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Neuropsychiatric Aspects of Hiv
Neuropsychiatric Aspects of Hiv
OF HIV/AIDS
PRESENTER: DR. N. MANJUSHA (2NDYR PG)
CHAIRPERSON: DR. K. NARASIMHA REDDI
(HOD)
SCHEME OF PRESENTATION :-
▪ INTRODUCTION
▪ EPIDEMIOLOGY
▪ ETIOLOGICAL AGENT
▪ ETIOLOGY AND CLASSIFICATION OF HIV/AIDS
▪ NEUROLOGICAL MANIFESTATIONS OF HIV
▪ PSYCHIATRIC MANIFESTATIONS OF HIV
▪ SPECIAL ISSUES IN HIV
▪ HIV SPECIFIC PSYCHOTHERAPEUTIC ISSUES
▪ CONCLUSION
▪ REFERENCES
INTRODUCTION :-
▪ The human immunodeficiency virus (HIV)
epidemic continues to be a major public health
problem > 20 years after the initial discovery of
the infection & of the routes by which it is
spread.
▪ Psychiatric disorders play a role in the epidemic
by increasing risk behaviour for infection &
decreasing access to treatment.
▪ HIV infection is an unfortunate consequence of
a defined set of behaviours that expose one
person to infectious body fluids from an already
infected person.
▪ Many of the behaviours that can result in HIV
infection are those that are associated with the
brain's reward systems.
▪ HIV: A retrovirus, previously called the human T-
cell lympho-tropic virus (HTLV).
▪ This virus infects cells important for the human
immune response, especially helper T cells, &
leaves its host vulnerable to opportunistic
infections.
▪ AIDS: A clinical syndrome defined by HIV
infection with certain associated signs & / or
symptoms, known as AIDS-defining conditions.
HISTORY :-
▪ One of the earliest documented HIV
infections was discovered in a preserved
blood sample taken in 1959 from a man
from Belgian Congo.
▪ In 1981 the AIDS epidemic was first
described in the medical literature, it was
in 1983 that the first articles were
published about the psychosocial /
psychiatric aspects of AIDS by Holtz &
colleagues.
▪ First psychiatrist to address these issues
was Stuart E. Nichols in his article in
Psychosomatics.
▪ HIV was originally recognized through a
series of case descriptions involving
young homosexual men with
Pneumocystis carinii (now Pneumocystis
jeroveci) pneumonia in the early 1980s in
Los Angeles.
EPIDEMIOLOGY :-
Category A includes :
▪ Bacillary angiomatosis
▪ Candidiasis , oropharyngeal (thrush)
▪ Candidiasis , vulvovaginal ; persistent,
frequent, / poorly responsive to therapy
▪ Cervical dysplasia (moderate or
severe)/cervical carcinoma in situ
▪ Constitutional symptoms, such as fever
(38.5°C) / diarrhea lasting >1 month
▪ Hairy leukoplakia, oral
▪ Herpes zoster (shingles), involving at least
two distinct episodes or more than one
dermatome
▪ Idiopathic thrombocytopenic purpura
▪ Listeriosis
▪ Pelvic inflammatory disease, particularly
if complicated by tubo-ovarian abscess
▪ Peripheral neuropathy.
Conditions Included as AIDS-Defining Illnesses
WHO Clinical Staging & Disease
Classification System
▪ Revised in 2007.
▪ Classifies HIV disease on the basis of clinical
manifestations that can be recognized &
treated by clinicians in diverse settings.
▪ It does not require a CD4 cell counts.
▪ This staging system is used in many countries to
determine eligibility for antiretroviral therapy,
particularly in settings in which CD4 testing is
not available.
NEUROLOGICAL COMPLICATIONS OF HIV
& AIDS
▪ Opportunistic infections
▪ CNS Neoplasms
▪ Direct CNS manifestations of HIV
▪ Peripheral Nervous system disorders
Opportunistic Infections :-
Toxoplasmosis
▪ Causative agent :- Toxoplasma gondii, a
protozoan acquired most commonly from
cat faeces / uncooked meat.
▪ Infection generally occurs in pts with <200
CD4 cells per microlitre.
Symptoms of CNS infection are:
▪ Fever
▪ change in level of alertness
▪ Headache
▪ focal neurological signs (approx 80 % of
cases)
▪ partial / generalized seizures (approx 30 % of
▪ CT & MRI scans usually show
multiple, ring-enhancing lesions
in the basal ganglia / at the
gray–white matter junction.
▪ P450 Inducers :-
nicotine/ cigarette smoking
carbamazepine
alcohol
▪ The nucleoside reverse transcriptase inhibitors
(NRTIs) are not metabolized significantly by the
P450 system, making them less vulnerable to
interactions with psychotropic medications.
▪ Zidovudine plasma levels, however, can be
increased by concurrent use of methadone/
valproic acid.
Antidepressants :-
▪ Interactions with anti-retrovirals are possible
with all selective serotonin reuptake inhibitors
by means of their potential to inhibit
cytochrome P450 enzymes.
▪ Because they are all metabolized by CYP
isoenzymes, there is the potential for increased
levels of selective serotonin reuptake inhibitors
when used in combination with enzyme
inhibitors.
▪ The combination of fluoxetine & ritonavir has
been shown to increase the concentration of
ritonavir.
▪ In a series of 5 cases of serotonin syndrome in
patients taking fluoxetine & antiretrovirals, the
most common culprit was ritonavir, which was
believed to increase fluoxetine levels.
▪ Fluvoxetine & paroxetine may cause toxicity
by increasing levels of protease inhibitors.
▪ Fluvoxamine may also cause toxicity through
increased levels of protease inhibitors.
▪ The role of TCAs in treating HIV-infected
patients is based on long-term experience
with them & the potential for capitalizing on
their side effects.
▪ For instance, a patient with AIDS who has
stomach distress from HAART, chronic
diarrhoea, & depression may benefit from
treatment with a TCA.
Benzodiazepines :-
▪ Of the benzodiazepines, alprazolam,
midazolam, & triazolam are dependent on CYP
3A4 for metabolism.
▪ Potent inhibitors of this CYP isoform , such as
ritonavir , can decrease clearance of these
drugs and result in over-sedation and possibly
death.
▪ The benzodiazepines oxazepam, lorazepam,
and temazepam are metabolized by
glucuronidation.
▪ Drugs that increase the activity of
glucuronidatioan, such as ritonavir or nelfinavir,
may lower the levels of these drugs.
▪ Additionally, the use of midazolam, along with
delavirdine (as well as protease inhibitors) may
increase its effect and lead to over-sedation.
Antipsychotics :-
▪ CYP inhibitors have the potential to
increase the concentration of the
antipsychotics, clozapine, & pimozide.
▪ For this reason, these drugs have been
contraindicated with anti-retrovirals with
CYP inhibition, such as ritonavir .
▪ In addition, the potential for toxicity
increase by CYP inhibitors exists in other
antipsychotics, including
chlorpromazine, haloperidol, olanzapine,
& risperidone .
CONCLUSION :-
▪ HIV & AIDS are closely related to
psychiatry with the infection giving rise to
many psychiatric problems & psychiatric
illnesses leading to risk of acquiring HIV.
▪ Hence the approach to such a situation
must be holistic with good coordination
b/w medical specialists & psychiatrists,
psychologists to bring maximum possible
benefit to people with such a difficult
illness.
References :-
▪ CTP-10th Edition.
▪ Lishman’s Organic Psychiatry 4th
Edition.
▪ Internet Articles.