Addiction Flashcards

1
Q

How would you define substance misuse? What are important aspects of a substance abuse Hx?

A

A pattern of substance use causing physical, mental, social or occupational dysfunction. ICD10 definitions vary by substance and type of disorder

Current Use:

  • > [TRAP] - Type, routes, amount and pattern
  • > Dependency
  • > Effect on life
  • > Past use
  • > Future use
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2
Q

What is withdrawal and what substances cause physical withdrawal?

A

Withdrawal = transient state whilst re-adjusting to lower levels of a drug in the body

Physical withdrawal only with: Alcohol, opiates and benzodiazepines

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3
Q

What is the epidemiology of substance misuse?

A

Males&raquo_space; Females

  • > 2x M for alcohol
  • > 4x M for substance

5.4% prevalence for alcohol and 14.6% for drug misuse (3% for dependence)

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4
Q

What are features of dependency according to ICD10?

A

Dependence syndrome = at least 3/+ of the below together in the last month

  • Tolerance (inc amount to get same effect)
  • Craving
  • Withdrawal (symptoms)
  • Problems controlling use
  • Continued use despite harm
  • Salience/primacy
  • Narrowing repetoire (loss of variation in use of substance)
  • Reinstatement after abstinence

‘SN RaW TUCH’

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5
Q

What are the normal and risk-stratified levels of alcohol consumption?

A

Normal - shouldn’t exceed over 14 units per week for M+F

Low risk = <14 units/week
Hazardous = 15-25 units/week
Harmful (alcohol misuse) = >35 units/week (i.e. >6 units a day)

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6
Q

What is the aetiology and epidemiology of alcohol abuse?

A

2:1 of males > females
5.4% lifetime prevalence
1% UK drink harmfully

Bio - genetics, ethnicity (E.Asians have lower dependency rates due to enzyme deficiency) and psychiatric illness (PDs, mania, depression, social phobia/anxiety)

Psychosocial - occupation (publicans, Drs, armed forces), social background, co-morbid psychiatric disorders

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7
Q

How may someone with alcohol dependence present?

A

Sx:

  • > Intoxication
  • > Withdrawal:
  • 4-12h after last drink = course tremor, sweating, insomnia, psychomotor agitation, anxiety, tachycardia, N&V, hallucinations (tactile, auditory)
  • ~36h (6-28h) = peak incidence of grand-mal/generalised tonic-clonic seizures
  • 48-72h - Delirium Tremens = disorientation, anterograde amnesia, Liliputian hallucinations of little people/animals, worse at night/fluctuations by hour, if severe then may have heavy sweating, fear, paranoid delusions, fever, sudden V collapse
  • > Dependence syndrome
  • > Psychotic disorder = alcoholic hallucinosis (auditory hallucinations, often persecutory derogatory), Liliputian hallucinations, morbid jealousy (delusion that partner is unfaithful)
  • > Amnesia = anterograde i.e in Korsakoff syndrome
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8
Q

What is one unit of alcohol?

A
unit = %ABV x volume/1000
OR
8g pure ethanol
OR
[amount of alcohol to be metabolised in 1h]
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9
Q

How would you Ix someone with a concerning alcohol history?

A

Ix:

  • > Full history (timeline) and physical exam (sx disease)
  • > Bedside obs
  • > SCREENING = CAGE screening (2/+ positive answers indicates further investigation*)
  • > Rating scale: 1st line, screening = AUDIT (alcohol use disorders identification test) - score >20 then do full assessment, 2nd line = SADQ (severity and dependence), FAST is the first 4Qs of AUDIT, often used in A&E (3/+ is positive), CIWA for withdrawal, APQ for nature and extent of problems from alcohol misuse

–> CAGE = have you tried to CUT down, have you ever been ANNOYED when someone criticises your drinking, have you ever felt GUILTY about drinking and have you ever needed a drink to get you going in the morning (EYE opener)?

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10
Q

How would you manage a patient generally for alcohol abuse+ what would warrant admission?

A

Mx:

  • Start by triaging the patient using AUDIT
  • MDT approach
  • Identify risks (driving, co-dependents, work)
  • Triage to admission detox regiment or community management
  • –> ADMISSION = acute alcohol withdrawal or Wernicke’s encephalopathy (ataxia, ophthalmoplegia, confusion)
  • —> Specialist management (alcohol addiction service) if less serious signs of dependence
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11
Q

How would you manage a patient with acute alcohol withdrawal? Acute vs Chronic, inpatient vs community, detox mx…?

A

Inpatient/Home depending on level of dependency:

  • > Inpatient = >30units a day or >30 on SADQ, PMH of epilepsy, DT, withdrawal-related seizures
  • > Community-based assisted withdrawal = >15units/day or >20 on AUDIT - have 2-4 meetings/week for up to 3w

Withdrawal regimen then progress to detox management:
-> Manage expectations that detox will be worst in first 48h and DON’T stop abruptly
-> Acute treatment (up to 7d)
= Inpatient: oral lorazepam +/- IV/IM Thiamine/Pabrinex on rapid reducing dose
= Community: oral chlordiazepoxide +/- IV/IM Thiamine/Pabrinex on reducing dose
** IF hypoglycaemic, give dextrose AFTER pabrinex as can precipitate Sx
-> Chronic treatment (after 7d - Detox management)
1st line = acamprosate or naltrexone
2nd line = disulfiram
+ Individualised psychosocial intervention plan:

BIOPSYCHOSOCIAL model for detox management^^:
Bio = Acamprosate (removes craving but increasing GABA) or Naltrexone (reduces high of alcohol) -> Difulfiram (causes bad hangover Sx as an irreversible acetaldehyde dehydrogenase inhibitor)

Psychosocial = FRAMES* intervention + Support (CGL, AA, Smart recovery), 1st line = motivational interviewing (establish goals, explore beliefs, encourage self-efficacy), 2nd line = psychosocial interventions like CBT, couples therapy, residential abstinence centres e.g. if homeless for max 3m

For those presenting with:

  • Alcohol withdrawal seizures (~36h) = IV lorazepam on rapid reducing dose
  • DT (48-72h) = Oral lorazepam AND IV/IM Thiamine/pabrinex
  • Wernicke’s (confusion, ophthalmoplegia, ataxia) = IV/IM Thiamine/Pabrinex

FRAMES = advice on drinking:
- feedback - responsibility - advice - menu - empathy - self-efficacy

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12
Q

What are some complications of alcohol abuse?

A

Bio:

  • Wernicke’s encephalopathy (reversible) due to B12 deficiency –> triad of ataxia, ophthalmoplegia, confusion (treated with IV/IM Pabrinex/Thiamine, if not can lead to …
  • Korsakoff’s psychosis (irreversible) –> anterograde+retrograde amnesia, confabulation, peripheral neuropathy, cerebellar degeneration
  • Liver disease, Varices + GI disease, pancreatitis
  • Seizures, dementia
  • Cancer - bowel, breast, oesophageal
  • HTN, cardiomyopathy
  • FAS in pregnancy

Psychological:

  • Depression, mania, anxiety disorder, psychosis, SH
  • Delusions and hallucinations
  • amnesia
  • Cognitive impairment

Social:

  • Family and relationship breakdown
  • Job loss/unemployment
  • Child neglect/abuse
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13
Q

What is the prognosis of alcohol abuse?

A

40% die prematurely
30% have lifelong alcohol problems
30% have favourable outcome

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14
Q

What are some types of opiate abuse? How do they exert their effect?

A

Opiates - from Papaver somniferum; types include:

  • HEROIN (brown, smack, skag, horse, gear)
  • Pethidine
  • Morphine, diamorphine, codeine, dihydrocodeine

Heroin is a mu opiate agonist –> immediate euphoria, diminished pain, detachment

ROA:

  • Smoking
  • Sniffing/snorting
  • Oral
  • IV (note complications like cellulitis, abcess, sepsis, IE and BBV, emboli and DVT)
  • IM/SC
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15
Q

What are some signs and symptoms of opiate abuse - intoxication (+OD), withdrawal and complications?

A

Sx:

Complications:
= DVT, IE and BBV such as HepC, cellulitis and abcesses, emboli, sepsis

Intoxication:

  • -> Euphoria and warmth -> sedation and bradycardia
  • -> Overdose = miosis/pinpoint pupils and low RR (Tx = IV NALOXONE)
  • -> Low dose SE = constipation, anorexia, decreased libido

Withdrawal symptoms:

  • Starts 6h after injection, peak at 36-48h, lasts 5-7d
  • Common sx = goosebumps, mydriasis, runs (D&V, lacrimation, rhinorrhoea), craving, insomnia, agitation, flu-like (fever, aches, cramps)
  • RARELY life-threatening
  • Due to noradrenergic storm
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16
Q

What Ix would you do in someone with opiate abuse?

A

Ix:

  • Full Hx and physical exam
  • Bedside obs
  • UDS (2d in urine)
  • Bloods = FBC (anaemia/infection), U&Es (malnutrition), LFTs (pre-meds), BBV tests (HBV, HCV, HIV)
  • Contact key worker before prescribing replacement opiates (note: opiate IV pain management does NOT increase relapse rates)
17
Q

How would you manage opiate abuse?

A

Mx:
- Similar to alcohol in that you triage for admission/treatment and MDT approach - D&A services:

According to NICE:

  • Appoint a key worker and develop a care plan (agree recovery goals and progress)
  • Harm reduction (vaccines and virus testing, needle-exchanges for IVDU as unlikely to get complete abstinence)
  • Health education (SMART recovery, NA, sleep hygiene and support)
  • Family/carer assessment
  • Discuss if they want to undergo an opioid substitution therapy (OST) ‘withdrawal’ OR ‘maintenance’ programme
  • -> 1st maintenance where goal is to stabilise lifestyle and reduce harm
  • -> 2nd detoxification where goal is abstinence and detox
  • -> For OST, admission may be necessary as give in a controlled environment for 3-6m and then if suitable, given some take-home medications:

Maintenance:
1st line = methadone (green liquid) or buprenophine (sub-lingual)
- if still using heroin, low dose methadone
- if wanting to stop heroin, high dose methadone or buprenoprhine
- offer naloxone for take-home and how to use

Detoxification:
MUST be committed to stopping, stable environment and on stable OST maintenance
- lasts 12w as an outpatient (4w inpatient)
- notify that they will lose tolerance if they start again so they should take a lot less
1st line = methadone or buprenophine + offer naloxone for home if needed
2nd line = Lofexidine (if rapid detox/mild dependence)
- Ultra-rapid detoxing regimens are not pleasant but exist (use naloxone)

Withdrawal symptom medications = clonidine, lofexidine, anti-diarrheals, anti-emetics

FOLLOW UP with drugs and alcohol service for at least 6m

  • look for withdrawal signs
  • check other drug use
  • ECG (QTc for those on methadone)
  • CBT to reduce relapse chance
  • Contingency management through frequent screenings (incentives for negative UDS)

Other types of detoxification = ultra rapid (<24h w GA - NOT offered), rapid (1-5d w moderate sedation - consider if pt requests) and accelerated detoxification (no sedation)–> uses naltrexone/naloxone (opioid antagonists)

18
Q

What is the active agent in cannabis + what are some other terms for it?

A

Cannabis has delta-9-tetrahydrocannabinol

Terms: grass/weed, hash, skunk and sinsemilla are strong types (w skunk the most commonly used)

19
Q

What are some signs of cannabis use?

A

Sx depend on expectations and original mood state:

  • > Spectrum ranges from euphoria and relaxation to paranoia, anxiety and panic
  • > Perceptual and time distortion
  • > Hunger
  • > Nausea and vomiting
20
Q

How would one use cannabis + what is the half-life?

A

Smoking - quicker onset, peaks at 30m, lasts 2-5h

PO - slower onset, lasts longer

21
Q

How would you Ix and Mx someone using cannabis? What are some complications?

A

Ix:
-> UDS (up to 4w)

Mx:

  • > Abstinence in those with major mental illness
  • > Irregular use can be free from major problems

Complications

  • > Use in developing years can cause schizophrenia
  • > Acute - can precipitate psychotic episode
  • > Chronic - anxiety/depressive illness, dysthymia
  • > NO physical dependency but mild withdrawal syndrome in heavy users (insomnia, anxiety, irritability)
22
Q

What are hallucinogens? Give 4 examples and how they act?

A

Hallucinogens produce a psychological (heightened perception, illusions) and physiological (dilated pupils, peripheral vasoconstriction, increased temperature) but no dependence

LSD - affects dopamine and 5-HT receptors, taken via ‘tabs’ –> euphoria/perceptual changes and trips lasting up to 12h

PCP (Phencyclidine, angel dust) - associated with violent outburst and ongoing psychosis, taken via liquid or powder which is snorted/smoked

Ketamine (special K) - similar structure to PCP, anaesthetic effect that can lead to unknowingly SH, small doses = disassociation, larger = hallucinations, synaethesia

Magic mushrooms (liberty cap) - eaten raw or drunk, small doses = euphoria, larger = euphoria (similar to LSD). Tolerance develops quickly so continued use is unlikely

23
Q

How may someone present on hallucinogens?

A

Sx:

  • Euphoria
  • Perceptual changes - hallucination, visual illusions, depersonalisation, derealisation
  • Synaesthesia (e.g. hear a smell)
  • Behavioural toxicity - acting on drug-induced beliefs i.e. being able to fly
  • SEs of drugs:
  • -> LSD: acute = due to behavioural toxicity, chronic = flashbacks, anxiety, depression
  • -> PCP: seratonergic/cholinergic (confusion, violence)
  • -> Ketamine: large amounts = nausea, ataxia, slurred speech
  • -> MM: behavioural toxicity, accidental poison consumption
24
Q

How would you manage hallucinogen use?

A

Mx:

  • > Health education
  • > Harm reduction (needle exchanges, vaccines/testing for BBV for other IVDU)
  • > Short term withdrawal relief as an inpatient with benzodiazepines
25
Q

What are stimulant drugs and give some examples and how they act?

A

Potentiate neurotransmission and increase cortical excitability –> increased alertness, endurance, reduced need for sleep + confidence

Cocaine

  • AKA Charlie, coke, snow
  • ROA = intranasal, IV

Crack cocaine

  • AKA rocks, base, freebase
  • ROA = concentrated smokeable form
  • Causes an immediate, extreme high but wears off quickly (5-10mins)
  • Highly addictive

Amphetamine

  • AKA speed
  • ROA = IV, PO, intranasal
  • Withdrawal meds include dexamphetamine

Khat

  • AKA Quat, chat
  • Mild stimulant, used in E. African communities
  • Causes psychosis

Ecstasy

  • AKA MDMA, E (3,4-methylenedioxymethamphetamine)
  • Causes 5HT release and blocks reuptake
  • Hallucinogenic + stimulant properties
  • Initial 3h rush, bruxism, agitation received by dancing/movement
  • hangover at 24-48h (fatigue, anorexia, depressed mood)
26
Q

How may someone on stimulants present? What are some SE’s of specific stimulant drugs?

A

Sx:

  • Increased alertness, endurance and confidence
  • Risky behaviour
  • Unpleasant ‘crash period’
  • No dependence apart from amphetamines

SEs:
–> Cocaine:
[acute] = arrhythmia, intense anxiety, HTN, impaired judgement
[chronic] = septal necrosis, foetal damage, delusions and psychosis, panic and anxiety , no dependence but can become ‘habit’
–> Amphetamines:
[acute] = tachycardia, arrhythmia, hyperpyrexia, irritability, post-use depression, quasi-psychotic state with visual, auditory and tactile hallucinations, v regular use associated with dependence
–> Ecstasy:
[acute] = increased sweating, nausea, vomiting, diminished potency despite increased libido, death associated with dehydration and hyperthermia

27
Q

How may someone who is undergoing cocaine withdrawal present?

A

Occurs in 2 stages:
[1] Crash phase - from 3h: depression, exhaustion, agitation and irritability
[2] Withdrawal - lasting 1-10w: cravings, irritability, anergia, poor concentration, insomnia, slowed movements

28
Q

How would you Ix and Mx someone with stimulant abuse?

A

Ix:

  • Full drug Hx and physical examination for signs of disease/chronic use
  • UDS (cocaine can last in urine for 5-7d)
  • Bloods - FBC for infection, BBV and HIV testing?

Mx:

  • Health education (support, + family and social help, NA)
  • Harm reduction (needle exchanges, BBV testing)
  • Short term withdrawal symptom relief can be provided with BDZ as an inpatient
29
Q

What are BDZ used for normally and what are the short-term and long-term risks of their use?

A

Uses of BDZ = sedation, hypnotic, anxiolytic, anticonvulsant, muscle relaxant (enhances GABA transmission)

Should only be used for a short time (2-4w)

Risks of BDZ use
[short-term] = drowsiness, reduced concentration
[long-term] = cognitive impairment, WORSENING OF anxiety and depression, DEPENDENCE, sleep disruption

30
Q

How may someone present with BDZ i) misuse ii) overdose and iii) withdrawal ?

A

i) Misuse
- Similar to alcohol; calm and mild euphoria
- Slurred speech, ataxia, stupor

ii) OD
- Respiratory depression, low GCS, low BP, mydriasis, hyporeflexia
- Tx = IV flumazenil

iii) Withdrawal
- Similar to alcohol; ANXIETY, tremor, insomnia, palpitations + tachycardia/tachypnoea, delusions, depersonalisation, irritably, hyperreflexia, ataxia, sweating, mydriasis, depression and anterograde amnesia, tinnitus, seizures
- Sudden withdrawal may present with a DT-like picture!!

31
Q

How would you Ix and Mx BDZ withdrawal and abuse?

A

Ix:

  • Full Hx and physical exam (neuro - reflexes, ataxia)
  • Hx –> use of BDZ, where from, how often/dose
  • Obs (HR, BP, RR)

Mx:
-> Address underlying need for BDZ (anxiety, sleep, depression) and the long term complications of use (cognitive impairment, anxiety, depression, insomnia)
-> Check willingness to withdraw and whether this can be done in primary care
-> Withdrawal Mx:
2 methods=
[1] Slow dose reduction
[2] Switch to equivalent dose of Diazepam and slow dose reduction (preferred: used in those on short-acting, potent BDZ such as lorazepam, and difficulty with physically tapering dose)
–> Withdraw 1/8th daily dose reduction every 2w
-> Advice:
- If done properly, there will be few, if any, withdrawal SEs
- Anxiety is the most common SE and is normal; treat with conservative mx such as relaxation/breathing techniques
- May take 3m-1y or longer
- Assess driving risk as can’t drive on certain amounts of BDZ (DONT drive if feeling drowsy)
- Offer CBT

**EG 1/8th daily dose reduction every 2 weeks – e.g. diazepam 40 mg per day:
• Reduce dose by 5 mg every 2 weeks until reaching 20 mg per day -> 8 weeks
• Reduce dose by 2 mg every 2 weeks until reaching 10 mg per day -> 10 weeks
• Reduce dose by 1 mg every 2 weeks until reaching 5 mg per day -> 10 weeks
• Reduce dose by 0.5 mg every 2 weeks until completely stopped -> 20 weeks
THEREFORE Estimated total withdrawal time = 30–60 weeks

NOTE: short acting BDZ e.g. lorazepam, long-acting e.g. chlordiazepoxide, diazepam

32
Q

How many people smoke in the UK and what is an indicator for abstinence?

A
  1. 7% of UK smoke

- > A CO level of =/< 10ppm indicates abstinence from smoking (5-9ppm)

33
Q

How would you manage smoking cessation? Conservative and Pharmacological?

A

Mx:

  • > Very brief advice (given anytime and anywhere)
  • ask about current and past smoking behaviour
  • Provide written AND verbal information on RISKS (cancer, CLD i.e. bronchitis, COPD, hospital admissions) and BENEFITS of stopping (whatever time you stop its beneficial, cost saving, health)
  • Advise options for smoking cessation like behavioural support and medication: refer to local cessation service if they wish to stop
  • If they don’t want to quit, enquire to a harm reduction policy i.e. use of NRT as most problems attributed to tobacco smoke, not nicotine and these NRTs provide nicotine slowly and less-addictively than smoking
  • > 1st line = ADVICE
  • Behavioural support and medication is best for stopping
  • Set a quit date and commit to it
  • First few days are most difficult, may experience withdrawal, but passes by 3-4d

-> 2nd line = MEDS
[] NRT varies on preference, but can’t prescribe in combination with medications. Types = lozenges, mouth spray, patches
- Start on agreed quit date
- 24h patches useful is smoking shortly after waking, on combined NRT so the patch is for ‘background craving’

[] Varenicline

  • Partial nicotine receptor agonist
  • Dose = 1mg BD, titrated up from 500mcg OD over 1w
  • Started 7-14d before quit date, whilst still smoking
  • Contraindicated in those <18y and those with renal disease

[] Buproprion
- Weak but selective DA and NA reuptake inhibitor
- 150mg BD, titrated up from 150mg OD over 1w
- Max use for 7-9w, then discontinue
Started 7-14d before quit date, whilst still smoking
- Contraindicated in those <18y, eating disorders, BPAD, cirrhosis, CNS disorders and seizures

DO NOT RECOMMEND E-CIGARETTES as unclear health impact

  • > Follow up - 2w if on NRT, 3-4w if on medications
  • Measure CO levels 4w after quitting
  • Check progress and withdrawal sx
  • If relapse/partial release then encourage and set new quit date