Who May ConsentThe determination of who has authority to consentto medical treatment is based on an evaluation of thecompetency of the patient. If competent, usually thepatient alone has the authority to consent. Competencyrefers to the ability to understand the nature andconsequences of one’s decisions. In the absence ofcontrary evidence, it may be assumed that the patientpresenting for treatment is competent. If the patient isi n c o m p e t e n t , e i t h e r b y r e a s o n o f s t a t u t o r yincompetence (e.g., a minor) or by reason of a physicalor mental impairment, the inquiry must turn towhoever has the legal capacity to consent on behalf ofthe patient. Parents and guardians will usually have theauthority to consent for their minor child or children.In many states, though not all, a husband or wife maygive consent for an incompetent spouse. It is the law ofthe state in which the hospital is located that controlsthe question of “substitute consent.”Forms of ConsentConsent for medical treatment should be obtainedthrough an open discussion between the provider andpatient during which the patient expressly agrees to theprocedure. The consent should then be documented byhaving the patient sign any appropriate forms and bythe provider noting any important details of thediscussion in the medical record.In certain limited circumstances, the consent of anindividual to simple medical treatment may be impliedfrom the circumstances. Implied consent arises byreasonable inference from the conduct of the patient orthe individual authorized to consent for the patient.Reliance on this form of consent is stronglydiscouraged except in the most routine, risk-freeexaminations and procedures.Witness to ConsentAny competent adult may witness the patient’sconsent. It is preferable that the witness be a staffmember of the hospital who is not participating in theprocedure. It is not advisable for a relative of thepatient to act as a witness.Duration of ConsentA consent is valid as long as there has been nomaterial change in the circumstances between the datethat consent was given and the date of the procedure. Itis desirable that a new consent be obtained if there is asignificant time lapse or if the patient has beendischarged and readmitted due to postponement of theprocedure.INCIDENT REPORTSWhen an event occurs that harms an individual,illustrates a potential for harm, or evidences seriousdissatisfaction by patients, visitors, or staff, then arisk-management incident has taken place. Examplesof such episodes could include the following:A patient’s family helps him out of bed despitedirections to the contrary by staff members. Thepatient falls and is injured.Excessive silver nitrate is put into the eyes of anewborn, impairing vision.The mother of the child complains about the carethat has been given to her child and informs astaff member that she is going to talk to herlawyer about what has happened.When a member of the staff becomes aware of anincident, he has a responsibility to make the hospitalcommand aware of the situation. The mechanism fordoing this is the incident report system. Incidentreports are designed to promptly document allcircumstances surrounding an event, to alert thecommanding officer, quality assurance coordinator,and other involved administrators and clinicians of apotential liability situation, and, in a broader sense, toestablish an information base on which to monitor andevaluate the number and types of incidents that takeplace in the facility.Because incident reports, by their very nature,contain a great deal of information that would be ofinterest to persons filing claims or lawsuits against theNavy for alleged substandard medical care, andbecause the law recognizes the need for hospitals tohave a reliable means of discovering and correctingproblems, most states have enacted laws that makeincident reports confidential. In other words, a personcannot obtain a copy of an incident report to help intheir legal action against the hospital.However, incident reports can lose their“protected” status if they are misused or mishandled. Itis important, therefore, to treat these reports like otherconfidential documents. You must strictly limit thenumber of copies made and the distribution of thereports. Do not include the report in the patient’streatment record. The report should be limited to thefacts and must not contain conclusions. Finally, the15-9
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