Chiong W, Kim AS, Huang IA, Farahany NA, Josephson SA. Testing the Presumption of Consent to Emergency Treatment for Acute Ischemic Stroke. JAMA. 2014;311(16):1689-1691. doi:10.1001/jama.2014.3302
In life-threatening emergencies involving incapacitated patients without surrogates, clinicians may intervene without obtaining informed consent, applying the presumption that reasonable people would consent to treatment in such circumstances. Whether this rationale applies to the treatment of acute ischemic stroke with intravenous thrombolysis is controversial because this intervention improves functional outcomes but is not life preserving.1
Nonetheless, the presumption of consent to thrombolysis for ischemic stroke has recently been endorsed by professional societies.2,3 Previous empirical studies of preferences for emergency treatment have been limited to surveys of convenience samples that were not demographically representative. We evaluated the presumption of consent by comparing preferences for treatment of acute ischemic stroke with thrombolysis and treatment of sudden cardiac arrest with cardiopulmonary resuscitation (CPR; in which the presumption of consent is generally accepted) in a nationally representative sample of older US adults.
This experiment was conducted between February 19 and March 3, 2013, as part of a broader study of treatment preferences using the GfK KnowledgePanel, a probability-based panel designed to be representative of the US population.4 Adults aged 50 years or older were randomly assigned to read 1 of 2 scenarios: in one they experienced a severe acute ischemic stroke and were brought to a hospital, and in the other they experienced an out-of-hospital cardiac arrest and were attended to by paramedics.
The stroke scenario included a graphical depiction of probabilistic risks and benefits of treatment with thrombolysis.5 The cardiac arrest scenario included a similar depiction of probabilistic outcomes after paramedic-initiated CPR.6 All participants were then asked whether they would want the treatment described, using a 4-point Likert scale (definitely yes, probably yes, probably no, or definitely no).
The institutional review board at the University of California, San Francisco, approved this study. All participants provided informed consent.
Responses were weighted to match the US population aged 50 years or older. Likert-scaled treatment preferences were dichotomized to yes or no for analysis. The influence of the clinical scenario (ischemic stroke vs cardiac arrest) on treatment preference was assessed using logistic regression.
In secondary analyses, we evaluated demographic and health predictors of treatment preference in both stroke and cardiac arrest using logistic regression. Exploratory multivariable logistic regression models were generated using backward stepwise selection at a P value threshold of .20. Statistical analyses were conducted using Stata version 12.1 (StataCorp). Two-tailed P < .05 was considered significant.
In the broader treatment preferences study, 2154 (63.0%) of 3418 fielded questionnaires were completed; half (n = 1100) of these participants were randomized to the 2 study conditions in the present experiment. Participants were demographically representative of US adults aged 50 years or older, with no significant differences between conditions (Table 1 and Table 2).
In population-weighted analyses, 76.2% (95% CI, 71.2%-80.6%) of older adults (419 of 545 participants) wanted thrombolysis for acute ischemic stroke, whereas 75.9% (95% CI, 71.1%-80.2%) of older adults (422 of 555 participants) wanted CPR for sudden cardiac arrest (P = .93). In multivariable models, female sex, divorced marital status, and lower educational attainment predicted refusal of thrombolysis (Table 1). Poorer physical health, previous stroke, and possession of a health care advance directive predicted refusal of CPR (Table 2).
When an incapacitated older patient’s treatment preferences are unknown and surrogate decision makers are unavailable, there are equally strong empirical grounds for presuming individual consent to thrombolysis for stroke as for presuming individual consent to CPR. Because the presumption of consent is generally accepted for CPR, this finding provides empirical support for policy positions recently taken by professional societies that favor the use of thrombolysis for stroke in emergency circumstances under a presumption of consent.
Even though such emergency presumptions are supported by the treatment preferences of most older adults, it is noteworthy that nearly one-quarter of older adults would not want either intervention. Also, our experiment was only designed to address the empirical basis of the ethical and legal presumption of consent. Policies regarding the applicability of this presumption must also be informed by normative considerations such as the role of clinical judgment and the values of life and independence.
Corresponding Author: Winston Chiong, MD, PhD, University of California, 675 Nelson Rising Ln, Ste 190, San Francisco, CA 94158 (email@example.com).
Author Contributions: Dr Chiong had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
Study concept and design: Chiong, Kim, Farahany, Josephson.
Acquisition, analysis, or interpretation of data: Chiong, Kim, Huang.
Drafting of the manuscript: Chiong, Huang.
Critical revision of the manuscript for important intellectual content: Chiong, Kim, Farahany, Josephson.
Statistical analysis: Chiong, Kim.
Obtained funding: Chiong.
Study supervision: Josephson.
Conflict of Interest Disclosures: The authors have completed and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Dr Kim reported receiving grants from SanBio Inc outside the submitted work. No other disclosures were reported.
Funding/Support: This work was supported by grant K23AG043553 from the National Institute on Aging, grant KL2TR000143 from the National Center for Advancing Translational Sciences, and by funding through the American Brain Foundation Clinical Research Training Fellowship Program. Data collection was provided by Time-sharing Experiments in the Social Sciences with National Science Foundation grant 0818839 (Jeremy Freese, PhD, and James Druckman, PhD, principal investigators). Time-sharing Experiments in the Social Sciences provided data collection using the GfK KnowledgePanel and survey weights for matching participants’ responses to the US Current Population Survey.
Role of the Sponsors: The sponsors had no role in the design of the study; analysis and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.
Additional Contributions: We gratefully acknowledge the technical contributions of Carolyn Chu, Stefan Subias, and other staff of GfK; and the assistance of Amy J. Markowitz, JD, and John M. Neuhaus, PhD (both with the University of California, San Francisco), in drafting the manuscript. None received compensation for their contributions.