Question 7 from the second paper of 2001 asks the candidates to list some drug withdrawal states which might be encountered in the ICU, and to list the principles of their management. The LITFL page on drug withdrawal states in the ICU is a good brief introduction, and closely resembles the college model answer. Greater detail than that is probably undesirable, as it may lead the candidate into confusion and despair. However, that is what we do here at Deranged Physiology.
Generally speaking, this topic is poorly covered in the critical care literature. One can find isolated articles dealing with alcohol or opiates, but little in the way of a broad overview. Even Oh's Manual fails to address this issue. The best resource for this seems to be Goldfranks' Manual of Toxicologic Emergencies (2007), where Chapter 15 deals with principles of withdrawal management. In this summary, I will use the structure offered by this resource; it cleverly organises its withdrawal syndromes by the receptor being affected. Another textbook chapter of note is Withdrawal Syndromes (Ch. 70) from the Ford's Clinical Toxicology (2001). These two chapters were used to compile the table below, and ensuing discussion of management principles. Of the published articles I have managed to scrape together, the most detailed seems to be Tetrault and O'Connor's "Substance abuse and withdrawal in the critical care setting" (Critical care clinics, 2008).
| Receptor system |
Drugs | Clinical withdrawal syndrome | Management options |
| GABAA | Alcohol Barbiturates Benzodiazepines Organic solvents |
CNS excitation (agitation, tremor, hallucinations, delirium, seizures) Autonomic stimulation (tachycardia, hypertension, hyperthermia, diaphoresis) |
Benzodiazepines Dexmedetomidine |
| GABAB | GHB Baclofen |
Dyskinesia, seizures, hypertension, hallucinations, psychosis, and coma. | Benzodiazepines |
| Opioid | Opiates | Diarrhoea, mydriasis, nausea, yawning, lacrimation, rhinorrhoea and piloerection. Increased autonomic sympathetic activity. Importantly, there is no seizures, fever, or altered mental status. |
Clonidine Dexmedetomidine |
| Adenosine | Caffeine | Head-ache (cerebral vasodilation), fatigue, and hypersomnia (motor inhibition) | - |
| Nicotinic acetylcholine receptor |
Nicotine | Agitation, insomnia, poor concentration, poor gut motility, poor feed tolerance. | Varenicline? |
| Noradrenenaline | Amphetamines | Agitation, dysphoria, somnolence | - |
| Dopamine | Cocaine | Anhedonia, irritability, exhaustion | - |
| Cannabinoid | Cannabis | Agitation, insomnia, poor gut motility | Mirtazapine ? |
In this context, "prevention" is not some sort of grassroots social work movement to gets the kids off their street drugs, but rather the push towards intelligent use of opiates and benzodiazepines in the ICU. Rationalising the infusions should prevent the development of iatrogenic withdrawal syndromes. Fortunately, the ICU environment typically does not favour true psychological addiction, as the pleasurable context of drug use is not present.
In this context, detection describes vigilant monitoring for drug withdrawal:
The supportive management of drug withdrawal aims to reduce the harm from the physiological and psychological consequences of withdrawal:
The aim is to replace the drug of addiction with a less harmful substance which offers submaximal receptor stimulation, so that the symptoms of withdrawl are ameliorated and the harm of pursuing the addiction is reduced. Examples of this include methadone and varenicline.