INTRODUCTION: Anesthesia-assisted rapid opioid detoxification (AAROD) is a controversial method of treating opioid dependence that involves sedating patients during a period of provoked withdrawal. Reported adverse outcomes of the procedure demonstrate the importance of recognizing the potential complications of AAROD. CASE PRESENTATION: We present a case of a 41-year-old male presenting with a subarachnoid hemorrhage following an AAROD procedure. CONCLUSION: This case report and discussion reviews the pathophysiology of opioid withdrawal syndrome, potential complications following AAROD, and important management considerations.
INTRODUCTION: Anesthesia-assisted rapid opioid detoxification (AAROD) is a controversial method of treating opioid dependence that involves sedating patients during a period of provoked withdrawal. Reported adverse outcomes of the procedure demonstrate the importance of recognizing the potential complications of AAROD. CASE PRESENTATION: We present a case of a 41-year-old male presenting with a subarachnoid hemorrhage following an AAROD procedure. CONCLUSION: This case report and discussion reviews the pathophysiology of opioid withdrawal syndrome, potential complications following AAROD, and important management considerations.
Emergency department (ED) visits and hospitalizations for opioid withdrawal have
occurred at an increasing rate over the past 20 years.1 Treatment of symptomatic withdrawal and opioid
dependence have been subjects of research for the past three decades.2 One such method involves acutely
precipitating withdrawal with opioid antagonists while ameliorating the symptoms
using sedatives, a treatment known as anesthesia-assisted rapid opioid
detoxification (AAROD). This treatment method, while sought after for its perceived
ease and short course, has been found to provide inconsistent rates of opioid
abstinence while being costlier and riskier compared to available alternatives.2 Additionally, little is known about
how to manage adverse effects of AAROD in the ED setting. Here, we present a case
describing the emergent treatment of a patient with subarachnoid hemorrhage after
AAROD.
CASE REPORT
A 41-year-old male with history of opioid and cocaine use disorders was brought to
the ED after being found unresponsive at an opioid detoxification center. The day
prior to admission, the patient underwent an observed AAROD where he received
buprenorphine while undergoing general anesthesia. After completion of treatment the
patient was transferred to a local center where he was observed by onsite staff,
receiving as-needed benzodiazepines for any continued withdrawal symptoms.
Subsequently, the patient began to complain of a severe headache and ataxia and
exhibited agitated behavior. Early the following morning he was found unresponsive
and in respiratory distress. Emergency medical services administered naloxone
without a change in his condition. A laryngeal mask airway was placed, and he was
transported to the ED.Upon arrival, the patient’s vitals were heart rate 152 beats per minute,
blood pressure 162/101 millimeters (mm) of mercury, respiratory rate 64 breaths per
minutes, oxygen saturation 100% on 15 liters of oxygen via a nonrebreather,
and temperature 37.9 Celsius. The patient was diaphoretic and had a Glasgow Coma
Scale score of three. His head was atraumatic, and his pupils were 3 mm and reactive
bilaterally. He had significant upper airway secretions, and lung auscultation
revealed diffuse bilateral rhonchi. His peripheral pulses were bounding and his skin
was mottled and pale. There was no evidence of traumatic injury. After he failed to
improve with an additional dose of naloxone, the patient was sedated and
intubated.An initial electrocardiogram (ECG) revealed supraventricular tachycardia that failed
to convert with administration of multiple doses of adenosine. Initial labs were
notable for a pH of 7.17, lactic acid of 8.0 millimoles per liter (mmol/L)
(reference range: 0.5 – 2.0 mmol/L), white blood cell count of 37.1 billion
per liter (bil/L) (3.5 – 10.1 bil/L) with left shift, and troponin of 16.38
nanograms per milliliter (ng/mL) (<0.3 ng/mL). Chest radiograph was significant
for diffuse pulmonary edema. A non-contrast head computed tomography (CT) revealed
extensive subarachnoid hemorrhage and right temporal intraparenchymal hemorrhage
with 5 mm of midline shift. A CT angiogram revealed a 3-mm right internal carotid
artery aneurysm as the source of the bleeding. Treatment with continuous nicardipine
infusion was initiated, and neurosurgery placed an external ventricular drain in the
ED.The patient was admitted to the surgical intensive care unit for aneurysmal repair.
Further conversation with family indicated no family history suggestive of cerebral
aneurysmal disease or known preceding symptoms. His procedure, completed
successfully, was complicated by a four-minute episode of pulseless electrical
activity cardiac arrest. He subsequently developed a right middle cerebellar artery
infarct with evidence of herniation. With poor neurologic prognosis, the family
chose comfort measures, and the patient died on hospital day three.
DISCUSSION
Opioid use disorder in the United States remains at an all-time high, with
hospitalization rates increasing 219% between 1998 (58.9 per 100,000) and
2016 (190.7 per 100,000).1 Opioid
withdrawal is a complicated neurobiological interaction caused by the decreased
responsiveness of opioid receptors in the brain from chronic use. In the locus
coeruleus, periaqueductal gray and rostral ventromedial medulla the lack of mu
opioid response leads to an overwhelming surge of noradrenaline and other
monoamines.3 These surges
produce electrolyte derangements and respiratory alkalosis, which have been linked
to episodes of cardiac arrest and seizure in previous opioid withdrawal cases.4,5 Outside of opioid withdrawal, massive catecholamine
surges have been documented as possible precipitants of subarachnoid
hemorrhage.6 Historically,
treatment regimens focused on treating the acute sympathetic overdrive with alpha-2
agonists and benzodiazepines and weaning patients with long-acting opioid agonists
such as methadone and buprenorphine.7 However, concerns of limited availability and length of treatment have
continued to push researchers and clinicians to search for additional
strategies.8What do we already know about this clinical entity?Anesthesia-assisted rapid opioid detoxification (AAROD) is a rare
treatment method of opioid use disorder with reported significant procedural
complications.What makes this presentation of disease reportable?This is the first reported case in the literature of AAROD complicated by
subarachnoid hemorrhage.What is the major learning point?Treatment of AAROD complications is based on reducing opioid withdrawal
symptoms from the pathologic sympathetic surge while providing long-acting
opioid agonists.How might this improve emergency medicine practice?Early recognition and prompt treatment of AAROD complications may lead to
improved outcomes in these patients.In the 1990s, the combination of difficulties prescribing long-acting opioids and the
desire for a faster resolution of opioid withdrawal symptoms led clinicians to
investigate opioid withdrawal induction in conjunction with sedation.8 The method described, known as
AAROD, involves precipitating withdrawal using various opioid antagonists while
sedating or anesthetizing patients to mask withdrawal symptoms. Although
pre-procedure evaluations are not standardized, a general medical exam, blood work,
ECG, and urine drug screen are often employed.2 Patients are typically excluded if there has been
recent cocaine use or significant medical or psychiatric disease history.2 While initial studies did show the
effectiveness of AAROD in transitioning patients to opioid abstinence.9 over the 20 years of its use
additional concerns have been raised on the safety and efficacy of AAROD.10–12A randomized clinical trial examining AAROD vs buprenorphine and clonidine alone
found equivalent rates of opioid abstinence, while AAROD conferred significantly
increased patient risks such as acute psychiatric disturbances, cardiac arrhythmias,
and pulmonary edema.2 A 2013 report
from the US Centers for Disease Control and Prevention detailed one New York City
AAROD clinic where seven of 75 patients experienced serious adverse events requiring
hospitalization with two resultant deaths.10 Additionally, two Cochrane reviews found AAROD to be equally
effective compared to traditional treatment options but with significantly higher
mortality, out-of-pocket patient cost, and medicolegal risk; the reviews recommended
avoidance of the technique.11,12 Currently, only
methadone and buprenorphine have shown consistent evidence for effective treatment
of opioid use disorders, with superior rates of long-term opioid abstinence compared
to AAROD, abstinence alone, naltrexone, alpha agonists, and benzodiazepines.2,14 Yet numerous AAROD programs still exist across
the country.Clinicians should maintain a broad differential when approaching critically ill
patients after AAROD. Evaluations should focus on potential neurologic, cardiac,
electrolyte, and metabolic abnormalities. Reported complications from the procedure
include the following: those due to opioid withdrawal symptoms, such as vomiting,
diarrhea, hypovolemia and electrolyte abnormalities; those related to adverse
effects of the resultant catecholamine surge; and complications arising from general
anesthesia.4,5 Documented adverse outcomes of
AAROD include severe psychiatric disturbances, aspiration, cardiac dysthymias,
cardiac arrest, respiratory arrest and death.10–12In our literature review, we did not find any previously documented cases of
subarachnoid hemorrhage following AAROD. Management should focus on reducing
withdrawal symptoms, decreasing the catecholamine surge, and providing additional
supportive care as necessary. Clonidine has been used to reduce sympathomimetic
hyperactivity. Adding short-acting opioid analgesics or increasing the frequency of
long-acting opioids are additional options.13 Pain management, which can be complicated by the
type and level of opioid antagonist used in the AAROD procedure, can be achieved by
non-opioid means including intravenous acetaminophen, dexmedetomidine, and
gabapentin.15 Early
utilization of these management options may confer improved outcomes for critically
ill post-AAROD patients.
CONCLUSION
Anesthesia-assisted rapid opioid detoxification is an uncommon and controversial
procedure used to treat opioid use disorder. This case of subarachnoid hemorrhage
precipitated by AAROD to our knowledge represents the first such documented instance
in the literature. Clinicians seeing patients brought to the ED after AAROD should
be aware of the potential for serious complications as outlined here. Strategies for
managing AAROD complications focuses on supportive care while decreasing withdrawal
symptoms and sympathetic surge. In addition, clinicians should remain educated on
best practices of opioid use disorder management including methods for using and
referring for buprenorphine and methadone treatments.