Literature DB >> 23408950

'The words will pass with the blowing wind': staff and parent views of the deferred consent process, with prior assent, used in an emergency fluids trial in two African hospitals.

Sassy Molyneux1, Maureen Njue, Mwanamvua Boga, Lilian Akello, Peter Olupot-Olupot, Charles Engoru, Sarah Kiguli, Kathryn Maitland.   

Abstract

OBJECTIVE: To document and explore the views and experiences of key stakeholders regarding the consent procedures of an emergency research clinical trial examining immediate fluid resuscitation strategies, and to discuss the implications for similar trials in future.
METHODS: A social science sub-study of the FEAST (Fluid Expansion As Supportive Therapy) trial. Interviews were held with trial team members (n = 30), health workers (n = 15) and parents (n = 51) from two purposively selected hospitals in Soroti, Uganda, and Kilifi, Kenya.
FINDINGS: Overall, deferred consent with prior assent was seen by staff and parents as having the potential to protect the interests of both patients and researchers, and to avoid delays in starting treatment. An important challenge is that the validity of verbal assent is undermined when inadequate initial information is poorly understood. This concern needs to be balanced against the possibility that full prior consent on admission potentially causes harm through introducing delays. Full prior consent also potentially imposes worries on parents that clinicians are uncertain about how to proceed and that clinicians want to absolve themselves of any responsibility for the child's outcome (some parents' interpretation of the need for signed consent). Voluntariness is clearly compromised for both verbal assent and full prior consent in a context of such vulnerability and stress. Further challenges in obtaining verbal assent were: what to do in the absence of the household decision-maker (often the father); and how medical staff handle parents not giving a clear agreement or refusal.
CONCLUSION: While the challenges identified are faced in all research in low-income settings, they are magnified for emergency trials by the urgency of decision making and treatment needs. Consent options will need to be tailored to particular studies and settings, and might best be informed by consultation with staff members and community representatives using a deliberative approach.

Entities:  

Mesh:

Year:  2013        PMID: 23408950      PMCID: PMC3569446          DOI: 10.1371/journal.pone.0054894

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


  27 in total

1.  Presumed consent in emergency neonatal research.

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

2.  What makes clinical research in developing countries ethical? The benchmarks of ethical research.

Authors:  Ezekiel J Emanuel; David Wendler; Jack Killen; Christine Grady
Journal:  J Infect Dis       Date:  2004-02-17       Impact factor: 5.226

3.  HIV vaccine trials: critical issues in informed consent.

Authors:  G Lindegger; L M Richter
Journal:  S Afr J Sci       Date:  2000-06       Impact factor: 2.197

4.  Trust and informed consent: insights from community members on the Kenyan coast.

Authors:  C S Molyneux; N Peshu; K Marsh
Journal:  Soc Sci Med       Date:  2005-02-12       Impact factor: 4.634

5.  Mortality after fluid bolus in African children with severe infection.

Authors:  Kathryn Maitland; Sarah Kiguli; Robert O Opoka; Charles Engoru; Peter Olupot-Olupot; Samuel O Akech; Richard Nyeko; George Mtove; Hugh Reyburn; Trudie Lang; Bernadette Brent; Jennifer A Evans; James K Tibenderana; Jane Crawley; Elizabeth C Russell; Michael Levin; Abdel G Babiker; Diana M Gibb
Journal:  N Engl J Med       Date:  2011-05-26       Impact factor: 91.245

Review 6.  Is the concept of informed consent applicable to clinical research involving critically ill patients?

Authors:  John M Luce
Journal:  Crit Care Med       Date:  2003-03       Impact factor: 7.598

7.  Inability to obtain deferred consent due to early death in emergency research: effect on validity of clinical trial results.

Authors:  Tim C Jansen; Jan Bakker; Erwin J O Kompanje
Journal:  Intensive Care Med       Date:  2010-08-06       Impact factor: 17.440

8.  Benefits and payments for research participants: experiences and views from a research centre on the Kenyan coast.

Authors:  Sassy Molyneux; Stephen Mulupi; Lairumbi Mbaabu; Vicki Marsh
Journal:  BMC Med Ethics       Date:  2012-06-22       Impact factor: 2.652

9.  Working with Concepts: The Role of Community in International Collaborative Biomedical Research.

Authors:  V M Marsh; D K Kamuya; M J Parker; C S Molyneux
Journal:  Public Health Ethics       Date:  2011-03-02       Impact factor: 1.940

Review 10.  Use of deferred consent for severely ill children in a multi-centre phase III trial.

Authors:  Kathryn Maitland; Sassy Molyneux; Mwamvua Boga; Sarah Kiguli; Trudie Lang
Journal:  Trials       Date:  2011-03-31       Impact factor: 2.279

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  22 in total

Review 1.  The intensive care medicine clinical research agenda in paediatrics.

Authors:  Mark J Peters; Andrew Argent; Marino Festa; Stéphane Leteurtre; Jefferson Piva; Ann Thompson; Douglas Willson; Pierre Tissières; Marisa Tucci; Jacques Lacroix
Journal:  Intensive Care Med       Date:  2017-03-17       Impact factor: 17.440

Review 2.  Pediatric clinical drug trials in low-income countries: key ethical issues.

Authors:  S M MacLeod; D C Knoppert; M Stanton-Jean; D Avard
Journal:  Paediatr Drugs       Date:  2015-02       Impact factor: 3.022

3.  Routine gastric residual volume measurement to guide enteral feeding in mechanically ventilated infants and children: the GASTRIC feasibility study.

Authors:  Lyvonne N Tume; Kerry Woolfall; Barbara Arch; Louise Roper; Elizabeth Deja; Ashley P Jones; Lynne Latten; Nazima Pathan; Helen Eccleson; Helen Hickey; Roger Parslow; Jennifer Preston; Anne Beissel; Izabela Andrzejewska; Chris Gale; Frederic V Valla; Jon Dorling
Journal:  Health Technol Assess       Date:  2020-05       Impact factor: 4.014

4.  Vulnerability, Agency, and the Research Encounter: Family Members' Experiences and Perceptions of Participating in an Observational Clinical Study in Kenya.

Authors:  Scholastica M Zakayo; Mary N Kimani; Gladys Sanga; Rita Njeru; Anderson Charo; James A Berkley; Judd L Walson; Maureen Kelley; Vicki Marsh; Sassy Molyneux
Journal:  J Empir Res Hum Res Ethics       Date:  2021-03-25       Impact factor: 1.978

5.  Health providers' perceptions of clinical trials: lessons from Ghana, Kenya and Burkina Faso.

Authors:  Vibian Angwenyi; Kwaku-Poku Asante; Abdoulaye Traoré; Lawrence Gyabaa Febir; Charlotte Tawiah; Anthony Kwarteng; Alphonse Ouédraogo; Sodiomon Bienvenue Sirima; Seth Owusu-Agyei; Egeruan Babatunde Imoukhuede; Jayne Webster; Daniel Chandramohan; Sassy Molyneux; Caroline Jones
Journal:  PLoS One       Date:  2015-05-01       Impact factor: 3.240

6.  Informed consent in paediatric critical care research--a South African perspective.

Authors:  Brenda M Morrow; Andrew C Argent; Sharon Kling
Journal:  BMC Med Ethics       Date:  2015-09-09       Impact factor: 2.652

7.  Fifteen-minute consultation: an evidence-based approach to research without prior consent (deferred consent) in neonatal and paediatric critical care trials.

Authors:  Kerry Woolfall; Lucy Frith; Angus Dawson; Carrol Gamble; Mark D Lyttle; Bridget Young
Journal:  Arch Dis Child Educ Pract Ed       Date:  2015-10-13       Impact factor: 1.309

8.  Benefits in cash or in kind? A community consultation on types of benefits in health research on the Kenyan Coast.

Authors:  Maureen Njue; Sassy Molyneux; Francis Kombe; Salim Mwalukore; Dorcas Kamuya; Vicki Marsh
Journal:  PLoS One       Date:  2015-05-26       Impact factor: 3.240

9.  Model for developing context-sensitive responses to vulnerability in research: managing ethical dilemmas faced by frontline research staff in Kenya.

Authors:  Sassy Molyneux; Priya Sukhtankar; Johnstone Thitiri; Rita Njeru; Kui Muraya; Gladys Sanga; Judd L Walson; James Berkley; Maureen Kelley; Vicki Marsh
Journal:  BMJ Glob Health       Date:  2021-07

10.  How parents and practitioners experience research without prior consent (deferred consent) for emergency research involving children with life threatening conditions: a mixed method study.

Authors:  Kerry Woolfall; Lucy Frith; Carrol Gamble; Ruth Gilbert; Quen Mok; Bridget Young
Journal:  BMJ Open       Date:  2015-09-18       Impact factor: 2.692

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