Rl. Jayes et al., DO-NOT-RESUSCITATE ORDERS IN INTENSIVE-CARE UNITS - CURRENT PRACTICESAND RECENT CHANGES, JAMA, the journal of the American Medical Association, 270(18), 1993, pp. 2213-2217
Objectives.-To describe the characteristics of patients with do-not-re
suscitate (DNR) orders and the frequency and timing of these orders in
a representative sample of intensive care units (ICUs) and to compare
practices from 1980 to 1990. Design.-Prospective inception cohort. Se
tting.-A total of 42 ICUs in 40 US hospitals with 200 or more beds; 26
randomly selected hospitals and 14 large, tertiary care hospitals tha
t volunteered to be studied. Participants.-A consecutive sample of 17
440 ICU admissions from 1988 to 1990.Measurements.-Patient demographic
characteristics, comorbid conditions, disease, and physiological abno
rmalities. Main Outcome Measures.-Frequency and timing of DN R orders;
ICU resource use before and after DNR orders; and patients' hospital
and ICU discharge status. Results.-Physicians wrote DNR orders for 157
7 ICU admissions (9%) (hospital range, 1.5% to 22%). Patients with ICU
DNR orders were older, more functionally impaired, had more comorbid
illness, a higher severity of illness, and required the usp of more IC
U resources compared with patients without DNR orders. Compared with d
ata from a similar survey from 1979 to 1982, ICU DNR orders were more
frequent in 1988 to 1990 (9% vs 5.4%; P<.001) and preceded 60% of all
in-unit deaths compared with only 39% in 1979 to 1982 (P<.001). Do-not
-resuscitate orders were written sooner (for 3.6% vs 2.0% of patients
on day 1 in the ICU) and patients with DNR orders remained in the ICU
longer in 1988 to 1990 (2.8 vs 1.4 days) than in 1979 to 1982, and had
lower ICU and hospital mortality rates (64% vs 74%, P<.001; and 85% v
s 94%, P<.001). Conclusions.-Over the last decade physicians and patie
nts' families set limits earlier and more frequently in cases likely t
o have poor outcomes. We attribute this change to a greater dialogue a
bout setting limits to care and a greater knowledge of treatment outco
mes among physicians and families. These changes in practice preceded
implementation of the Patient Self-determination Act, designed to ensu
re patient autonomy for decisions about life-sustaining therapy.