I do not believe that the perspective of the patient is the most important determinant as to whether an adverse event has occurred. Basing patient safety strictly by adverse events that occur deemphasizes any errors that occur that do not lead to harm. Such errors, especially of the "near miss" category where the errors would most certainly have led to serious harm if they hadn't have been caught beforehand and prevented are never reported to the patient, yet it is vital to determine the root causes behind these errors. In other cases, errors actually happen that do not lead to harm, such as giving the wrong dose of the right medication or a dose of a harmless, yet incorrect medication such as acetaminophen (Ransom, 2008, p. 244).
The very definition of "adverse event" includes a great number of actual medical treatments simply because some form of harm or injury occurs to the patient. No errors at all occur in the delivery of care. There is just risk involved. "Some argue that such events are not adverse and should not be considered as harm; instead, they see such events as known complications or risks of certain procedures and interventions (Ransom, 2008, p. 244)."
The very nature of practicing medicine entails risk, much of which is not within the control of the medical providers. I am referring to patient compliance, which is not only an issue pertinent to this topic of reporting adverse advents, but also to the adoption of Accountable Care Organizations that will hold physicians responsible for outcomes despite patients themselves having a large responsibility for their own health. Patients often choose to not follow doctors' orders correctly and engage in self-destructive practices, further balancing the scales toward adverse events occuring beyond where they exist already due to natural complications due to things such as post surgical infection or medication intolerance.
Americans want Rolls Royce medical care for the price of a Honda, if not for free. Despite signing legal forms acknowledging the risks involved with medical and surgical interventions, many expect miracles and are willing to find an attorney willing to gamble on a settlement offer when not satisfied with the outcomes.
I do not believe that patients, as lay people, are qualified to determine the occurrence of adverse events. Epidemiologists or others professionally trained in collecting such data are better qualified. Ideally, a group of professionals that is impartial to the process could be inserted into the process that could also address the problems of underreporting that occurs in medical institutions of errors and adverse advents.
Reference:
Ransom, R.R., Joshi, M.S., Nash, D.B., and Ransom, S.B. (2008). The
healthcare quality book, 2nd Ed., vision, strategy, and tools. Chicago,
IL: Health Administration Press.