ulcers, and the lack of immediate feedback on whether these interventions do anything to substantially offload at risk areas. Previous studies have been inconsistent in their findings of an association between duration of surgery and HAPU occurrence, with results ranging from a negative association to a positive association. This study seeks to better understand the interface pressures between the patient and his or her support surface and how this relates to the development of pressure ulcers. This data will provide critical insight into the physiologic targets healthcare providers should use to develop better pressure ulcer prevention programs and ultimately lead to a reduction in the incidence of pressure ulcers. The primary outcome will be the interface pressure trend on the sacrum throughout the duration of time a patient is on the operating table and how that is correlated with pressure ulcer development. The effect of Braden scale score and other patient characteristics and the relationship between total length of time on the operating table and pressure ulcer development, and healthcare provider intervention in response to the pressure reading if in the second part of the study healthcare providers are not blinded to the pressure data. This study will measure the interface pressure between a patient and his or her support surface in the operating room for prolonged (>2 hour) operative cases. Eligible patients will receive an adhesive padded bandage (similar to Mepilex Gentle Border) that collects interface pressure data. When the patient is being positioned in the operating room, this bandage will be applied to the sacrum. At the completion of the case the bandage will be removed and the status of the skin will be recorded and a photo of the sacrum will be taken for documentation. Skin status will be reassessed at 24 hours and at 1 week at regularly scheduled follow-ups with the surgeon. Pressure ulcer development will then be correlated with interface pressure characteristics during the operative case, using demographic data to check homogeneity between the experimental and control groups. If at interim analysis there is a clear relationship between a pressure threshold and pressure ulcer development, the second portion of the study will not blind healthcare providers to the live data. They would be able to see the pressure measurement and reposition the patient to effectively offload. While retrospectively this has been investigated, there is currently no substantial prospective, randomized study. This study will significantly add to strengthening the body of evidence regarding pressure ulcer development, specifically the relationship between the magnitude of interface pressure between the patient and the support surface for what duration of time leads to the development of a pressure ulcer.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Pressure Ulcer, Signs and Symptoms
    Keywords
    Pressure ulcer, Monitoring, Pressure, Physiologic feedback

    7. Study Design

    Primary Purpose
    Diagnostic
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Masking Description
    The investigator and outcomes assessors will be masked to the pressure data during the operating room and follow-up.
    Allocation
    N/A
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Monitoring patch, no display
    Arm Type
    Experimental
    Arm Description
    Participants in this condition will receive a padded bandage that monitors pressure over time. In this arm, healthcare providers will not be able to view the pressure data collected.
    Intervention Type
    Device
    Intervention Name(s)
    Patch
    Intervention Description
    A bandage applied to the sacrum with pressure offloading characteristics and pressure monitoring components in a low-profile housing.
    Primary Outcome Measure Information:
    Title
    Interface pressure (mmHg) over time (minutes)
    Description
    The interface pressure trend on the sacrum throughout the duration of time a patient is on the operating table and how that is correlated with pressure ulcer development
    Time Frame
    Duration of the surgery (>120 min, <1440 min)
    Secondary Outcome Measure Information:
    Title
    Pressure ulcer development
    Description
    Skin will be checked immediately after the surgery and at 1 week using National Pressure Ulcer Advisory Panel (NPUAP) pressure ulcer staging system (grades I-IV).
    Time Frame
    1 week
    Title
    Effect of Braden Scale
    Description
    The relationship between interface pressure (mmHg), pressure ulcer development and Braden Scale Score (0-23).
    Time Frame
    1 week
    Title
    Effect of Body Weight (kg)
    Description
    The relationship between interface pressure (mmHg), pressure ulcer development and body weight (kilograms).
    Time Frame
    1 week
    Title
    Effect of Body Mass Index (kg/m^2)
    Description
    The relationship between interface pressure (mmHg), pressure ulcer development and body mass index (kg/m^2).
    Time Frame
    1 week
    Title
    Effect of Age (years)
    Description
    The relationship between interface pressure (mmHg), pressure ulcer development and age (years).
    Time Frame
    1 week
    Title
    Effect of American Society of Anesthesiologists Score (I-IV)
    Description
    The relationship between interface pressure (mmHg), pressure ulcer development and American Society of Anesthesiologists Score (I-VI).
    Time Frame
    1 week
    Title
    Number of Repositioning events
    Description
    The number of times a patient is repositioned (defined by a greater than 50% change in the interface pressure (mmHg)) throughout the duration of the surgery.
    Time Frame
    Duration of the surgery (>2 h, <24 h)

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients undergoing an operation that is scheduled to last more than 2 hours Exclusion Criteria: Existing sacral pressure ulcer, undergoing a cardiac procedure, or inability to provide informed consent.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Justin Sacks, MD
    Organizational Affiliation
    Johns Hopkins University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    Citation
    Berlowitz D, VanDeusen Lukas C, Parker V, Niederhauser A, Silver J, Logan C, Ayello E, Zulkowski K. 2012. Preventing Pressure Ulcers in Hospitals: A Toolkit for Improving Quality of Care. Rockville, MD: Agency for Healthcare Research and Quality; 2011. Rockville, MD: Agency for Healthcare Research and Quality.
    Results Reference
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    Monitoring Physiologic Data in the Development of Pressure Ulcers

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