TITLE: AUTHOR:

Therapeutic hypothermia following cardiac arrest Jeffrey A. Tice, MD Assistant Professor of Medicine Division of General Internal Medicine Department of Medicine University of California San Francisco

PUBLISHER:

California Technology Assessment Forum

DATE OF PUBLICATION:

February 16, 2011

PLACE OF PUBLICATION:

San Francisco, CA

THERAPEUTIC HYPOTHERMIA FOLLOWING CARDIAC ARREST A Technology Assessment INTRODUCTION The California Technology Assessment Forum (CTAF) was asked to assess the evidence for the use of mild therapeutic hypothermia in comatose patients after cardiac arrest. Since 2002, when two randomized trials were published in the New England Journal of Medicine (NEJM),1,2 the use of therapeutic hypothermia has steadily increased in emergency rooms and intensive care units around the world.3,4 Despite recommendations to use therapeutic hypothermia for post-cardiac arrest management of patients presenting with ventricular fibrillation or ventricular tachycardia from the International Liaison Committee on Resuscitation in 20035 and the American Heart Association in 20056, use of the technology has been inconsistent. BACKGROUND Cardiac Arrest Cardiac arrest, the cessation of effective contraction of the heart confirmed by the absence of a pulse, occurs over 250,000 times annually in the United States.7 Patients usually become unconscious within seconds and the majority do not report any symptoms prior to the cardiac arrest.8-10 Among those treated by emergency medical services, the survival to hospital discharge is only about 8%. Patients with an initial rhythm of ventricular tachycardia have a somewhat better prognosis (21% survive to hospital discharge).7 The time to return of spontaneous circulation (ROSC) is the primary predictor of meaningful recovery from cardiac arrest. Considerable public health resources have been directed at teaching the public cardiopulmonary resuscitation (CPR) in order to shorten the time until the return of circulation. The most effective intervention to restore circulation is defibrillation. Thus CPR education stresses early activation of emergency medical services and the use of automatic external defibrillators when available. Patients who survive cardiac arrest often have significant neurological deficits. The majority are comatose for at least an hour following cardiac arrest and fewer than half have a good neurological recovery.4 Outcomes from cardiac arrest are primarily assessed using a five-point scale: the Pittsburgh Cerebral 2

Performance Categories (CPC).11,12 In brief, the five categories are defined as follows: 1 good cerebral performance, capable of normal life with at most minor neurological deficits; 2 moderate cerebral disability, but conscious, alert and able to perform the activities of daily life although the person may suffer hemiplegia and permanent memory or mental changes; 3 severe cerebral disability, conscious, but usually institutionalized because of the degree of dependence on others for the activities of daily life; 4 comatose / vegetative state; and 5 certified brain death. Most commonly, the scale is dichotomized with categories one and two representing a good outcome and categories three through five representing a poor outcome.11,12 Once circulation has been restored after cardiac arrest, the primary goal of therapy is to maximize the chance for recovery by minimizing damage to the brain and other organ systems. This is primarily done with supportive treatment and careful monitoring in the intensive care unit (ICU). Therapeutic Hypothermia Hypothermia is usual divided into three categories: mild (33 to 35 C), moderate (28 to 32 C), and severe (<28 C). Animal studies demonstrated that mild to moderate hypothermia markedly decreases central nervous system damage after cardiac arrest.13-17 These studies also reported that neurologic damage is minimized by initiating hypothermia as close to the return of spontaneous circulation as possible.18-20 However hypothermia is not without risk. When temperatures drop below 32 C there is a significant increase in the risk for bradycardia and ventricular arrhythmias that are difficult to treat.6,21 Hypothermia is associated with thrombocytopenia, interference with clotting factors and thus an increased risk for bleeding.22,23 Additionally, hypothermia suppresses the immune system, raising the risk for systemic infections including sepsis and pneumonia.24,25 The biological mechanisms underlying the beneficial effects of hypothermia are not completely understood. It is hypothesized that hypothermia causes a reduction in cerebral oxygen demand, slowing deleterious enzymatic reactions, decreasing free radical production, and limiting the release of excitatory neurotransmitters.14,15,19,26 This in turn should help to maintain the integrity of the blood brain barrier, maintain the supply of adenosine triphosphate, and decrease intracranial pressure. There are many approaches to cooling the patients and maintaining hypothermia. Early studies used of ice packs positioned around the patients head and body. Cooling mattresses and blankets, temperature controlled gel packs, cold water immersion, cooling helmets, rapid infusion of cold fluids, direct cooling of the patients blood via hemofiltration, endovascular cooling devices, and nasopharyngeal evaporative 3

cooling have all been used in the clinical trials described below. There is no agreement on the optimal rate or method for cooling patients. The bodys homeostatic mechanisms to maintain body temperature through peripheral vasoconstriction and shivering would blunt the effect of any of these therapeutic approaches, particularly those utilizing surface cooling. Patients who are treated with therapeutic hypothermia are generally paralyzed with neuromuscular blocking drugs to avoid the shivering response and thus patients must be intubated and sedated. Core body temperature also needs to be monitored to insure that the target temperature is reached and that patients are not over-cooled. The gold standard for monitoring core temperature requires a pulmonary artery catheter, but it is rarely used because of the risks involved. More commonly, endotracheal or bladder temperature monitors are used as patients are routinely intubated and have Foley catheters in place. These approaches to core temperature monitoring all have limitations, but are reasonable surrogate measures. After 12 to 24 hours from the initiation of hypothermia, patients are allowed to slowly warm up over about eight hours. This process is generally passive by selectively reducing the application of whatever cooling method is being used, followed by a reduction in sedation and neuromuscular blockade once the temperature rises above 35 C. Heated blankets and other devices are sometimes used. TECHNOLOGY ASSESSMENT (TA) TA Criterion 1: The technology must have final approval from the appropriate government regulatory bodies. Surface cooling products have received FDA 510(K) marketing clearance for general indication of temperature reduction when clinically indicated. Most recently, the Arctic Sun 5000 Temperature Management System by Medivance received 510(K) clearance in July 2010. No catheter based product has received FDA 510(K) clearance specifically for use after cardiac arrest. Cather-based cooling products that have received FDA marketing clearance for other indications (e.g., during neurosurgery and recovery, during cardiac surgery and recovery, for fever reduction) are being used off-label following cardiac arrest. TA Criterion 1 is met.

TA Criterion 2: The scientific evidence must permit conclusions concerning the effectiveness of the technology regarding health outcomes.

The Medline database, Embase, Cochrane clinical trials database, Cochrane reviews database and the Database of Abstracts of Reviews of Effects (DARE) were searched using the key words cardiac arrest, cardiopulmonary arrest, or resuscitation. The results were crossed with the results from a search on hypothermia or cooling. The search was performed for the period from 1945 through January 2011 (see Appendix for details). The bibliographies of systematic reviews and key articles were manually searched for additional references. References were also solicited from the manufacturers and local experts. The abstracts of citations were reviewed for relevance and all potentially relevant articles were reviewed in full. This review focuses on the essential patient oriented outcomes: survival and good neurologic recovery. The search identified 1,081 potentially relevant trials. After elimination of duplicate and non-relevant references including animal model studies, 112 articles were reviewed in full. These references included 57 case series27-83, 24 controlled studies3,84-105, and seven randomized trials.1,2,74,106-110 For the controlled studies and randomized trials, studies without a comparison group that did not receive hypothermia were excluded. Three randomized trials74,108,110 that evaluated the use of hypothermia in the pre-hospital setting were included even though many of the patients in the control group received therapeutic hypothermia once they arrived at the hospital. One randomized trial reported only in abstract form,111 two randomized trials of therapeutic hypothermia during cardiac arrest112,113, and two trials with no usual care arm45,114 were excluded.

Figure: Selection of studies for inclusion in review

1081 potentially relevant References screened 268 duplicate citations excluded 554 excluded: not hypothermia; not cardiac arrest) 259 abstracts for assessment 147 studies excluded (Editorials, reviews, abstracts, no clinical outcomes) 112 studies for full text review 25 studies excluded

88 studies included in assessment: 7 RCTs 24 Controlled studies 57 Case series

Level of Evidence: 1 through 5. TA Criterion 2 is met.

TA Criterion 3: The technology must improve net health outcomes. The key health outcomes following cardiac arrest are survival and good neurologic function as assessed by the CPC scale described above. The assessment will focus on the results from the published randomized trials, but the case series and non-randomized, controlled literature will be summarized in order to better assess the incidence of adverse effects and the real world effectiveness of therapeutic hypothermia. Randomized trials comparing hypothermia to control The data from the randomized trials are described in Tables 1 through 4 below. The first four trials compare therapeutic hypothermia to usual care and the last three investigate the utility of initiating therapeutic 6

hypothermia by emergency medical services prior to the arrival of the participant at the hospital. Table 1 summarizes the methodological characteristics of the trials that determine the quality of the trials. Table 2 summarizes the participant characteristics, the details of the intervention and control, the inclusion and exclusion criteria, and the length of follow-up for the primary outcomes. Table 3 describes the primary outcomes of the trials and Table 4 describes the reported adverse events.

Table 1: Randomized trials of therapeutic hypothermia - Study quality Study Randomization Allocation concealment Groups comparable Outcome assessment blinded Yes Yes Follow-up > 80% Intention to treat analysis Quality

In hospital hypothermia Hachimi-Idrissi 2001 HACA 2002

Yes Yes

Yes Yes

Yes No: More diabetes, CHD, bystander CPR in control No: more women and bystander CPR in hypothermia Yes

Yes 100% Yes 99% at 6 months. Yes

Yes Yes

Fair Largest, highest quality study Poor

Bernard 2002

No Even / Odd days Yes

No

Yes

Yes

Laurent 2005

Yes

NR

Yes

Yes

Fair

Pre-hospital therapeutic hypothermia Kim 2007 Yes Kamarainen 2009 Yes

Yes Yes

Yes No: 58% versus 22% received CPR Yes

No NR

Yes Yes

Yes No: 14% of randomized patients excluded from analysis Yes

Fair Poor

Bernard 2010

Yes

Yes

Yes

Yes, 100%

Good

Table 2: Randomized trials of therapeutic hypothermia - Study description Study N Intervention Target temp Time to TT Length cooled Helmet. 34 C. 3 hours. To TT or maximum 4 hours. Cooling blanket / mattress/ air. 32 to 34 C. 8 hours. 24 hours. Ice packs. 33 C. 2 hours. 12 hours. HF w/ blood cooling. 32 to 33 C. 4 hours. 18 hours. Control Inclusion criteria Exclusion Criteria Follow-up Comment

Location Age Multicenter? % Female In hospital hypothermia Hachimi-Idrissi 30 2001 75 years Belgium 39% No HACA 2002 Europe Yes Bernard 2002 Australia Yes Laurent 2005 France Yes 275 59 years 24% 77 66 years 33% 42 54 years 19%

Standard ICU care

OOH Asystole or PEA Comatose Age > 18 Temp > 30 C OOH + IH VF or VT Comatose Witnessed arrest Age 18 to 75 OOH VFib Comatose Age 18 for M Age 50 for F OOH VF or Asystole Comatose Age 18 to 75

Pregnant Coagulopathy Cardiogenic shock Pregnant Coagulopathy T < 30 C MAP < 60 x 30 minutes Terminal illness Cardiogenic shock

14 days

Standard ICU care

6 months

The majority of patients in the cooling arm also were treated with ice packs.

Standard ICU care

Hospital discharge

HF to maintain temperature at 37 C

Pregnant Terminal illness > 10 min to CPR > 50 min CPR to ROSC

6 months

Study Location Multicenter?

N Age % Female

Intervention Target temp Time to TT Length cooled

Control

Inclusion criteria

Exclusion Criteria

Follow-up

Comment

Pre-hospital therapeutic hypothermia Kim 2007 125 2L 4 C NS. NA. Seattle, WA 66 years NA. Yes 19% Until Hospital.

OOH T < 34 C All rhythms Following ROSC commands Age 18 IV access Kamarainen 2009 43 4 C RL infusion. Usual care OOH Pregnant 33 C. All rhythms Trauma Finland 61 years ROSC > 9 min GCS > 5 Yes 5% Age 18 Cardiogenic IV access shock Bernard 2010 234 2L 4 C RS. Usual care OOH Not intubated NA. including VFib T < 34 C Australia 63 years NA. therapeutic Comatose Pregnant Yes 15% Until Hospital. hypothermia in ROSC >10 min ICU. Age 15 IV access Target temp, method of cooling, average temperature, time to cool, time to ROSC, age, sex, %VF, length of hypothermia VF VT HF OOH NA NR NS RS Ventricular fibrillation Ventricular tachycardia Hemofiltration Out of hospital cardiac arrest Not applicable Not reported Normal saline Ringers solution ROSC CPR ICU TT IH MAP IV GCS

Usual care

Hospital discharge

62% of the patients also received hypothermia therapy in ICU

Hospital discharge

Hospital discharge

Return of spontaneous circulation Cardiopulmonary resuscitation Intensive Care Unit Target temperature In hospital Mean arterial pressure Intravenous Glasgow coma scale

10

Table 3: Randomized trials of therapeutic hypothermia - Study outcomes Study Study group, n Survival, n (%) Good recovery, n (%) 2 (14%) 0 (0%) 75 (55%) 54 (39%) 21 (49%) 9 (26%) 7 (32%) 9 (45%) NR 49 (78%) 48 (77%) Survival to arrival at hospital 8 (42%) 8 (44%) 56 (47%) 61 (53%) Outcomes at 6 months. Survival to hospital discharge was 45% in both groups (10/22 vs. 9/20). Trend towards better outcomes in patients with VF (66% versus 45% discharged alive) Cooling was faster, but no improvement in outcomes. Other outcomes Comment

In hospital hypothermia Hachimi-Idrissi Hypo 2001 Control HACA 2002 Hypo Bernard 2002 Laurent 2005 Control Hypo Control Hypo Control

16 14 137 138 43 34 22 20

3 (19%) 1 (7%) 81 (59%) 62 (45%) 21 (49%) 11 (32%) 7 (32%) 9 (45%) 21 (32%) 18 (29%) 8 (42%) 8 (44%) 56 (47%) 62 (53%)

Outcomes at hospital discharge. High mortality because of initial rhythms. These are outcomes at 6 months.

Pre-hospital therapeutic hypothermia Kim 2007 Hypo 63 Control Kamarainen 2009 Bernard 2010 Hypo Control Hypo Control 62 19 18 118 116

11

Table 4: Randomized trials of therapeutic hypothermia - Potential harms from hypothermia Study Study group, n 16 14 136 137 43 34 22 20 Arrhythmia 0 (0%) 0 (0%) 49 (36%) 44 (32%) 0 (0%) 1 (3%) 6 (27%) 2 (10%) NR NR Pneumonia 0 (0%) 0 (0%) 50 (37%) 40 (29%) NR Sepsis 0 (0%) 0 (0%) 17 (13%) 9 (7%) NR Bleeding 0 (0%) 0 (0%) 35 (26%) 26 (19%) 0 (0%) 0 (0%) NR NR Pancreatitis 0 (0%) 0 (0%) 1 (1%) 2 (1%) NR Other 0 (0%) 0 (0%)

In hospital hypothermia Hachimi-Idrissi Hypo 2001 Control HACA 2002 Hypo Bernard 2002 Control Hypo Control Laurent 2005 Hypo Control

0 (0%) 0 (0%)

Pre-hospital therapeutic hypothermia Kim 2007 Hypo 63 0 (0%) Control Kamarainen 2009 Bernard 2010 Hypo Control Hypo Control 62 19 18 118 116 0 (0%) 0 (0%) 0 (0%)

0 (0%) 0 (0%) 0 (0%) 0 (0%)

0 (0%) 0 (0%) 0 (0%) 0 (0%)

0 (0%) 0 (0%) 0 (0%) 0 (0%)

0 (0%) 0 (0%) 0 (0%) 0 (0%)

0 (0%) 0 (0%) 0 (0%) 0 (0%)

12

Hachimi-Idrissi and colleagues published the first randomized trial106 of therapeutic hypothermia. In this single site feasibility study in Brussels, the investigators randomized 30 participants greater than 18 years old who presented with asystole or pulseless electrical activity (PEA) and remained comatose following ROSC. They used a cooling helmet filled with aqueous glycerol to rapidly cool the participants brain to a target temperature of 34 C. Once their bladder temperature reached 34 C or cooling had been ongoing for four hours, the participants were allowed to passively rewarm. The trial randomized 16 participants to the hypothermia group and 14 participants to the usual care group. Baseline characteristics were similar in the two groups. The median age of the participants was 75 years and the median time from collapse to ROSC was 33 minutes. On arrival to the emergency room (ER), the median temperature of the participants was 35.7 C. In the hypothermia group, three participants survived at least two weeks, of whom two had a good neurologic recovery. Only one participant in the usual care group survived and that individual had a poor neurologic recovery. The difference in survival (19% versus 7%) was not statistically significant, but the trial was underpowered to detect a difference. The high mortality is consistent with the poor prognosis for cardiac arrest with an initial rhythm of asystole or PEA. No treatment related adverse events were identified. The Hypothermia After Cardiac Arrest Study (HACA) was published in the NEJM in 1992.1 This multicenter European trial randomized 275 patients and remains the largest and best quality study published to date. The study enrolled patients ages 18 to 75 years who had a witnessed arrest with a first rhythm of ventricular fibrillation (VF) or ventricular tachycardia (VT) and remained comatose after ROSC. The participants were followed for six months for the primary outcome. Participants in the hypothermia group were cooled with a device using a mattress and blanket to deliver cold air over the entire body. Ice packs were also used to cool 70% of the participants in the hypothermia group. The target temperature in the hypothermia group was 32 to 34 C and the participants were maintained at this temperature for 24 hours from the time cooling was initiated. Participants were then allowed to rewarm passively. Participants had similar baseline characteristics (age 59 years, 24% female, 22 minutes to ROSC) except that the hypothermia group had fewer patients with diabetes (8% versus 19%), coronary heart disease (32% versus 43%), and CPR from a bystander (43% versus 49%). Survival at six months was higher in the hypothermia group (59% versus 45%, p = 0.02, number needed to treat (NNT) to save one life equal to seven). Similarly, the proportion of patients with a good neurological outcome at six months was greater in the hypothermia group (55% versus 39%, p = 0.009). These differences remained statistically significant after adjustment for baseline variables, including those with important differences between the two groups. The rate of complications did not differ between the two groups (70% versus 73%, p=0.70), but there was a trend towards more sepsis in the hypothermia group (13% versus 7%, p NS). It is likely that overall mortality was much lower in this trial than in the prior trial because patients presenting the initial rhythms required for randomization in HACA (VF, VT) 13

have a much better prognosis than patients presenting with asystole or PEA. The investigators also performed detailed cognitive and neuropsychological testing on 45 of the patients who survived three months.109 There were no statistically significant differences between the two groups, although trends favored the hypothermia group. Overall, 67% of the survivors in the hypothermia group had either mild or no cognitive defects compared with 44% in the control group (p NS). A second, smaller Australian study on hypothermia was published by Bernard and colleagues in the same issue of the NEJM.2 This study enrolled 84 patients with an out of hospital cardiac arrest with a first rhythm of VF who remained comatose after ROSC. The age cutoff was 18 years for men, but 50 years for women in order to minimize the likelihood of pregnancy. It was not a true randomized trial on odd numbered days, participants were treated with hypothermia and on the even numbered days they received standard therapy. Participants in the hypothermia group (n = 43) were cooled with ice packs to the head, neck, torso and limbs. Limited cooling was initiated by emergency medical services before arriving at the hospital. The target temperature in the hypothermia group was 33 C and the participants were maintained at this temperature for 12 hours from arrival at the hospital. After 18 hours, the patients were actively warmed over six hours. Participants in the control group (n = 34) were paralyzed and sedated with the same protocol as the hypothermia group, but their target temperature was 37 C. The primary outcome was survival to discharge with discharge home or to a rehabilitation facility considered a good outcome. Discharge to a long term nursing facility and in-hospital death was considered poor outcomes. A blinded specialist in rehabilitation medicine evaluated the patient and made the decision about where patients were discharged. The participants in both groups were similar at baseline (age 66 years, 26 minutes to ROSC) except that the hypothermia group had fewer men (58% versus 79%, p = 0.05) and fewer participants who received CPR from a bystander (49% versus 71%, p = 0.05). There was a non-significant trend towards higher survival at hospital discharge in the hypothermia group (49% versus 32%, p = 0.145). The primary outcome in the study, the proportion of patients with a good neurological outcome at hospital discharge, was greater in the hypothermia group (49% versus 26%, p = 0.046). In bivariate analyses, the participants age and the time from collapse to ROSC were both significantly associated with the primary outcome. After adjustment for these two variables in multivariate logistic regression, the odds ratio for a good neurologic outcome for hypothermia was 5.25 (95% CI 1.5 to 18.8, p = 0.011). No multivariate model adjusting for the baseline differences in sex and bystander CPR were reported. There were no important adverse events associated with hypothermia. One patient in the control group developed 3rd degree heart block requiring a transvenous pacemaker and no patients in either arm experienced significant bleeding complications. The last of the published trials directly evaluating therapeutic hypothermia to treatment without hypothermia was a three-arm multicenter trial in France.107 This study enrolled 61 patients between the ages of 18 and 14

75 with an out of hospital cardiac arrest with a first rhythm of VF or asystole who remained comatose after ROSC. Patients were randomized to high volume hemofiltration with or without hypothermia or to usual care without hemofiltration or hypothermia. For the purposes of this assessment, comparing the hemofiltration plus hypothermia group to the hemofiltration alone group isolates the independent effect of hypothermia. Participants in the hypothermia group (n = 22) were cooled by external cooling of their blood during hemofiltration. The target temperature in the hypothermia group was 32 to 33 C and the participants were maintained at this temperature for 18 hours. After 18 hours, the patients were allowed to warm passively. Participants in the control hemofiltration only group (n = 34) were paralyzed, sedated, and received hemofiltration with the same protocol as the hypothermia group, but their target temperature was 37 C. The primary outcome of the study was survival at six months and the secondary outcome was survival with a favorable neurologic outcome (CPC score of one or two). Baseline characteristics were similar in the two groups (age 54 years, 19% female), although there was a trend towards a shorter time to ROSC in the hypothermia group (16 minutes versus 25 minutes, p NS). There was a trend towards lower survival at six months in the hypothermia group (32% versus 45%, p NS), although survival at hospital discharge was 45% in both groups. Survival at six months was significantly higher in both of these groups compared to the control group who received usual care without hemofiltration or hypothermia (21% survival, p = 0.018). Similarly, there was a trend towards fewer participants with a good neurological outcome at six months in the hypothermia group compared with the hemofiltration alone group (32% versus 45%, p NS). There was a trend toward more ventricular tachycardia in the hypothermia group (27% versus 10%), but no other adverse events were reported. The quality of the randomized trials was somewhat uneven. None of the trials could feasibly blind treating personnel to the treatment intervention, which raises the possibility of differential co-interventions that could impact survival. Given the paucity of known effective interventions following cardiac arrest, this is unlikely to have had a large impact on the outcomes. Follow-up was nearly 100% for the primary outcomes in all of the trials and all used an intention to treat analysis. Three of the four trials used appropriate randomization and allocation concealment, but Bernard and colleagues2 used a pseudo-randomization scheme (odd and even day assignment), which could have introduced selection bias. Two of the trials were too small to have sufficient statistical power to demonstrate significant results.106,107 Finally, in the largest study,1 the HACA trial, there were baseline differences in the characteristics of the two study groups despite randomization. When the investigators adjusted for these differences in a secondary analysis, the results remained significant in favor of hypothermia, but the imbalances introduce some uncertainty about the quality of the trial. In addition to the methodological concerns, there was significant heterogeneity in the patient populations 15

studied and the methods used to cool the study participants. Only one study included participants presenting with an initial rhythm of PEA106, two allowed participants with asystole106,107, and two focused primarily on participants with VF.1,2 It is important to note that all of the trials excluded patients younger than 18 years, so the results only apply to adults. Cooling was done with four different approaches: a cooling helmet, ice bags, cool air delivered by a mattress and blanket device, and external cooling of blood during hemofiltration. The target temperature was similar in all four trials (32 to 34 C), but the length of time that participants were cooled varied from three hours to 24 hours. In addition, the time to reach the target temperature varied from two to eight hours. Finally, a non-standard intervention, hemofiltration, was used in both the hypothermia group and the control group in one of the trials. The lack of consistency in the patient populations and approaches to cooling make it difficult to combine the results of these trials. The two largest trials that reported statistically significant benefits excluded patients who presented with PEA and asystole and they cooled patients for 12 to 24 hours. Meta-analyses of randomized trials Despite the small number of randomized trials and the heterogeneity of the populations, interventions, and results, there have been a relatively large number of systematic reviews and meta-analyses of therapeutic hypothermia following cardiac arrest.115-121 Using individual patient data from the trials, the Cochrane review115 found that patients in the hypothermia group were more likely to reach a best cerebral performance categories score of one or two (RR, 1.55; 95% CI 1.22 to 1.96) and were more likely to survive to hospital discharge (RR, 1.35; 95% CI 1.10 to 1.65) compared to standard post-resuscitation care. The review did not find any important differences in the rates of adverse events between the hypothermia and standard care groups. All of the other meta-analyses agreed with the conclusions of the Cochrane review except Nielsen et al120, which agreed that the evidence suggested both an improvement in mortality and neurologic outcomes, but concluded that quality of the evidence was low because the methodological issues discussed above raised important concerns about systematic and random errors. They called for additional large, well-designed randomized trials to address this uncertainty. Several of the reviews highlight the limitations in the evidence for patients presenting with rhythms other than ventricular fibrillation and the need to avoid fever in the control group as fever may be associated with neurologic damage. Ongoing trials will address some of these issues. Ongoing trials of therapeutic hypothermia There are a many ongoing trials indexed on ClinicalTrials.gov. The largest is an international trial, the Target Temperature Management After Cardiac Arrest study, which is randomizing 850 participants resuscitated from an out of hospital cardiac arrest to a target temperature of 33 C or a target temperature of 36 C. 16

Other trials are investigating the utility of hypothermia in pediatric patients, comparing internal versus external cooling devices, and evaluating the impact of inducing hypothermia during prior to the return of spontaneous circulation. These trials should help address many of the questions not yet answered by the published clinical trials. Observational studies comparing hypothermia to control Because of the uncertainties raised by the methodologic issues in the published randomized trials, it is important to carefully evaluate the results of the observational studies of therapeutic hypothermia. Since the publication of the two studies in 2002 in the NEJM, many organizations began to use therapeutic hypothermia to treat comatose survivors of cardiac arrest. These organizations have published a number of small studies of less than 100 patients that compare the survival and neurologic outcomes in patients treated with therapeutic hypothermia to historical controls.3,41,84-105,122 The results consistently favored therapeutic hypothermia and almost all of the studies reported differences in survival and neurological outcome were statistically significant. Since these are non-randomized trials, they are subject to potential selection bias and confounding. In particular, improvements over time in the management of patients in the ICU following cardiac arrest other than therapeutic hypothermia may explain some of the observed improvements in survival. These comparative studies are important to consider in evaluating therapeutic hypothermia because there were relatively few participants in the published randomized trials. Furthermore, these comparative studies reflect the experience in larger community practices, not just centers with particular expertise and interest in hypothermia. They also present data on subgroups underrepresented in the randomized trials such as patients with an in-hospital arrest or patients presenting with PEA or asystole. The largest of the studies are described below. Arrich and colleagues41 published data on 585 patients (462 treated with hypothermia, 123 controls) followed in the prospective European Resuscitation Council Hypothermia After Cardiac Arrest Registry. There were many significant differences between the two groups: the hypothermia group was more likely to have suffered an out of hospital arrest (91% versus 53%, p<0.001); was more likely to have a first rhythm of VF or VT (68% versus 37%, p<0.001); and had a longer time from collapse to ROSC (23 minutes versus 17 minutes, p<0.001). Survival was higher in the hypothermia group (57% versus 32%, p<0.001), but this was not adjusted for the baseline differences in the patients nor was any matched analysis or propensity score adjusted analysis presented. Among patients with an in-hospital arrest (n= 43 hypothermia, n=58 control), there was a trend towards lower survival in the hypothermia group (39% versus 60%, p=0.30). However, in the subgroup of patients presenting with PEA or asystole (n= 124 hypothermia, n=73 control), survival was higher in the hypothermia group (35% versus 19%, p=0.023). The majority of the patients in the 17

hypothermia group were treated with an endovascular device (75%). The remaining 25% were cooled with ice packs, cooling blankets, and cold fluids. In the hypothermia group, 3% had significant bleeding and 6% had an arrhythmia within seven days of cooling. The adverse event rates in the control group were not presented. Don et al assessed the survival and neurologic outcome in 491 consecutive patients in Seattle, Washington.98 Therapeutic hypothermia with ice packs, cooling blankets, or cooling pads was initiated in 204 patients. Multivariable logistic regression was used to adjust for baseline differences in the two groups. Survival to hospital discharge was improved with hypothermia in the subgroup of patients who presented with an initial rhythm of VF (OR 1.88, 95% CI 1.03-3.45), but not in patients with other initial rhythms (OR 1.17, 95% CI 0.66-2.05). In the adjusted analyses, patients in the subgroup presenting with VF who were treated with hypothermia had favorable neurologic outcomes (OR 2.62, 95% CI 1.1-6.27). There was no significant benefit in patients whose initial rhythm was PEA or asystole. The largest comparative analysis was recently published by van der Wal and colleagues3 using data on patients who were comatose following cardiac arrest in the Dutch National Intensive Care Evaluation database. They compared outcomes in 3770 patients treated with therapeutic hypothermia to outcomes in 1547 historical controls from the same database. They adjusted their analysis for the Simplified Acute Physiology Score II, age, gender, in- versus out-of-hospital arrest, and a propensity score for receiving hypothermia. Characteristics of the two groups were remarkably similar: their average age (63.6 versus 64.3 years), sex (35.9% female in both groups), use of vasopressors (77.1% versus 77.2%), and median Glasgow coma scale (three in both groups) did not differ significantly. Crude survival was 35% in the hypothermia group and 28% in the control group. In the adjusted analysis, use of hypothermia was associated with a 20% lower odds of in-hospital death (OR 0.80, 95% CI 0.65 to 0.98, p = 0.029). No adverse outcomes data were reported, but the ICU length of stay (3.0 days versus 2.6 days) and total hospital stay (6.0 versus 5.0 days) increased significantly (p<0.001 for both comparisons). Kagawa et al recently published a comparative study (110 patients treated with hypothermia, 290 controls) that looked carefully at the impact of time to ROSC on the relative benefit of therapeutic hypothermia.103 In their initial analysis, the hypothermia group had a higher rate of favorable neurological outcome (39% vs. 14%, P < 0.001) and higher 30-day survival (48% vs. 16%, P < 0.001). The differences were particularly strong when the time from collapse to ROSC was greater than 15 minutes. For example, the rates of favorable neurological outcome in patients with ROSC between 15 and 20 minutes was 64% vs. 17%, P < 0.01 and for patients with ROSC between 25 and 30 minutes the were 50% vs. 7%, P = 0.02. The investigators used propensity scoring to adjust for baseline differences between the two groups. In that 18

analysis, the benefits of therapeutic hypothermia on favorable neurological outcome was only significant for patients with time to ROSC greater than 15 minutes (p<0.001). If these findings are replicated within randomized trials of hypothermia, they may be used to better target the use of therapeutic hypothermia. In summary, the comparative data confirm that therapeutic hypothermia can improve survival after cardiac arrest in the community setting. Most of the studies reported no increase in adverse effects potentially associated with hypothermia such as bleeding, arrhythmias, infections, or poor glycemic control. The benefits appear to be primarily in patients presenting with ventricular fibrillation as their first rhythm. Further study is needed to evaluate whether therapeutic hypothermia is beneficial in patients presenting with asystole or PEA. Similarly, some of the comparative data suggested that the benefit of hypothermia is primarily in patients with out-of-hospital cardiac arrest with a time from collapse to return of spontaneous circulation of greater than 15 minutes. It would be helpful to see subgroup analyses within the completed and ongoing randomized trials to better define which patients benefit most from therapeutic hypothermia. Case Series A large number of case series have been published describing individual institutions, regions or countries experience with therapeutic hypothermia.27-40,42-83 Most case series were small and focused on the feasibility of implementing therapeutic hypothermia or describing new techniques and devices for lowering body temperature. Large case series add real-world data to randomized trials and can help to more precisely define known adverse events, identify rare adverse events, and evaluate long term outcomes. Nielsen and colleagues67 reported on 986 patients entered into the prospective Hypothermia Registry representing 34 centers in seven countries. All patients with ROSC following out-of-hospital cardiac arrest who were comatose were entered into the registry. There were no exclusion criteria. Hypothermia was initiated and maintained by a variety of methods including ice packs, cold fluid infusion, air cooling, circulating water blankets, and intravascular devices. The patients median age was 63 years and 36% were female. The initial rhythm was VT or VF in 70%, asystole in 22%, and PEA in 7%. The median time to ROSC was 20 minutes. Therapeutic hypothermia was started a median of 90 minutes following the arrest and the target temperature (< 34 C) was reached after a median of 260 minutes. At hospital discharge survival was 56% and 434 (44%) patients had a good neurological outcome. At long-term follow-up (greater than six months) survival was 50% and 447 (46%) patients had a good neurological outcome. Long-term survival was higher in patients initially presenting with VT or VF (61%) than in patients presenting with asystole (25%) or PEA (27%). In multivariate modeling, the factors significantly associated with a poor longterm outcome included older age, longer time to ROSC, lower Glasgow Coma Scale on admission, unwitnessed arrest, and an initial rhythm of asystole (all p < 0.001). Notably, neither the time to initiation of 19

hypothermia (p=0.48), nor the time to reach the target temperature (p=.91) were associated with a poor outcome. Arrhythmias were a common adverse event (33%) with 13% of patients experiencing bradycardia, 9% atrial fibrillation, 9% VT, and 7% VF. Infectious complications included pneumonia (46%), sepsis (4%), and other infections (4%). Bleeding requiring transfusions occurred in 4% and only 0.2% of patients had intracerebral bleeding. Because there was not a control group treated, it is impossible to determine whether there is an excess of any of these adverse events. However, the incidence of arrhythmias was comparable to that observed in both the control and hypothermia group in the HACA trial.1 The observed bleeding may be due in part to hypothermia, but 49% of the patients underwent emergent coronary angiography and 31% of the patients received some form of percutaneous coronary intervention. Thus, at least half of the patients received heparin and at least one third were placed on long-term anti-platelet therapy. The rate of pneumonia was higher than that observed in the HACA trial, but the rate of sepsis was lower. Randomized trials evaluating pre-hospital therapeutic hypothermia The three most recent randomized trials74,108,110 summarized in Tables 1 through 4 evaluated the impact of pre-hospital initiation of hypothermia in order to shorten the time from ROSC to hypothermia. Animal model data suggested that this should improve clinical outcomes.18-20 The quality of the trials was somewhat variable. None of the trials could blind study personnel to the intervention. Only Kim et al108 did not blind the outcome assessment. Kamarainen et al110 was the smallest of the trials, had large differences in baseline characteristics, and failed to analyze the data by intention-to-treat. The most recent trial, by Bernard et al,74 included more patients than the other two combined and was the highest quality of the three. All three of the trials used up to two liters of intravenous fluids chilled to 4 C (normal saline or Ringers solution) to initiate hypothermia. At arrival to the hospital, temperatures in the hypothermia group were approximately 1 C lower than the control group in all three trials even though the majority of patients in the hypothermia groups did not receive the full two liters of cold fluid. None of the trials found a benefit to hypothermia in improving survival to hospital discharge. In Kim et al,108 there was a slight trend toward higher survival in the hypothermia group (32% versus 29%), particularly in patients presenting with VF (66% versus 45%). However, survival trends went in the opposite direction in the randomized trials of Kamarainen110 (42% versus 44%) and Bernard74 (47% versus 53%). Notably, Bernard et al only randomized patients presenting with VF.74 Thus the trend identified in the subgroup analyses of Kim et al108 was not confirmed in the larger, higher quality trial. It is also interesting that the large observational Hypothermia Registry, there was no association of time to initiation of hypothermia with survival or good neurologic outcome, contradicting the findings in one much smaller case series (n=49) that had suggested a benefit to earlier initiation of 20

hypothermia.72 There may be negative consequences from the rapid infusion of chilled fluids intravenously, although none were identified in these three studies. The volume of fluid may increase the risk for heart failure and in animal models, the infusion of cold saline reduces coronary perfusion pressure.21,24 Further trials may investigate alternative methods for initiating hypothermia in the pre-hospital setting. Until new randomized trials are published that convincingly demonstrate a survival benefit, pre-hospital initiation of hypothermia should remain investigational.

Summary Four randomized trials have been published that directly compare therapeutic hypothermia to the same level of ICU care without hypothermia. In 2002, the NEJM published one good quality randomized trial1 and one pseudo-randomized trial2 that reported 14% to 17% absolute improvements in survival and 16% to 23% absolute improvements in neurologic outcomes compared to standard ICU care. Thus, for every seven comatose patients treated with therapeutic hypothermia following cardiac arrest, one additional patient would survive with meaningful quality of life. There were non-significant trends towards increased arrhythmias, infection, and bleeding in patients randomized to hypothermia. However, even if some patients were harmed by these adverse events, the net benefit in terms of patient survival and quality of life strongly favored the hypothermia intervention. Both of these trials cooled patients to a target temperature between 32 and 34 C using external cooling methods for a total of 12 to 24 hours. The study population in these two trials was similar: adults at least 18 years old who presented with an initial rhythm of VF or VT. The other two randomized trials106,107 were smaller and one reported trends towards worse outcomes in patients randomized to therapeutic hypothermia. The patient populations in these two trials differed from the two trials that found benefit. Both of the trials included patients who presented with asystole and one of the trials included patients with PEA and excluded patients with VF or VT. The hypothermia interventions were also quite different. The first used a cooling helmet for only three to four hours.106 The other randomized trial107 used external cooling of the patients blood during hemofiltration and the control group was also treated with hemofiltration, which is not an established therapy for post-cardiac arrest management. These differences in patient populations and in cooling techniques are likely to be responsible for the differences in outcomes. Thus current randomized trials only support using external cooling methods for 12 to 24 hours in comatose survivors of out of hospital cardiac arrest in whom the presenting rhythm is VF or VT. Because of the relative weakness in the quality of the randomized trial data for therapeutic hypothermia and the small number of patients studied, it was helpful to review the observational literature for evidence that 21

hypothermia improves outcomes outside the investigational setting. Recent studies that compared outcomes in survivors of cardiac arrest treated with hypothermia to historical or contemporary controls reported improvements in survival of a similar magnitude to the initial randomized trials. They also suggest that the largest benefit from therapeutic hypothermia is in the subgroup of patients presenting with VF or VT who have ROSC more than 15 minutes after the initial cardiac arrest. Some of the larger observational studies reported that therapeutic hypothermia did not improve outcomes in patients suffering cardiac arrest while in the hospital or in patients with asystole or PEA as their presenting rhythm, although the data were not consistent across all observational studies. Thus, the results of observational studies essentially echoes the findings of the randomized trials. Three additional randomized trials74,108,110 failed to demonstrate any improvements in patient outcomes when pre-hospital therapeutic hypothermia was evaluated. The largest case series of therapeutic hypothermia also failed to find an association between the time to induction of hypothermia and clinical outcomes. These results suggest that the currently studied approach to pre-hospital therapy, the infusion of cold normal saline or Ringers solution, does not improve outcomes and should not be recommended on a routine basis. In summary, randomized trial and comparative studies support the use of therapeutic hypothermia with a target temperature of 32 to 34 C for 12 to 24 hours in adult comatose survivors of out of hospital cardiac arrest who present with VF or VT. Further study is needed to extend the indication beyond this patient population. The optimal method for therapeutic hypothermia also remains unclear.

TA Criterion 3 is met.

TA Criterion 4: The technology must be as beneficial as any established alternatives. There is no established alternative to therapeutic hypothermia for the care of post-cardiac arrest patients other than standard ICU care. Approaches such as hemofiltration and aggressive maintenance of normothermia remain investigational. The clinical trials discussed above under TA 3 demonstrated improved survival and neurologic outcome in patients treated with therapeutic hypothermia compared to patients treated with standard ICU care. Thus TA criterion 4 is met. TA Criterion 4 is met. 22

TA Criterion 5: The improvement must be attainable outside of the investigational setting. Therapeutic hypothermia is not straightforward to administer. Patients are usually paralyzed to prevent shivering and thus the patients often need to be intubated and sedated. In addition, the patients core temperature must be carefully monitored to maintain the target temperature without over-cooling the patient, which would increase the likelihood of arrhythmias, infection, bleeding, and electrolyte abnormalities. However, most intensive care units are able to provide this level of care. Most of the randomized trials were multi-institutional. The many published case series and comparative observational studies demonstrate the feasibility of therapeutic hypothermia at care facilities in many countries around the world and demonstrate improvements in survival and neurologic outcome compared with historical controls. TA Criterion 5 is met.

CONCLUSION One good quality randomized trial of therapeutic hypothermia1 and one pseudo-randomized trial2 published in 2002 reported 14% to 17% absolute improvements in survival and 16% to 23% absolute improvements in neurologic outcomes compared to standard ICU care. Thus, for every seven comatose patients treated with therapeutic hypothermia following cardiac arrest, approximately one additional patient would survive with meaningful quality of life. There were trends towards increased arrhythmias, infection, and bleeding in patients randomized to hypothermia, but these were not large enough to offset the observed improvements in overall survival and neurologic outcome. Both of these trials cooled patients to a target temperature between 32 and 34 C using external cooling methods for 12 to 24 hours. These two trials also limited their study population to adults at least 18 years old who presented with an initial rhythm of VF or VT. However, the two other published randomized trials106,107 had lower survival rates and one reported a trend towards worse outcomes in patients randomized to therapeutic hypothermia. One included only patients presenting with asystole or PEA and used a cooling helmet for three hours.106 The other randomized trial107 included patients presenting with either VF or asystole, but compared hypothermia achieved by external cooling of the blood during hemofiltration to hemofiltration alone. The differences in patient populations and in the methods used to cool patients may be responsible for the differences in outcomes. Subsequent observational studies that compared outcomes in survivors of cardiac arrest treated with 23

hypothermia to historical or contemporary controls reported improvements in survival of a similar magnitude to the initial randomized trials. They also suggest that the largest benefit from therapeutic hypothermia is in the subgroup of patients presenting with VF or VT who have ROSC more than 15 minutes after the initial cardiac arrest. Some of the larger observational studies reported that therapeutic hypothermia did not improve outcomes in patients suffering cardiac arrest while in the hospital or in patients with asystole or PEA as their presenting rhythm, although the data were not consistent across all observational studies. Finally, three randomized trials74,108,110 failed to demonstrate any benefit to pre-hospital therapeutic hypothermia using cold intravenous fluids. The largest case series of therapeutic hypothermia also failed to find an association between the time to induction of hypothermia and clinical outcomes. These results contradict animal studies that demonstrated less nerve cell death in the brain and higher survival in animals treated with rapid induction of hypothermia after ROSC. In conclusion, there is modest evidence supporting the use of therapeutic hypothermia with a target temperature of 32 to 34 C for 12 to 24 hours in adult comatose survivors of out of hospital cardiac arrest who present with VF or VT. Current evidence supports the use of external methods to cool patients. Randomized trials are needed to evaluate whether therapeutic hypothermia should be extended to other patient populations including children under the age of 18 years, patients suffering cardiac arrest in the hospital, and patients presenting with asystole or PEA. Additional areas of uncertainty include the best methods for inducing and maintaining hypothermia, the optimal target temperature, how long to maintain hypothermia, and whether the risks of hypothermia outweigh the benefits in patients with ROSC in less than 15 minutes. Ongoing randomized trials are addressing many of these questions. RECOMMENDATION It is recommended that use of therapeutic hypothermia in comatose adults following cardiac arrest with a first rhythm of ventricular fibrillation or ventricular tachycardia meets CTAF Technology Assessment Criteria 1 through 5 for safety, effectiveness and improvement in health outcomes. February 16, 2011 This is the first review of this technology by the California Technology Assessment Forum

The California Technology Assessment Forum voted to approve the recommendation as presented.

24

RECOMMENDATIONS OF OTHERS American Heart Association In October, 2002, the Advanced Life Support Task Force of the International Liaison Committee on Resuscitation (ILCOR) recommended that unconscious adult patients with spontaneous circulation after outof-hospital cardiac arrest should be cooled to 32C to 34C for 12 to 24 hours when the initial rhythm was ventricular fibrillation (VF) and that cooling patients might be of benefit to those with other rhythms and inhospital cardiac arrest. In 2005, AHA cited two nonrandomized studies that indicate the possible benefit of hypothermia for adults following in-and out-of-hospital cardiac arrest from all other rhythms. The 2010 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care states that therapeutic hypothermia has been shown to improve outcomes for comatose adult victims of witnessed out-of-hospital cardiac arrest due to ventricular fibrillation. Blue Cross Blue Shield Association (BCBSA) The BCBSA Technology Evaluation Center has not conducted an assessment of Therapeutic Hypothermia Used in Cardiac Arrest. Centers for Medicare and Medicaid Services (CMS) Neither a National Coverage Determination nor a Local Coverage Determination (CA) was found in a review of the CMS web site Society of Critical Care Medicine (SCCM) The SCCM (www.sccm.org) has been invited to attend the meeting and to provide an opinion regarding the use of this technology. The American Society of Hypothermic Medicine (ASHM) The ASHM (www.asfhm.com) was invited to attend the meeting and to provide an opinion regarding the use of this technology

25

The American College of Emergency Physicians (ACEP) ACEP was invited to attend the meeting and to provide an opinion regarding the use of this technology.

ABBREVIATIONS CTAF NEJM ROSC CPR CPC ICU DARE RCT CHD NR TT OOH IH T MAP NS HF NA GCS RS IV PEA VT California Technology Assessment Forum New England Journal of Medicine Return of spontaneous circulation Cardiopulmonary resuscitation Cerebral performance categories Intensive care unit Database of Abstracts of Reviews of Effects Randomized controlled trial Coronary heart disease Not reported Target temperature Out of hospital cardiac arrest In hospital Temperature Mean arterial pressure Normal saline Hemofiltration Not applicable Glasgow coma scale Ringers solution Intravenous Pulseless Electrical Activity Ventricular tachycardia 26 HACA VF ER NNT Hypothermia after cardiac arrest Ventricular fibrillation Emergency room Number needed to treat

APPENDIX: Search strategy PubMed:

Search Most Recent Queries #7 Search #3 OR #4 OR #5 OR #6 #6 Search heart arrest[majr] AND hypothermia, induced[majr] AND (treatment outcome[mh] OR prognosis[mh:noexp]) NOT ((animals[mh] NOT humans[mh]) OR review[pt]) #5 Search #2 AND (outcome OR outcomes OR prognosis) Limits: Comparative Study, Multicenter Study, Research Support, American Recovery and Reinvestment Act, Research Support, N I H, Extramural, Research Support, N I H, Intramural, Research Support, Non U S Gov't, Research Support, U S Gov't, Non P H S, Research Support, U S Gov't, P H S #4 Search #2 AND (controlled clinical trials as topic[mh] OR systematic*[tiab] OR cohort stud* OR observational stud* OR observation stud* OR controlled stud* OR control stud* OR experimental stud*) #3 Search #2 Limits: Meta-Analysis, Randomized Controlled Trial, Controlled Clinical Trial #2 Search #1 NOT (animals[mh] NOT humans[mh]) #1 Search (heart arrest[mh] OR heart arrest[tiab] OR cardiac arrest[tiab] OR cardiopulmonary arrest[tiab] OR asystole[mh] OR asystole[tiab] OR resuscitation[mh:noexp] OR resuscitation[tiab] OR cardiopulmonary resuscitation[mh] OR cardiopulmonary resuscitation[tiab] OR advanced cardiac life support[mh] OR advanced cardiac life support[tiab] OR heart standstill[tiab] OR sudden cardiac death[tiab] OR death, sudden, cardiac[mh] OR heart massage[mh] OR heart massage[tiab] OR reanimation[tiab]) AND (hypothermia, induced[mh] OR "induced hypothermia"[tiab] OR "moderate hypothermia"[tiab] OR "mild hypothermia"[tiab] OR "therapeutic hypothermia"[tiab] OR "artificial hypothermia"[tiab] OR "extracorporeal hypothermia"[tiab] OR "resuscitative hypothermia"[tiab] OR hibernation OR cooling[tiab] OR chilling[tiab] OR refrigeration OR body temperature[mh] OR body temperature[tiab])

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EMBASE.com

Search Queries

Access the Embase Info site if you have questions about this message or other features of this service. Please do not reply to this email. No. Query #5 #4 AND ('cohort analysis'/de OR 'controlled clinical trial'/de OR 'controlled study'/de OR 'observational study'/de OR 'outcomes research'/de OR 'prospective study'/de OR 'randomized controlled trial'/de OR 'systematic review'/de) #4 #3 NOT ([animals]/lim NOT [humans]/lim) #3 #1 AND #2 #2 'induced hypothermia'/de OR 'induced hypothermia':ab,ti OR 'moderate hypothermia':ab,ti OR 'mild hypothermia':ab,ti OR 'therapeutic hypothermia':ab,ti OR 'artificial hypothermia':ab,ti OR 'extracorporeal hypothermia':ab,ti OR 'resuscitative hypothermia':ab,ti OR hibernation:ab,ti OR 'cooling'/de OR cooling:ab,ti OR chilling:ab,ti OR refrigeration:ab,ti OR 'body temperature'/de OR 'body temperature':ab,ti #1 'heart arrest'/de OR 'heart arrest':ab,ti OR 'cardiac arrest':ab,ti OR 'cardiopulmonary arrest':ab,ti OR 'asystole'/de OR asystole:ab,ti OR 'resuscitation'/de OR resuscitation:ab,ti OR 'cardiopulmonary resuscitation':ab,ti OR 'advanced cardiac life support':ab,ti OR 'heart standstill':ab,ti OR 'sudden cardiac death':ab,ti OR 'sudden death'/de OR 'sudden death':ab,ti OR 'heart massage'/de OR 'heart massage':ab,ti OR reanimation:ab,ti Results 477 Date 21 Dec 2010

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ID

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Hits Edit Delete

(heart arrest OR cardiac arrest OR cardiopulmonary arrest OR asystole OR resuscitation OR advanced cardiac life support OR #1 heart standstill OR sudden cardiac death OR death sudden cardiac 207 edit delete OR heart massage OR reanimation):ti,ab,kw and (hypothermia):ti,ab,kw
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