Literature DB >> 1881731

Informational needs of parents of sick neonates.

N B Perlman1, J L Freedman, R Abramovitch, H Whyte, H Kirpalani, M Perlman.   

Abstract

Sixty-one parents of 43 neonates in a neonatal intensive care unit were interviewed within 3 days of their first conference with the neonatologist to assess their needs for medical information. The conference with the physician and the interview with the investigator were audiotaped. Information given by the physician and information recalled by the parents was categorized and rated by the investigator. The physicians gave very detailed information about diagnosis in 77% of cases whereas 39% of the parents recalled diagnostic information in great detail. Respective percentages for prognosis were 16 and 33; for current management (eg, investigation, therapy), 28 and 66; and for cause of illness, 16 and 18. The statistical significance of the differences between the very detailed information int he physician-parent conferences and in the parent-investigator interviews was, by category, less than .002, less than .041, less than .004, and not significant, respectively. Information in the respective categories was described as "most helpful" by 20%, 67%, 90%, and 8% of parents. All but one of the parents stated that they wanted the whole truth. Physician uncertainty in providing information was significantly associated with severity of illness. It is concluded that while parents wanted information in all categories, they paid most attention to that relating to management. Physician-parent discordances with respect to information about management, diagnosis, and prognosis suggest directions for future investigation of the optimal content of information for parents in this context.

Mesh:

Year:  1991        PMID: 1881731

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  12 in total

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Authors:  M Cuttini; M Rebagliato; P Bortoli; G Hansen; R de Leeuw; S Lenoir; J Persson; M Reid; M Schroell; U de Vonderweid; M Kaminski; H Lenard; M Orzalesi; R Saracci
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  1999-09       Impact factor: 5.747

2.  Presumed consent in emergency neonatal research.

Authors:  D J Manning
Journal:  J Med Ethics       Date:  2000-08       Impact factor: 2.903

3.  Neonatal research: the parental perspective.

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Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  2004-07       Impact factor: 5.747

4.  Families' views on ward rounds in neonatal units.

Authors:  R Bramwell; M Weindling
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  2005-09       Impact factor: 5.747

5.  Parents' informational needs at the birth of a baby with a surgically correctable anomaly.

Authors:  L Aite; A Zaccara; A Trucchi; A Nahom; B Iacobelli; P Bagolan
Journal:  Pediatr Surg Int       Date:  2006-01-21       Impact factor: 1.827

6.  Communicating with parents of high-risk infants in neonatal intensive care.

Authors:  Wendy Yee; Sue Ross
Journal:  Paediatr Child Health       Date:  2006-05       Impact factor: 2.253

7.  A Medicaid eHealth program: an analysis of benefits to users and nonusers.

Authors:  Charles Safran; Grace Pompilio-Weitzner; Kathryn D Emery; Louis Hampers
Journal:  AMIA Annu Symp Proc       Date:  2005

8.  Proxy consent in neonatal care--goal-directed or procedure-specific?

Authors:  Donal Manning
Journal:  Health Care Anal       Date:  2005-03

9.  Predicting outcome in very low birthweight infants using an objective measure of illness severity and cranial ultrasound scanning.

Authors:  P W Fowlie; W O Tarnow-Mordi; C R Gould; D Strang
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  1998-05       Impact factor: 5.747

10.  From powerlessness to empowerment: Mothers expect more than information from the prenatal consultation for preterm labour.

Authors:  Nathalie Gaucher; Antoine Payot
Journal:  Paediatr Child Health       Date:  2011-12       Impact factor: 2.253

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