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1.
PLoS One ; 17(1): e0260978, 2022.
Article in English | MEDLINE | ID: mdl-35073333

ABSTRACT

BACKGROUND: The incidence of keratinocyte carcinomas is high and rapidly growing. Approximately 80% of keratinocyte carcinomas consist of basal cell carcinomas (BCC) with 50% of these being considered as low-risk tumors. Nevertheless, 83% of the low-risk BCC patients were found to receive more follow-up care than recommended according to the Dutch BCC guideline, which is one visit post-treatment for this group. More efficient management could reduce unnecessary follow-up care and related costs. OBJECTIVES: To study the efficacy, cost-utility, and budget impact of a personalized discharge letter for low-risk BCC patients compared with usual care (no personalized letter). METHODS: In a multi-center intervention study, a personalized discharge letter in addition to usual care was compared to usual care in first-time BCC patients. Model-based cost-utility and budget impact analyses were conducted, using individual patient data gathered via surveys. The outcome measures were number of follow-up visits, costs and quality adjusted life years (QALY) per patient. RESULTS: A total of 473 first-time BCC patients were recruited. The personalized discharge letter decreased the number of follow-up visits by 14.8% in the first year. The incremental costs after five years were -€24.45 per patient. The QALYs were 4.12 after five years and very similar in both groups. The national budget impact was -€2,7 million after five years. CONCLUSIONS: The distribution of a personalized discharge letter decreases the number of unnecessary follow-up visits and implementing the intervention in a large eligible population would results in substantial cost savings, contributing to restraining the growing BCC costs.


Subject(s)
Aftercare/economics , Carcinoma, Basal Cell/therapy , Skin Neoplasms/therapy , Adult , Aged , Aged, 80 and over , Carcinoma, Basal Cell/economics , Cost-Benefit Analysis , Female , Humans , Male , Middle Aged , Models, Economic , Netherlands , Patient Discharge Summaries , Practice Guidelines as Topic , Precision Medicine , Quality-Adjusted Life Years , Skin Neoplasms/economics , Standard of Care , Technology Assessment, Biomedical
2.
J Neurosci Methods ; 224: 1-12, 2014 Mar 15.
Article in English | MEDLINE | ID: mdl-24365047

ABSTRACT

BACKGROUND: To investigate the pathophysiology of temperature hypersensitivity in neuropathic pain rodent models, it is essential to be able to quantify the phenotype as objective as possible. Current temperature sensitivity measuring paradigms are performed during exposure to external factors, i.e. light, sound and smell, which modulate behavior significantly. In addition the present outcome measure for temperature hypersensitivity in rodents is the examination of the hind paw lift upon exposure to a certain temperature, which reflects more a reflex-flexion than an experience of pain. NEW METHOD: Therefore the Rotterdam Advanced Multiple Plate (RAMP) was developed to assess cold hyperalgesia and allodynia objectively in freely behaving neuropathic pain rats, which measures the avoidance for certain temperatures and monitoring the location of the rat with an infrared camera while excluding external environmental influences such as light and sound. RESULTS: Compared to sham rats, the spared nerve injury (SNI) rats demonstrated a higher preference for the comfortable plate (27 °C) when the other three plates were set at 5 °C, 14 °C, 17 °C and 19 °C. We were unable to detect heat hyperalgesia and allodynia with the RAMP. COMPARISON WITH EXISTING METHOD: The paw withdrawal method displays similar results during cold hypersensitivity measurements as observed with the RAMP. The SNI group did display heat hypersensitivity during the paw withdrawal test. CONCLUSIONS: The results indicate that the RAMP is able to quantify cold hyperalgesia and allodynia in neuropathic pain rats while resolves some of the problems of conventional temperature sensitivity measuring paradigms in rodents.


Subject(s)
Cold Temperature/adverse effects , Hyperalgesia/diagnosis , Pain Measurement/methods , Pain Threshold/physiology , Wakefulness , Analysis of Variance , Animals , Disease Models, Animal , Hyperalgesia/etiology , Male , Neuralgia/complications , Pain Measurement/instrumentation , Psychophysics , Rats , Rats, Wistar , Reproducibility of Results , Time Factors
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