Informed consent in pediatric neurology

Seminars in Pediatric Neurology

Volumn 9, Issue 1, 2002, Pages 10-18

  Bernat, James L ^a,b  

^a DARTMOUTH MEDICAL SCHOOL   (United States)

^b DARTMOUTH HITCHCOCK MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHILD PARENT RELATION; CLINICAL RESEARCH; DECISION MAKING; DOCTOR PATIENT RELATION; EMERGENCY TREATMENT; GENETIC ANALYSIS; HUMAN; ILLNESS BEHAVIOR; INFORMED CONSENT; LEGAL ASPECT; MALPRACTICE; MEDICAL PRACTICE; NEUROLOGIC DISEASE; PEDIATRICS; REVIEW;

EID: 0036121527     PISSN: 10719091     EISSN: None     Source Type: Journal    
DOI: 10.1053/spen.2002.30333     Document Type: Article

References (48)

1. Consent issues in the management of cerebrovascular diseases
2. Minors' rights to consent to medical care
3. Basic ethical concepts in neurological practice
4. Moral theory in neurological practice
5. The ideal of shared decision making between physicians and patients
6. The framing of decisions and the psychology of choice
7. The influence of the probability of survival on patients' preferences regarding cardiopulmonary resuscitation
8. Barriers to informed consent
9. How informed is signed consent?
10. Informed proxy consent: Communication between pediatric surgeons and surrogates about surgery
11. Counseling patients to counsel physicians on future care in the event of patient incompetence
12. Beyond advance directives - Health care surrogate laws
13. Minors' consent to treatment: A developmental perspective
14. Minors' assent or dissent to medical treatment
15. The competency of children and adolescents to make informed medical decisions
16. Children as decision makers: Guidelines for pediatricians
17. Affirming the decisions adolescents make about life and death
18. A model act for consent of minors for health services
19. The minor's fight to consent to medical treatment: A corollary of the constitutional right of privacy
20. Informed consent and medical ethics
21. Informed consent, parental permission, and assent in pediatric practice
22. Health care decision making by children: Is it in their best interest?
23. The pre-adult health decision-making model: Linking decision-making directedness/orientation to adolescent health-related attitudes and behaviors
24. Consent for medical services for children and adolescents
25. Guidelines for urgent care in school
26. Minor rights and wrongs
27. In their own hands: Adolescent refusals of medical treatment
28. Parents' perceptions of decision making for children
29. Collision between law and ethics: Consent for treatment with adolescents
30. Challenging parental decisions to overtreat children
31. Minors, medical treatment, and interspousal disagreement: Should Solomon split the child?
32. The role of adolescents in decisions concerning their cancer therapy
33. Case consultation: When to invoke state agencies to treat: The cases of a minor and a mentally disabled adult
34. Legal aspects of transfusion of Jehovah's Witnesses
35. Jehovah's Witnesses and transfusion: The pediatric perspective
36. Genetic testing for children and adolescents: Who decides?
37. Research with children
38. Ethical considerations in pediatric oncology
39. In loco parentis: Minimal risk as an ethical threshold for research upon children
40. Empirical examination of the ability of children to consent to clinical research