Guest guest Posted January 30, 2010 Report Share Posted January 30, 2010 Dear Members, Ethical issues of pharmacogenetic testing in germ-line testing: - 1) It tests for genetic mutations and allele distributions that are inheritable. 2) Once a patient has gained knowledge about his own genotype, this may also give him knowledge about his relatives. Relatives may not want to know about their risk for a particular condition or about the effectiveness of a treatment for them. Indeed, a relative has the right not to know these things about their genotype. This raises a difficult issue, as it is impossible to legally regulate the distribution of this information once it has been given to a patient. 3) The desire to not want knowledge of one’s own genotype carries additional problems. Because of the risk of receiving a non-responder profile to many drugs, and the associated increase in insurance costs and other problems outlined above, a patient may not want to be genotyped. 4) With a pharmacogenomic profile- Physicians are put in a difficult position. By giving the patient in question the bulk drug, he is in fact providing inferior treatment and exposing the patient to possible ADRs, because he has not been tested. Similarly, if the physician gives the patient a genotype-specific drug, there is risk of ADRs because it is unknown whether the patient matches the genetic profile of those for whom the drug was designed. If ADRs do arise, even in the situation of the bulk drug, there is the question of responsibility. Should the physician be held responsible, or should the responsibility lie on the shoulders of the patient? These issues could cause subtle changes in the doctor-patient relationship. RegardsDr Sanjay Yallappa ChoudhariJR2,Dept of PharmacologyGMC, Nagpur Your Mail works best with the New Optimized IE8. Get it NOW!. Quote Link to comment Share on other sites More sharing options...
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