GUIDELINES: INFORMED CONSENT

1 SAMA Copyright20121 GUIDELINES: INFORMED CONSENTIt has long been part of South African law that a patient must provide INFORMED CONSENT for allmedical treatment (diagnostic or therapeutic) on him/her (Stoffberg v Elliot, 1912). Basically, INFORMED CONSENT means thatsufficient information is provided to the patient to make aninformed decision and that the patient actually understands the information and the implicationsof acting on that information. INFORMED CONSENT relates to a person s right to human dignity andautonomy.

2 The medical practitioner has the duty to obtain the CONSENT , as s/he is in a position toanswer questions and provide further to the HPCSA guidelines for Good Practice in the Health care professions, there aregeneral and ethical guidelines which must be adhered to for a practitioner to be practicing withinthe ethical and legal boundaries which is required not only by law, but also by moral following Guideline Booklets are worthy to note:-Booklet 9 in its entirety discusses Seeking a Patiens INFORMED CONSENT and what the ethicalconsiderations from other Booklets regarding INFORMED CONSENT :Booklet 1 : General Ethical guidelines for the Health Care ProfessionsHealth care practitioners should: Give their patients the information they ask for or needabouttheir condition, itstreatment and prognosis.

3 Give information to their patients in the way they can best understand it. Theinformation must be given in a language that thepatient understands and in a mannerthattakesinto account the patient s level of literacy, understanding, values and beliefsystems. Refrain from withholding from their patients any information, investigation, treatment ofprocedure the health carepractitioner knowswould be in the patient s best interest. Apply the principle of INFORMED CONSENT as an on-going process Allow patients access to their medical records SAMA Copyright20122 Booklet 2: National Patient s Rights CharterInformed CONSENT :Everyone has a right to be given full and accurate information about the nature of one s illnesses,diagnostic procedures, the proposed treatment and risks associated therewith and the 6: General Ethical guidelines for Health ResearchersInformed CONSENT :Health researchers should always.

4 Give research participants sufficient information about the nature and effect of theresearch in particular the effect of the research on the participants including itsconsequences, risks and benefits to enable them to make an INFORMED choice abouttheir participation. Give research participants the information they ask for and need about their researchparticipation Remember that responsibility for the well-being of research participants always restswith the health researcher not the research participant even thought the latter havegiven CONSENT Give information to research participants in a language that the participant understandsand in a manner that takesinto accountthe participant s level of literacy, understanding,values and personal belief systems.

5 Participation at all times should be voluntary and notcoerced. Use caution when obtaining INFORMED CONSENT where the research participant is in adependent relationship with thehealthresearcher or is in a situation where he or shemay consentunderduress. In such cases, INFORMED CONSENT should be obtained by a well- INFORMED health care practitioner who is not engaged in the research and who iscompletely independent of this relationship Refrain from purposefullywithholdingfrom research participants any information,investigation or procedure that health care practitioners know is in the best interests ofthe participants Obtain the CONSENT of legally authorized representatives in cases of research participantswho cannot CONSENT for themselves, children.

6 Mentallychallenged, elderly and theunconscious. These groups should not be included in research unless the research is SAMA Copyright20123necessary to promote the health of the population represented and unless this researchcannot instead be performed on legally competent persons Remember that the principle of INFORMED CONSENT should be viewed as an ongoingprocess in that research participants are entitled to change their minds. Moreover, theconsent process should bereinforced during the trial Inform research participants of theirrightto abstain from participating in the study, or towithdraw from participating in the study by revoking their CONSENT at any time.

7 Without suffering prejudice or reprisal Allow competent research participantsunimpededaccessthroughoutthe researchperiod to information concerning the research Inform participants of the limits to the confidentiality of the information about themgathered during the research bodies such as the National Health Research EthicsCouncil, the HPCSA, and theMedicinesControl Council mayreviewor inspect data. Adhere to the principle of INFORMED CONSENT by keeping proper documentation. Afterensuring that the research participant understand the information, the health researchershould obtain the participant s freely given INFORMED consentin writing.

8 If the consentcannot be obtained in writing, the non-written CONSENT must be fully documented andwitnessed. Both verbal and written INFORMED consentmust be obtained unless there aregood reasons for not doing so. Where the research participant is not literate verbalconsent should be obtained in the presence of an independent literate witness whoshould verify this in writing. Where the independent witness is not literate, the consentprocess should be audio-visually following are elements of INFORMED CONSENT : CONSENT must be voluntary and without constraint; In the case of a HIV test, CONSENT should preferably be written, although CONSENT may beimplied; CONSENT must not conflict with good morals or the Constitution; The patient must be capable of consenting; The patient must give the CONSENT personally, unless proxy CONSENT is applicable (see below).

9 The patient should know why the medical practitioner needs the results of the test; There should be sufficient information on the diagnosis, proposed treatment, expectedbenefits, risks, alternative treatment, probable results, etc; SAMA Copyright20124 The patient must actually understand, there is likelyto be a need for an interpreter or atleast sensitivity that the patient may not actually understand everything and arrangementsshould be made so as to assist the process of a number of cases a patient may not be able or capable of giving INFORMED CONSENT .

10 In terms ofthe Child Care Act a child that is older than 14 years may independently CONSENT to means that such a child can CONSENT to a HIV test without his/her parents/guardian person who is older than 18 years may CONSENT to any operations. Schools, whether they arepublic or private, may not test learners without the CONSENT as required by the Child Care Act andit is likely that,even if CONSENT is obtained in the school setting, such tests may be found toviolate the human rights of the learners teacher will also not be able to provide CONSENT on behalf of a learner.