The skin has many important functions; including protection from harmful substances and microbes, prevention of loss of body water, and temperature control. It is therefore essential to maintain the health and integrity of the skin. Healthy adults are usually able to assess and care for their own skin, however, at extremes of age and during periods of illness skin assessment and care may need to be carried out by carers or healthcare professionals. If skin assessment is to be undertaken, the individual should be informed of the reasons and procedures so that they can consent and participate where able. Skin assessment requires moving the individual in order to examine the skin and therefore healthcare providers should use appropriate moving and handling techniques and equipment to prevent harm to themselves or the individual. It is also important that skin assessment is carried out in the right environment where there is good (preferably natural) lighting to observe the colour and texture of the skin and where a person's privacy, dignity and warmth can be respected (see NICE clinical guideline 138 ‘Patient experience’). Show The assessment for potential tissue damage includes an observation of the skin for changes in colour compared with the surrounding skin or in comparison to the skin on the contralateral side of the body. It should be noted that in some cases deep tissue injury can occur before any changes on the surface of the skin are discernible; grade 3 and 4 pressure ulcers may therefore develop without prior superficial skin damage. For full details see review protocol in Appendix C. This review focuses on the clinical effectiveness of skin assessment as part of a larger number of interventions for pressure ulcer prevention. The prognostic ability of skin assessment tools is reported separately. One randomised trial by Vanderwee (2007) was included in this review.215 Evidence from this study is summarised in the clinical GRADE evidence profile below (Table 15). See also the study selection flow chart in Appendix D, forest plots in Appendix I, study evidence tables in Appendix G and exclusion list in Appendix J. View in own window
The study also allowed calculation of the sensitivity and specificity: the details informing the 2 × 2 table are given in the evidence table and the forest plot is given in Appendix O. Sensitivity and specificity results are as follows:
In this context, sensitivity and specificity are likely to be confounded by preventative treatment – it is unclear if a high value of sensitivity can be attributed to the relative lack of success of the preventative treatment or the success of the risk assessment method. Therefore the false negative rate for the 2 test-and-treat interventions was considered and this is reported in the GRADE table above. The evidence showed that, of the 251 assessed to be at-risk in the control group (Braden then NBE), 219 people were identified on the basis of having a Braden score less than 17and 32 of 572 (6%) people with a Braden score above 17 were identified using skin assessment. The study does not compare using the Braden score head-to-head with skin assessment. No relevant economic evaluations of skin assessment techniques were identified. One economic evaluation13 was identified which included use of skin assessment as part of a more complex skin care protocol, but this was not considered useful in informing the cost effectiveness of skin assessment. No RCTs or cohort studies were identified. Recommendations were developed using a modified Delphi consensus technique. Further details can be found in Appendix N. No relevant economic evidence was identified. 8.2.5.1. Clinical (adults)
8.2.5.2. Economic (adults)
8.2.5.3. Clinical (neonates, infants, children and young people)
8.2.5.4. Economic (neonates, infants, children and young people)
For full details see review protocol in Appendix C. The second approach is applied in this review, but there are confounding factors in the prognostic review due to preventative treatment. Five studies were included in the review.36,107,144,146,213 Odds ratios for the predictive effect of different skin assessment factors on pressure ulcer incidence are reported, with emphasis on those calculated from multivariable regression analyses. Sensitivity and specificity were calculated using the raw data as presented in the individual studies. The evidence is summarised in the clinical GRADE evidence profile below (Table 3). See also the study selection flow chart in Appendix D, forest plots in Appendix O, study evidence tables and the quality assessment table in Appendix G and O, and the exclusion list in Appendix J. Evidence was also considered from a further study (Compton 2008),36 that also conducted multivariable analysis of different skin assessment features, but by nurse assessment rather than using skin assessment tools. If preventative measures are used as a consequence of skin assessment findings, the probability that an individual will develop a pressure ulcer at the start of the study will not remain constant through the study. The use of effective targeted prevention will alter the assessment of predictive ability. The results should therefore be considered with caution where preventative treatment was given, but not taken into account in the analysis. The studies varied according to their use of preventative measures:
None of the studies took preventative treatment into account in the results. View in own window
No relevant economic evaluations were identified. No RCTs or cohort studies were identified. Recommendations were developed using a modified Delphi consensus technique. Further details can be found in Appendix N. No relevant economic evaluations were identified. 8.4.5.1. Clinical (adults)
8.4.5.2. Economic (adults)
8.4.5.3. Clinical (neonates, infants, children and young people)
8.4.5.4. Economic (neonates, infants, children and young people)
View in own window c Healthcare professionals should be aware that non-blanchable erythema may present as colour changes or discolouration, particularly in darker skin tones or types. View in own window
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