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Volumn 364, Issue 9434, 2004, Pages 560-561

Intrapartum prevention of meconium aspiration syndrome

Author keywords

[No Author keywords available]

Indexed keywords

AMNION FLUID; ARTIFICIAL VENTILATION; ASPIRATION PNEUMONIA; COMMUNITY; CONSULTATION; HUMAN; INFORMED CONSENT; LABOR; MECONIUM; NOTE; PERINATAL CARE; PRIORITY JOURNAL; STAINING;

EID: 4143151006     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(04)16863-3     Document Type: Note
Times cited : (7)

References (11)
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    • Niermeyer S, Kattwinkel J, Van Reempts P, et al. International guidelines for neonatal resuscitation: an excerpt from the guidelines 2000 for cardiopulmonary resuscitation and emergency cardiovascular care - international consensus on science. Pediatrics 2000; 106: e29-44. http://www.pediatrics.org/ cgi/content/full/106/3/e29 (accessed July 7, 2004).
    • (2000) Pediatrics , vol.106
    • Niermeyer, S.1    Kattwinkel, J.2    Van Reempts, P.3
  • 2
    • 0031834803 scopus 로고    scopus 로고
    • The Cochrane Collaboration: Evaluation of health care and services using systematic reviews of randomized controlled trials
    • Dickersin K, Manheimer E. The Cochrane Collaboration: evaluation of health care and services using systematic reviews of randomized controlled trials. Clin Obstet Gynecol. 41:1998;315-331
    • (1998) Clin Obstet Gynecol , vol.41 , pp. 315-331
    • Dickersin, K.1    Manheimer, E.2
  • 3
    • 0030839611 scopus 로고    scopus 로고
    • Making sense of randomization; Responses of parents of critically ill babies to random allocation of treatment in a clinical trial
    • Snowdon C, Garcia J, Elbourne D. Making sense of randomization; responses of parents of critically ill babies to random allocation of treatment in a clinical trial. Soc Sci Med. 45:1997;1337-1355
    • (1997) Soc Sci Med , vol.45 , pp. 1337-1355
    • Snowdon, C.1    Garcia, J.2    Elbourne, D.3
  • 4
    • 0034676823 scopus 로고    scopus 로고
    • Obtaining informed consent to neonatal randomised controlled trials: Interviews with parents and clinicians in the Euricon study
    • Mason SA, Allmark PJ, for the Euricon Study Group. Obtaining informed consent to neonatal randomised controlled trials: interviews with parents and clinicians in the Euricon study. Lancet 2000; 356: 2045-51.
    • (2000) Lancet , vol.356 , pp. 2045-2051
    • Mason, S.A.1    Allmark, P.J.2
  • 5
    • 0037713715 scopus 로고    scopus 로고
    • Consent for clinical research in the neonatal intensive care unit: A retrospective survey and a prospective study
    • Burgess E, Singhal N, Amin H, McMillan DD, Devrome H. Consent for clinical research in the neonatal intensive care unit: a retrospective survey and a prospective study. Arch Dis Child Fetal Neonatal Ed. 88:2003;F280-F286
    • (2003) Arch Dis Child Fetal Neonatal Ed , vol.88
    • Burgess, E.1    Singhal, N.2    Amin, H.3    McMillan, D.D.4    Devrome, H.5
  • 7
    • 0031575969 scopus 로고    scopus 로고
    • Consent is not always practical in emergency treatments
    • Morley C. Consent is not always practical in emergency treatments. BMJ. 314:1997;1480
    • (1997) BMJ , vol.314 , pp. 1480
    • Morley, C.1
  • 8
    • 0033863910 scopus 로고    scopus 로고
    • Presumed consent in emergency neonatal research
    • Manning DJ. Presumed consent in emergency neonatal research. J Med Ethics. 26:2000;249-253
    • (2000) J Med Ethics , vol.26 , pp. 249-253
    • Manning, D.J.1
  • 9
    • 0038105272 scopus 로고
    • Informed consent - Legally effective and prospectively obtained
    • Aug 12
    • Ellis GB. Informed consent - legally effective and prospectively obtained. OPRR Rep, Aug 12, 1993: No 93-3.
    • (1993) OPRR Rep , vol.93 , Issue.3
    • Ellis, G.B.1
  • 10
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    • 45 CFR 46 116(d) and 46 102 (i).
    • Department of Health and Human Services. Protection of Human Research subjects. 45 CFR 46 116(d) and 46 102 (i). http://ohsr.od.nih.gov/guidelines/ 45cfr46.html (accessed July 7, 2004).
    • Protection of Human Research Subjects
  • 11
    • 0001122640 scopus 로고    scopus 로고
    • Protection of human subjects: Informed consent and waiver of informed consent requirements in certain emergency research - Final rules (codified at 21 CFR 50 et al.; 45 CFR 46)
    • Department of Health and Human Services/ Food and Drug Administration/Office of the Secretary. Protection of human subjects: informed consent and waiver of informed consent requirements in certain emergency research - final rules (codified at 21 CFR 50 et al.; 45 CFR 46). Federal Register 1996; 61: 51497-533.
    • (1996) Federal Register , vol.61 , pp. 51497-51533


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.