Roger D. Feldman (ed.), American Health Care: Government, Market Processes, and the Public Interest (New Brunswick and London: Transaction Publishers, The Independent Institute, 2000, $39.95 cloth, $24.95 paper). Pp. 444. ISBN 1 560 00430 4, 0 765 80676 2.

2001 ◽  
Vol 35 (3) ◽  
pp. 499-550
Author(s):  
BENJAMIN GRAY
Author(s):  
Karsten Vrangbæk

Scandinavian health systems have traditionally been portrayed as relatively similar examples of decentralised, public integrated health systems. However, recent decades have seen significant public policy developments in the region that should lead us to modify our understanding. Several dimensions are important for understanding such developments. First, several of the countries have undergone structural reforms creating larger governance units and strengthening the state level capacity to regulate professionals and steer developments at the regional and municipal levels. Secondly, the three Nordic countries studied experienced an increase in the purchase of voluntary health insurance and the use of private providers. This introduces several issues for the equality of users and the efficiency of the system. This paper will investigate such trends and address the question: Is the Nordic health system model changing, and what are the consequences for trust, professional regulation and the public interest?


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Kayla Gordon

Mandatory reporting legislation is designed to clarify when to report and ensure that all cases of child maltreatment are reported. However, while mandated reporting is well meaning and in the public interest, many practical difficulties for health care professionals and families reduce its effectiveness. Therefore, Ontario mandatory reporting legislation is falling short of its purpose of eliminating underreporting to protect children. This paper outlines this problem and offers some potential solutions.


2020 ◽  
pp. 1-14
Author(s):  
Johan W. van de Gronden ◽  
Mary Guy

Abstract Part of the controversy surrounding competition and health care stems from the complexity connected with delineating the applicability of competition law – encompassing both the provisions governing anticompetitive agreements and abuse of dominance and the state-aid rules. Cases determined at the European Union (EU) level within the past 30 years have developed a broad framework, and notable trends have emerged – for example, a distinction between health care providers and managing bodies (purchasers). The former have been subject to an ‘abstract’ test and the latter to a more sophisticated ‘concrete’ test. In this paper, we chart the development of the EU courts’ approach to developing the ‘undertaking’ concept in health care and examine the current EU competition law framework with a view to identifying future directions. van de Gronden has recently identified a ‘three-prong’ test of exemption from competition law in connection with the recent CEPPB case: firstly, where the supply of services is predominantly dependent upon public financing; secondly, the public funding aims to achieve a public interest goal and thirdly, the activities concerned are closely related to this public interest goal. We examine this test in a health care context, drawing on our findings regarding Dutch competition reforms.


2012 ◽  
Vol 19 (1, 2 & 3) ◽  
pp. 2011
Author(s):  
Gillian Calder

I have entitled my five-minute comment: “Insite: Right Answer, Wrong Question.”1 The focus of my comments is on the division-of-powers approach used in the reasoning of Justice Huddart of the British Columbia Court of Appeal. Although asked to determine whether the legislative regime at issue was enacted validly, that is, whether it was either federal or provincial—the question that she wanted to answer, and did answer, was whether the matter should be federal or provincial. My reading of the majority reasons is that Justice Huddart (with Justice Rowles concurring) used the doctrine of interjurisdictional immunity (“IJI”) to reach the conclusion that she deemed to be the just outcome—that “the supervision of self-injections of illegally-possessed drugs in a provincially authorized and supported health care facility is dictated by the public interest in health care”2 and thus falls exclusively within provincial jurisdiction.


Author(s):  
William Roche

Regulation of the medical profession has a long history in the United Kingdom but a number of high profile failures of National Health Service (NHS) organisations to deliver safe health care and the unlawful killing of more than 200 patients by one rogue doctor have led to a clamour for change. Many of these tragedies have been the subject of public inquiries and have created significant public disquiet about the role and effectiveness of the medical regulator. United Kingdom governments have responded to these inquiries by means of a combination of strengthening professional regulation and the introduction of new mechanisms of appeal against the sanctions imposed on doctors by tribunals. The historical development of medical regulation is reviewed and the more recent changes to address the public interest and crises in the confidence in the regulation of health care are described.


PEDIATRICS ◽  
1969 ◽  
Vol 44 (3) ◽  
pp. 312-314
Author(s):  
Alfred Yankauer

In contrast to the prevailing tenor of less than a decade ago, few voices can be heard today reassuring the public or the professional that the American "health care system" is itself in good health. Having dealt with the aged through Medicare, the national spotlight now focuses on children who form the other major segment of our "poverty population." Analyses and complaints, proposals and programs flow forth at an accelerating pace. Two types of programs are discussed in the current issues of Pediatrics-one as a proposal presented to the American Academy of Pediatrics last fall, and the other as a report of work in progress.


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