| Literature DB >> 29499693 |
Dorien T Beeres1, Darren Cornish2, Machiel Vonk3, Sofanne J Ravensbergen4, Els L M Maeckelberghe5, Pieter Boele Van Hensbroek6, Ymkje Stienstra4.
Abstract
BACKGROUND: With a large number of forcibly displaced people seeking safety, the EU is facing a challenge in maintaining solidarity. Europe has seen millions of asylum seekers crossing European borders, the largest number of asylum seekers since the second world war. Endemic diseases and often failing health systems in their countries of origin, and arduous conditions during transit, raise questions around how to meet the health needs of this vulnerable population on arrival in terms of screening, vaccination, and access to timely and appropriate statutory health services. This paper explores the potential role of the principle of reciprocity, defined as the disposition 'to return good in proportion to the good we receive, and to make reparations for the harm we have done', as a mid-level principle in infectious disease screening policies. MAIN TEXT: More than half of the European countries implemented screening programmes for newly arrived asylum seekers. Screening may serve to avoid potential infectious disease risks in the receiving countries as well as help identify health needs of asylum seekers. But screening may infringe upon basic rights of those screened, thus creating an ethical dilemma. The use of the principle of reciprocity can contribute to the identification of potential improvements for current screening programmes and emphasizes the importance of certain rights into guidelines for screening. It may create a two way moral obligation, upon asylum seekers to actively participate in the programme, and upon authorities to reciprocate the asylum seekers' participation and the benefits for the control of public health.Entities:
Keywords: Asylum seeker; Infectious diseases; Migration; Reciprocity; Screening
Mesh:
Year: 2018 PMID: 29499693 PMCID: PMC5834863 DOI: 10.1186/s12910-018-0256-7
Source DB: PubMed Journal: BMC Med Ethics ISSN: 1472-6939 Impact factor: 2.652
Wilson and Jungner screening criteria [40]
| 1. The condition sought should be an important health problem. | |
| 2. There should be an accepted treatment for patients with recognized disease. | |
| 3. Facilities for diagnosis and treatment should be available. | |
| 4. There should be a recognizable latent or early symptomatic stage. | |
| 5. There should be a suitable test or examination. | |
| 6. The test should be acceptable to the population. | |
| 7. The natural history of the condition, including development from latent to declared disease, should be adequately understood. | |
| 8. There should be an agreed policy on whom to treat as patients. | |
| 9. The cost of case-finding (including diagnosis and treatment of patients diagnosed) should be economically balanced in relation to possible expenditure on medical care as a whole. | |
| 10. Case-finding should be a continuing process and not a “once and for all” project |
Synthesis of emerging screening criteria proposed over the past 40 years [25]
| 1. The screening programme should respond to a recognized need. | |
| 2. The objectives of screening should be defined at the outset. | |
| 3. There should be a defined target population. | |
| 4. There should be scientific evidence of screening programme effectiveness. | |
| 5. The programme should integrate education, testing, clinical services and programme management. | |
| 6. There should be quality assurance, with mechanisms to minimize potential risks of screening. | |
| 7. The programme should ensure informed choice, confidentiality and respect for autonomy. | |
| 8. The programme should promote equity and access to screening for the entire target population. | |
| 9. Programme evaluation should be planned from the outset. | |
| 10. The overall benefits of screening should outweigh the harm. |