The first national study of patient safety in Canadian hospitals estimates that 7.5 per cent of people hospitalized in Canada have experienced an adverse event as a result of their care. "The Canadian Adverse Events Study: the incidence of adverse events in hospital patients in Canada", to be published in the May 25 edition of the Canadian Medical Association Journal, found that the overall rate of adverse events in 2000 was 7.5 per 100 patient admissions, not including pediatric, obstetric or psychiatric admissions.
This rate suggests that 185,000 of the almost 2.5 million medical and surgical admissions in Canada in 2000 were associated with an adverse event - defined as an unintended injury or complication resulting in death, disability or prolonged hospital stay caused by health care management rather than the patient's underlying condition. Researchers from seven Canadian universities, led by the University of Toronto (U of T) and the University of Calgary (U of C), analysed the adverse event rate after reviewing 3,745 adult patient charts, randomly selected from 20 acute care hospitals across five provinces (B.C., Alberta, Ontario, Quebec and Nova Scotia).
The study also found that:
- the majority of adverse events resulted in temporary disability or prolonged hospital stay
- five per cent of patients who experienced adverse events were udged to have a permanent disability
- adverse events were associated with death in 1.6 per cent of patients admitted to acute care hospitals
- surgical care accounted for the largest number of adverse events
- close to 37 per cent of adverse events in the study were potentially preventable. Based on this, the researchers estimate there were 70,000 preventable adverse events across the country in 2000.
"Our study indicates that care in Canadian hospitals is safe for the vast majority of patients," says Prof. Ross Baker, PhD, principal investigator of the study and professor of health policy, management and evaluation at U of T. "However, certain patients are experiencing injuries and complications related to their care, some preventable. The good news is, this study gives hospitals a clearer picture of the scope and nature of this issue and will help them to determine why these problems are occurring and to develop strategies to address them." "It would be a mistake to focus on the performance of individual health care providers when interpreting these findings," says Dr. Peter Norton, head of family medicine at U of C and co-principal investigator of the study. "We recommend that hospitals and health providers focus on system-wide changes - such as ensuring that medications don't look or sound alike - to reduce the number and likelihood of adverse events."
This research provides the first national estimate of adverse events across a range of teaching and community hospitals using methods comparable to recent studies in other countries. Those studies reported adverse events rates ranging from 2.9 per cent in the United States to 16.6 per cent in Australia. This variation is at least partly explained by differences in study methods. The Canadian study also found that teaching hospitals had a higher rate of adverse events than other hospitals.
The authors attribute this to several factors, including: patients with more complex illnesses may be treated in teaching hospitals; the complexity of care in teaching hospitals means patients may receive care from several care providers, thereby increasing the potential for adverse events relating to communication and coordination of care. The study was jointly funded by the Canadian Institute for Health Information (CIHI) and the Canadian Institutes of Health Research (CIHR).