Pressure Ulcer
Conditions
Keywords
bed linens
Brief summary
This study will use a traditional parallel randomization design with patients in five medical intensive care units at the Cleveland Clinic to evaluate the efficacy of silk-like bed sheets and underpads for prevention of Unit-Acquired Pressure Ulcers (UAPU). Adult hospitalized patients in beds with standard bed linens versus those with silk-like linens will be compared for 1) rate of development of UAPU, 2) time to develop the first UAPU, and the maximum severity of any UAPU that develop. Bed linens will be changed per unit protocol. Patient characteristics will be summarized using frequencies and percentages for categorical factors and means, standard deviations, percentiles and median and range for continuous measures. For the primary outcome of unit-acquired pressure ulcer rate, generalized linear mixed models, assuming a Poisson distribution for the outcome, and unit length of stay as an offset will be used. For the time to event analysis, frailty models will be used to assess whether time to first pressure ulcer differs between treatment types. Generalized linear mixed models will be used for other secondary endpoints, including maximum severity of observed pressure ulcers
Detailed description
Although there has been a large amount of research published on contributing factors to pressure ulcers, there has been little research related to the role that bed linens play in affecting moisture, friction, and shear that may lead to development of unit-acquired pressure ulcers (UAPU) for patients in acute care settings. This study will use a traditional parallel randomized design with patients in five medical intensive care units at the Cleveland Clinic to evaluate the efficacy of silk-like bed sheets and underpads for prevention of Unit-Acquired Pressure Ulcers (UAPU). Patients were randomly assigned by personnel who were blinded to the intervention based on bed availability. Nurses will assess all patients on standard bed linens and silk-like linens for development of UAPU. Adult hospitalized patients in beds with standard bed linens versus those with silk-like linens will be compared for 1) rate of development of UAPU, 2) time to develop the first UAPU, and the maximum severity of any UAPU that develop. Upon entry into the study, all patients will be assessed for baseline skin integrity by the admitting nurse. Demographic data (MRN; unit name; type of linen on bed; admitting diagnosis; dates of admission/discharge; age; gender; race; weight; Braden score; date, location, and stages of UAPU development; lab values (albumin, total protein); and categories of the Charlson Comorbidity Index will be recorded on data collection form by research nurse. Bed linens will be changed per unit protocol. A sample size of 3456 patients is estimated. Patient characteristics will be summarized using frequencies and percentages for categorical factors and means, standard deviations, percentiles and median and range for continuous measures. Comparisons of these patient characteristics, including Braden score, Charlson comorbidity index, unit length of stay and hospital length of stay, will be compared between linen types using generalized linear mixed effect models. For the primary outcome of unit-acquired pressure ulcer rate, generalized linear mixed models, assuming a Poisson distribution for the outcome, and unit length of stay as an offset will be used. In these models, linen type and study period will be used as fixed effects and each unit will be included as a random effect. For the time to event analysis, frailty models will be used to assess whether time to first pressure ulcer differs between treatment types. Generalized linear mixed models will be used for other secondary endpoints, including maximum severity of observed pressure ulcers.
Interventions
Synthetic moisture-wicking fabric
Sponsors
Study design
Intervention model description
Of 5 Medical ICUs at 1 quaternary care medical center, patients were assigned to groups based on bed availability by personnel who were blinded to linens used on those units.
Eligibility
Inclusion criteria
* All patients admitted into the medical intensive care unit during the one year study period
Exclusion criteria
* Patients who are transferred from one study unit to another study unit, data for their days on the second unit will be measured only if the second unit is in the same study arm as the sending unit * Patients who are in the prone position * Patients remaining on a unit past the two week washout period, will not be included in the crossover arm
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Rate of Development of Unit-acquired Pressure Ulcers | During MICU admission | Total count of the number of patients who developed unit acquired pressure ulcers during the study (count) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| The Time to Develop the First Unit-acquired Pressure Ulcer | Days from admission to HAPI | The number of days spent in the intensive care unit prior to the development of a pressure ulcer |
| Maximum Severity of Unit Acquired Pressure Injury (UAPI) | During MICU admission | HAPI staged by trained clinical nurses using the National Pressure Advisory Panel (NPUAP) staging definitions in which Stage 1 is the least severe with severity progressing through Stage 2, 3, 4, and unstageable. Unstageable is an evolving type of pressure injury evolving into a Stage 3 or 4. |
Countries
United States
Participant flow
Pre-assignment details
Eleven patients refused the synthetic linens.
Participants by arm
| Arm | Count |
|---|---|
| Silk-like Linen Patients cared for on silk-like linen. | 1,626 |
| Standard Cotton Linen Patients cared for on standard cotton linen | 1,706 |
| Total | 3,332 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 |
|---|---|---|---|
| Overall Study | Withdrawal by Subject | 11 | 0 |
Baseline characteristics
| Characteristic | Total | Standard Cotton Linen | Silk-like Linen |
|---|---|---|---|
| Admission Type Direct Admission | 80 Participants | 37 Participants | 43 Participants |
| Admission Type Emergency Department | 1449 Participants | 729 Participants | 720 Participants |
| Admission Type Inpatient | 852 Participants | 452 Participants | 400 Participants |
| Admission Type Outside | 944 Participants | 484 Participants | 460 Participants |
| Age, Continuous | 60.1 years STANDARD_DEVIATION 16.3 | 60.3 years STANDARD_DEVIATION 16 | 60 years STANDARD_DEVIATION 16.6 |
| Albumin, mg/dL | 3.1 mg/dL STANDARD_DEVIATION 0.7 | 3.0 mg/dL STANDARD_DEVIATION 0.7 | 3.1 mg/dL STANDARD_DEVIATION 0.71 |
| APACHE | 66.9 calculated score (high= high acuity) STANDARD_DEVIATION 28.2 | 66.4 calculated score (high= high acuity) STANDARD_DEVIATION 27.8 | 67.5 calculated score (high= high acuity) STANDARD_DEVIATION 28.7 |
| Braden Score | 15.4 units on a scale STANDARD_DEVIATION 3.1 | 15.4 units on a scale STANDARD_DEVIATION 3.1 | 15.5 units on a scale STANDARD_DEVIATION 3.1 |
| Charlson Comorbidity Index 0 | 591 Participants | 282 Participants | 309 Participants |
| Charlson Comorbidity Index 1-2 | 1289 Participants | 690 Participants | 599 Participants |
| Charlson Comorbidity Index 3-4 | 890 Participants | 439 Participants | 451 Participants |
| Charlson Comorbidity Index 5 or more | 557 Participants | 293 Participants | 264 Participants |
| Diagnostic Category Cardiovascular | 1015 Participants | 510 Participants | 505 Participants |
| Diagnostic Category Gastrointestinal | 467 Participants | 250 Participants | 217 Participants |
| Diagnostic Category Hematologic | 249 Participants | 104 Participants | 145 Participants |
| Diagnostic Category Other | 446 Participants | 256 Participants | 190 Participants |
| Diagnostic Category Respiratory | 999 Participants | 491 Participants | 508 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Black or African American | 1037 Participants | 499 Participants | 538 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 181 Participants | 103 Participants | 78 Participants |
| Race (NIH/OMB) White | 2114 Participants | 1104 Participants | 1010 Participants |
| Sex: Female, Male Female | 1565 Participants | 796 Participants | 769 Participants |
| Sex: Female, Male Male | 1765 Participants | 909 Participants | 856 Participants |
| Total Protein, mg/dL | 6.2 mg/dL STANDARD_DEVIATION 1.03 | 6.2 mg/dL STANDARD_DEVIATION 1.01 | 6.2 mg/dL STANDARD_DEVIATION 1.05 |
| Weight; kgs | 85.4 kgs STANDARD_DEVIATION 30.1 | 85.4 kgs STANDARD_DEVIATION 30.6 | 85.5 kgs STANDARD_DEVIATION 29.7 |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | — / — | — / — |
| other Total, other adverse events | 2 / 1,626 | 0 / 1,706 |
| serious Total, serious adverse events | 0 / 1,626 | 0 / 1,706 |
Outcome results
Rate of Development of Unit-acquired Pressure Ulcers
Total count of the number of patients who developed unit acquired pressure ulcers during the study (count)
Time frame: During MICU admission
Population: Total count and percentage of patients who developed a hospital acquired pressure injury (HAPI)
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Silk-Like Linen | Rate of Development of Unit-acquired Pressure Ulcers | 45 Participants |
| Standard Cotton Linen | Rate of Development of Unit-acquired Pressure Ulcers | 42 Participants |
Maximum Severity of Unit Acquired Pressure Injury (UAPI)
HAPI staged by trained clinical nurses using the National Pressure Advisory Panel (NPUAP) staging definitions in which Stage 1 is the least severe with severity progressing through Stage 2, 3, 4, and unstageable. Unstageable is an evolving type of pressure injury evolving into a Stage 3 or 4.
Time frame: During MICU admission
Population: For all patients, maximum stage of HAPI during medical intensive care unit (MICU) stay
| Arm | Measure | Category | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Silk-Like Linen | Maximum Severity of Unit Acquired Pressure Injury (UAPI) | Stage 1 | 6 Participants |
| Silk-Like Linen | Maximum Severity of Unit Acquired Pressure Injury (UAPI) | Stage 2-4 | 20 Participants |
| Silk-Like Linen | Maximum Severity of Unit Acquired Pressure Injury (UAPI) | Unstageable | 15 Participants |
| Silk-Like Linen | Maximum Severity of Unit Acquired Pressure Injury (UAPI) | No HAPI | 1585 Participants |
| Standard Cotton Linen | Maximum Severity of Unit Acquired Pressure Injury (UAPI) | No HAPI | 1660 Participants |
| Standard Cotton Linen | Maximum Severity of Unit Acquired Pressure Injury (UAPI) | Stage 1 | 9 Participants |
| Standard Cotton Linen | Maximum Severity of Unit Acquired Pressure Injury (UAPI) | Unstageable | 15 Participants |
| Standard Cotton Linen | Maximum Severity of Unit Acquired Pressure Injury (UAPI) | Stage 2-4 | 22 Participants |
The Time to Develop the First Unit-acquired Pressure Ulcer
The number of days spent in the intensive care unit prior to the development of a pressure ulcer
Time frame: Days from admission to HAPI
Population: Number of days from admission to first HAPI for patients who developed a HAPI
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Silk-Like Linen | The Time to Develop the First Unit-acquired Pressure Ulcer | 6 days |
| Standard Cotton Linen | The Time to Develop the First Unit-acquired Pressure Ulcer | 6 days |