G-BA resumes method evaluation of synchronous balneo phototherapy in atopic dermatitis in outpatient settings in Germany

20

Feb 2018

According to §135 of the Social Code Book V, the Joint Federal Committee (G-BA) takes decisions about which outpatient services are part of the social health insurance (SHI) in Germany. Synchronous balneo phototherapy in atopic dermatitis was evaluated by the G-BA over 12 years ago for the first time. However, the assessment of the method was paused in 2008 due to a lack of sufficient evidence to make a reimbursement decision. Since then, synchronous balneo phototherapy had been included in Annex III of the outpatient benefit directive, which lists methods that are excluded from reimbursement until their assessment can be completed.

In the previous evaluation, evidence suggested that patients with psoriasis vulgaris profit from bath and UV light therapy (balneo-phototherapy) to a higher degree than from UVB light therapy alone. In patients with atopic dermatitis, indications of an additional benefit exist. However, this only applies to so-called synchronous balneo phototherapy, where the patient is exposed to UV radiation during a bath. In its last report from December 2006, IQWiG concluded that the different types of lights used make a comparison and a summarising evaluation of balneo-phototherapy difficult. Although 11 trials were identified that fulfilled the inclusion and exclusion criteria, these trials included 11 different treatment comparisons.

On February 15th 2018, the G-BA decided to resume its evaluations. To support the final decision, the Institute for Quality and Efficiency in Health Care (IQWiG) will perform a health technology assessment (HTA). According to the project time plan, the HTA report is expected to be completed in October 2019 and the final decision by G-BA is planned in February 2020. The result will determine the reimbursement of synchronous balneo phototherapy in atopic dermatitis in outpatient settings.

The decision document and project time plan are available here.

Subscribe to our newsletter delivered every second week not to miss important reimbursement information.

The latest related news

24

Mar 2022

The HTA body of the Tuscany Regional Healthcare issues two types of documents: HTA forms and motivational forms. With a regional decree 2472 of February 10, 2022, Tuscany Regional Healthcare has published assessments of five medical devices of various therapeutic areas, such as cardiovascular and peripheral vascular areas.

Read more

22

Mar 2022

On February 17, 2022, the Federal Joint Committee (G-BA) has decided to include the method of matrix-associated autologous chondrocyte implantation (M-ACI) on the knee joint in the case of symptomatic cartilage damage in the lists of reimbursed procedures in the hospital and ambulatory settings.

Read more

15

Mar 2022

The Belgian Health Care Knowledge Center (KCE) initiated a study aimed at defining a clear and transparent procedure for the evaluation of digital health technologies in Belgium.

Read more

11

Mar 2022

On February 07, 2022, the Dental and Pharmaceutical Benefits Agency has announced the withdrawal of the assessments of the PhysioMem PM 100 and CardioMem CM 100 XT and the finalization of the assessments of the Zenicor ECG, Coala Heart Monitor Pro, and KardiaMobile. For the conducted assessments, it was outlined that the portable devices provide more limited information than standard ECG measurements; therefore, it was mainly estimated for atrial fibrillation.

Read more

10

Mar 2022

In February 2022, the Finnish Coordinating Center for Health Technology Assessment announced the release of the seven accomplished rapid hospital assessments performed by the Helsinki, Tampere, and Oulu University Hospital. The accomplished rapid HTAs concern the diagnostic imaging, e-Health, endocrine, endoscopy, men’s health, neuromodulation technology groups.

Read more