How are you taking part in this consultation?

You will not be able to change how you comment later.

You must be signed in to answer questions

    The content on this page is not current guidance and is only for the purposes of the consultation process.

    3 Evidence

    Clinical evidence

    The main clinical evidence comprises 7 studies

    3.1 The evidence assessed by the external assessment centre (EAC) included 7 studies; 3 were full text peer reviewed publications (Gefan et al. 2018; O'Brian et al. 2018; Raizman et al. 2018) and 4 were abstracts (Hancock and Lawrance 2018; Okonkwo et al. 2017; Okonkwo et al. 2018; O'Keefe et al. 2019). The studies included 2,213 patients at risk of developing pressure ulcers in secondary care. Two of the studies were before and after comparative studies, the remaining 5 studies were single-arm observational studies. For full details of the clinical evidence, see section 3 of the assessment report.

    The 2 before and after studies are relevant to the decision problem and report pressure ulcer incidence

    3.2 Both studies compared pressure ulcer incidence before and after using SEM Scanner 200 as a risk assessment tool to be used alongside standard care. Both studies reported reduced pressure ulcer incidence after using the SEM Scanner 200. Neither study included a detailed description of the protocol used for assessment and management in the standard care arm. Also, there was heterogeneity in the reporting of pressure ulcer incidence, with only 1 study including stage 1 pressure ulcers. These limitations made it difficult to be certain about how well SEM Scanner 200 works when used as the only test.

    Diagnostic accuracy is reported in 3 of the observational studies but they use an inappropriate reference standard

    3.3 All studies reporting the diagnostic accuracy of the SEM Scanner 200 used visual skin assessment (a standard clinical measure for detecting pressure ulcers based on visual signs of skin deterioration) as a reference standard. The SEM Scanner 200 is intended to detect subepidermal moisture changes before visual evidence of pressure ulcers is present and is not a diagnostic test for pressure ulcers. The EAC noted the use of visual skin assessment for measuring the diagnostic accuracy of SEM scanner may underestimate the specificity of the SEM scanner because non-visible damage correctly identified by SEM scanner would be recorded as a false positive.

    In 3 of the observational studies SEM Scanner 200 detects subepidermal moisture changes earlier than visual skin assessment

    3.4 All 3 studies reported that subepidermal moisture changes indicating pressure-induced damage were detected earlier than visible signs of skin deterioration reported by visual skin assessment. The studies provided no additional information about the effect of these findings on clinical management or on the clinical benefits of earlier detection.

    Cost evidence

    The company's model compares the costs of using of SEM Scanner 200 plus standard care with using standard care alone

    3.5 The company submitted 10 studies relevant to the economic assessment of SEM Scanner 200. The EAC reviewed the literature and found 1 study (Burns et al. unpublished) that it considered to be relevant to the decision problem. The company used a decision tree, based on NICE's clinical guideline on pressure ulcers: prevention and management, to assess the effect of SEM Scanner 200 on the cost of preventing pressure ulcers, over a 1-year time horizon. In this model, the heels and sacrum of each patient were assessed and categorised as low risk, at risk or at high risk. Patients assessed to be at risk or at high risk had repositioning every 6 or 4 hours, respectively. The key clinical parameters were identified as an assumed pressure ulcer incidence of 4.09% in the at risk group and an incidence rate of 1.637% in the standard care arm and 0.509% in the SEM scanner arm (a 68% reduction). Parameters were from the unpublished Hancock and Lawrance (2018) before and after study.

    The EAC updates costs in the company model

    3.6 The company used a cost of £18 per hour for band 5 nursing time as stated in the NICE costing statement for pressure ulcers published in 2014. The EAC considered this source to be outdated and updated the cost to £37 per hour (Curtis and Burns 2018). The EAC also added a 3.5% depreciation rate for the device that had not been included in the company submission.

    The updated company model results in cost savings of £59 per person from reduced pressure ulcer incidence

    3.7 The company model resulted in cost savings of £59 per patient. Sensitivity analyses applied to the assumed percentage pressure ulcer reduction found SEM Scanner 200 to be cost-neutral at a 28% reduction in pressure ulcer incidence. The company model included the costs of 1 scanner per 9 beds for 210 beds. The model showed that the increased costs for preventive measures were offset by cost savings related to the reduced need for pressure ulcer treatment. Results were reported to be robust to sensitivity analyses, however, the results were not presented. The EAC noted there was uncertainty around estimates sourced from an unpublished study used to populate the company model.

    The EAC modelled the cost of SEM Scanner 200 using preferred assumptions, the technology was cost incurring by £45 per person

    3.8 The EAC used the predicted number of positive stage 1 pressure ulcers, the prevalence of pressure ulcers and the diagnostic accuracy of the combination of SEM Scanner 200 and visual skin assessment to calculate a pressure ulcer incidence of 8.05%. The model assumed that 50% of stage 1 pressure ulcers would progress to stage 2 without diagnosis and treatment and that 36.5% would do so with diagnosis and treatment. The EAC acknowledged that this model did not adequately capture any potential benefit of earlier identification of pressure-induced damage. The EAC's base case resulted in the technology being cost incurring by £45 per person when using SEM Scanner plus visual skin assessment compared with visual skin assessment alone.