Professional Documents
Culture Documents
DISUSUN OLEH:
Kevin Fidiasrianto
PEMBIMBING:
dr. Dharmadi Agus, Sp.KJ
About 275 million people worldwide (5.6 per cent of the global population
aged 15–64 years) used drugs at least once during 2016. Overdose deaths contribute
to between roughly a third and a half of all drug-related deaths. Approximately one in
ten people who use illicit drugs is suffering from a form of a drug use disorder,
including drug dependence. Almost half of people with drug dependence inject drugs
and of them more than 10% are living with HIV, and the majority are infected with
hepatitis C. Drug use disorders are a major global health problem. Drug use disorders
are a serious health issue, with a significant burden for individuals affected and their
families. There are also significant costs to society including lost productivity,
security challenges, crime, increased health care costs, and a myriad of negative
social consequences. The social cost of illicit drug use is estimated at up to 1.7% of
GDP in some countries (World Drug Report, 2016). Caring for individuals with drug
use disorders places a heavy burden on public health systems of Member States and
therefore improving treatment systems by making them the best they can be. This
would undoubtedly benefit not only the affected individuals, but also their
communities and the whole society. Unfortunately, outdated views about drug use
disorders persist in many parts of the world. Stigma and discrimination that is
commonly applied to drug dependent individuals and to professionals working with
them have significantly compromised the implementation of quality treatment
interventions in this area, undermining the development of treatment facilities, the
training of health professionals and the investment in recovery programs. Even
though the evidence clearly shows that drug use disorders are best managed within a
public health system, similarly to other medical problems such as HIV infection or
hypertension, the inclusion of addiction treatment in the health care system is still
very difficult in many countries where a huge gap exists between science, policy and
the clinical practice. In some countries drug use disorders are still seen as a primarily
criminal justice problem, and agencies of the Ministry of Interior, Ministry of Justice
or Ministry of Defense are still responsible for affected individuals, without the
supervision or engagement of the Ministry of Health. Using only law enforcement
strategies and methods is unlikely to result in sustained positive effects. Only
treatment that has at its core an understanding of drug dependence as a primarily
multifactorial biological and behavioral disorder, that can be treated using medical
and psychological approaches, can improve chances of a recovery from the disorder
and reduce (drug-) related consequences.
CHAPTER 2 : LITERATURE REVIEW
Opioid overdose
Due to their effect on the part of the brain which regulates breathing, opioids in high
doses can cause respiratory depression and death. An opioid overdose can be
identified by a combination of three signs and symptoms referred to as the “opioid
overdose triad”. The symptoms of the triad are:
pinpoint pupils
unconsciousness
respiratory depression.
Combining opioids with alcohol and sedative medication increases the risk of
respiratory depression and death, and combinations of opioids, alcohol and sedatives
are often present in fatal drug overdoses.
Because of their capacity to cause respiratory depression, opioids are responsible for
a high proportion of fatal drug overdoses around the world. The number of opioid
overdoses has increased in recent years, in part due to the increased use of opioids in
the management of chronic non-cancer pain. In the United States of America alone in
2016, there were an estimated 63 632 deaths due to drug overdose, which is a 21%
increase from previous years. This was largely due to a rise in deaths associated with
prescription opioids. This group of opioids (excluding methadone) was implicated in
19 413 deaths in the country, more than double the number in 2015.
Emergency responses to opioid overdose
Death following opioid overdose is preventable if the person receives basic life
support and the timely administration of the opioid antagonist naloxone. Naloxone,
which is effectively an antidote to opioid overdose, will completely reverse the
effects of an opioid overdose if administered in time. Naloxone is effective when
delivered by intravenous, intramuscular, subcutaneous, and intranasal routes of
administration. Naloxone has virtually no effect in people who have not taken
opioids.
2. Alcohol
As with all emergency patients, initial treatment should focus on the airway,
breathing, and circulation. Gastric decontamination is rarely necessary for any of the
alcohols. An exception to this may be a patient who presents immediately after
ingestion of a toxic alcohol in whom one might reasonably expect to be able to
recover a significant amount of the toxin via aspiration through a nasogastric tube.
Treatment of ethanol and isopropanol intoxication is largely supportive. [1] Because of
the hemorrhagic gastritis that can follow isopropanol ingestion, H2 blockade or
proton-pump inhibitors may be helpful. Hemodialysis, while effective, is rarely
indicated, and should only be used in the setting of profound hemodynamic
compromise. [9]
If ethylene glycol overdose is suspected, the patient should also receive 100
mg of intravenous thiamine every 6 hours and 50 mg of pyridoxine every 6 hours.
The purpose of the thiamine and pyridoxine is to shunt metabolism of glyoxylic acid
away from oxalate and favor the formation of less toxic metabolites.
Ethanol infusions are not only labor intensive, but once the costs of the
frequent blood glucose and serum ethanol level assays are accounted for, ethanol
antidotal therapy is frequently more expensive than fomepizole. Ethanol has also
[7]
been associated with more frequent adverse reactions than fomepizole. Thus,
because of the lower overall cost and the ease of administration and safety
considerations, fomepizole has become the preferred antidote for methanol or
ethylene glycol poisoning. [8]
Signs and symptoms of MDMA intoxication manifest across multiple body systems
and includes :
The TTM posits that individuals move through six stages of change:
precontemplation, contemplation, preparation, action, maintenance, and termination.
Termination was not part of the original model and is less often used in application of
stages of change for health-related behaviors. For each stage of change, different
intervention strategies are most effective at moving the person to the next stage of
change and subsequently through the model to maintenance, the ideal stage of
behavior.
Treatments for prescription drug abuse tend to be similar to those for illicit drugs
that affect the same brain systems. For example, buprenorphine, used to treat heroin
addiction, can also be used to treat addiction to opioid pain medications. Addiction to
prescription stimulants, which affect the same brain systems as illicit stimulants like
cocaine, can be treated with behavioral therapies, as there are not yet medications for
treating addiction to these types of drugs.
Many treatment programs employ both individual and group therapies. Group
therapy can provide social reinforcement and help enforce behavioral contingencies
that promote abstinence and a non-drug-using lifestyle. Some of the more established
behavioral treatments, such as contingency management and cognitive-behavioral
therapy, are also being adapted for group settings to improve efficiency and cost-
effectiveness. However, particularly in adolescents, there can also be a danger of
unintended harmful (or iatrogenic) effects of group treatment—sometimes group
members (especially groups of highly delinquent youth) can reinforce drug use and
thereby derail the purpose of the therapy. Thus, trained counselors should be aware of
and monitor for such effects. Because they work on different aspects of addiction,
combinations of behavioral therapies and medications (when available) generally
appear to be more effective than either approach used alone.
Finally, people who are addicted to drugs often suffer from other health (e.g.,
depression, HIV), occupational, legal, familial, and social problems that should be
addressed concurrently. The best programs provide a combination of therapies and
other services to meet an individual patient’s needs. Psychoactive medications, such
as antidepressants, anti-anxiety agents, mood stabilizers, and antipsychotic
medications, may be critical for treatment success when patients have co-occurring
mental disorders such as depression, anxiety disorders (including post-traumatic
stress disorder), bipolar disorder, or schizophrenia. In addition, most people with
severe addiction abuse multiple drugs and require treatment for all substances abused.
PHARMACOTHERAPIES
Opioid Addiction
Tobacco Addiction
1. Nicotine Replacement Therapy (NRT) A variety of formulations of
nicotine replacement therapies (NRTs) now exist, including the
transdermal nicotine patch, nicotine spray, nicotine gum, and nicotine
lozenges. Because nicotine is the main addictive ingredient in tobacco, the
rationale for NRT is that stable low levels of nicotine will prevent
withdrawal symptoms—which often drive continued tobacco use—and
help keep people motivated to quit. Research shows that combining the
patch with another replacement therapy is more effective than a single
therapy alone
2. Bupropion (Zyban®) was originally marketed as an antidepressant
(Wellbutrin). It produces mild stimulant effects by blocking the reuptake
of certain neurotransmitters, especially norepinephrine and dopamine. A
serendipitous observation among depressed patients was that the
medication was also effective in suppressing tobacco craving, helping
them quit smoking without also gaining weight. Although bupropion’s
exact mechanisms of action in facilitating smoking cessation are unclear,
it has FDA approval as a smoking cessation treatment.
3. Varenicline (Chantix®) is the most recently FDA-approved medication
for smoking cessation. It acts on a subset of nicotinic receptors in the brain
thought to be involved in the rewarding effects of nicotine. Varenicline
acts as a partial agonist/antagonist at these receptors this means that it
midly stimulates the nicotine receptor but not sufficiently to trigger the
release of dopamine, which is important for the rewarding effects of
nicotine. As an antagonist, varenicline also blocks the ability of nicotine to
activate dopamine, interfering with the reinforcing effects of smoking,
thereby reducing cravings and supporting abstinence from smoking.
Alcohol Addiction
1. Naltrexone blocks opioid receptors that are involved in the rewarding
effects of drinking and the craving for alcohol. It has been shown to
reduce relapse to problem drinking in some patients. An extended
release version, Vivitrol—administered once a month by injection—is
also FDA-approved for treating alcoholism, and may offer benefits
regarding compliance
2. Acamprosate (Campral®) acts on the gamma-aminobutyric acid
(GABA) and glutamate neurotransmitter systems and is thought to
reduce symptoms of protracted withdrawal, such as insomnia, anxiety,
restlessness, and dysphoria. Acamprosate has been shown to help
dependent drinkers maintain abstinence for several weeks to months,
and it may be more effective in patients with severe dependence.
3. Disulfiram (Antabuse) interferes with degradation of alcohol, resulting
in the accumulation of acetaldehyde, which, in turn, produces a very
unpleasant reaction that includes flushing nausea, and palpitations if a
person drinks alcohol. The utility and effectiveness of disulfiram are
considered limited because compliance is generally poor. However,
among patients who are highly motivated, disulfiram can be effective
and some patients use it episodically for high-risk situations, such as
social occasions where alcohol is present. It can also be administered
in a monitored fashion, such as in a clinic or by a spouse, improving
its efficancy.
4. Topiramate is thought to work by increasing inhibitory (GABA)
neurotransmission and reducing stimulatory (glutamate)
neurotransmission, although its precise mechanism of action is not
known. Although topiramate has not yet received FDA approval for
treating alcohol addiction, it is sometimes used off-label for this
purpose. Topiramate has been shown in studies to significantly
improve multiple drinking outcomes, compared with a placebo.
BEHAVIORAL THERAPIES
1. Kraut JA, Kurtz I. Toxic alcohol ingestions: clinical features, diagnosis, and
management. Clin J Am Soc Nephrol. 2008 Jan. 3(1):208-25.
2. Brent J, McMartin K, Phillips S, et al. Fomepizole for the treatment of
ethylene glycol poisoning. Methylpyrazole for Toxic Alcohols Study Group.
N Engl J Med. 1999 Mar 18. 340(11):832-8.
3. Brent J, McMartin K, Phillips S, et al. Fomepizole for the treatment of
methanol poisoning. N Engl J Med. 2001 Feb 8. 344(6):424-9.
4. Burns MJ, Graudins A, Aaron CK, et al. Treatment of methanol poisoning
with intravenous 4-methylpyrazole. Ann Emerg Med. 1997 Dec. 30(6):829-32.
5. Megarbane B, Borron SW, Baud FJ. Current recommendations for treatment
of severe toxic alcohol poisonings. Intensive Care Med. 2005 Feb. 31(2):189-
95.
6. Lepik KJ, Levy AR, Sobolev BG, Purssell RA, DeWitt CR, Erhardt GD.
Adverse drug events associated with the antidotes for methanol and ethylene
glycol poisoning: a comparison of ethanol and fomepizole. Ann Emerg Med.
2009 Apr. 53(4):439-450.e10. .
7. Thanacoody RH, Gilfillan C, Bradberry SM, Davies J, Jackson G, Vale AJ, et
al. Management of poisoning with ethylene glycol and methanol in the UK: a
prospective study conducted by the National Poisons Information Service
(NPIS). Clin Toxicol (Phila). 2016. 54 (2):134-40.
8. Ghannoum M, Hoffman RS, Mowry JB, Lavergne V. Trends in toxic alcohol
exposures in the United States from 2000 to 2013: a focus on the use of
antidotes and extracorporeal treatments. Semin Dial. 2014 Jul. 27(4):395-401.
9. Slaughter RJ, Mason RW, Beasley DM, Vale JA, Schep LJ. Isopropanol
poisoning. Clin Toxicol (Phila). 2014 Jun. 52(5):470-8.
10. [Guideline] Caravati EM, Erdman AR, Christianson G, Manoguerra AS,
Booze LL, Woolf AD, et al. Ethylene glycol exposure: an evidence-based
consensus guideline for out-of-hospital management. Clin Toxicol (Phila).
2005. 43 (5):327-45.