CAPÍTULO XVII De las bajas de alumnos
SECCIÓN CUARTA Usuarios
Withdrawal Symptoms
Te sudden stopping of opioids after prolonged use or
Te sudden stopping of opioids after prolonged use or
intake of opioid antagonists like naltrexone can produce
intake of opioid antagonists like naltrexone can produce
withdrawal
withdrawal symptomssymptoms. . Te Te short-term short-term use use of of opioidsopioids
decreases the activity of noradre
decreases the activity of noradrenergic neurons and thenergic neurons and the
long-term use results in compensatory hyperactivity.
long-term use results in compensatory hyperactivity.
When opioids
When opioids are suddenly are suddenly stopped, there stopped, there are symptomsare symptoms
of rebound noradrenergic hyperactivity. Tis hypothe-
of rebound noradrenergic hyperactivity. Tis hypothe-
sis also explains the mechanism of action of clonidine
sis also explains the mechanism of action of clonidine
(alpha-2 adrenergic receptor agonist, which decreases
(alpha-2 adrenergic receptor agonist, which decreases
norepinephrine release) in management of opioid with-
norepinephrine release) in management of opioid with-
drawal.
drawal.
Te
Te withdrawal withdrawal symptoms symptoms usually usually appear appear aroundaround
6–8 hours
6–8 hoursQQafter the last dose, peak during the secondafter the last dose, peak during the second
or third day and subside during the next 7–10 days. Te
or third day and subside during the next 7–10 days. Te
withdrawal from
withdrawal from opioids opioids produces produces aaflu-like syndromeflu-like syndromeQQ
with
with the the following following symptomssymptoms..
1.
1.LacrimationLacrimationQQ,,rhinorrhearhinorrheaQQ, sweating,, sweating,diarrheadiarrheaQQ
2.
2. Ya Yawning wning and and piloerectionpiloerectionQQ
3.
3.Pupillary dilationPupillary dilationQQ
4. M
4. Muscle cramps and generalized bodyauscle cramps and generalized bodyacheche
5.
5.InsomniaInsomniaQQ, anxiety, hypertension and tachycardia, anxiety, hypertension and tachycardia
6. N
6. Nausea, vomiting and anorexia.ausea, vomiting and anorexia.
Treatment
Treatment
A.
A.DetoxificationDetoxification: In this stage, the main focus is on: In this stage, the main focus is on
the manage
the management of withdrawal symptoms. Tement of withdrawal symptoms. Te
medications used are usually long acting opioids like
medications used are usually long acting opioids like
methadone
methadoneQQ oror buprenorphinebuprenorphine. Both medications,. Both medications,
in view of their agonist action at opioid receptors,
in view of their agonist action at opioid receptors,
suppress the withdrawal symptoms. Other opioids
like dextropropoxyphene can also be used. Usually
like dextropropoxyphene can also be used. Usually
detoxification medicines are required for 2-3 weeks.
detoxification medicines are required for 2-3 weeks.
Another method
Another method is use ofis use ofclonidineclonidineQQ for detoxification. for detoxification.
However, clonidine provides considerably less reduction
However, clonidine provides considerably less reduction
in symptoms in comparison to buprenorphine or metha-
in symptoms in comparison to buprenorphine or metha-
done. Clonidine is thus mostly used as an adjunct to
done. Clonidine is thus mostly used as an adjunct to
methadone or buprenorphine during detoxification.
methadone or buprenorphine during detoxification.
Accelerated
Accelerated detoxificationdetoxification: In this method, initially low: In this method, initially low
doses of naltrexone is given to patient. Naltrexone being
doses of naltrexone is given to patient. Naltrexone being
an opioid antagonist, produces severe withdrawal symp-
an opioid antagonist, produces severe withdrawal symp-
toms. After that, clonidine is used to control the symp-
toms. After that, clonidine is used to control the symp-
toms. Tis method reduces the detoxification period to
toms. Tis method reduces the detoxification period to
4-5 days.
4-5 days.
B.
B.Maintenance treatment Maintenance treatment : It follows the detoxification: It follows the detoxification
and the aim is to prevent the relapse. Tere are two
and the aim is to prevent the relapse. Tere are two
different pharmacological approaches for mainte-
different pharmacological approaches for mainte-
nance phase.
nance phase.
•
• Opioid substitution therapy Opioid substitution therapy : In this method, the: In this method, the
illicit, parenterally administered and short acting
illicit, parenterally administered and short acting
opioids (like heroin) are
opioids (like heroin) are replaced by medically safe,replaced by medically safe,
orally taken and long acting opioids. Te long act-
orally taken and long acting opioids. Te long act-
ing opioids such as
ing opioids such asmethadonemethadone, buprenorphine are, buprenorphine are
mostly used. Levo alpha acetylmethadol was also
mostly used. Levo alpha acetylmethadol was also
used in past, however it has since been stopped as
used in past, however it has since been stopped as
it is known to cause torsades de pointes.
it is known to cause torsades de pointes.
Tese
Tese orally orally used used opioids opioids are are given given at at govern-govern-
ment approved centres. Tough the patient conti-
ment approved centres. Tough the patient conti-
nues to remain depen
nues to remain dependent, however he is protecteddent, however he is protected
from medical consequence of parenteral opioids
from medical consequence of parenteral opioids
(like HBV, HIV infection) and does not need to
(like HBV, HIV infection) and does not need to
indulge in cri
indulge in criminal activities to fund the illicit opi-minal activities to fund the illicit opi-
oid use.
oid use.
•
• Opioid antagonist treatment Opioid antagonist treatment :: NaltrexoneNaltrexoneQQ can be can be
given to the patient after detoxification is complete.
given to the patient after detoxification is complete.
Te rationale is that naltrexone will block the opi-
Te rationale is that naltrexone will block the opi-
oid receptors and any opioid use would fail to pro-
oid receptors and any opioid use would fail to pro-
duce the euphoric response and hence would not
duce the euphoric response and hence would not
be repeated.
be repeated.
• Nonpharmacological approaches like cognitive
• Nonpharmacological approaches like cognitive
behavioral therapy, narcotic anonymous (12 step
behavioral therapy, narcotic anonymous (12 step
self help groups), family therapy and group therapy
self help groups), family therapy and group therapy
are also useful.
are also useful.
C.
C.Overdose treatment Overdose treatment : Te opioids are lethal in over-: Te opioids are lethal in over-
dose. Te drug of choice for treatment of opioid over-
dose. Te drug of choice for treatment of opioid over-
dose is i.v.
dose is i.v.naloxonenaloxoneQQ(short acting opioid antagonist).(short acting opioid antagonist).
CANNABIS
CANNABIS
Cannabis is derived from the hemp plant,
Cannabis is derived from the hemp plant, cannabiscannabis sativa
sativa. Te plant has several varieties named after the. Te plant has several varieties named after the
regions where it is found (e.g. cannabis sativa indica in
regions where it is found (e.g. cannabis sativa indica in
India, cannabis sativa americana in USA). Cannabis is
India, cannabis sativa americana in USA). Cannabis is thethe
most commonly used illegal drug
most commonly used illegal drug QQ in the world and in in the world and in
India. Te street names include joints, marijuana, grass,
India. Te street names include joints, marijuana, grass,
pot, weed, etc.
pot, weed, etc.
Te
Te active active ingredient, ingredient, which which is is responsible responsible for for thethe
psychoactive effects of cannabis is
psychoactive effects of cannabis is dd-9 tetrahydrocan--9 tetrahydrocan-
nabinol (HC)
nabinol (HC)QQ. Te various preparations of cannabis. Te various preparations of cannabis
includes.
includes.
Table 2:
Table 2: THC concentration in various cannabis preparations. THC concentration in various cannabis preparations.
C Caannnnaabbiis s pprreeppaarraattiioonn TTHHC C ccoonntteennt t ((%%)) B Bhhaanng (g (ddeerriivveed fd frroom m ddrriieed ld leeaavveess)) 11 Ga Gannjja (a (ddeerriivveed fd frroom im innflfloorreesscceennccee)) 11––22
Hashish/Charas (derived from resinous
Hashish/Charas (derived from resinous
exudates) exudates) 8–14 8–14 Ha Hash sh oioil (l (lilipipid sd sololububle le plplanant et extxtraractct)) 1515–4–400
Te cannabis can be ingested orally or is more com-
Te cannabis can be ingested orally or is more com-
monly smoked. It is unsuitable for
monly smoked. It is unsuitable for intravenous use becauseintravenous use because
of poor solubility in water and risk of anaphylaxis due to
of poor solubility in water and risk of anaphylaxis due to
undissolved particulate matter.
undissolved particulate matter.
Intoxication
Intoxication
It is characterized by euphoria, subjective sense of
It is characterized by euphoria, subjective sense of
slowing of time, sense of floating in air,
slowing of time, sense of floating in air, reddening ofreddening of
conjunctiva
conjunctivaQQ (due to dilatation of conjunctival blood (due to dilatation of conjunctival blood
vessels),
vessels), increased appetiteincreased appetite and dryness of mouth. and dryness of mouth.
Other symptoms include depersonalization, derealiza-
Other symptoms include depersonalization, derealiza-
tion,
tion,synesthesiasynesthesiaQQ (cross over of sensory perceptions. For (cross over of sensory perceptions. For
example, patient may report that he is
example, patient may report that he is “seeing” music and“seeing” music and
“hearing” lights).
“hearing” lights).
Sometimes,
Sometimes, after after consumption consumption of of cannabis, cannabis, the the per-per-
son might feel restless, fearful, extremely anxious (similar
son might feel restless, fearful, extremely anxious (similar
to panic attack) and may feel that he is about to go crazy.
to panic attack) and may feel that he is about to go crazy.
Tis unpleasant experience is known as
Tis unpleasant experience is known as“bad trip”“bad trip”QQ..
Withdrawal Symptoms
Withdrawal Symptoms
It was earlier believed that cannabis doesn’t cause physi-
It was earlier believed that cannabis doesn’t cause physi-
cal dependence and produces no withdrawal symptoms,
cal dependence and produces no withdrawal symptoms,
however recent studies have shown that there are mild
however recent studies have shown that there are mild
withdrawal symptoms
withdrawal symptoms within within 1-2 1-2 weeks weeks of of cessation andcessation and
include insomnia, anxiety, decreased appetite, irritability,
include insomnia, anxiety, decreased appetite, irritability,
etc.