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Optimalisatie van de werkingsprocessen van het Bijzonder ... - KCE

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154 Special Solidarity Fund <strong>KCE</strong> Reports 133<br />

• The category of “chronically ill children” should be exten<strong>de</strong>d to “all<br />

chronically ill patients”.<br />

• The off label use of drugs.<br />

• The social and financial situation of the patient should be taken into<br />

account in the reimbursement amount. Otherwise the SSF doesn’t cover<br />

what the term suggests.<br />

• For some “social” categories no limitation in the reimbursement may be<br />

applied.<br />

• The restriction to “one parent guidance” to other countries is<br />

problematic and emotionally unacceptable.<br />

9.10.6.2 Limitation of the SSF intervention domains<br />

On the question “Which elements should to your opinion be exclu<strong>de</strong>d from the<br />

current SSF system?” all respon<strong>de</strong>nts answered that there was no reason to reduce the<br />

existing intervention domains of the SSF. On the contrary, the suggestion was given to<br />

inclu<strong>de</strong> current SSF cases as much as possible into the regular health insurance system<br />

and to look for solutions for all medical treatments not covered by the current system.<br />

The SSF has a role to play in the i<strong>de</strong>ntification, the communication and formulation of<br />

suggestions for inclusion of treatments into the regular health system.<br />

Five respon<strong>de</strong>nts explicitly suggested including the category of “chronically ill children”<br />

into the regular health insurance coverage. The inclusion of costs for medical treatment<br />

abroad was mentioned once.<br />

9.10.7 Experience with the SSF/knowledge of the SSF procedure<br />

The respon<strong>de</strong>nts <strong>de</strong>scribed their view on the different steps and parties involved in the<br />

SSF procedure.<br />

• Many respon<strong>de</strong>nts reported that the complete file (<strong>de</strong>claration on honor,<br />

scientific articles, medical information, invoice, …) is submitted to the<br />

local sickness fund of the patient. One interviewee reported that the SSF<br />

files are submitted directly to the national level (medical director) of the<br />

sickness funds. One social worker indicated the possibility to send the SSF<br />

file directly to the SSF.<br />

• Among respon<strong>de</strong>nts knowing that files are submitted in a first step to the<br />

local sickness funds, some reported the internal transfer from the local<br />

sickness funds (advisory physician) to the national level (medical director).<br />

Consequently, many respon<strong>de</strong>nts believe that the local advisory physicians<br />

submit the files directly to the SSF and are not aware of the intermediate<br />

step within the sickness funds.<br />

• It is not clear who the <strong>de</strong>ciding authority is for SSF files: the advisory<br />

physician of the local sickness fund <strong>de</strong>ci<strong>de</strong>s, or a committee of advisory<br />

physicians that meets once every two to three months; Some<br />

respon<strong>de</strong>nts refer also to a committee without further specification.<br />

• Almost all respon<strong>de</strong>nts indicate that they are not involved or informed on<br />

the outcome and further follow-up of a SSF file. There is only feedback<br />

and communication with the local sickness funds when documents are<br />

missing. Contacts with the SSF or the sickness funds at national level<br />

(medical directors) don’t exist.<br />

• Social services are not informed about the final outcome of a SSF file<br />

unless the patient informs them that the SSF file is rejected and the<br />

patient is still confronted with the financial problem linked to the cost of<br />

the medical treatment.<br />

• One respon<strong>de</strong>nt received the information from the sickness funds that<br />

the financial cost needs to exceed €2000 before a SSF reimbursement can<br />

be accepted.

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