Consent and Intensive Care: Is It Possible?
L. B
ERGGRENThe intensive care environment is complex and sometimes confusing to both patients and their relatives. Decisions concerning diagnosis, treatment, and prognosis are often made in emergency situations with insufficient underly- ing information. Also, the clinical situation sometimes imposes great strain upon the intensive care physician and the assisting team. The discussion of different potential treatment options with relatives or patients might thus be both difficult and stressful and not the main priority. Furthermore, most patients admitted to the intensive care unit (ICU) are not competent and a priori excluded from any possibility of autonomous decision making. Today, in medical practice in general, there is a shift from paternalism towards shared decision making. Also, legislation in many countries mandates informed consent. The problems in the ICU setting are obvious. When and what to tell patients and relatives can be contentious issues and are influenced by the physician’s beliefs, knowledge, and attitudes just as much as more objective patient factors, making the situation even harder in clinical ICU practice.
Meaning of Informed Consent
Informed consent is the process by which a person authorises medical treat- ment after discussion with clinicians regarding the nature, indications, bene- fits, and risks of treatment [1]. It has obvious ethical and legal implications.
There are three broad aspects of intensive care practice for which consent is
relevant. The first relates to invasive procedures, the second to treatment and
diagnosis options and strategies, and the third to research participation. The
third aspect, however important, is beyond the scope of this paper. As previ-
ously stated, consent is often and regularly given by relatives or proxies. More
than half of all consents were given by proxies in a recent study from a North
American university ICU. This did not change after an intervention with introduction of a standardised consent form [2]. However, it is an open ques- tion as to what extent surrogate decision making actually reflects the will of the patient, especially in an emotionally stressful situation. The problem might not be that difficult when physicians are considering consent to com- mon routine procedures, but it’s immense when they are dealing with end-of- life issues. Another problem with surrogate decision making is the identifica- tion of the surrogates. Who are actually the surrogates? There are obvious personal, cultural, and societal differences concerning the preferences and recognition of proxies. Thus, surrogate decision making in the ICU is ulti- mately also a question of moral and ethical justification.
There are certain problems with obtaining consent for routine procedures.
How to act if the surrogates refuse to allow the placing of a necessary central line for the safe delivery of vasoactive drugs? Are the relatives also able to refuse an arterial line or the appropriate antibiotic regimen? Clearly this approach has the potential to collapse into absurdity [3].
Consent for Commonly Performed Procedures
Consent to routine or everyday invasive procedures is often presumed under the general consent to ICU treatment. This is clearly not always the case. The practice differs substantially between and within countries. A recent study from the United States showed no uniform practice of consent for commonly performed invasive procedures between 173 ICU training program directors.
The rate of consent for vascular access procedures ranged from 20 to 90%.
The rates of obtaining consent for Foley catheterisation or nasogastric intu- bation was less than 10%. Consent was routinely obtained for GI endoscopy, bronchoscopy, and medical research [4]. The situation in Europe is the same, with a wide variation in practice between countries. In a postal survey, Vincent showed that 50% of ICU physicians required written informed con- sent for surgery, but only a few required consent for routine procedures like arterial lines. There were significant differences between different countries.
The ICU physicians from Northern Europe, the Netherlands, and Scandinavia were more likely to accept ‘no’ or only oral consent for procedures, while German and British ones preferred written consent. Another interesting find- ing was that only 32% of ICU physicians would provide full information on an iatrogenic incident, but more than 70% felt they actually should. Again, geographically there were significant differences between doctors from the Netherlands and Scandinavia who were more likely to give complete infor- mation, and those from Greece, Spain, and Italy who were less likely [5]. The conclusion was that ICU physicians were not completely honest with their
6 L. Berggren