Optimization of informed consent for umbilical cord blood banking

Objective: The purpose of this project was to evaluate the informed consent process for donation to a public umbilical cord blood bank. Study Design: Telephone interviews were conducted with 170 women who had given consent to donate their newborn infants' umbilical cord blood. Results: Of the 1...

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Veröffentlicht in:American journal of obstetrics and gynecology 2002-12, Vol.187 (6), p.1642-1646
Hauptverfasser: Sugarman, Jeremy, Kurtzberg, Joanne, Box, Tamara L., Horner, Ronnie D.
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container_end_page 1646
container_issue 6
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container_title American journal of obstetrics and gynecology
container_volume 187
creator Sugarman, Jeremy
Kurtzberg, Joanne
Box, Tamara L.
Horner, Ronnie D.
description Objective: The purpose of this project was to evaluate the informed consent process for donation to a public umbilical cord blood bank. Study Design: Telephone interviews were conducted with 170 women who had given consent to donate their newborn infants' umbilical cord blood. Results: Of the 170 women who were contacted, 96.8% of the women reported that all their questions had been answered. Nevertheless, approximately one third of the respondents did not consider themselves to be in research, and almost one quarter of the respondents did not know how to contact the umbilical cord blood bank if they or their infant became seriously ill. Further, a substantial proportion of the respondents did not understand the full range of alternatives to donation and incorrectly endorsed potential benefits. Conclusion: Informed consent could be optimized by (1) having those personnel who obtain consent emphasize that banking involves research and to explain the true benefits of donation, (2) ensuring that parents know how and when to contact the umbilical cord blood bank after donation, and (3) using phone surveys to continue assessments and to monitor changes in the process. (Am J Obstet Gynecol 2002;187:1642-6.)
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Study Design: Telephone interviews were conducted with 170 women who had given consent to donate their newborn infants' umbilical cord blood. Results: Of the 170 women who were contacted, 96.8% of the women reported that all their questions had been answered. Nevertheless, approximately one third of the respondents did not consider themselves to be in research, and almost one quarter of the respondents did not know how to contact the umbilical cord blood bank if they or their infant became seriously ill. Further, a substantial proportion of the respondents did not understand the full range of alternatives to donation and incorrectly endorsed potential benefits. Conclusion: Informed consent could be optimized by (1) having those personnel who obtain consent emphasize that banking involves research and to explain the true benefits of donation, (2) ensuring that parents know how and when to contact the umbilical cord blood bank after donation, and (3) using phone surveys to continue assessments and to monitor changes in the process. (Am J Obstet Gynecol 2002;187:1642-6.)</description><identifier>ISSN: 0002-9378</identifier><identifier>EISSN: 1097-6868</identifier><identifier>DOI: 10.1067/mob.2002.127307</identifier><identifier>PMID: 12501077</identifier><identifier>CODEN: AJOGAH</identifier><language>eng</language><publisher>Philadelphia, PA: Mosby, Inc</publisher><subject>Adult ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Bioethics ; Biological and medical sciences ; Blood Banks ; Blood Donors ; Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis ; Continental Population Groups ; Educational Status ; ethics ; Ethics, Medical ; Female ; Fetal Blood ; Health Knowledge, Attitudes, Practice ; Humans ; Income ; Informed Consent ; Medical sciences ; survey ; Surveys and Questionnaires ; Telephone ; Time Factors ; Transfusions. Complications. Transfusion reactions. 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Study Design: Telephone interviews were conducted with 170 women who had given consent to donate their newborn infants' umbilical cord blood. Results: Of the 170 women who were contacted, 96.8% of the women reported that all their questions had been answered. Nevertheless, approximately one third of the respondents did not consider themselves to be in research, and almost one quarter of the respondents did not know how to contact the umbilical cord blood bank if they or their infant became seriously ill. Further, a substantial proportion of the respondents did not understand the full range of alternatives to donation and incorrectly endorsed potential benefits. Conclusion: Informed consent could be optimized by (1) having those personnel who obtain consent emphasize that banking involves research and to explain the true benefits of donation, (2) ensuring that parents know how and when to contact the umbilical cord blood bank after donation, and (3) using phone surveys to continue assessments and to monitor changes in the process. (Am J Obstet Gynecol 2002;187:1642-6.)</description><subject>Adult</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Bioethics</subject><subject>Biological and medical sciences</subject><subject>Blood Banks</subject><subject>Blood Donors</subject><subject>Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis</subject><subject>Continental Population Groups</subject><subject>Educational Status</subject><subject>ethics</subject><subject>Ethics, Medical</subject><subject>Female</subject><subject>Fetal Blood</subject><subject>Health Knowledge, Attitudes, Practice</subject><subject>Humans</subject><subject>Income</subject><subject>Informed Consent</subject><subject>Medical sciences</subject><subject>survey</subject><subject>Surveys and Questionnaires</subject><subject>Telephone</subject><subject>Time Factors</subject><subject>Transfusions. Complications. Transfusion reactions. 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Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Bioethics</topic><topic>Biological and medical sciences</topic><topic>Blood Banks</topic><topic>Blood Donors</topic><topic>Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis</topic><topic>Continental Population Groups</topic><topic>Educational Status</topic><topic>ethics</topic><topic>Ethics, Medical</topic><topic>Female</topic><topic>Fetal Blood</topic><topic>Health Knowledge, Attitudes, Practice</topic><topic>Humans</topic><topic>Income</topic><topic>Informed Consent</topic><topic>Medical sciences</topic><topic>survey</topic><topic>Surveys and Questionnaires</topic><topic>Telephone</topic><topic>Time Factors</topic><topic>Transfusions. Complications. Transfusion reactions. 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Study Design: Telephone interviews were conducted with 170 women who had given consent to donate their newborn infants' umbilical cord blood. Results: Of the 170 women who were contacted, 96.8% of the women reported that all their questions had been answered. Nevertheless, approximately one third of the respondents did not consider themselves to be in research, and almost one quarter of the respondents did not know how to contact the umbilical cord blood bank if they or their infant became seriously ill. Further, a substantial proportion of the respondents did not understand the full range of alternatives to donation and incorrectly endorsed potential benefits. Conclusion: Informed consent could be optimized by (1) having those personnel who obtain consent emphasize that banking involves research and to explain the true benefits of donation, (2) ensuring that parents know how and when to contact the umbilical cord blood bank after donation, and (3) using phone surveys to continue assessments and to monitor changes in the process. (Am J Obstet Gynecol 2002;187:1642-6.)</abstract><cop>Philadelphia, PA</cop><pub>Mosby, Inc</pub><pmid>12501077</pmid><doi>10.1067/mob.2002.127307</doi><tpages>5</tpages></addata></record>
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source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Adult
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Bioethics
Biological and medical sciences
Blood Banks
Blood Donors
Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis
Continental Population Groups
Educational Status
ethics
Ethics, Medical
Female
Fetal Blood
Health Knowledge, Attitudes, Practice
Humans
Income
Informed Consent
Medical sciences
survey
Surveys and Questionnaires
Telephone
Time Factors
Transfusions. Complications. Transfusion reactions. Cell and gene therapy
umbilical cord blood banking
title Optimization of informed consent for umbilical cord blood banking
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