
A Call to Move Beyond the Numbers in DNAR Orders Research
Author(s) -
Dainty Katie N.
Publication year - 2020
Publication title -
journal of the american heart association
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.494
H-Index - 85
ISSN - 2047-9980
DOI - 10.1161/jaha.119.015657
Subject(s) - cardiopulmonary resuscitation , psychology , medicine , sociology , resuscitation , emergency medicine
D o not attempt resuscitation orders (DNAR) have been the topic of many studies in many fields, for many years. As Burns et al stated in their 25-year review of DNR orders, “few initials in medicine today evoke as much symbolism or controversy as the DNR order.” It is a complicated procedural entity that is often counted as binary (yes or no); however, its execution is heavily influenced by persuasive sociocultural constructs such as sex, age, culture, religion, and relationships —not only of the patient, but also of the substitute decision maker(s) and healthcare providers involved. The publication of the first DNR orders in the literature in 1976 was a significant transition in the delivery of medical care; rather than ordering the start of a therapeutic intervention, this was the first order prohibiting a medical therapy. Since then many papers have been published looking at various associations in order to determine whether there are trends in who has or should have a DNAR order and what the timing was or should be, although the majority are retrospective, quantitative analyses of registry/administrative data. In this issue of the Journal of the American Heart Association (JAHA), Perman et al use data from the Get With The Guidelines—Resuscitation Registry to look at the association between de novo DNAR (any time after return of spontaneous circulation [ROSC]), within 12 hours of ROSC, or within 72 hours of ROSC) by sex, and the association between sex and survival to discharge accounting for DNAR for in-hospital cardiac arrest. Their cohort included 30 454 (42.4%) women, who were slightly more likely to establish DNAR orders any time after ROSC (45.0% versus 43.5%; ARR [Absolute Risk Reduction] 1.15 [95% CI: 1.10–1.20]; P<0.0001). Of those with DNAR, women were more likely to be DNAR within the first 12 hours (51.8% versus 46.5%; ARR 1.40 [1.30–1.52]; P<0.0001) and within 72 hours after ROSC (75.9% versus 70.9%; ARR 1.35 [1.26–1.45]; P<0.0001). However, they did not find a difference in survival to hospital discharge between women and men (34.5% versus 36.7%; ARR 1.00, 95% CI 0.99– 1.02, P=0.74). This is a very well-written paper using a robust national database, but after reading it I found myself still asking the “So what?” question. What knowledge do these statistics impart that helps us understand the impact of the execution of DNAR orders at a certain time, in certain people? Not unlike previous papers, we see that women are more likely to have a DNAR status initiated earlier than their male counterparts. However, the complexities of how and why the DNAR orders were implemented for those women at that time (earlier), the nature of the discussions and decision-making factors that were considered, etc are absent from this type of study, which leaves the reader still wanting for an explanation. While the excellent work presented by Perman et al is important to begin to draw attention to a potential sex/ gender association (or in this case a lack of association regarding survival), it also draws attention to the need to look at more than just epidemiology and statistics when investigating what are complex, socially mediated questions in health care. We need to lean more heavily on a mixed methods approaches to put meat on the numerical bones and truly understand the reasons behind the choices and timing of initiation of DNAR status in all patients. Registry data research looking at variations in care can quantify differences between groups, but the issue becomes whether a difference equates to a problem. In the case of sex differences such as those described by Perman et al, there may be very good explanations for why the women in this cohort were put on DNAR status when they were, but we do not have a way to know that from the registry. And if we decide that such a sex difference (or any other inequality for that matter) is indeed problematic, how can we begin to understand the root of the problem or what interventions or changes should be made in order to reverse the problem without understanding the answers to the why and how questions? Quantitative research methods are a powerful tool for measuring and analyzing large amounts of data and for understanding relationships between dependent and The opinions expressed in this article are not necessarily those of the editors or of the American Heart Association. From the North York General Hospital, The University of Toronto, Toronto, Ontario, Canada. Correspondence to: Katie N. Dainty, PhD, North York General Hospital, 4001 Leslie St, Room LE-140, Toronto, Ontario, Canada M2K 3E1. E-mail: katie.dainty@utoronto.ca J Am Heart Assoc. 2020;9:e015657. DOI: 10.1161/JAHA.119.015657. a 2020 The Author. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.