Lesson
Map the Infection to Every Exposed Surface
N. gonorrhoeae occupies mucosal sites independently. Symptoms at one site do not reveal what is happening at another.
- Gram-negative diplococcus
- Mucosal attachment
- Silent carriage
- Ascending infection
- Dissemination
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Start with site biology
Gonococci attach to columnar epithelium at the cervix, urethra, rectum, pharynx, and conjunctiva. Antigenic variation and local inflammation support reinfection rather than durable immunity.
Expect silence
Cervical, rectal, and pharyngeal infection is often asymptomatic. Urethritis can cause dysuria and discharge, but symptom absence cannot close the diagnosis.
Recognize ascent
Untreated cervical infection can ascend into PID, infertility, ectopic pregnancy, and chronic pelvic pain. Epididymitis and local complications can occur in other anatomy.
Keep dissemination visible
Bloodstream spread is uncommon but can produce skin lesions, tenosynovitis, polyarthralgia, septic arthritis, meningitis, or endocarditis even when genital symptoms are absent.
Quick check
Lesson
Pair Each Question With the Right Specimen
NAAT answers whether gonococcal nucleic acid is present at a sampled site. Culture answers the additional resistance question when a viable isolate matters.
- Urine or vaginal NAAT
- Rectal NAAT
- Pharyngeal NAAT
- Culture
- AST
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Use site-specific NAAT
Collect an assay-approved vaginal, cervical, urine, rectal, or pharyngeal specimen from every exposed site. Patient-collected swabs can improve access when validated.
Preserve culture when needed
Culture is less sensitive than NAAT but supplies the viable isolate required for antimicrobial susceptibility testing. Transport and incubation conditions matter.
Test the connected infections
Every gonorrhea diagnosis should trigger chlamydia, syphilis, and HIV testing. Offer HIV PrEP when the HIV result is negative and clinical context supports it.
Interpret after treatment carefully
A positive pharyngeal NAAT at the early edge of follow-up can reflect residual nucleic acid. Confirm with culture before retreatment when possible.
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Lesson
Deliver Exact Ceftriaxone Exposure in One Visit
The CDC regimen is simple only after weight, site, allergy, pregnancy, and chlamydia status are known.
- 500 mg IM
- 1 g IM
- 150 kg threshold
- Chlamydia status
- Direct observation
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Dose below 150 kg
Give ceftriaxone 500 mg IM once for uncomplicated cervical, urethral, rectal, or pharyngeal infection in adolescents and adults weighing less than 150 kg.
Dose at or above 150 kg
Give ceftriaxone 1 g IM once when weight is at least 150 kg. Document weight rather than estimating around the threshold.
Address chlamydia deliberately
If chlamydia has not been excluded, add doxycycline 100 mg orally twice daily for 7 days in a nonpregnant adult. Pregnancy follows its own chlamydia pathway.
Close administration safely
Review severe beta-lactam reactions, use trained IM technique, prepare for immediate reactions, and use on-site directly observed dosing when possible.
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Lesson
Treat the Pharynx as the Resistance Boundary
Pharyngeal infection is often silent, harder to eradicate, and a potential reservoir for resistance. It has no reliable CDC alternative to ceftriaxone.
- Oral exposure
- Ceftriaxone
- No reliable alternative
- Test of cure
- Three-month retest
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Test after oral exposure
A patient with urogenital or rectal gonorrhea who reports oral exposure should also receive pharyngeal testing.
Use the reliable regimen
Give ceftriaxone 500 mg IM once below 150 kg or 1 g IM once at or above 150 kg. Severe ceftriaxone reaction requires expert consultation.
Prove cure
Obtain culture or NAAT 7 to 14 days after treatment. Testing at 7 days can produce more false-positive NAAT results, so confirm a positive NAAT with culture before retreatment when possible.
Retest for reinfection
Routine test of cure is not needed for correctly treated uncomplicated urogenital or rectal disease, but every treated patient should be retested at 3 months.
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Lesson
Place Every Alternative Inside Its Boundary
Alternative and newly approved oral therapies expand access for selected uncomplicated urogenital infection. They do not erase site, population, resistance, or label limits.
- Cefixime
- Gentamicin plus azithromycin
- Zoliflodacin
- Gepotidacin
- Current label
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Use cefixime for availability
If ceftriaxone is unavailable, cefixime 800 mg orally once is an alternative for selected uncomplicated urogenital or rectal infection. It is not an equivalent pharyngeal regimen.
Use the allergy regimen narrowly
For a severe cephalosporin allergy, gentamicin 240 mg IM plus azithromycin 2 g orally once can be considered. Vomiting and weaker pharyngeal evidence limit the regimen.
Know zoliflodacin
FDA approved Nuzolvence 3 g orally once in December 2025 for uncomplicated urogenital gonorrhea in eligible patients at least 12 years old and weighing at least 35 kg. Avoid use in pregnancy, obtain pregnancy testing when applicable, and follow the label's reproductive precautions.
Know gepotidacin
FDA approved Blujepa 3,000 mg orally followed by another 3,000 mg about 12 hours later for uncomplicated urogenital gonorrhea in eligible patients at least 12 years old and weighing at least 45 kg who have few or no treatment alternatives. Check QT, cholinergic, interaction, and administration warnings.
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Lesson
Protect Pregnancy, Birth, and the Newborn
Maternal screening, immediate treatment, partner care, and newborn prophylaxis form one prevention chain. Established neonatal disease is a systemic emergency.
- Prenatal screening
- Weight-based ceftriaxone
- Pregnancy chlamydia plan
- Ocular prophylaxis
- Neonatal therapy
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Use the gonorrhea regimen in pregnancy
Give ceftriaxone 500 mg IM once below 150 kg or 1 g IM once at or above 150 kg. Severe cephalosporin allergy requires specialist consultation.
Do not default to doxycycline
When chlamydia is not excluded in pregnancy, use pregnancy-appropriate chlamydia guidance rather than automatically adding doxycycline.
Prevent neonatal disease
Screen patients younger than 25 and older patients with increased risk early in pregnancy, then repeat in the third trimester when risk remains. Ensure treatment and partner management are complete.
Treat disease, not just prophylaxis
Purulent neonatal conjunctivitis can progress rapidly and requires systemic evaluation and ceftriaxone or cefotaxime therapy. Routine ocular prophylaxis does not treat established infection.
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Lesson
Recognize the Systemic Pattern Before the Source Is Visible
DGI frequently presents through skin, tendon, and joint findings while the mucosal source remains asymptomatic.
- Pustular lesions
- Tenosynovitis
- Polyarthralgia
- Septic arthritis
- Deep-site infection
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Recognize arthritis-dermatitis syndrome
Look for petechial or pustular acral lesions, asymmetric polyarthralgia, tenosynovitis, or oligoarticular septic arthritis.
Collect the complete specimen set
Obtain NAAT and culture from all exposed mucosal sites plus blood, synovial fluid, skin, or CNS sites as clinically indicated. Test recovered isolates for susceptibility.
Treat sustained infection
Use ceftriaxone 1 g IM or IV every 24 hours for arthritis-dermatitis disease. After substantial improvement for 24 to 48 hours, AST-guided oral step-down can complete at least 7 total days.
Escalate CNS or valve infection
Use ceftriaxone 1 to 2 g IV every 12 to 24 hours. Treat meningitis for 10 to 14 days and endocarditis for more than 4 weeks with infectious-disease consultation.
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Lesson
Preserve the Isolate Before It Disappears
A repeat positive test can reflect reinfection, inadequate exposure, wrong site therapy, or true resistance. The workup must preserve the evidence needed to distinguish them.
- Reinfection
- Culture
- AST
- Expert consultation
- Public-health report
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Audit the original treatment
Verify product, dose, weight, site, route, timing, vomiting, adherence, chlamydia management, symptoms, and partner treatment.
Separate reinfection from failure
Most apparent failures are reinfections. Review sexual exposure after treatment and whether partners received effective therapy.
Preserve resistance evidence
Collect culture, preferably with simultaneous NAAT, from every relevant site before retreatment when true failure is plausible. Send isolates for AST.
Escalate within 24 hours
Consult an infectious-disease or STI expert and report suspected cephalosporin treatment failure through local or state public health to CDC within 24 hours.
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Lesson
Close the Transmission System
Treatment succeeds at the population level only when partners, retesting, screening, HIV prevention, and barriers to care are addressed together.
- Sixty-day partners
- Seven-day abstinence
- Three-month retest
- HIV PrEP
- Doxy PEP
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Manage partners
Evaluate, test, and presumptively treat partners from the preceding 60 days. Consider expedited partner therapy only when lawful and timely evaluation is unlikely.
Give exact abstinence guidance
Avoid sex for 7 days after treatment and until all partners are treated and symptoms have resolved.
Schedule retesting and screening
Retest at 3 months. Screen sexually active women younger than 25 annually, older women by risk, and MSM at exposed sites at least annually or every 3 to 6 months when risk is increased.
Integrate HIV and doxy PEP
Test for HIV and offer PrEP when appropriate. Discuss doxy PEP with MSM and transgender women who had a bacterial STI in the prior 12 months, using 200 mg within 72 hours after sex and no more than 200 mg per 24 hours.
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Lesson
Make Site, Host, and Public Health One Decision
A complete plan moves from exposure to specimen, regimen, administration, follow-up, partner care, and surveillance without dropping a handoff.
- Site
- Host
- Drug
- Follow-up
- Ownership
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Connect anatomy, susceptibility, host factors, follow-up, and transmission control.
Name every site
Document exposed and infected anatomy, specimen method, symptoms, and complications before choosing therapy.
Name every host modifier
Record weight, pregnancy, age, allergy phenotype, kidney and auditory risk, interactions, immune status, and ability to return.
Name every drug boundary
Separate CDC standard therapy, availability alternatives, severe-allergy options, and 2025 site-specific oral approvals.
Name every owner
Assign treatment, test of cure when required, three-month retesting, partner services, public-health reporting, HIV prevention, and urgent return precautions.
Quick check
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.