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Simpkin AJ, Rooshenas L, Wade J, et al. Development, validation and evaluation of an instrument for active monitoring of men with clinically localised prostate cancer: systematic review, cohort studies and qualitative study. Southampton (UK): NIHR Journals Library; 2015 Jul. (Health Services and Delivery Research, No. 3.30.)

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Development, validation and evaluation of an instrument for active monitoring of men with clinically localised prostate cancer: systematic review, cohort studies and qualitative study.

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Appendix 1Development of active monitoring system

The model developed in Chapter 3 was included in an AMS through the MS Excel software, such that serial PSAs could be entered and displayed for men following an AM/AS programme. Interviews with men on AM/AS, urologists and oncologists included a demonstration of the system.

The main interface allows entry of date of birth, Gleason score, PSA test date and result. The Excel sheet then calculates one of a number of options. The first is the average trend of PSA for a similar man (i.e. with the same PSA, age and Gleason score at diagnosis) with clinically localised prostate cancer, as shown in the green line in Figure 10. There is also the option to show the average trend along with 95% reference range for a similar man without PCa, as shown in the blue and orange lines of Figure 10. Using a simple interface, men can compare their own PSA results with the average PSA growth of similar men with and without prostate cancer.

FIGURE 10. The PSARR system for a simulated individual, showing average PSA trend (blue, short dash) plus 95% reference range (orange) for men without PCa, as well as average PSA trend for men with PCa (green, long dash).

FIGURE 10

The PSARR system for a simulated individual, showing average PSA trend (blue, short dash) plus 95% reference range (orange) for men without PCa, as well as average PSA trend for men with PCa (green, long dash).

Initially, we intended to use the 95% reference range for men without PCa as the method that would alert men with PCa to rapidly rising PSA. After discussion with the steering group, the use of reference ranges of men with PCa were taken forward for use in the comparison of Chapter 5.

Note that data presented are simulated to be indicative of men with PCa. The names given are fictitious and are not representative of any men in any of the cohorts.

Copyright © Queen’s Printer and Controller of HMSO 2015. This work was produced by Simpkin et al. under the terms of a commissioning contract issued by the Secretary of State for Health. This issue may be freely reproduced for the purposes of private research and study and extracts (or indeed, the full report) may be included in professional journals provided that suitable acknowledgement is made and the reproduction is not associated with any form of advertising. Applications for commercial reproduction should be addressed to: NIHR Journals Library, National Institute for Health Research, Evaluation, Trials and Studies Coordinating Centre, Alpha House, University of Southampton Science Park, Southampton SO16 7NS, UK.

Included under terms of UK Non-commercial Government License.

Bookshelf ID: NBK305580

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