4th Pediatric Infectious Diseases Conference
 
 
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Pedi Poll
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Should teicoplannin, colistin be used in case of neonatal sepsis where culture does not reveal any organism_?
No, it should be used only after drug sensitivity report
Yes, under guidance of an infectious disease expert
POST-EXPOSURE PROPHYLAXIS (PEP)
Post Exposure Prophylaxis(PEP)
PEP Occupational Exposure Management Resources
Occupational Exposure Management Resources
Dr Tripti Pensi
Professor of Pediatrics, Dr.R.M.L Hospital, New Delhi

Continued...

Considerations in initiating anti-retroviral therapy for PEP
Physicians considering the initiation of anti-retroviral therapy in an attempt to reduce the risk for HIV infection in an exposed person should take the following steps in consultation with an expert in the use of anti-retroviral agents:


  • Evaluate the HIV status and risk behaviour history of the reported source of HIV exposure.
  • Provide medical care, supportive counselling and prevention services to persons who are determined to be HIV infected when they seek care for a potential HIV exposure.
  • Evaluate the risk for HIV transmission (if there is convincing evidence of HIV infection in the reported source). Physician should determine the specifics of the risk event (e.g. no condom, torn condom, whether receptive or insertive partner, injection before or after others, number of persons sharing injection equipment) and the presence or absence of factors that would modify risk (e.g. vaginal or anal tears or bleeding, visible genital ulcers or other evidence of an active STD, or bleach treatment of injection equipment).
  • Determine the time elapsed between exposure and presentation for medical care. Although animal studies indicate that anti-retroviral agents are most effective within 1 - 2 hours of exposure and probably not effective when started later than 24 - 36 hours after exposure, the interval during which therapy can be beneficial for humans is unknown
  • Evaluate the frequency of HIV exposure. Uninfected persons who request anti-retroviral agents should be evaluated for sexual, injecting drug use and other behaviours that might lead to recurrent HIV exposures. Anti-retroviral therapy is not a replacement for adherence to behaviours that reduce the risk of HIV exposure.

Provide counselling and obtain informed consent. Because post-exposure prophylaxis is an experimental therapy of unproven efficacy, informed consent should be obtained and recorded in the medical charts of all persons prescribed anti-retroviral agents following non-occupational exposure. Such consent should document the patient's understanding of

  • The need to initiate or resume relevant HIV risk-reduction behaviours (e.g. condom use and /or drug treatment)
  • The limited knowledge about the effectiveness and toxicity of anti-retroviral treatment for non-occupational exposure.
  • The known side effects of the medications being prescribed.
  • The name and phone number of a source for follow up medical care
  • The frequency and timing of recommended follow up HIV testing
  • The signs and symptoms associated with acute HIV seroconversion; and
  • The need for adherence to prescribed medications to maximise efficacy and reduce the risk for infection with a drug resistant variant.

Persons younger than 16 years at the time of exposure should be evaluated (before therapy is initiated) by paediatricians, family physicians or other clinicians expert in the specific medical needs, consent issues and other factors involved in their treatment, including the use of anti-retroviral medicines for children and adolescents.

If anti-retroviral therapy is used, drug toxicity monitoring should include a complete blood count and renal and hepatic function tests when therapy is initiated and again 2 week after the patient begins to take the medications. It is possible that anti-retroviral therapy during early HIV infection could benefit the patient by reducing the initial level of viral replication (i.e. the set point) and decreasing the extent of lymph node infiltration. Thus, for patients with the highest risk exposures, health care providers may consider continuing therapy until HIV test results are received from a specimen drawn after 28 days of treatment. Patients should be monitored for signs and symptoms of acute HIV infection during therapy. If such conditions develop, the patient should be tested for HIV (p24 antigen, HIV viral load assays) during their 4-week course of therapy with confirmation by standard HIV antibody tests. Persons who become infected while taking anti-retroviral therapy should be advised to continue taking the medication pending transfer to a health care provider who specialises in long term HIV care.

There has been apprehension that availability of PEP may cause people to stop practising safe sex or stop safer needle use. HIV negative persons may wonder, "why bother with condoms or clean rig" when therapy to prevent HIV is available. HIV transmission could increase with these attitudes. So it must be emphasized through media campaign and counselling that no PEP therapy is 100% effective, it has its own side effects and it needs strict adherence. Hence the stress should be on preventive measures through safe sex and safer needle use.

Last updated on 01-06-2005 Vol 2 Issue 6 Art # 27

How to cite this url

Pensi T.Post-Exposure Prophylaxis (PEP).Pediatric Oncall [serial online] 2005 [cited 2005 June 1];2. Art # 27 . Available from:


Last created on: 23rd February 2001



 
 
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