Death
is an everyday occurrence in the critical care
unit. The dying frequently do so in critical
care units. For many, life-support interventions
have not helped to mitigate their suffering,
but have rather added the agony and burden of
a prolonged dying process. Death, which we all
wish to be peaceful and to occur in the presence
of loved ones, has become artificial, away from
the family surrounded by the paraphernalia of
modern critical care. Prolonged and futile life
support has undoubtedly imposed enormous economic
strain on patients and families. Potentially
salvageable patients can be denied ICU care
when scarce beds and resources are consumed
in a futile search of cure where death appears
inevitable. Setting goals appropriate to clinical
situations of poor prognosis are an integral
part of critical care. Quality critical care
requires that the practice be well grounded
in ethical principles and that the ICU staff
are trained in the skills of end of life care.
A consensus regarding the practices relating
to EOL care in Indian ICUs should eventually
lead to the evolution of appropriate legislation
in keeping with the changing needs of critical
care practice.
Position Statement of the Indian Society
of Critical Care Medicine
Mani RK, Amin P, Chawla R, Divatia JV, Kapadia
F, Khilnani P, Myatra SN, Prayag S, Rajagopalan
R, Todi SK, Uttam R, Balakrishnan S, Dalmia
A, Kuthiala A. Limiting life-prolonging interventions
and providing palliative care towards the end-of-life
in Indian intensive care units. Indian J Crit
Care Med 2005;9:96-107
Checklist
for initiating EOL discussions
1. Advanced age coupled with a poor premorbid
state due to chronic debilitating diseases,
e.g., advanced chronic obstructive pulmonary
disease (COPD) requiring home oxygen and/or
bilevel pressure support or with severe impairment
of quality of life; advanced interstitial lung
disease on oxygen therapy with failed medical
treatment, chronic renal failure requiring long-term
dialysis, chronic liver disease, advanced congestive
heart failure.
2. Catastrophic illnesses with organ dysfunctions
unresponsive to a reasonable period of aggressive
treatment.
3. Prolonged coma (in the absence of brain death)
due to acute nonreversible causes or chronic
vegetative state.
4. Incurable chronic severe neurological states
rendering meaningful life unlikely, e.g., progressive
dementia, quadriplegia with ventilator dependency.
5. Progressive metastatic cancer where treatment
has failed or patient refuses treatment.
6. Post cardio-respiratory arrest, nonrestoration
of comprehension after a few days.
7. Comparable clinical situations coupled with
a physician prediction of low probability of
survival.
8. Patient/family preference to limit life support
or refusal to accept life support.
Recommendations
1. The physician has a duty to disclose to the
capable patient or family, the patient’s
poor prognosis with honesty and clarity when
further aggressive support appears nonbeneficial.
The physician should initiate discussions on
the treatment options available including the
option of no specific treatment.
2. When the fully informed capable patient or
family desires to consider palliative care,
the physician should offer the available modalities
of limiting life-prolonging interventions. The
patient or family should be clearly made aware
of the available options for the use of life-sustaining
supports as follows:
3. The physician must discuss the implications
of forgoing aggressive interventions through
formal conferences with the capable patient
or family, and work towards a shared decision-making
process. Thus, he accepts patient’s autonomy
in making an informed choice of therapy, while
fulfilling his/her obligation to provide beneficent
care.
4. Pending consensus decisions or in the event
of conflicts between the physician’s recommendations
and the family’s wishes, all existing
supportive interventions should continue. The
physician however, is not morally obliged to
institute new therapies against his/her better
clinical judgment.
5. The discussions leading up to the decision
to withhold life-sustaining therapies should
be clearly documented in the case records, to
ensure transparency and to avoid future misunderstandings.
Such documentation should mention the persons
who participated in the decision-making process
and the treatments withheld or withdrawn.
6. The overall responsibility for the decision
rests with the attending physician/intensivist
of the patient, who must ensure that all members
of the caregiver team including the medical
and nursing staff agree with and follow the
same approach to the care of the patient.
7. If the capable patient or family consistently
desires that life support be withdrawn, in situations
in which the physician considers aggressive
treatment nonbeneficial, the treating team is
ethically bound to consider withdrawal within
the limits of existing laws.
8.
In the event of withdrawal or withholding of
support, it is the physician’s obligation
to provide compassionate and effective palliative
care to the patient as well as attend to the
emotional needs of the family.
ABSTRACT
46. Limitation and withdrawal of intensive
therapy at the end of life: practices in intensive
care units in Mumbai, India. Kapadia F, Singh
M, Divatia J, et al. Crit Care Med. 2005 Jun;33(6):1272-5.
Objective : To describe the practices in intensive
care units in Mumbai hospitals regarding limitation
and withdrawal of care at the end of life. Design:
Review of prospectively collected data. Settings
: Intensive care units of four major hospitals
(two private tertiary referral general hospitals,
one mixed public and private cancer referral
hospital, and one large public hospital). Patients
: Hospital and intensive care unit patients
who died during the study period. Intervention
: None. Measurements and main results : We measured
the percentage of hospital deaths occurring
inside and outside intensive care units and
the incidence of withholding intubation, withholding
other therapy, and withdrawing therapy for deaths
in the intensive care unit. The proportion of
hospital deaths that occurred in an intensive
care unit was 14% in the cancer hospital, 23%
in the public hospital, and 58-73% in the two
private hospitals
(chi-square test for trends, p < .0001).
Of the 143 deaths that occurred in intensive
care unit, limitation of care occurred in 49
patients. Twenty-five percent of these patients
were not intubated terminally, 67% were initially
intubated and ventilated but failed to recover
and subsequently had no further escalation of
therapy, and 8% had withdrawal of therapy. Therapy
was limited in 19% of deaths in the public hospital
intensive care unit (odds ratio, 0.44; 95% confidence
interval, 0.2-0.97) vs. 40%, 41%, and 50% of
deaths in the other three intensive care units.
Conclusions: Therapy is limited in a significant
proportion of intensive care unit patients.
Significant differences in the practice of limitation
of therapy exist between public and private
hospitals. Lack of access to a limited number
of intensive care unit beds, especially in the
public hospital, may constitute implicit limitation
of care.