If a healthcare provider sustains a needlestick injury, they should immediately wash the area, alert their supervisor to initiate injury reporting, and identify the source patient to determine if testing is needed. They should then report to employee health services and give consent for baseline HIV, hepatitis B, and hepatitis C testing. Post-exposure prophylaxis for HIV should begin within 2 hours according to CDC guidelines, and follow-up testing should occur at 6 weeks, 3 months, 6 months, and possibly 1 year. The exposure should be fully documented for the provider and employer's records.
Original Description:
POSTEXPOSURE PROPHYLAXIS FOR HEALTH CARE PROVIDERS
If a healthcare provider sustains a needlestick injury, they should immediately wash the area, alert their supervisor to initiate injury reporting, and identify the source patient to determine if testing is needed. They should then report to employee health services and give consent for baseline HIV, hepatitis B, and hepatitis C testing. Post-exposure prophylaxis for HIV should begin within 2 hours according to CDC guidelines, and follow-up testing should occur at 6 weeks, 3 months, 6 months, and possibly 1 year. The exposure should be fully documented for the provider and employer's records.
If a healthcare provider sustains a needlestick injury, they should immediately wash the area, alert their supervisor to initiate injury reporting, and identify the source patient to determine if testing is needed. They should then report to employee health services and give consent for baseline HIV, hepatitis B, and hepatitis C testing. Post-exposure prophylaxis for HIV should begin within 2 hours according to CDC guidelines, and follow-up testing should occur at 6 weeks, 3 months, 6 months, and possibly 1 year. The exposure should be fully documented for the provider and employer's records.
POSTEXPOSURE PROPHYLAXIS FOR HEALTH CARE PROVIDERS
If you sustain a needle stick injury, take the following actions immediately:
Wash the area with soap and water.
Alert your supervisor and initiate the injury-reporting system used in the setting. Identify the source patient, who may need to be tested for HIV, hepatitis B, and hepatitis C. (State laws will determine if written informed consent must be obtained from the source patient prior to his or her testing.) Report to the employee health services, the emergency department, or other designated treatment facility. Give consent for baseline testing for HIV, hepatitis B, and hepatitis C. Get post-exposure prophylaxis for HIV in accordance with CDC guidelines. Start the prophylaxis medications within 2 hours after exposure. Make sure that you are being monitored for symptoms of toxicity. Practice safer sex until follow-up testing is complete. Follow up with post-exposure testing at 6 weeks, 3 months, and 6 months and perhaps 1 year. Document the exposure in detail for your own records as well as for the employer. Take the psychosocial support offered or seek support outside of the employment setting.
Classification of antiretroviral agents
Name of the drugs Food Interactions Adverse Effects Nucleoside Reverse Take without regard to Hypersensitivity reaction, which can Transcriptase Inhibitors (NRTIs) meals. Alcohol increases be fatal; symptoms may include fever, Abacavir (ABC) ziagen. abacavir levels 41%. rash, nausea, vomiting malaise or Truvada (FTC/TDF) zalcitabine Abacavir has no effect on fatigue, loss of appetite, and (ddC) Hivid alcohol. respiratory symptoms such as sore throat, cough, shortness of breath. Non-Nucleoside reverse Take without regard to Rash (rare cases of Stevens-Johnson Transcriptase inhibitors meals. syndrome have been reported), Delavirdine (DLV) rescriptor increased transaminase levels, efavirenz (EFV) Sustiva headaches Protease inhibitors High fat-meal decreases GI intolerance, nausea, vomiting, Amprenavir (APV) Agenerase blood concentration diarrhea, rash, oral paresthesias, 21%; can be taken with hyperlipidemia, transaminase or without food, but elevation, hyperglycemia, fat high-fat meal should be maldistribution, possible increased avoided. bleeding episodes in patients with haemophilia. Fusion Inhibitors Injected subcutaneously, Local injection site reactions-almost Enfuvirtide (T-20) Fuzeon so meals are not an issue. 100% of patients (pain, erythema, induration, nodules and cysts, pruritus, ecchymosis); increased rate of bacterial pneumonia; hypersensitivity reaction-symptoms may include rash, fever, nausea, vomiting, chills, rigors, hypotension, or elevated serum transaminases; may recur on challenge Integrase strand transfer No food restrictions Diarrhea, nausea, headache, and fever inhibitor identified have been reported. Raltegravir (RAL) Isentress Multiclass combination products Atripla (EFV/FTC/TDF)
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