Potential Impact of a Verbal Prehospital DNR Policy

Abstract

Background. Forgoing resuscitation in prehospital cardiac arrest has previously required a written prehospital do-not-resuscitate (DNR) order. Some emergency medical services (EMS) agencies, including Los Angeles County (LAC), have implemented policies allowing surrogate decision makers to verbally request to forgo resuscitation. The impact of a verbal DNR policy is unclear, given the absence of information about how often cardiac arrest occurs at home, or in the presence of a family member. Objective. To determine the prevalence of written DNR forms, rate of resuscitation, location of cardiac arrest, andavailability of a family member in nontraumatic cardiac arrest prior to implementation of the new policy in LAC. Methods. All prehospital run sheets for nontraumatic cardiac arrest in LAC were reviewed for the first seven days of each month (August 2006–January 2007) for DNR status, location of cardiac arrest, presence of family members, andwhether resuscitation was attempted. Results. Of the 897 cardiac arrests, 492 occurred at home, 111 in a public place, and93 in a nursing home (location was unknown for 201). Fifty-five patients (6%) had a written DNR order, although it was not always available. Of these 55 patients, ten were resuscitated, the majority of the time because the family could not produce the paperwork. A family member was listed as present 29% of the time (261 of 897 cases). A medical history was obtained in an additional 465 cases (52%), indicating that someone familiar with the patient's medical history was present more than half the time, even when a family member was not mentioned. Conclusions. A written DNR order is uncommonly used in the prehospital setting as a reason to forgo resuscitation in LAC. Even when family members state that the patient has a DNR order, patients are often resuscitated. A majority of cardiac arrests occurs at the patient's home, andin many cases in the presence of family members, some of whom may be able to express a patient's preferences regarding end-of-life care