Lesson
Follow an Intracellular Pathogen Across Mucosal Sites
C. trachomatis alternates between an infectious elementary body and a replicating intracellular reticulate body. Local symptoms can be absent while tissue injury continues.
- Elementary body
- Reticulate body
- Silent infection
- Ascending disease
- Reinfection
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Follow the developmental cycle
Elementary bodies enter susceptible epithelial cells, reorganize into replicating reticulate bodies, then produce new elementary bodies for release and transmission.
Expect asymptomatic disease
Urogenital and rectal infection is frequently silent. Screening is therefore a prevention intervention, not merely a response to symptoms.
Recognize reproductive injury
Untreated cervical infection can ascend and cause PID, ectopic pregnancy, infertility, and chronic pelvic pain. Some apparently uncomplicated infections already include subclinical upper-tract disease.
Do not expect durable immunity
Repeat infection is common, especially when partners remain untreated. Each repeat infection can add reproductive risk.
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Lesson
Match Every Exposure to the Right NAAT Specimen
NAAT is the preferred diagnostic method, but its answer is limited to the site and specimen collected.
- Vaginal swab
- First-catch urine
- Rectal swab
- Pharyngeal result
- Screening interval
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Choose optimal urogenital specimens
Patient-collected or clinician-collected vaginal swabs are optimal for many women. First-catch urine is preferred for many men, with urethral or meatal options when appropriate.
Test exposed extragenital sites
Use a validated rectal NAAT after rectal exposure. Routine pharyngeal chlamydia screening is not recommended, but a positive result reported by a combined assay should be treated.
Screen by age and risk
Screen sexually active women younger than 25 annually and older women with increased risk. Screen MSM at exposed sites at least annually and every 3 to 6 months when risk is increased.
Let point-of-care testing improve stewardship
Rapid NAAT can shorten time to treatment, reduce unnecessary empiric antibiotics, and improve partner treatment when available.
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Lesson
Use Doxycycline as the Cross-Site Standard
Doxycycline provides the most reliable efficacy across urogenital, rectal, and oropharyngeal infection in nonpregnant adolescents and adults.
- 100 mg twice daily
- Seven days
- Full-course dispensing
- Esophageal safety
- Alternatives
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Use the preferred regimen
Give doxycycline 100 mg orally twice daily for 7 days. A delayed-release 200 mg once-daily formulation for 7 days is an effective but more costly alternative formulation.
Counsel for absorption and injury prevention
Take with a full glass of water, remain upright, use sun protection, and separate from antacids or supplements containing polyvalent cations.
Place azithromycin correctly
Azithromycin 1 g orally once is an adherence alternative, not equal cross-site therapy. Directly observe the dose and plan post-treatment evaluation when rectal infection is possible.
Place levofloxacin correctly
Levofloxacin 500 mg orally daily for 7 days is effective but carries tendon, nerve, CNS, glycemic, QT, aortic, pregnancy, and interaction boundaries.
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Lesson
Treat the Compartments That Can Reseed Infection
Rectal infection can coexist with urogenital disease, including in women who do not report receptive anal sex. Inadequate rectal cure can contribute to repeat urogenital infection.
- Rectal efficacy
- Autoinoculation
- Proctitis
- Oropharyngeal detection
- HIV PrEP
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Use the efficacy difference
A randomized rectal-chlamydia trial reported 100 percent microbiologic cure with doxycycline and 74 percent with azithromycin. This difference drives the preferred regimen.
Do not infer site from history alone
Concomitant rectal infection in women is common and does not track reliably with reported anal exposure. Persistent rectal infection can reseed the urogenital tract.
Separate uncomplicated proctitis from LGV
Bloody discharge, tenesmus, mucosal ulceration, severe pain, genital ulcers, or buboes require the LGV pathway rather than a routine 7-day course.
Treat a detected pharyngeal result
Routine screening is not recommended because prevalence and clinical significance are low, but detected infection can transmit and should be treated, with doxycycline favored when appropriate.
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Lesson
Treat Pregnancy and Prove Eradication
Pregnancy changes the preferred drug and creates a mandatory cure checkpoint because persistent maternal infection threatens both patients.
- Azithromycin
- Amoxicillin alternative
- Four-week cure test
- Three-month retest
- Third-trimester rescreen
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Use the recommended pregnancy regimen
Give azithromycin 1 g orally once. Observe the dose when possible and reassess when vomiting or absorption is uncertain.
Use amoxicillin as an alternative
Amoxicillin 500 mg orally three times daily for 7 days is an alternative. Persistence concerns keep it behind azithromycin.
Prove cure at the correct time
Obtain NAAT about 4 weeks after completion. Testing earlier can detect nonviable organisms. Retest again at 3 months for reinfection.
Screen across pregnancy
Screen at the first prenatal visit when younger than 25 or at increased risk, repeat in the third trimester when risk continues, and screen at delivery when prenatal testing was missed.
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Lesson
Recognize Eye Disease and Afebrile Pneumonia on Time
Perinatal cervical exposure can cause conjunctivitis at 5 to 12 days or a subacute afebrile pneumonia at 1 to 3 months. Prenatal treatment is the strongest prevention.
- Five to twelve days
- Systemic therapy
- Staccato cough
- Eosinophilia
- Pyloric stenosis
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Recognize conjunctivitis
Consider chlamydia in every infant 30 days or younger with conjunctivitis, especially with maternal infection. Collect conjunctival cells, not exudate alone, and test for gonorrhea.
Treat systemically
Give erythromycin base or ethylsuccinate 50 mg/kg/day divided four times daily for 14 days. Azithromycin 20 mg/kg daily for 3 days is a shorter alternative with limited evidence.
Recognize pneumonia
Look for staccato cough, tachypnea, hyperinflation, bilateral diffuse infiltrates, and eosinophilia in an afebrile infant aged 1 to 3 months. Collect a nasopharyngeal specimen.
Follow both efficacy and safety
Erythromycin efficacy is about 80 percent, so a second course can be necessary. Monitor infants younger than 6 weeks for infantile hypertrophic pyloric stenosis after either macrolide.
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Lesson
Recognize Invasive Chlamydia Before It Scars
LGV serovars invade lymphatic tissue and can cause destructive proctocolitis, strictures, fistulas, genital ulcer disease, and painful inguinal buboes.
- Bloody proctitis
- Tenesmus
- Mucosal ulcer
- Bubo
- Twenty-one days
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Identify the clinical syndrome
Presume LGV with rectal chlamydia plus bloody discharge, tenesmus, mucosal ulceration, or severe proctitis, or with a genital ulcer and severe inguinal lymphadenopathy or bubo.
Use extended doxycycline
Give doxycycline 100 mg orally twice daily for 21 days. Aspiration through intact skin or drainage can be needed for fluctuant buboes.
Place alternatives carefully
Azithromycin 1 g weekly for 3 weeks or erythromycin base 500 mg four times daily for 21 days are alternatives. Consider cure testing after the less-validated azithromycin regimen.
Close the invasive pathway
Follow clinically until resolution, test HIV, gonorrhea, and syphilis, offer HIV PrEP when appropriate, and retest for chlamydia at 3 months.
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Lesson
Separate Cure Testing From Reinfection Testing
Nonpregnant patients usually do not need routine test of cure, but every treated patient needs a reinfection plan and partner closure.
- No early NAAT
- Three-month retest
- Sixty-day partners
- Most recent partner
- EPT
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Do not test too early
Avoid routine NAAT before 4 weeks. In nonpregnant patients, cure testing is reserved for questionable adherence, persistent symptoms, or suspected reinfection.
Retest at 3 months
Schedule retesting at treatment regardless of whether the patient believes partners were treated. If that is impossible, retest at the next visit within 12 months.
Manage every relevant partner
Evaluate, test, and presumptively treat partners from the preceding 60 days, plus the most recent partner even when the last contact was earlier.
Use EPT within its limits
Consider expedited partner therapy when lawful and timely evaluation is unlikely, while giving written allergy, adverse-effect, and complication warnings.
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Lesson
Close Sex, Partners, HIV Risk, and Doxy PEP Together
The treatment course is one part of a longitudinal prevention system. Exact abstinence timing, partner completion, HIV prevention, and repeat screening prevent the next infection.
- Seven days
- Partner completion
- HIV test
- PrEP
- Doxy PEP
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Give exact abstinence instructions
Avoid sex for 7 days after single-dose azithromycin or until the 7-day doxycycline course is complete, symptoms resolve, and partners are treated.
Test linked infections
Test for gonorrhea, syphilis, and HIV. Offer HIV PrEP to appropriate HIV-negative patients, especially MSM with rectal chlamydia.
Use doxy PEP within guidance
Discuss with MSM and transgender women who had syphilis, chlamydia, or gonorrhea in the previous 12 months. Use doxycycline 200 mg within 72 hours after sex, no more than 200 mg per 24 hours.
Reassess the prevention plan
Repeat site-specific STI testing and reassess doxy PEP need every 3 to 6 months, while reviewing esophageal safety, cations, photosensitivity, adherence, and antimicrobial resistance.
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Lesson
Own the Whole Pathway From Specimen to Return Visit
A complete plan names the infected and exposed sites, regimen, pregnancy status, cure checkpoint, reinfection test, partners, and prevention owner.
- Site
- Host
- Regimen
- Timeline
- Ownership
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Connect intracellular biology, anatomy, treatment, follow-up, and prevention.
Name every site
Document which anatomy was exposed, which specimen was collected, which result was positive, and which complication was excluded.
Name every host modifier
Record pregnancy, age and weight for pediatric care, allergy, adherence, swallowing, interactions, HIV status, and access.
Name every timeline
Write the last dose, required test of cure when applicable, 3-month retest, partner window, and safe return to sexual activity.
Name every owner
Assign maternal-newborn communication, partner services, EPT materials, HIV PrEP, doxy PEP reassessment, and escalation for pelvic, testicular, rectal, ocular, or respiratory danger signs.
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Module test
Check the connections.
Each attempt draws 10 questions from the complete 130 question bank.
Each attempt draws a fresh set and rearranges the answer choices.
References
Current clinical foundation.
Lecture material was synthesized with the following contemporary guidance. Verify local policy and current guidance before applying clinical information.