Title: Alcohol Withdrawal Syndromes
1Alcohol Withdrawal Syndromes
2Case Presentation
- 43 y/o AAM with a hx, HTN, and long term ETOH
abuse, who presented to the Urology service after
being seen in the ED for Hematuria, and being
diagnosed with a renal mass. He was 1 day s/p
nephrectomy. He was on epidural pain medications
per pain control. He was reported to be agitated
when the nursing staff evaluated him.The
3Case Presentation
- The Urology team evaluated the patient and after
realizing that he had not had a drink in 36 hours
they called for a Medicine consult for management
of DTs.
4Definitions
- Alcoholism chronic alcohol abuse, dependence, or
addiction chronic excessive drinking of
alcoholic beverages resulting in impairment of
health and/or social or occupational functioning,
and increasing adaptation to the effects of
alcohol requiring increasing doses to achieve and
sustain a desired effect specific signs or
symptoms of withdrawal are usually shown on
sudden cessation of such drinking. - Alcoholic One who suffers from alcoholism. One
who abuses or is dependent on alcohol (Stedmans
26th ed.)
5Alcoholism in the United States
- Alcoholism is a common condition, with
complications that will eventually confront all
clinicians. - Estimated 10-18 million Alcoholics in the U.S. in
1990. - 15-20 of hospitalized and primary care patients.
- Studies show that b/w 13 and 71 percent of
patients develop symptoms of ETOH withdrawal
6Various Presentations of Acute ETOH Withdrawal
- Minor Withdrawal Symptoms
- -occur w/i 6 hours of cessation
- -insomnia, tremulousness, mild anxiety, GI upset,
diaphoresis, HA, palpitations, and anorexia. - -usually resolve w/i 24-48 hrs.
- -vary from episode to episode
7Various Presentations of Acute ETOH Withdrawal
- Withdrawal Seizures
- -w/i 48 hours of last drink
- -generalized tonic-clonic
- -3 of chronic alcoholics develop this
- -3 of those who seize develop Status Epilepticus
8Various Presentations of Acute ETOH Withdrawal
- Alcoholic Hallucinosis
- - 12- 24 hr. onset after last drink
- - usually visual
- - Resolve w/i 24-48 hr.
- - NOT synonymous with DTs
- other signs may or may not be present
- time course is different
- not usually associated with clouding of the
sensorium
9Various Presentation of Acute ETOH Withdrawal
- Delirium Tremens
- - 5 of patients who withdraw
- - typically begin b/w 48 and 96 hours
- - typically last 1-5 days
- - longer periods requiring massive doses of
medications have been described (Wolf et. Al 1993)
10Delirium Tremens
- - Early figures of associated mortality were as
high as 37 - - Now mortality is felt to be 5. This is likely
due to earlier diagnosis, improved
pharmacological, and non-pharmocologic
management, and improved treatment of co-morbid
conditions.
11Delirium Tremens
- -Mortality risk is greater
- 1. Elderly
- 2. Concomitant lung Dz
- 3. Core body temp 104
- 4. Co-existing liver Dz.
- - Death is usually due to arrhythmia or secondary
complications. (pneumonia,liver failure)
12DT Risk Factors
- History of sustained drinking
- Previous DTs
- 30
- Greater number of days since last drink
- Presence of other illnesses
13Hallmarks of DTs
- Hallucinations
- Disorientation
- Tachycardia
- Hypertension
- Low Grade Fever
- Agitation
- Diaphoresis
14Hallmarks of DTs
- Elevated cardiac indices, oxygen delivery and
oxygen consumption - Hyperventilation and Respiratory alkalosis which
result in reduced cerebral blood flow - Sensorium Clouding
15Other Char. Of Delirium Tremens
- Fluid and electrolyte concerns
- Hypokalemia is common
- Hypomagnesemia - may predispose to sz. Activity
- Hypophosphatemia - may be present and contribute
to heart failure and rhabdomyolysis.
16Non-Pharmacological Management Principals
- PT should be closely monitored
- -Ideally a quiet and protective setting, unless
pt. Is at higher risk for complications, then
they should be in a ICU. - Frequent evaluation by nursing AND medical staff
- Other conditions may mimic DT infection, OD,
trauma, hepatic failure, GIB
17Non-Pharmacological Management Principals cont.
- Appropriate diagnostic testing LP, CMP,
Cultures etc. - Mechanical Restraints in the swimmers position
for pt. Protection - Correction of volume and Electrolyte deficits
- Thiamine, MVT, Folate given regularly
18Pharmacological Management
19Pharmacological Management
- Working Group on Pharmacological Management of
Alcohol Withdrawal - - JAMA July 9,1997
- - Goal was to establish evidence based
guidelines for the treatment of Alcohol
withdrawal syndromes -
20Working Group Outcomes Studied
- 1. Severity of withdrawal syndrome
- 2. Alcohol Withdrawal Delirium
- 3. Withdrawal Seizures
- 4. Completion of withdrawal
- 5. Entry into Rehab
- 6. Cost
21Working Group on ETOH Withdrawal Syndromes cont.
- Prospective controlled trials with documented
reporting of the endpoint in question were
investigated further. - Available literature that addressed one of the
clinical endpoints listed were assimilated and
reviewed to formulate the pharmacological
guidelines.
22CIWA-Ar
- Clinical Institute Withdrawal Assessment -
revised version (CIWA-Ar) - - Structured Severity Assessment Scale
- -Objective Scale for use by health care personel
to evaluate patients at risk for developing
alcohol withdrawal syndromes, and quantify the
severity of withdrawal.
23CIWA-Ar
- Well documented reliability, reproducibility, and
validity when based on comparison with ratings by
experienced clinicians - First used in ETOH detox, and psychiatric units
- Studies have proven usefulness in general
medical/surgical wards
24CIWA-Ar
- High scores are predictive of development of
seizures and delirium!! - Scale is currently being used with strict
protocalls for medication administration at many
non-teaching facilities - Using the CIWA-Ar was found to reduce patient
effect from over-sedation cost of hospitalization
by avoiding unnecessary use of medications
25CIWA-Ar
26Dosing of Pharmacological Agents
- Dosing Schedules which are acceptable
- 1. Fixed - most useful in high risk pts.
- 2. Symptom Triggered - Based on certain
CIWA-Ar scores. - 3. Front Loaded - Auto taper method. Not in
Working Group Recommendations, but supported by
other studies
27Working Group Recommendations on Choice of Agent
- -Benzodiazepines recommended
- 1. Long acting may be more effective in
controlling seizures - 2. Long acting contributes to smoother withdrawal
and less rebound - 3. Short acting have lower risk of oversedation
28Working Group on ETOH Withdrawal Syndromes cont
- 4. Certain Benzos have higher potential for abuse
- 5. Cost varies considerably
29Working Group Recommendations
- 1. Mild Symptoms (CIWA-Ar score option is non-pharmacological supportive therapy
and cont. monitoring. - Moderate Symptoms (score 8-15) symptomatic
administration of medications, with hourly
assessment. Regimen recommended - 1.Librium 50-100 mg
- 2.Valium 10-20 mg
- 3.Ativan 2-4 mg.
30Dosing of Pharmacological Agents
- Severe Symptoms (score 15) - Provide Fixed
scheduled medications in the amounts necessary to
control symptoms. Regimen Recommended - 1.Librium50 mg q 6 hrs. x 4 doses then 25 mg q
6 hrs. x 4 doses - 2.Valium 10 mg q 6 hrs. x 4 doses then 5 mg q
6x 8 doses - 3.Ativan 2 mg q 6 x 4 doses then 1 mg q6 x 8
doses. - Additional PRN dosing if necessary
31Dosing of Pharmacological Agents
- 2. For pts. With a hx of Sz. Provide 1 of the
proposed fixed regimens on presentation,
regardless of the severity of withdrawal. - (monitoring and symptomatic tx is reasonable)
- 3. Early treatment of those with severe
co-morbidities is warranted.
32More Recent Evidence on DT Management
- Pts. In DTs should receive IV diazepam 5-10 mg
every 5 minutes until pt. Is awake but calm. - Continue parenteral administration of Diazepam
until pt. Is no longer delirious and absorption
from gut is reliable.
33Other Agents Examined
- Beta Blockers, clonidine, and Carbamazepine - Not
to be used as mono-therapy because they do not
protect against delirium or seizures - Neuroleptics - Only in conjunction with benzos
for hallucinations. May increase seizures - Magnesium - not recommended
- Ethyl ETOH - NOT recommended due to lack of
controlled studies and well known adverse effects - Thiamine - Administer at initial evaluation.
34Back to Our Case
- Pt. was seen by the internal medicine consult
team. He was found to be mildly sedated from pain
medicines but would answer questions. He had mild
pain from incision site, but otherwise had no
tremors, nausea, diaphoresis, or signs of
anxiety/agitation. He had no visual or auditory
hallucinations. Physical exam was benign.
35Case Presentation
- The CIWA-Ar score was used in assessing the
patient, and he was found to have a CIWA-Ar of 0.
The urology team was notified of findings and a
copy of the CIWA-Ar scale was applied to his
chart.
36Summary
- ETOH withdrawal is a common problem facing
internists - Has a wide range of presentations
- DTs, being the most severe form must be treated
as a medical emergency with monitoring, frequent
pt. assessment, and both pharmacological and
non-pharmacological strategies
37Summary
- Clinical assessment tools, such as the CIWA-Ar
are useful and should be considered when
assessing pts who ETOH withdrawal is suspected
in, to help guide medication administration. - Clinical guidelines exist for medical treatment
of withdrawal and should be followed