Background Data about the frequency of adverse events related to inapp
ropriate care in hospitals come from studies of medical records as if
they represented a true record of adverse events. In a prospective, ob
servational design we analysed discussion of adverse events during the
care of all patients admitted to three units of a large, urban teachi
ng hospital affiliated to a university medical school. Discussion took
place during routine clinical meetings. We undertook the study to enh
ance understanding of the incidence and scope of adverse events as a b
asis for preventing them. Methods Ethnographers trained in qualitative
observational research attended day-shift, weekday, regularly schedul
ed attending rounds, residents' work rounds, nursing shift changes, ca
se conferences, and other scheduled meetings in three study units as w
ell as various departmental and section meetings. They recorded all ad
verse events during patient care discussed at these meetings and devel
oped a classification scheme to code the data. Data were collected abo
ut health-care providers' own assessments about the appropriateness of
the care that patients received to assess the nature and impact of ad
verse events and how health-care providers and patients responded to t
he adverse events. Findings Of the 1047 patients in the study, 185 (17
.7%) were said to have had at least one serious adverse event; having
an initial event was linked to the seriousness of the patient's underl
ying illness. Patients with long slays in hospital had more adverse ev
ents than those with short stays. The likelihood of experiencing an ad
verse event increased about 6% for each day of hospital stay. 37.8% of
adverse events were caused by an individual, 15.6% had interactive ca
uses, and 9.8% were due to administrative decisions. Although 17.7% of
patients experienced serious events that led to longer hospital stays
and increased costs to the patients, only 1.2% (13) of the 1047 patie
nts made claims for compensation. Interpretation This study shows that
there is a wide range of potential causes of adverse events that shou
ld be considered, and that careful attention must be paid to errors wi
th interactive or administrative causes. Healthcare providers' own dis
cussions of adverse events can be a good source of data for proactive
error prevention.