2020 performance
Reports on healthcare service assessments – developed in 1H2020.
Qualification of healthcare services into the health benefit package:
- next-generation whole-exome sequencing in diagnostics of genetic disorders (health problem card 8) in outpatient specialist care;
- clinical exome sequencing (panel of > 4.500 genes with well-documented clinical significance) using next-generation sequencing in diagnostics of genetic disorders (health problem card 5) in outpatient specialist care;
- gene expression profiling (GEP) in oncological diagnostics (health problem card 2) in outpatient specialist care;
- electrochemotherapy (ECT) – verification of recommendation No. 49/2013 of 29.04.2013 on qualification of healthcare services into the health benefit package as part of hospital treatment.
Changes of health technologies:
- in oncology in the following indications: C53, C54, C56 gynaecological neoplasms in primary healthcare, outpatient specialist care, inpatient care;
- C64 – renal cancer in primary healthcare, outpatient specialist care, inpatient care;
- C67 – bladder cancer in primary healthcare, outpatient specialised care, inpatient care;
- Decision problem analysis on changing health technologies in all cardiology guaranteed benefits (I00-I99) in primary healthcare, outpatient specialist care, hospital treatment.
Changes in service provision organisation:
- development (in consultation with stakeholders) of comprehensive oncological care in urooncological neoplasms: kidney cancer, bladder cancer;
- development (in consultation with stakeholders) of a comprehensive oncological care system in gynaecological neoplasms: cervical, endometrial, ovarian malignant cancers;
Other tasks commissioned by the Minister of Health:
- report on validity of introducing check-ups of 60-year-olds as a guaranteed healthcare service;
- report on validity of allowing GPs to commission the following diagnostic tests: ferritin and vitamin D-25-OH levels; Borellia afzelli, Borellia burgdorferi;
- development of a concept for the organisation and scope of preventive examinations for 40-years-olds and older people;
- report on the validity of changing the continuous glycaemic monitoring service: financing Roche’s Eversense system as a guaranteed service;
- report on the validity of financing the following medicinal product from public funds: Jakavi (ruxolitinib) in the indication: chronic mucocutaneous candidiasis (ICD-10: D84.8) with STAT1 and NFC1 mutations – under emergency access to medicines;
- report on validity of financing the following medicinal product from public funds: IMFINZI (durvalumab) in the indication: unresectable non-small cell lung cancer PD-L1 positive (ICD-10: C34) – under emergency access to medicines;
- report on validity of financing the following medicinal product from public funds: Cyramza (ramucirumab) in the indication: generalised gastric adenocarcinoma (ICD-10: C16.8) – under emergency access to medicines;
- report on the rationalisation proposal made by Coloplast Sp. z o.o. and the national consultant in the field of paediatric urology on ensuring greater accessibility to medical devices for disabled children – hydrophilic urinary catheters in the healthcare system in Poland.
*Ladies and Gentlemen
We inform you that the materials and results of the discussions posted on the Agency’s website are the result of the conceptual work and analytical process carried out by the team of the Agency for Health Technology Assessment and Tariff System based on the EBM paradigm, including: search, selection, synthesis and interpretation of scientific evidence, or the data analysis carried out.
In connection with the above, we would like to inform you that the use of analytical material or the results of the discussion, in accordance with good practice, should be accompanied by information on the source in the form: [title of presentation / report], AOTMiT, Warsaw, June 2024]