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AACN18_4_397-403 10/20/07 14:23 Page 397<br />

397<br />

AACN Advanced Critical Care<br />

Volume 18, Number 4, pp.397–403<br />

© 2007, AACN<br />

<strong>How</strong> <strong>to</strong> <strong>Withdraw</strong> <strong>Mechanical</strong> <strong>Ventilation</strong><br />

A Systematic Review <strong>of</strong> the Literature<br />

Margaret L. Campbell, PhD, RN, FAAN<br />

ABSTRACT<br />

Eight published accounts about ventila<strong>to</strong>r<br />

withdrawal spanning 1992–2004 were selected<br />

for review. Articles were selected if<br />

they contained data that described the<br />

processes comprising the withdrawal <strong>of</strong><br />

mechanical ventilation as a terminal illness<br />

event. The purpose <strong>of</strong> this article is <strong>to</strong> synthesize<br />

the existing evidence about<br />

processes for the compassionate withdrawal<br />

<strong>of</strong> mechanical ventilation from<br />

Artificial ventilation has been used for<br />

decades <strong>to</strong> support breathing when patients<br />

experienced acute or chronic respira<strong>to</strong>ry<br />

failure. Beginning with negative pressure ventilation<br />

(iron lungs) during the polio epidemic,<br />

clinicians had the means <strong>to</strong> prolong life. Modern<br />

ventila<strong>to</strong>rs provide a variety <strong>of</strong> modes and<br />

mechanisms for supporting even patients with<br />

the most severe pulmonary impairments.<br />

In 1975, a young woman named Karen Ann<br />

Quinlan existed in a persistent vegetative state.<br />

Her life was prolonged with mechanical ventilation<br />

and enteral feedings. Her parents recognized<br />

that her prognosis for functional neurologic<br />

recovery was poor, and they requested<br />

withdrawal <strong>of</strong> the ventila<strong>to</strong>r. Karen’s physicians<br />

had never faced this type <strong>of</strong> request and<br />

would have found no support in the pr<strong>of</strong>essional<br />

literature for how <strong>to</strong> respond. The clinicians<br />

believed that Karen would die without<br />

the ventila<strong>to</strong>r and that by acting <strong>to</strong> remove it,<br />

they would be complicit in her death.<br />

Karen’s condition and her parent’s request<br />

were given a great deal <strong>of</strong> ethical and legal<br />

intensive care unit patients, including measures<br />

<strong>of</strong> distress, premedication, medication<br />

during withdrawal, withdrawal methods,<br />

extubation considerations, duration <strong>of</strong> survival,<br />

and relationship <strong>of</strong> opioids or benzodiazepines<br />

<strong>to</strong> duration <strong>of</strong> survival. Practice<br />

recommendations will be suggested.<br />

Keywords: dyspnea, dying, life supports,<br />

mechanical ventilation, terminal weaning,<br />

terminal care, withdrawal<br />

attention. In 1976, the New Jersey Supreme<br />

Court ruled in favor <strong>of</strong> the ventila<strong>to</strong>r withdrawal.<br />

To the surprise <strong>of</strong> her physicians, she<br />

was able <strong>to</strong> sustain herself with spontaneous<br />

breathing and lived 10 more years in a vegetative<br />

state with enteral feeding and hydration<br />

before dying from pneumonia.<br />

The 1970s were characterized by a proliferation<br />

<strong>of</strong> new and improving life-sustaining<br />

therapies and the continued evolution <strong>of</strong> critical<br />

care as a specialty. The development <strong>of</strong> ethical<br />

standards and the creation <strong>of</strong> legal statutes<br />

lagged behind the expansion and implementation<br />

<strong>of</strong> life-sustaining therapies. The 1980s<br />

featured “right <strong>to</strong> die” cases resolved in the<br />

courts and the formulation <strong>of</strong> ethical standards<br />

<strong>to</strong> guide this type <strong>of</strong> care decision. 1<br />

Margaret L. Campbell is Palliative Care Nurse Practitioner,<br />

Detroit Receiving Hospital, Associate Direc<strong>to</strong>r <strong>of</strong> Research,<br />

Center <strong>to</strong> Advance Palliative Care Excellence, and Assistant<br />

Pr<strong>of</strong>essor-Research, Center for Health Research, College <strong>of</strong><br />

Nursing, Wayne State University, 5557 Cass Ave, Detroit, MI<br />

48202 (Mcampbe3@dmc.org).


AACN18_4_397-403 10/20/07 14:23 Page 398<br />

CAMPBELL AACN Advanced Critical Care<br />

Numerous cases across the country found<br />

their way in<strong>to</strong> the courts, providing the basis<br />

for case law and eventually statutes <strong>to</strong> guide<br />

clinical decision making. A Presidential Commission<br />

<strong>to</strong> address ethical issues in medicine<br />

was formed; one <strong>of</strong> their reports addressed decisions<br />

<strong>to</strong> forgo life-sustaining treatment. 2 The<br />

Commission examined how decisions were<br />

made <strong>to</strong> forgo therapy, clarified the issues, and<br />

suggested appropriate procedures for making<br />

decisions that are the basis for current practice.<br />

By the early 1990s, clinical standards,<br />

policies, and procedures about forgoing lifesustaining<br />

therapy were in wide use and reflected<br />

broad agreement about the underlying<br />

principles regarding these decisions. The Patient<br />

Self-Determination Act was introduced<br />

<strong>to</strong> provide federal statu<strong>to</strong>ry support <strong>of</strong> the patient’s<br />

right <strong>to</strong> use advance directives. 3<br />

Currently, decisions are made every day <strong>to</strong><br />

forgo life-sustaining therapies. In the vast majority<br />

<strong>of</strong> cases, all parties directly involved—<br />

patients, families, and clinicians—are in agreement<br />

with the decision. Referral <strong>to</strong> a court or<br />

an ethics committee is not necessary, except in<br />

cases characterized by dispute.<br />

Before 1990, the critical care literature focused<br />

on ethical and legal decision making<br />

about forgoing mechanical ventilation. There<br />

was little empiric evidence <strong>to</strong> guide the process;<br />

the “ought <strong>to</strong>” was described but not the “how<br />

<strong>to</strong>.” The earliest article that suggested a method<br />

for ventila<strong>to</strong>r withdrawal was published in<br />

1983 on the basis <strong>of</strong> the processes used in one<br />

unit. Grenvik distinguished terminal weaning<br />

from conventional weaning because terminal<br />

weaning proceeds despite deteriorating vital<br />

signs and other variables. He recommended<br />

continued evaluation <strong>of</strong> blood gases during terminal<br />

weaning <strong>to</strong> moni<strong>to</strong>r the patient’s progress<br />

<strong>to</strong>ward death or successful weaning. Additionally,<br />

he suggested that some patients should remain<br />

intubated if airway obstruction and disconcerting<br />

airway sounds can be anticipated. 4<br />

More recently, Rubenfeld and Crawford<br />

suggested that ventila<strong>to</strong>r withdrawal be treated<br />

similarly <strong>to</strong> other processes or procedures undertaken<br />

in the intensive care unit (ICU). 5 For<br />

example, a plan should be developed for the<br />

ventila<strong>to</strong>r withdrawal that considers what<br />

processes will occur and in what order. Who<br />

will be responsible for those processes?<br />

Some critical care units have turned <strong>to</strong> pro<strong>to</strong>cols,<br />

standing orders, or algorithms <strong>to</strong> guide<br />

the process <strong>of</strong> ventila<strong>to</strong>r withdrawal and an<br />

398<br />

ideal pro<strong>to</strong>col should reflect the state <strong>of</strong> the<br />

science. Thus, the purpose <strong>of</strong> this article is <strong>to</strong><br />

systematically review and synthesize extant evidence<br />

about the processes <strong>of</strong> ventila<strong>to</strong>r withdrawal,<br />

in other words the “how <strong>to</strong>.” This article<br />

does not include a summary <strong>of</strong> the<br />

evidence about communicating <strong>to</strong> make the<br />

decision or caring for families as those <strong>to</strong>pics<br />

are presented in other articles in this issue <strong>of</strong><br />

AACN Advanced Critical Care.<br />

Method<br />

Two electronic databases, MEDLINE (1980<br />

<strong>to</strong> February 2007) and CINAHL (1982 <strong>to</strong><br />

February 2007), were searched for studies in<br />

English using the keywords mechanical ventilation<br />

and withdrawal, life support withdrawal,<br />

ventila<strong>to</strong>r withdrawal, and terminal<br />

weaning. The search yielded 207 citations, <strong>of</strong><br />

which 35 articles reflected the purpose <strong>of</strong> the<br />

review and were selected for evaluation for<br />

inclusion/exclusion criteria. Studies were included<br />

if the target population was mechanically<br />

ventilated adults having ventilation<br />

withdrawn as a part <strong>of</strong> terminal illness care.<br />

Articles were excluded if the data were collected<br />

from a mixed sample <strong>of</strong> patients having<br />

ventilation withdrawn or withheld, if the<br />

sample was less than 12 patients, or if the article<br />

described one or more case reports.<br />

Table 1 summarizes the 8 articles included in<br />

this review.<br />

Data were extracted <strong>to</strong> predesigned summary<br />

tables under the following headings: author(s),<br />

year <strong>of</strong> publication, study design, sample<br />

size, measures <strong>of</strong> distress, premedication or<br />

medication during withdrawal, withdrawal<br />

method(s), extubation considerations, duration<br />

<strong>of</strong> survival, and correlation <strong>of</strong> survival<br />

with administration <strong>of</strong> opioids and sedatives.<br />

Because <strong>of</strong> variability in data extracted, it was<br />

not possible <strong>to</strong> combine the findings <strong>of</strong> different<br />

studies and, therefore, summaries <strong>of</strong> the<br />

variables are reported.<br />

<strong>How</strong> Is Dyspnea or Respira<strong>to</strong>ry<br />

Distress Measured?<br />

Dyspnea, also known as “breathlessness,” is a<br />

nociceptive phenomenon defined as “a subjective<br />

experience <strong>of</strong> breathing discomfort that<br />

consists <strong>of</strong> qualitatively distinct sensations that<br />

vary in intensity. The experience derives from<br />

interactions among multiple physiological, psychological,<br />

social and environmental fac<strong>to</strong>rs,<br />

and may induce secondary physiological and


AACN18_4_397-403 10/20/07 14:23 Page 399<br />

VOLUME 18 • NUMBER 4 • OCTOBER–DECEMBER 2007 HOW TO WITHDRAW MECHANICAL VENTILATION<br />

Table 1: Studies Included in Review <strong>of</strong> the Literature<br />

Authors Year Design N<br />

Faber-Langendoen 1992 Retrospective, descriptive 14<br />

and Bartels 6<br />

Daly et al 7 1996 Retrospective, descriptive 42<br />

Campbell et al 8 1999 Prospective, descriptive, 31<br />

correlational<br />

Mayer and Koss<strong>of</strong>f 9 1999 Retrospective, descriptive, 32<br />

correlational<br />

Ankrom et al 10 2001 Retrospective, descriptive 13<br />

O’Mahony et al 11 2003 Retrospective, descriptive 21<br />

Rocker et al 12 2004 Prospective, descriptive 155<br />

Chan et al 13 2004 Retrospective, descriptive 75<br />

Abbreviation: N, study sample size.<br />

behavioral responses.” 14(p321) Dyspnea can be<br />

perceived and verified only by the person experiencing<br />

it. Many patients who are undergoing<br />

ventila<strong>to</strong>r withdrawal are cognitively impaired<br />

or unconscious as a result <strong>of</strong> underlying<br />

neurologic lesions or hemodynamic, metabolic,<br />

or respira<strong>to</strong>ry dysfunction that produce<br />

cognitive impairment or unconsciousness. 15<br />

Respira<strong>to</strong>ry distress has been characterized as<br />

an observable (behavioral) corollary <strong>to</strong> dyspnea;<br />

the physical and emotional suffering that<br />

results from the experience <strong>of</strong> asphyxiation<br />

that is characterized by behaviors that can be<br />

observed and measured. 16,17 Dyspnea or respira<strong>to</strong>ry<br />

distress is anticipated during ventila<strong>to</strong>r<br />

withdrawal and should be the focus <strong>of</strong> patient<br />

interventions during the process.<br />

Neuromuscular blocking agents (NMBA)<br />

are being used with less frequency in the ICU;<br />

however, when in use, it is impossible <strong>to</strong> assess<br />

the patient’s comfort. Thus, NMBA should be<br />

discontinued with evidence <strong>of</strong> patient neuromuscular<br />

recovery before ventila<strong>to</strong>r withdrawal.<br />

18–20 In some cases, the duration <strong>of</strong> action<br />

<strong>of</strong> these agents is prolonged, such as when<br />

the patient has liver or renal failure and impaired<br />

clearance. Therefore, although controversial,<br />

withdrawal can proceed with careful<br />

attention <strong>to</strong> ensuring patient comfort if an unacceptable<br />

delay in withdrawing mechanical<br />

ventilation occurs because <strong>of</strong> protracted effects<br />

<strong>of</strong> NMBA. 20<br />

Daly et al conducted a chart review and indicated<br />

that medications given during ventila-<br />

399<br />

<strong>to</strong>r withdrawal were titrated <strong>to</strong> maintain a<br />

respira<strong>to</strong>ry rate less than 30 breaths per<br />

minute, or <strong>to</strong> an unspecified appearance <strong>of</strong><br />

comfort. 7 Campbell et al used 3 measures for<br />

distress in a prospective observation study.<br />

The bispectral index <strong>of</strong> EEG, Bizek agitation<br />

scale (BAS), 21 and the COMFORT scale 22 were<br />

used simultaneously <strong>to</strong> assess patients for respira<strong>to</strong>ry<br />

distress, and they strongly correlated<br />

with each other. 8 The measures used were not<br />

specific <strong>to</strong> respira<strong>to</strong>ry distress: BIS is a measure<br />

<strong>of</strong> wakefulness, BAS is an agitation scale,<br />

and the COMFORT scale is intended <strong>to</strong> measure<br />

distress in infants.<br />

O’Mahoney et al reported after retrospective<br />

chart review that initiating or escalating<br />

sedation or analgesia was done if the patient<br />

showed unspecified signs <strong>of</strong> dyspnea, agitation,<br />

or anxiety, and <strong>to</strong> keep the respira<strong>to</strong>ry<br />

rate below 28 breaths/minute. 11 Additionally,<br />

they reported that sedating medications were<br />

administered if the respira<strong>to</strong>ry rate increased<br />

by 50% over baseline or if accessory muscle<br />

use or nasal flaring was apparent.<br />

Subjectivity characterizes the measures<br />

used. Nurse-nurse interrater reliability was not<br />

measured or reported in the previous studies,<br />

nor were operational definitions provided for<br />

“distress,” “signs <strong>of</strong> dyspnea,” “anxiety,” or<br />

“agitation.” Skill is required <strong>to</strong> detect nuances<br />

<strong>of</strong> behaviors, particularly when the patient is<br />

unable <strong>to</strong> validate the nurse’s assessment. Evidence<br />

is needed <strong>to</strong> reliably identify the behaviors<br />

that signify respira<strong>to</strong>ry distress, especially


AACN18_4_397-403 10/20/07 14:23 Page 400<br />

CAMPBELL AACN Advanced Critical Care<br />

when patients are unable <strong>to</strong> reliably provide a<br />

self-report about their experience. Recent investigation<br />

<strong>of</strong> the reliability and validity <strong>of</strong> a<br />

Respira<strong>to</strong>ry Distress Observation Scale suggests<br />

that there may be common behaviors displayed<br />

by patients in response <strong>to</strong> hypercarbia,<br />

hypoxemia, or inspira<strong>to</strong>ry effort, including<br />

tachycardia, tachypnea, accessory muscle use,<br />

restlessness, nasal flaring, grunting at end-expiration,<br />

and a fearful facial expression. 23<br />

Some would argue that routine premedication<br />

with opioids and sedatives will prevent distress<br />

during ventila<strong>to</strong>r withdrawal, however, many<br />

clinicians fear hastening patient death and are<br />

reluctant <strong>to</strong> medicate without clear evidence <strong>of</strong><br />

patient distress.<br />

Recommendation<br />

More studies are needed <strong>to</strong> identify reliable behaviors<br />

that signify respira<strong>to</strong>ry distress when<br />

the patient is unable <strong>to</strong> generate a self-report.<br />

Brain-dead patients by definition will not<br />

show distress, cough, gag, or breath during or<br />

following ventila<strong>to</strong>r withdrawal, and sedation<br />

or analgesia is not indicated. Coma<strong>to</strong>se patients<br />

are unlikely <strong>to</strong> demonstrate distress except<br />

for, perhaps, tachypnea and tachycardia. 8<br />

Initiation and escalation <strong>of</strong> sedatives and opioids<br />

should be guided by patient behaviors.<br />

Premedication<br />

Four investiga<strong>to</strong>rs reported about premedication.<br />

Campbell et al recommended premedication<br />

with morphine and/or a benzodiazepine<br />

if the patient showed signs <strong>of</strong> distress before<br />

withdrawal or if the conscious patient desired<br />

medication. Because subjects in the sample<br />

were coma<strong>to</strong>se, only 13% <strong>of</strong> patients were<br />

premedicated; an average Glasgow Coma<br />

Scale (GCS) score <strong>of</strong> 7 was reported for those<br />

premedicated and 4 for those with no premedication.<br />

8 Investiga<strong>to</strong>rs at the University <strong>of</strong><br />

Washing<strong>to</strong>n reported progressive escalation<br />

<strong>of</strong> infusions <strong>of</strong> opioids or benzodiazepines in<br />

the 8 hours preceding a planned ventila<strong>to</strong>r<br />

withdrawal. The justification for dose escalation<br />

was not reported from this retrospective<br />

review. 13 Ankrom et al reported that “small”<br />

doses <strong>of</strong> morphine and a benzodiazepine<br />

were given before ventila<strong>to</strong>r withdrawal, but<br />

doses and indications were not reported. 10<br />

O’Mahoney reported premedication if the<br />

patient was alert or had a his<strong>to</strong>ry <strong>of</strong> recent<br />

agitation before the withdrawal. 11<br />

400<br />

Medication During or<br />

After <strong>Withdraw</strong>al<br />

Variance in reporting characterized the descriptions<br />

<strong>of</strong> medications used during ventila<strong>to</strong>r<br />

withdrawal. All investiga<strong>to</strong>rs used an opioid,<br />

usually morphine, and some used a benzodiazepine<br />

occasionally or always. Table 2 is a<br />

summary <strong>of</strong> the morphine characteristics<br />

reported across investigations. As seen, doses<br />

ranged from very small <strong>to</strong> very large. As discussed,<br />

most studies did not report how distress<br />

was measured or how dose escalation was<br />

determined.<br />

Recommendation<br />

As is the standard with pain management, opioids<br />

should be initiated <strong>to</strong> signs <strong>of</strong> distress and<br />

the advice <strong>to</strong> “start low and titrate slowly” is<br />

sage. Anticipa<strong>to</strong>ry premedication is a sound<br />

practice if distress is already evident and if distress<br />

can be anticipated. There is no justification<br />

for medicating a brain-dead patient, and<br />

one could argue that the patient in coma with<br />

only minimal brainstem function is also unlikely<br />

<strong>to</strong> experience distress. Doses that correspond<br />

<strong>to</strong> cus<strong>to</strong>mary dosing for the treatment<br />

<strong>of</strong> dyspnea should guide dosing during ventila<strong>to</strong>r<br />

withdrawal. Documentation <strong>of</strong> the signs <strong>of</strong><br />

distress and rationale for dose escalation is important<br />

<strong>to</strong> ensure continuity across pr<strong>of</strong>essional<br />

caregivers and <strong>to</strong> prevent overmedication<br />

and the appearance <strong>of</strong> hastening death.<br />

Weaning Method<br />

Terminal extubation is characterized by ceasing<br />

ventila<strong>to</strong>ry support and removing the endotracheal<br />

tube in one step. Extubation was<br />

the only method used in 2 studies. 9,11, Terminal<br />

weaning is a process <strong>of</strong> step-wise, gradual reductions<br />

in oxygen and ventilation, terminating<br />

with placement on a t-piece or with extubation.<br />

Rapid terminal weaning was the only<br />

method used in one study with an average<br />

weaning interval <strong>of</strong> 15 minutes. 8 In 2 studies,<br />

investiga<strong>to</strong>rs reported various methods used<br />

with no rationale provided for choice <strong>of</strong><br />

method. 6,7<br />

In a survey <strong>of</strong> physician practices related <strong>to</strong><br />

ventila<strong>to</strong>r withdrawal, investiga<strong>to</strong>rs found<br />

that surgeons and anesthesiologists preferred<br />

terminal weaning compared with internists<br />

and pediatricians who preferred extubation. 24<br />

It is interesting <strong>to</strong> note that physician rather<br />

than patient characteristics contributed <strong>to</strong>


AACN18_4_397-403 10/20/07 14:23 Page 401<br />

VOLUME 18 • NUMBER 4 • OCTOBER–DECEMBER 2007 HOW TO WITHDRAW MECHANICAL VENTILATION<br />

Table 2: Summary <strong>of</strong> Reports <strong>of</strong> Morphine Administered During Ventila<strong>to</strong>r <strong>Withdraw</strong>al<br />

Author(s) Total morphine (duration) Average hourly dose Range <strong>of</strong> dosing<br />

Faber-Langendoen NR NR 0–80 mg/h<br />

and Bartels 6<br />

Daly et al 7 NR NR 1–59 mg/h<br />

Campbell et al 8 36 � 10 mg (24 h from 5.5 mg/h NR<br />

beginning <strong>of</strong> withdrawal)<br />

Mayer and Koss<strong>of</strong>f 9 6–456 mg (30 h from 6.3 mg/h 2.5–20 mg/h<br />

beginning <strong>of</strong> withdrawal)<br />

Ankrom et al 10 206 � 265 mg (patient survived NR NR<br />

�30 min) 78 � 14 mg (patient<br />

survived longer than 30 min)<br />

O’Mahoney et al 11 12 mg (extubation until death) 6 mg/h 1–50 mg/h<br />

Rocker et al 12 24 mg (4 h before death) 24 mg/h median 2–340 mg/h<br />

Chan et al 13 81 mg (24 h before death) Increased from 4 mg/h NR<br />

<strong>to</strong> 16.2 mg/h during<br />

interval before<br />

withdrawal<br />

Abbreviation: NR, not reported.<br />

choice <strong>of</strong> method. There are no known investigations<br />

that compare these methods.<br />

Recommendation<br />

With no comparative evidence <strong>to</strong> support one<br />

method over another, it is difficult <strong>to</strong> make a<br />

recommendation. Rapid terminal weaning<br />

may afford the clinician with the most control<br />

because it allows for careful, sequential adjustments<br />

<strong>to</strong> the ventila<strong>to</strong>r with precise titration <strong>of</strong><br />

medications <strong>to</strong> ensure patient comfort. Continuous<br />

patient moni<strong>to</strong>ring with readily accessible<br />

opioids and sedatives will afford the patient<br />

and family comfort regardless <strong>of</strong> method<br />

employed.<br />

Extubation Considerations<br />

Campbell et al were the only investiga<strong>to</strong>rs who<br />

recommended extubation as a separate decision<br />

based on the patient’s airway integrity,<br />

volume <strong>of</strong> pulmonary secretions, and ability <strong>to</strong><br />

experience distress. Of coma<strong>to</strong>se patients,<br />

35% were extubated after rapid terminal<br />

weaning. Of note, survival was longer for<br />

those who were extubated (85.3 � 35 hours)<br />

compared with the patients who remained<br />

intubated (12.95 � 4.96 hours; P � .01). 8<br />

Rocker reported no significant difference in<br />

duration <strong>of</strong> survival when the patients who<br />

were extubated (median 1.1 hours) were com-<br />

401<br />

pared with those who had either a tracheos<strong>to</strong>my<br />

or endotracheal tube maintained<br />

(median 1.2 hours). 12<br />

Recommendation<br />

Removal <strong>of</strong> the endotracheal tube should be<br />

performed whenever possible because <strong>of</strong> patient<br />

comfort and the aesthetic appearance <strong>of</strong><br />

the patient. <strong>How</strong>ever, in some cases, airway<br />

compromise can be anticipated, such as when<br />

the patient has a swollen, protuberant <strong>to</strong>ngue,<br />

or has no gag or cough reflexes. In cases <strong>of</strong> airway<br />

compromise, the disconcerting noises<br />

may be more distressing <strong>to</strong> the attendant family<br />

than the presence <strong>of</strong> the tube. Aerosolized<br />

racemic epinephrine is a useful intervention <strong>to</strong><br />

reduce stridor after extubation. Family counseling<br />

about usual noises that can be expected<br />

and cause no distress should be done prior <strong>to</strong><br />

extubation.<br />

Duration <strong>of</strong> Survival<br />

All the investiga<strong>to</strong>rs reported about duration<br />

<strong>of</strong> survival. In 4 studies, patients who died following<br />

ventila<strong>to</strong>r withdrawal comprised the<br />

sample; thus 100% <strong>of</strong> patients died. 9,12,13,25 All<br />

the patients who were withdrawn died in 2<br />

studies, 7,10 and 2 brain-dead patients were included<br />

in the sample from Daly et al. 7<br />

Campbell et al reported that <strong>of</strong> 31 coma<strong>to</strong>se


AACN18_4_397-403 10/20/07 14:23 Page 402<br />

CAMPBELL AACN Advanced Critical Care<br />

patients, 2 patients (6%) survived <strong>to</strong> hospital<br />

discharge, and O’Mahoney et al discharged 3<br />

<strong>of</strong> 21 (14%) patients after ventila<strong>to</strong>r withdrawal.<br />

8,11<br />

Across studies the duration <strong>of</strong> survival<br />

ranged from 2 minutes <strong>to</strong> 9 days after ventila<strong>to</strong>r<br />

withdrawal. Median survival across<br />

studies ranged from 35 minutes 13 <strong>to</strong> 7.5<br />

hours. 9 Campbell et al reported no relationship<br />

between duration <strong>of</strong> survival and use <strong>of</strong><br />

sedation/analgesia, GCS score, or PaO 2/FiO 2<br />

but there was a significant inverse correlation<br />

with illness severity measured with<br />

APACHE II 26 (r ��0.42, P � .05). 8 Mayer<br />

et al also found no relationship between duration<br />

<strong>of</strong> survival and GCS score. 9 Ankrom<br />

et al reported no correlation between analgesia<br />

use and duration <strong>of</strong> survival; however,<br />

patients who died in less than 30 minutes received<br />

an average <strong>to</strong>tal morphine dose <strong>of</strong><br />

206 � 265 mg morphine, and those who<br />

died more than 30 minutes after withdrawal<br />

received an average <strong>of</strong> 78 � 111 mg morphine.<br />

10 This suggests a clinical significance,<br />

although the analysis with a small sample<br />

and a large standard deviation may not have<br />

yielded a statistical significance.<br />

Of note, both Campbell et al and Chan et al<br />

reported no significant relationship between<br />

analgesia/sedation and duration <strong>of</strong> survival. 8,13<br />

<strong>How</strong>ever, with similar average reported GCS<br />

scores (5.3 vs 4), Campbell reported an average<br />

<strong>to</strong>tal morphine dose <strong>of</strong> 36 mg for the 24hour<br />

period after withdrawal and an average<br />

survival <strong>of</strong> 24.2 hours (median 2.3 hours).<br />

This contrasts sharply with the average <strong>to</strong>tal<br />

morphine dose <strong>of</strong> 81 mg for the 24-hour period<br />

before death and the median survival after<br />

ventila<strong>to</strong>r withdrawal <strong>of</strong> 35 minutes<br />

(range, 1 minute <strong>to</strong> 14.8 hours).<br />

Summary<br />

Small samples and largely retrospective chart<br />

reviews characterize the body <strong>of</strong> evidence<br />

about processes for ventila<strong>to</strong>r withdrawal.<br />

Thus, it seems fair <strong>to</strong> say that the evidence is<br />

largely lacking <strong>to</strong> predict the best method that<br />

ensures patient comfort without hastening<br />

death. Palliation versus hastening death may<br />

be difficult <strong>to</strong> distinguish in this context because<br />

the patients are <strong>of</strong>ten near death before<br />

the ventila<strong>to</strong>r is withdrawn. The cited research<br />

is not conclusive <strong>to</strong> make recommendations<br />

in all cases <strong>of</strong> ventila<strong>to</strong>r withdrawal.<br />

Therefore, a number <strong>of</strong> suggested processes<br />

402<br />

may be useful in this clinical context as well as<br />

with a team approach <strong>to</strong> the procedure and<br />

patient care.<br />

First, a common measure <strong>of</strong> dyspnea or respira<strong>to</strong>ry<br />

distress should be identified and used<br />

across clinicians <strong>to</strong> guide the initiation and escalation<br />

<strong>of</strong> opioids or sedatives, such as noting<br />

the presence <strong>of</strong> behaviors specific <strong>to</strong> respira<strong>to</strong>ry<br />

distress. Additionally, moni<strong>to</strong>ring the patient<br />

for signs <strong>of</strong> affective distress, such as fear,<br />

is essential. Brain-dead patients do not experience<br />

or display signs <strong>of</strong> distress.<br />

Premedication or medication during and<br />

following withdrawal <strong>of</strong> mechanical ventilation<br />

with opioids and benzodiazepines is<br />

useful if the patient is experiencing distress<br />

before withdrawal or likely <strong>to</strong> experience distress<br />

during or after. Brain-dead patients do<br />

not require medication because there is no<br />

distress. Coma<strong>to</strong>se patients may require little<br />

or no analgesia or sedation unless objective<br />

signs <strong>of</strong> respira<strong>to</strong>ry distress are apparent.<br />

Doses should be initiated according <strong>to</strong> the patient’s<br />

<strong>to</strong>lerance and escalated only <strong>to</strong> signs or<br />

reports <strong>of</strong> distress.<br />

Every attempt should be made <strong>to</strong> extubate<br />

patients after ceasing mechanical ventilation<br />

because the endotracheal tube is a source <strong>of</strong><br />

iatrogenic discomfort. <strong>How</strong>ever, in some<br />

cases, particularly when the patient is unresponsive,<br />

it may be best <strong>to</strong> keep the endotracheal<br />

tube, such as when the <strong>to</strong>ngue is<br />

swollen, when gag and cough reflexes are absent,<br />

or when there is a large volume <strong>of</strong> pulmonary<br />

secretions. Studies are needed <strong>to</strong> identify<br />

best methods.<br />

References<br />

1. Meisel A. The legal consensus about forgoing life-sustaining<br />

treatment: its status and its prospects. Kennedy<br />

Inst Ethics J. 1993;2:309–335.<br />

2. President’s Commission for the Study <strong>of</strong> Ethical Problems<br />

in Medicine and Behavioral Research. Deciding <strong>to</strong><br />

Forego Life-Sustaining Treatment. Washing<strong>to</strong>n, DC: US<br />

Government Printing Office; 1983.<br />

3. Omnibus Budget Reconciliation Act. Washing<strong>to</strong>n, DC:<br />

Government Printing Office; 1990.<br />

4. Grenvik A. “Terminal weaning”: discontinuance <strong>of</strong> lifesupport<br />

therapy in the terminally ill patient. Crit Care<br />

Med. 1983;11:394–395.<br />

5. Rubenfeld GD, Crawford SW. Principles and practice <strong>of</strong><br />

withdrawing life-sustaining treatment in the ICU. In:<br />

Curtis JR, Rubenfeld GD, eds. Managing Death in the<br />

ICU: The Transition From Cure <strong>to</strong> Comfort. New York:<br />

Oxford University Press; 2001:127–147.<br />

6. Faber-Langendoen K, Bartels DM. Process <strong>of</strong> forgoing<br />

life-sustaining treatment in a university hospital: an empirical<br />

study. Crit Care Med. 1992;20(5):570–577.<br />

7. Daly BJ, Thomas D, Dyer MA. Procedures used in withdrawal<br />

<strong>of</strong> mechanical ventilation. Am J Crit Care. 1996;<br />

5:331–338.


AACN18_4_397-403 10/20/07 14:23 Page 403<br />

VOLUME 18 • NUMBER 4 • OCTOBER–DECEMBER 2007 HOW TO WITHDRAW MECHANICAL VENTILATION<br />

8. Campbell ML, Bizek KS, Thill M. Patient responses during<br />

rapid terminal weaning from mechanical ventilation:<br />

a prospective study. Crit Care Med. 1999;27(1):73–77.<br />

9. Mayer SA, Koss<strong>of</strong>f SB. <strong>Withdraw</strong>al <strong>of</strong> life support in the<br />

neurological intensive care unit. Neurol. 1999;52(8):<br />

1602–1609.<br />

10. Ankrom M, Zelesnick L, Bar<strong>of</strong>sky I, Georas S, Finucane<br />

TE, Greenough WB, III. Elective discontinuation <strong>of</strong> lifesustaining<br />

mechanical ventilation on a chronic ventila<strong>to</strong>r<br />

unit. J Am Geriatr Soc. 2001;49(11):1549–1554.<br />

11. O’Mahony S, McHugh M, Zallman L, Selwyn P. Ventila<strong>to</strong>r<br />

withdrawal: procedures and outcomes. J Pain Symp<strong>to</strong>m<br />

Manag. 2003;26:954–961.<br />

12. Rocker GM, Heyland DK, Cook DJ, Dodek PM,<br />

Kutsogiannis DJ, O’Callaghan CJ. Most critically ill patients<br />

are perceived <strong>to</strong> die in comfort during withdrawal<br />

<strong>of</strong> life support: a Canadian multicentre study. Can J<br />

Anesth. 2004;51:623–630.<br />

13. Chan JD, Treece PD, Engelberg RA, et al. Narcotic and<br />

benzodiazepine use after withdrawal <strong>of</strong> life support: association<br />

with time <strong>to</strong> death? Chest. 2004;126:286–293.<br />

14. <strong>American</strong> Thoracic Society. Dyspnea. Mechanisms, assessment,<br />

and management: a consensus statement.<br />

<strong>American</strong> Thoracic Society. Am J Respir Crit Care Med.<br />

1999;159(1):321–340.<br />

15. Campbell ML, Thill MC. Impact <strong>of</strong> patient consciousness<br />

on the intensity <strong>of</strong> the do-not-resuscitate therapeutic<br />

plan. Am J Crit Care. 1996;5(5):339–345.<br />

16. Campbell ML. Terminal dyspnea and respira<strong>to</strong>ry distress.<br />

Crit Care Clin. 2004;20(3):403–417.<br />

403<br />

17. Campbell ML. Fear and pulmonary stress behaviors <strong>to</strong><br />

an asphyxial threat across cognitive states. Res Nurs<br />

Health. In press.<br />

18. Rush<strong>to</strong>n C, Terry PB. Neuromuscular blockade and ventila<strong>to</strong>r<br />

withdrawal: ethical controversies. Am J Crit Care.<br />

1995;4:112–115.<br />

19. Truog RD, Burns JP. To breathe or not <strong>to</strong> breathe. J Clin<br />

Ethics. 1994;5(1):39–42.<br />

20. Truog RD, Campbell ML, Curtis JR, et al. Recommendations<br />

for end-<strong>of</strong>-life care in the intensive care unit. Crit<br />

Care Med. In press.<br />

21. Bizek K. Optimizing sedation in critically ill, mechanically<br />

ventilated patients. Crit Care Nurs Clin North Am.<br />

1995;7:315–325.<br />

22. Ambuel B, Hamlett KW, Marx CM, Blumer JL. Assessing<br />

distress in pediatric intensive care environments:<br />

the COMFORT scale. J Pediatr Psychol. 1992;17:<br />

95–109.<br />

23. Campbell ML. Psychometric testing <strong>of</strong> a respira<strong>to</strong>ry distress<br />

observation scale. J Palliat Med. In press.<br />

24. Faber-Langendoen K. The clinical management <strong>of</strong> dying<br />

patients receiving mechanical ventilation. A survey <strong>of</strong><br />

physician practice. Chest. 1994;106(3):880–888.<br />

25. Faber-Langendoen K, Spomer A, Ingbar D. A prospective<br />

study <strong>of</strong> withdrawing mechanical ventilation from<br />

dying patients. Am J Respir Crit Care Med. 1996;<br />

153:45.<br />

26. Knaus WA, Drapter EA, Wagner DP, Zimmerman JE.<br />

APACHE II: a severity <strong>of</strong> disease classification system.<br />

Crit Care Med. 1985;13:818–829.


AACN18_4_404-405 17/11/07 1:19 Page 404<br />

Test writer: John P. Harper, MSN, RN, BC<br />

Contact hours: 1.0<br />

Category: A, Synergy CERP A<br />

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CE Test Form<br />

<strong>How</strong> <strong>to</strong> <strong>Withdraw</strong> <strong>Mechanical</strong> <strong>Ventilation</strong>: A Systematic<br />

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AACN18_4_404-405 17/11/07 1:19 Page 405<br />

CE Test Questions<br />

<strong>How</strong> <strong>to</strong> <strong>Withdraw</strong> <strong>Mechanical</strong> <strong>Ventilation</strong>: A Systematic<br />

Review <strong>of</strong> the Literature<br />

Objectives:<br />

Upon completion <strong>of</strong> this article, the reader will be able <strong>to</strong>:<br />

1. Identify 3 patient behaviors that signify respira<strong>to</strong>ry distress.<br />

2. Describe 2 weaning methods for ventila<strong>to</strong>r withdrawal.<br />

3. Discuss the processes for compassionate withdrawal <strong>of</strong> mechanical ventilation.<br />

1. Which <strong>of</strong> the following patients was involved in a US<br />

Supreme Court ruling in favor <strong>of</strong> ventila<strong>to</strong>r withdrawal?<br />

a. Karen Andrews<br />

b. Nancy Cruzan<br />

c. Terry Schiavo<br />

d. Karen Ann Quinlan<br />

2. Which <strong>of</strong> the following patient rights is provided for in<br />

the Patient Self-Determination Act?<br />

a. Advance directives<br />

b. Ventila<strong>to</strong>r withdrawal<br />

c. Removal <strong>of</strong> feeding tube<br />

d. Physician-assisted suicide<br />

3. Which <strong>of</strong> the following symp<strong>to</strong>ms is anticipated during<br />

ventila<strong>to</strong>r withdrawal and should be the focus <strong>of</strong><br />

interventions during the withdrawal process?<br />

a. Pain<br />

b. Death<br />

c. Dyspnea<br />

d. Agitation<br />

4. Which <strong>of</strong> the following behaviors may be displayed by<br />

patients in response <strong>to</strong> hypercarbia or hypoxemia?<br />

a. Facial grimacing<br />

b. Nasal flaring<br />

c. Grunting during inspiration<br />

d. Stridor<br />

5. Which <strong>of</strong> the following should guide initiation and<br />

escalation <strong>of</strong> sedatives and opioids during ventila<strong>to</strong>r<br />

withdrawal?<br />

a. Routine administration throughout the withdrawal process<br />

b. Blood pressure<br />

c. Signs <strong>of</strong> respira<strong>to</strong>ry distress<br />

d. Glascow coma scale<br />

6. Which <strong>of</strong> the following medications was most<br />

commonly used by investiga<strong>to</strong>rs during ventila<strong>to</strong>r<br />

withdrawal?<br />

a. Morphine<br />

b. Lorazepam<br />

c. Fentanyl<br />

d. Prop<strong>of</strong>ol<br />

405<br />

7. Which <strong>of</strong> the following weaning intervals was used by<br />

investiga<strong>to</strong>rs during rapid terminal weaning?<br />

a. 1 <strong>to</strong> 5 minutes<br />

b. 15 <strong>to</strong> 20 minutes<br />

c. 30 <strong>to</strong> 45 minutes<br />

d. 60 <strong>to</strong> 90 minutes<br />

8. The terminal extubation method <strong>of</strong> weaning:<br />

a. is based on physician preference.<br />

b. should not be used if strider is present.<br />

c. is the safest method <strong>of</strong> withdrawal <strong>of</strong> mechanical ventila<strong>to</strong>r.<br />

d. should be done without the administration <strong>of</strong> opioids or<br />

benzodiazepines.<br />

9. Which <strong>of</strong> the following is a useful aerosol medication<br />

<strong>to</strong> reduce stridor after extubation?<br />

a. Epinephrine<br />

b. Metaproterenol<br />

c. Ephedrine<br />

d. Ipratroprium bromide<br />

10. Which <strong>of</strong> the following had a significant inverse<br />

correlation with duration <strong>of</strong> survival after ventila<strong>to</strong>r<br />

withdrawal?<br />

a. Ramsey sedation scale score<br />

b. Glascow coma scale score<br />

c. PaO2/FIO2 ratio<br />

d. APACHE II score<br />

11. Which <strong>of</strong> the following would not preclude extubation<br />

after ceasing mechanical ventilation?<br />

a. Swollen <strong>to</strong>ngue<br />

b. Absent gag reflex<br />

c. Stridor<br />

d. Increased secretions<br />

12. Which <strong>of</strong> the following was the smallest average<br />

hourly dose <strong>of</strong> morphine used by investiga<strong>to</strong>rs for<br />

ventila<strong>to</strong>r withdrawal?<br />

a. 3 mg/h<br />

b. 5.5 mg/h<br />

c. 6 mg/h<br />

d. 8.5 mg/h

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