Consent Article
Consent Article
Consent Article
Bhatt
M.D. (O&G) ; PGDMLS
Medico-legal consultant
Rainbow Women’s Hospital
1st Floor A wing
Swami Shivanand Society
Chakala Road
Nr Cigarette Factory
Andheri East
Mumbai 400099
Mob: 9833966522
We are living in the era of consumer awareness and evidence based practice. These
are two essential elements of any service based industry. Delivery of a health care is
no longer considered as a divine work and complications are not accepted as an ACT
OF GOD, rather the expectations for standard and safety from health care providers
are ranking among the tops in list.
The American examples inspired India as well and in case of Indian medical
association v. V.P. Shantha. (1995) 6 scc 651 The apex court gave decision that
patient is a consumer and health care providers can be sued for deficiencies in the
services in consumer courts. Though the result of the professional services are not
guaranteed and are dependent upon many factors which are beyond the control of
service providers, the Supreme Court held that the success or failure shall not be
made the subject of legal scrutiny but a minimum degree of professional skill and care
expected from an averagely skilled professional in discharge of his duty shall be
regulated.
The concept of the standard of care was further enhanced by the requirements of
documentations. Consent to the treatment forms an important medico-legal document.
Supreme Court of India in its landmark judgment of Sameera Kohli VS Dr Prabha
Manhanda elaborated its views on the topic of consent.
WHAT IS CONSENT?
“Two or more persons are said to consent, when they agree upon the
same thing in same sense”. i.e. “PARTIES AD IDEM”
TYPES OF CONSENT
Implied
Nothing is said or explained but both the parties understand the object.
eg. Patient coming to your chamber, it is implied that he/she has come
for examination and you can go ahead with history taking and
examination without any consent of your patient. Implied consent will
help you till examination of the patient, for any further investigations or
treatment informed consent is must
• On 9/5/95 the appellant an unmarried lady aged 44 yrs visited the clinic of Dr.
Prabha Manchanda
• C/o Prolonged menstrual Bleeding for 9 days
• The doctor examined the patient and advised Ultrasound test on the same day.
• After examining the reports, the respondent had a discussion with the appellant
and advised her to come on the next day i.e. 10/05/1995 for a Laparoscopy test
under General Anaesthesia for making an affirmative diagnosis
• On 10/05/1995, the appellant went to the respondent’s clinic with her mother.
• On admission the appellant’s signature were taken on
1. Admission & Discharge Card
2. Consent form for hospital admission and medical treatment
3 Consent form for surgery reading as consent for “diagnostic and
operative laparoscopy. Laparotomy may be needed”
(i) A doctor has to seek and secure the consent of the patient before commencing
a ’treatment’ (the term ’treatment’ includes surgery also). The consent so
obtained should be real and valid, which means that : the patient should have
the capacity and competence to consent; his consent should be voluntary; and
his consent should be on the basis of adequate information concerning the
nature of the treatment procedure, so that he knows what is consenting to.
(ii) The ’adequate information’ to be furnished by the doctor (or a member of his
team) who treats the patient, should enable the patient to make a balanced
judgment as to whether he should submit himself to the particular treatment or
not. This means that the Doctor should disclose
(a) nature and procedure of the treatment and its purpose, benefits and effect;
(b) alternatives if any available;
(c) an outline of the substantial risks; and
(d) adverse consequences of refusing treatment.
But there is no need to explain remote or theoretical risks involved, which may
frighten or confuse a patient and result in refusal of consent for the necessary
treatment. Similarly, there is no need to explain the remote or theoretical risks
of refusal to take treatment which may persuade a patient to undergo a fanciful
or unnecessary treatment. A balance should be achieved between the need for
disclosing necessary and adequate information and at the same time avoid the
possibility of the patient being deterred from agreeing to a necessary treatment
or offering to undergo an unnecessary treatment.
(iii) Consent given only for a diagnostic procedure, cannot be considered as
consent for therapeutic treatment. Consent given for a specific treatment
procedure will not be valid for conducting some other treatment procedure. The
fact that the unauthorized additional surgery is beneficial to the patient, or that it
would save considerable time and expense to the patient, or would relieve the
patient from pain and suffering in future, are not grounds of defense in an
action in tort for negligence or assault and battery. The only exception to this
rule is where the additional procedure though unauthorized, is necessary
in order to save the life or preserve the health of the patient and it would
be unreasonable to delay such unauthorized procedure until patient
regains consciousness and takes a decision.
(iv) There can be a common consent for diagnostic and operative procedures
where they are contemplated. There can also be a common consent for a
particular surgical procedure and an additional or further procedure that may
become necessary during the course of surgery.
(v) The nature and extent of information to be furnished by the doctor to the patient
to secure the consent need not be of the stringent and high degree mentioned
in Canterbury but should be of the extent which is accepted as normal and
proper by a body of medical men skilled and experienced in the particular field.
It will depend upon the physical and mental condition of the patient, the nature
of treatment, and the risk and consequences attached to the treatment.
After this landmark case on CONSENT, many cases were filed against doctors for
improper or absent consent and decided in favor of patient
(1) Mrs Zeba Hamid Vs Hajela Hospital and ors. (National Commission)
Jst Kulshreshta/Mrs Pramila S Kumar
Judgment
o Bleeding is no negligence
o Deviation from route consented is not acceptable ; unless it is life saving
Rs. 1,25,00,000/- (one crore twenty five lacs) and for pain and
suffering Rs. 25,00,000 (twenty five lacs)
There is an Indian Medical Council Act; 1956 for the consent (Section – 33 clause 13)
There are certain Acts which includes consent as an annexure of the act itself and in
such case one must take consent on that particular form and not on any other consent
form. PCPNDT ACT (Form G ); MTP ACT (Form C) etc.
Consent in IPC
Act not intended to cause grievous hurt-87 or death-88 done with consent in
good faith for person’s benefit
“Nothing, which is not intended to cause death, is an offence by reason of any harm
which it may cause, or be intended by the doer to cause, or be known by the doer to
be likely to cause, to any person for whose benefit it is done in good faith, and who
has given a consent, whether express or implied to suffer that harm, or to take the risk
of that harm.”
Negative Consent:
When patient is not ready to take the treatment offered by you, please take negative
consent of the patient for the same and if patient do not sign it then get it signed by
the witness eg. other patient or relatives of some patient. This will help you in saving
yourself in case of litigation by proving contributory negligence of the patient.
At the end, looking at the legal expectations for the consent, there is a serious
need to develop standard consents for various common operations. Just few common
lines written as a consent for surgery has stopped standing the test of law after the
landmark judgment. So give as much importance to documentation as you give to the
surgery or treatment itself because in the eyes of law “the thing which is not
documented never happened”.
Further Reading: