The TURN Study: Is there a difference in pressure ulcer incidence with 2, 3, or 4 hour turning of nursing facility residents? Nancy Bergstrom, Susan D. Horn, Mary Pat Rapp, Anita Stern, Ryan Barrett, Michael D. Watkiss
Jan 18, 2018
The TURN Study: Is there a difference in pressure ulcer incidence with 2, 3, or 4 hour turning of nursing facility
residents?
Nancy Bergstrom, Susan D. Horn,Mary Pat Rapp, Anita Stern,
Ryan Barrett, Michael D. Watkiss
Purpose of Study
Is there a significant difference in the incidence of pressure ulcers among moderate and high risk nursing facility residents cared for on a high density foam mattress when repositioning occurs every 2, compared to every 3 or 4 hours?
Hypothesis• It is hypothesized that there is no difference in
pressure ulcer incidence among moderate or high risk residents randomly assigned to repositioning every 2-, compared with every 3- or 4 hours.
Randomized Controlled Trial
• Random allocation– High risk ( 2, compared with 3 or 4 hour turn)– Moderate risk (2, compared with 3 or 4 hour turn)
• 3 week follow up• Weekly and final skin assessment (blinded)• Outcome PrU on coccyx, sacrum, heels• Stage 1 must be present on 2 days
The Intervention
• Random assignment to turning schedule• Turning clock kept in bedside folder• Documentation (24- hr safety checklist: skin
observation, position in bed, position of heels in bed, time spent in chair, bathing, meal intake, continence care)
• Fidelity measures (% on time turning, % position agreement between CNA and Supervisor)
• Shift handoff
Outcome Assessors
• Trained in risk assessment using the Braden Scale
• Trained using video, vignettes, observation• Prior to study to determine selection and risk• Weekly throughout study
• Trained in skin assessment• Blinded to turning frequency• Assessed for PUs weekly
Facility Criteria
• Provide basic good care• Use high density foam mattresses (mattress
provided to all participants in Canada due to variability in existing surfaces)
• Willingness to provide staff time to participate• Initial screening of residents verify number of
eligible, at risk subjects
Resident Criteria
• Newly admitted (within 7 days), or• Long term (> 90 days)• Age > 65 years• At risk for PrUs
• Moderate risk (Braden scores 13, 14)• High risk (Braden scores 10-12)
• No PrUs at outset• High density foam mattress
Sample Size
• Assuming a change from 4% incidence to 8% would be considered significant, a one-tailed test, and an alpha of .05, the power to detect such a difference is 0.82 for 900 participants.
Lost to follow-up: (n=26)
Hospitalized: (n=8), Died: (n=1), Discharged: (n=2), Withdrew: (n=10), Other: (n=5)
Enrollment
Analyzed (n=295) Did not receive allocated intervention: (n=4)
Assessed for eligibility (n= 6240) Excluded (n=5273) Not meeting inclusion criteria (n= 4840) Declined to participate (n= 204) Other reasons (n= 229)
Analyzed (n=321) Did not receive allocated intervention: (n=14)
Lost to follow-up: (n=35)
Hospitalized: (n=8), Died: (n=6), Discharged: (n=2), Withdrew: (n=14), Other: (n=5)
Lost to follow-up: (n=28)
Hospitalized: (n=13), Died: (n=2), Discharged: (n=8), Withdrew: (n=5)
Analyzed (n=326) Did not receive allocated intervention: (n=7)
Analyzed
Randomized (n=967)
Allocation
Follow-up
Allocated to intervention (n=335)
Received allocated intervention (n=321)Did not receive allocated intervention: (n=14) Death:(n=2), Hospitalized(n=1),Other(n=3),Participant Choice:(n=8)
Allocated to intervention (n=333)
Received allocated intervention (n=326)Did not receive allocated intervention: (n=7) Hospitalized:(n=1), Participant Choice: (n=6)
Allocated to intervention (n=299)
Received allocated intervention (n=295)Did not receive allocated intervention: (n=4) Hospitalization: (n=2), Participant Choice: (n=1), Other: (n=1)
2 Hour Turn Group
3 Hour Turn Group
4 Hour Turn Group
CharacteristicsVariable All (N=942) Mod Risk
(N=617)High Risk(N=325)
P=(T-test)
Age (years)(M + SD)
85 (7.7) 85 (7.7) 85 (7.7) 0.36
Braden (M + SD)
12.8 (1.1) 13.6 (0.5) 11.4 (0.7) <.001
Canada
US
505 (53.6)437 (46.4)
336 (54.4)281 (45.5)
169 (52.0)156 (48.0)
0.49
CharacteristicsVariable All (N=942) Mod Risk
(N=617)High Risk(N=325)
P=(T-test)
Female # (%)
731 (77.6) 464 (75.2) 267 (82.2) 0.017
Race # (%)
White Black Asian Hispanic
758 (80.5) 55 ( 5.8)101 (10.7) 22 ( 2.3)
506 (82.0) 37 ( 6.0) 59 ( 9.6) 14 ( 2.3)
252 (77.5) 18 ( 5.5) 42 (12.9) 8 ( 2.5)
0.056
CharacteristicsVariable All (N=942) Mod Risk
(N=617)High Risk(N=325)
P=(T-test)
Diagnosis # (%) Dementia Cerebro Diabetes Cardio Musculo Thyroid Nutrition
672 (72.5)341 (36.8)252 (27.2)713 (76.9)506 (54.6)167 (18.0) 18 ( 1.9)
421 (69.0)216 (35.4)173 (28.4)491 (80.5)333 (54.6)111 (18.2) 5 (0.82)
251 (79.2)125 (39.4) 79 (24.9)222 (70.0)173 (54.6) 56 (17.7) 13 ( 4.1)
0.0010.2510.2770.0010.9990.8580.001
LOS # (%)
0.231
Long Short
814 (86.4)128 (13.6)
527 (85.4) 90 (14.6)
287 (88.3) 38 (11.7)
Analysis• 942 participants, power 80%, and 1-tailed
type I error of p<0.05, to detect a difference of about 4% between turning schedules
• Moderate risk, 3 hour turn group was significantly different
• Chi square/Fisher’s exact test• ANOVA• Original prediction 4% incidence/group
Incidence of PrU by Risk and Turning Group
Group Ulcers/Group% Ulcers
Ulcers2-hour% Ulcers
Ulcers3-hour% Ulcers
Ulcers 4-hour% ulcers
Group (p=)
All participants
19/942(2.02%)
8/321(2.49)
2/326(0.61%)
9/295(3.05%)
(0.07)
Moderate Risk
13/617(2.11%)
6/210(2.86%)
0/209 (0%)
7/198(3.54%)
(0.03)
High Risk 6/325(1.85%)
2/111(1.80%)
2/117(1.71%)
2/97(2.06%)
(0.98)
Moderate vs. High
(0.73)
Discussion
EVIDENCE FOR TURNING
Study Braden Scale Score
Support Surface
2-hour 3-hour 4-hour 6-hour
Defloor et. al. 2005Belgium
Mean 13.0 + 2
Standard Visco elastic mattress
9/63 (14%) 14/58 (24%)2/66 (3%) stage 2
10/63 (15.9%)Stage 2
Vanderwee et. al., 2007 Belgium
Mean 15.0 + 3
Visco elastic foam overlay (7 cm), 2-4-2 turns
17/122 stage 2 (13.9%) stage 3 or 4(2.5%)
22/113 Stage 2 (19.5%)Stage 3 or 4 (1.8%)
Moore et al., 2011Scotland
Braden Activity and Mobility Subscales
99% had powered redistribution device
2/99 (2%) 7/114 (6%)
TURN StudyUS & Canada
BradenModerate Risk (13-14)High Risk(10-12)
Visco elastic, high density foam mattresses
Moderate:6/210 (2.86%)High:2/111 (1.8%)
Moderate:0/209 (0.00%)High:2/117 (1.71%)
Moderate:7/198 (3.54%)High:2/97 (2.06%)
Study Braden Scale Score
Support Surface
2-hour 3-hour 4-hour
Defloor et. al. 2005
Mean 13.0 + 2 Visco elastic
mattress2/66 (3%) stage 2
TURN Study BradenModerate Risk (13-14)High Risk(10-12)
Visco elastic, high density foam mattresses
Moderate:6/210 (2.86%)High:2/111 (1.8%)
Moderate:0/209 (0.00%)High:2/117 (1.71%)
Moderate:7/198 (3.54%)High:2/97 (2.06%)
Conclusions
Implementation
Turn Q 3 or 4 hours, IF…1. High density foam mattress 2. Braden risk scores 10 – 143. Using guideline based care:
(chair cushions, nutrition, briefs, careful vigilant staff)
Implementation
3. Use Checklist to ensure safety and consistency of care
4. Use Checklist to monitor care and change care plan if needed
5. Monitor outcomes on a pilot basis