Arzthaftungsrecht/Medical Malpractice Law

1982 ◽  
Vol 30 (4) ◽  
pp. 704
Author(s):  
John G. Fleming ◽  
Dieter Giesen
1984 ◽  
Vol 4 (4) ◽  
pp. 401-414 ◽  
Author(s):  
Harold Bursztajn ◽  
Robert M. Hamm ◽  
Thomas G. Gutheil ◽  
Archie Brodsky

2018 ◽  
pp. 241-258
Author(s):  
CHARLES L. BECKER ◽  
SHANIN SPECTER ◽  
THOMAS R. KLINE

2018 ◽  
pp. 241-258
Author(s):  
Charles L. Becker ◽  
Shanin Specter ◽  
Thomas R. Kline

1979 ◽  
Vol 7 (3) ◽  
pp. 391-393
Author(s):  
Donald Dawidoff

2004 ◽  
Vol 11 (5) ◽  
pp. 489-499 ◽  
Author(s):  
Ümit N Gündoğmuş ◽  
Erdem Özkara ◽  
Samiye Mete

Medical malpractice has attracted the attention of people and the media all over the world. In Turkey, malpractice cases are tried according to both criminal and civil law. Nurses and midwives in Turkey fulfill important duties in the distribution of health services. The aim of this study was to reveal the legal procedures followed in malpractice allegations and malpractice lawsuits in which nurses and midwives were named as defendants. We reviewed 59 nursing and midwifery lawsuits reported to the Higher Health Council between 1993 and 1998. Health professionals were held liable in 59% of the lawsuits. Midwives had the highest percentage of malpractice liability (52%), followed by physicians (29%) and nurses (19%). To reduce potential liability, nurse education should be improved, a nursing malpractice law should be enacted, and instructions for nursing procedures should be formulated.


2007 ◽  
Vol 14 (1) ◽  
pp. 47-59 ◽  
Author(s):  
Dieter Hart

AbstractMedicinal products are associated with risks as well as potential therapeutic benefits. This is reflected by the legal requirements for patient information on drug therapy which can be differentiated into general product information, regulated by pharmaceutical (i. e. product safety) law, and individual patient information on the treatment with the product, which is subject to medical malpractice law. The physician's duty to inform the patient comprises therapeutic information as well as information required for informed consent. Therapeutic information intends to empower the patient to comply with the requirements of treatment and to protect him/her against preventable danger and risk; it is part of the medical treatment, aimed at the individual patient and his/her personal situation. Information required for informed consent enables the patient to a self-determined decision on the treatment offered; it can be divided into information on the course of treatment and risk information. Product information and treatment information complement each other; the former should be the basis of individual information on the concrete treatment, provided by the physician in a mandatory oral conversation with the patient. Product information cannot replace the physician's individual information about the treatment.


1989 ◽  
Vol 37 (4) ◽  
pp. 838 ◽  
Author(s):  
John G. Fleming ◽  
Dieter Giesen

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