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َّ ِ الر ْح
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INFECTIOUS DISEASE
THANKS BY DR: SHAAFI
LUCTURE: HIV INFECTION AND AIDS
• ASSIGMENT GROUP A
• GROUP NAMES……..
• HUSSEIN HASHIM NOR [LEADR]
• ABDULLAHI OSMAN ABDI
• ABDULLAHI HABIB HSJI
• ABDISAMAD MOHAMED ABDI
• SALIM ABDULLAHI MOHAMED
1:ABDULLAHI HABIIB HAJI [DR HABIIB CADDE]
PULMONARY TUBERCULOSIS
BACTERIAL PNEUMONIA
MISCELLANEOUS CAUSES OF PULMONARY INFILTRATES
NERVOUS SYSTEM AND EYE DISEASE
COGNITIVE IMPAIRMENT
SPACE-OCCUPYING LESIONS
STROKE
MENINGITIS
1. Pulmonary tuberculosis
Tuberculosis is the most common cause of admission in
countries with a high tuberculosis incidence. Pulmonary
tuberculosis in patients with mild immune suppression
typically presents as in HIV-uninfected patients, with a
chronic illness and apical pulmonary cavities (p. 518).
However, in patients with CD4 counts below 200
cells/mm3 , there are four important differences in the
clinical presentation of pulmonary tuberculosis:
Tuberculosis progresses more rapidly, with a subacute or even acute presentation. The
diagnosis therefore needs to be made and therapy commenced promptly. A trial of
empirical therapy is often justifed while awaiting the results of mycobacterial cultures.
The chest X-ray appearance alters: cavities are rarely seen, pulmonary infiltrates are
no longer predominantly in apical areas, and pleural effusions and hilar or
mediastinal lymphad.
Sputum smears, which are positive in most HIV-uninfected adults with pulmonary
tuberculosis, are negative in more than half of patients. The main reason for this is the
absence of pulmonary cavities.
Many patients have disseminated tuberculosis, sometimes with a classic miliary pattern
on chest X-ray, but more commonly presenting with atypical pulmonary infiltrates
together with extrapulmonary tuberculosis. The most common sites of concomitant
extrapulmonary tuberculosis are the pleura and lymph nodes. A rapid diagnosis can be
made with the urine lipoarabinomannan lateral flow assay.
Initial Chest x-ray showing pulmonary infiltrates in the right lung
especially in the right mid and lower lung zones indicative of pulmonary
edema.
2. Bacterial pneumonia
The incidence of bacterial pneumonia is increased about 100-fold by HIV
infection. The severity, likelihood of bacteraemia, risk of recurrent pneumonia
and mortality are all increased compared with HIV-negative patients. The
aetiology is similar to that of community-acquired pneumonia in HIV-uninfected
patients with comorbidity: S. pneumonia is the most common cause, followed by
Haemophilus influenzae, Enterobacterales (e.g. Klebsiella pneumoniae) and
Staphylococcus aureus.
The prevalence of atypical bacteria in PLWH with pneumonia is
similar to that in the general population. Treatment is with a broad-spectrum β-
lactam (e.g. ceftriaxone, amoxicillin–clavulanate), with the addition of a
macrolide if the pneumonia is severe)
Typical Bacterial Pneumonia Imaging
Pneumocystis pneumonia: typical chest X- chest X-ray of pulmonary tuberculosis in advanced HIV infection.
ray appearance. Note the interstitial Lower-zone iniltrates and hilar or mediastinal nodes in a patient with a
bilateral infiltrate. CD4 count of < 200 cells/mm3
3. Miscellaneous causes of pulmonary infltrates
5. Cognitive impairment
HIV-associated neurocognitive disorders HIV is a neurotropic virus
and invades the CNS early during infection. Meningoencephalitis may
occur at seroconversion. PLWH often have abnormalities on
neuropsychiatric testing. The term HIV-associated neurocognitive
disorder (HAND) describes a spectrum of disorders:
6. Space-occupying lesions
Space-occupying lesions in AIDS patients typically present over days to weeks. The most
common cause is toxoplasmosis. As toxoplasmosis responds rapidly to therapy, a trial of
anti-toxoplasmosis therapy should be given to all patients presenting with space-occupying
lesions while the results of diagnostic tests are being awaited.
7. Stroke
There is a higher incidence of stroke in patients with HIV disease. Atherosclerosis is
accelerated by the presence of inflammation due to the immune response to HIV, which is not
completely suppressed by ART, and by dyslipidaemia caused by some antiretroviral drugs.
HIV vasculopathy, which is thought to be a vasculitis, can also cause a stroke. It is important
to exclude tuberculous meningitis and meningovascular syphilis in all PLWH who present
with a stroke.
8. Meningitis
Cryptococcal meningitis
Trials in patients not on ART showed that preventive therapy, either with isoniazid or
combinations of rifamycins with isoniazid, reduces the risk of tuberculosis only in PLWH
with a positive tuberculin skin test. The usual duration of isoniazid preventive therapy is 6
months. Rifampicin or rifapentine combined with isoniazid for 12 weeks has been shown to
be at least as effective as 6–12 months of isoniazid.
32. Immunisation
There are significant problems associated with vaccination in HIV infection. First, vaccination
with live organisms is contraindicated in patients with severe immune suppression. Secondly,
immune responses to vaccination are impaired in PLWH (people living with HIV). If the CD4
count is below 200 cells/mm3 , then immune responses to immunisation are poor. Therefore,
it is preferable to wait until the CD4 count has increased to more than 200 cells/mm3 on ART
before immunisation is given; this is essential if live virus vaccines are used. All patients
should be given a conjugate pneumococcal vaccine and annual influenza vaccination.
Hepatitis B vaccination should be given to those who are not immune.