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HIV Guide
 Zambia HIV National Guidelines
 


Introduction  

HIV Counseling and Testing  

Sexually Transmitted Infections (STIs)  

General Principles of Antiretroviral Therapy for Chronic HIV Infection in Adults and Adolescents  

When to Start ARV Therapy for Chronic HIV Infection in Adults and Adolescents  

Initial Regimen for ARV Therapy  

Adherence  

Baseline evaluation and Monitoring  

Calculations: Ideal Body Weight, Body Mass Index and Creatinine Clearance  

ARV Therapy for Individuals with Tuberculosis Co-Infection  

Adverse Effects and Toxicity  

Immune Reconstitution Inflammatory Syndrome (IRIS)  

Changing or Stopping ART  

Treatment Failure  

Stopping ARV Therapy  

Post Exposure Prophylaxis  

Cotrimoxazole Prophylaxis  

WHO Staging in Adults and Adolescents  

Nutrition Care and Support  

Palliative Care in HIV and AIDS  

 Guide Editors
 Editor In Chief
    Joel E. Gallant, MD, MPH

Pharmacology Editor
    Paul Pham, PharmD, BCPS

Zambia Guideline Team
   Peter Mwaba MMed PhD FRCP
   Alywn Mwinga MMed
   Isaac Zulu MMed MPH
   Velepie Mtonga MMed
   Albert Mwango MBChB
   Jabbin Mulwanda MMed FCS
 

 

 

Pathogens>Bacteria>
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Neisseria gonorrhoeae

Khalil G. Ghanem, M.D.
02-14-2008

  • All patients with gonorrhea should be offered routine counseling and testing for HIV infection.
  • Dx based on syndromic presentation; Cx, hybridization probes, NAATs not routinely available. 
  • Recent report from S. Africa found resistance to penicillin: 16%; tetracycline: 36%; ciprofloxacin: 7%. 
  • Rates of resistance not published for Zambia; uinolone resistance has risen elsewhere in the world but not well-documented in Africa.
  • Recommended Rx in Zambia: Adults -  ciprofloxacin 500 mg PO x1; Pregnancy -  spectinomycin 2g IM x1; Children and adolescents (<17 yrs old) - spectinomycin 40 mg/kg IM x1 (maximum of 2g).
  • Alternative Rx in Zambia: Adults - spectinomycin 2g IM x1 OR cefixime 400 mg PO x1; Pregnancy - cefixime 400 mg PO x1 OR ceftriaxone 250 mg IM x1; Children and adolescents (<17 yrs old) - ceftriaxone 125 mg IM x1 (if > 45 kg, use adult dose) OR cefixime 8 mg /kg PO x1 (if > 45 kg, use adult dose).
Zambia Information Author: David Riedel, M.D.

MICROBIOLOGY

  • Non-motile, non-spore-forming, gram-negative diplococcus
  • Infects cuboidal & columnar epithelium leading to a vigorous PMN response.
  • Selective growth media (Thayer-Martin & New York City) most common; Cx still considered standard in Dx of GC infection in settings that can process specimens appropriately. Swabs from urethral, cervical, rectal, pharyngeal, & ocular sites can be Cx'd.
  • Non-amplified molecular testing, including EIA & DNA hybridization probes, are most commonly used Dx methods. Cervical & urethral swabs can be tested.
  • Nucleic acid amplification tests (NAATs), including PCR, strand displacement assay (SDA), & transcription-mediated amplification (TMA), may be performed on urethral swabs, cervical swabs, urine, & self-collected vaginal swabs.

CLINICAL

  • Sx in men: acute urethritis (purulent urethral discharge, dysuria) is predominant manifestation; incubation 2-7d; 10% of epididymitis in young men due to GC; asymptomatic infection less common than in women (up to 30%)
  • Sx in women: asymptomatic (up to 90% in some studies); vaginal discharge, dysuria, spotting. PID is serious complication of ascending infection.
  • Anorectal: May be only site of infection in up to 40% of MSM & 5% of women. Sx may include tenesmus, purulent discharge, & rectal bleeding, though most asymptomatic.
  • Disseminated GC infection (DGI): asymmetrical migratory polyarthritis (knees, elbows), tenosynovitis, & dermatitis (hemorrhagic papules/pustules); blood Cx positive in 50%; >80% of mucosal Cx are positive; joint fluid findings: >50,000 PMNs & Cx usually positive.
  • Gram stain (urethra) >90% sensitive in symptomatic men, less sensitive (40-60%) in women (endocervical site) & asymptomatic men (~50-70% sens); NAATs have >95% sensitivity & ~99% specificity in both symptomatic & asymptomatic pts.
  • NAATs from oropharyngeal or rectal sites not currently FDA licensed; Cx is standard diagnostic test.

SITES OF INFECTION

  • GU: urethritis, epididymitis, cervicitis, Skene's & Bartholin's gland infections, endometritis, salpingitis, pelvic peritonitis & tubo-ovarian abscess.
  • CV: DGI ; endocarditis (rare)
  • GI: gingivitis (rare), pharyngitis, proctitis, & perihepatitis (Fitz-Hugh-Curtis syndrome).
  • Musculoskeletal: osteomyelitis (rare) & septic arthritis
  • Eyes: conjunctivitis.
  • CNS: meningitis (very rare)

TREATMENT

Drug Resistance

  • ~18% of strains in the U.S. resistant to PCN, TCN, or both.
  • Fluoroquinolone-resistant N. gonorrhoeae (FQRNG) strains are widespread in Asia, Pacific islands (Hawaii), California, England, & Wales.
  • Increase in FQRNG in men who have sex w/ men (MSM) throughout U.S. in 2003 (~5% of isolates among MSM) .
  • Increase in azithromycin resistance in the past several years (~3% in 2002)
  • Cephalosporin (ceftriaxone and cefixime) resistance in U.S. very low.
General Principles

  • Prevention: condoms highly effective at preventing transmission.
  • Treatment recommendations for HIV-infected pts similar to uninfected pts.
  • Single dose therapy is preferred.
  • PCN & TCN should not be used
  • FQs should not be used to treat pts who have traveled (or whose partners have traveled) to areas w/ high rates of FQRNG (see above)
  • FQs should not be used to treat infections in MSM
  • Treat for concomitant Chlamydia trachomatis infection with doxycycline 100 mg PO bid x 7d OR azithromycin 1 g PO x1 dose unless Chlamydia definitively ruled out by NAATS.
Antimicrobial Therapy

Drug Comments

DrugRecommendations/Comments
Azithromycin 1 g used for co-treatment of C. trachomatis not adequate for GC. 2 g dose FDA-approved for GC but cost and high rate of GI distress limit clinical applicability.
Ceftriaxone No clinically significant resistance to ceftriaxone documented in U.S.
Ciprofloxacin Not to be used in MSM or in pts who have traveled to California, Hawaii, or Asia.
Spectinomycin Less effective cure rates for oropharyngeal GC.

FOLLOW UP

  • No test of cure necessary after Rx
  • Repeat NAATs should not be performed within 2 wks after Rx as persistent nucleic acid can give false-positive results.
  • All sex partners in past 60 d should be tested and treated presumptively if follow-up uncertain.
  • Persistent Sx despite adequate therapy & no re-exposure warrants Cx with susceptibility testing
  • Outpatient Rx of PID warrants F/U within 72 hrs to ensure clinical improvement.

OTHER INFORMATION

REFERENCES

REFERENCED WITHIN THIS GUIDE


 
Diagnosis
 


Complications of Therapy


Malignancies


Miscellaneous


Opportunistic Infections


Organ System

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Antimicrobial Agents


Antiretrovirals


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Guidelines
 


Zambia HIV National Guidelines

Management
 


Antiretroviral Therapy


Laboratory Testing


Miscellaneous

Pathogens
 


Bacteria


Fungi


Parasites


Viruses

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