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Management of Gonorrhea
and Chlamydia in Patients
with HIV
www.hivguidelines.org
Purpose of the Guideline
• Increase the numbers of NYS residents with HIV and gonococcal
or chlamydial coinfection who are identified and treated with effective
interventions.
• Reduce gonorrhea and chlamydia rates in support of the NYSDOH
Prevention Agenda 2013-2018 goals.
• Reduce the growing burden of morbidity associated with gonococcal
and chlamydial infections.
• Integrate current evidence-based clinical recommendations into the
healthcare-related implementation strategies of the Ending the Epidemic
initiative, which seeks to end the AIDS epidemic in NYS by the end of 2020.
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
Recommendations:
Transmission and Prevention
 Clinicians should inform patients with HIV infection about the risk
of acquiring or transmitting chlamydia, gonorrhea, and other STIs from
close physical contact with all sites of possible exposure, including
the penis, vagina, mouth, or anus. (A3)
 When patients with HIV infection are diagnosed with gonococcal or
chlamydial infections, clinicians should educate patients about the
following: risk-reduction strategies, including the value of correct
condom use (A2); the potential for oral transmission of gonorrhea and
chlamydia (A3); the benefits of identifying STIs early (A3); and the need
for prompt evaluation and treatment of partners (A3).
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
Description of Risk Status
for Sexual Exposure to Gonorrhea and Chlamydia
Risk Level Description
No/Low Risk Patient reports no sexual activity or sex only within a mutually monogamous
relationship within the year prior
Moderate Risk Patient reports a new sex partner within the year prior
High Risk Patient self-identifies as being at high risk of sexually transmitted infections
(STIs) and/or reports any of the following for self or sex partner(s):
• Multiple or anonymous sex partners
• Bacterial STI diagnosed since last STI screening
• Participation in sex parties or sex in other high-risk venues
• Participation in any type of transactional sex
• Use of recreational substances during sex
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
Recommendation:
Obtaining a Sexual History
 Clinicians should ask all patients about sexual behaviors and
new sex partners at each routine monitoring visit to assess for
risk behaviors that require repeat or ongoing screening.
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
Who to Screen?
• All patients with HIV infection should be serologically screened for
gonorrhea and chlamydia at least once per year.
• MSM who engage, or whose partners may engage, in continued high-risk
behavior should be serologically screened for gonorrhea and chlamydia at
least every 3 months.
• The diagnosis of another bacterial STI in a patient with HIV infection or a
patient’s sex partner should prompt a clinician to perform gonorrhea and
chlamydia screening tests and to consider more frequent screening for
gonorrhea and chlamydia.
• Pregnant patients with HIV infection should be serologically screened for
gonorrhea and chlamydia at the first prenatal visit.
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
Recommendations: Screening Frequency
 For MSM and transgender women who have sex
with men, clinicians should perform 3-site
screening (genital, pharyngeal, rectal) at the
following intervals:
• At first visit and annually thereafter if the
patient is at low risk of infection. (A2)
• At first visit and every 3 months thereafter if
the patient is at high risk of infection. (A2)
 For all other patients, clinicians should perform
genital screening (urine/urethra, vagina/cervix)
and extragenital screening (pharyngeal and/or
rectal) at sites of contact at the following
intervals:
• At first visit and annually thereafter if the
patient is at low risk of infection. (A2)
• At first visit and every 3 months thereafter
if the patient is at high risk of infection. (A2)
 Clinicians should serologically screen pregnant patients with HIV infection for gonococcal and chlamydial
infections at the first prenatal visit. (A2)
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
Key Points: Screening Frequency
 Because most gonorrheal and chlamydial infections are asymptomatic, regular screening is essential to
protect patients’ health and prevent the spread of STIs. This is an essential component of patient
education.
 Gonococcal and chlamydial screening at least every 3 months is recommended for all individuals at high
risk of exposure, including those who:
• Have, or whose partners may have, multiple
or anonymous sex partners
• Engage, or whose partners may engage, in
sexual activity at sex parties or other high-risk
venues
• Are, or whose partners may be, involved in
transactional sex (i.e., sex workers and their
clients)
• Have been diagnosed with a bacterial STI in the
previous 12 months
• Report recreational substance use during sexual
activity
• Self-identify as at high risk for STIs
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
When to Consider 3-Site Screening
• This Committee supports routine 3-site
(urine, pharyngeal, and rectal)
screening in sexually active MSM and
MtF transgender women who have sex
with men.
• Screening at 3 sites (i.e., genital,
pharyngeal, and rectal) is
recommended for patients who are
included in recognized high-risk groups
and for those who report exposure at
extragenital sites.
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
• Information about the patient’s sexual behaviors
informs decisions about the frequency and type
(genital only or 3-site) of screening and points
clinicians to key areas to address in risk-
reduction counseling.
• The recommendation for extragenital (3-site)
screening should be discussed with the patient.
For individuals who opt out of 3-site screening,
testing based on the patient’s reported sites of
anatomical exposure should be performed and
documented in the medical record.
Recommendations:
Presentation of Symptomatic Infection
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
 When patients with HIV present with symptoms suggestive of gonococcal
or chlamydial infection, clinicians should perform diagnostic testing
as recommended in the guideline. (A1)
 Clinicians should include lymphogranuloma venereum (LGV) infection in the
differential diagnosis for patients who test positive for rectal chlamydial infection
or who present with such symptoms as rectal pain, tenesmus, bloody rectal
discharge, or isolated, atypical perianal ulcerative lesions and adenopathy. (A2)
Key Point: Although LGV occurs only sporadically in the U.S., outbreaks of LGV
proctocolitis have been reported among MSM in New York and other U.S. cities,
and many of these cases occurred in individuals with HIV.
Recommendations:
Laboratory-Based Diagnosis
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
 Clinicians should obtain NAAT (preferred) on samples collected from genital
and extragenital sites (A1); if NAAT is not available, then clinicians should:
• Send alternative samples for culture in accordance with the protocols of
the laboratory performing the analysis, with the understanding that
culture is significantly less sensitive than NAAT. (A1)
 If a patient has a known exposure to a cephalosporin-resistant strain,
clinicians should obtain samples for both culture/susceptibility and NAAT
testing from the patient and his/her sex partner(s). (A3)
 Clinicians should perform syphilis testing for any patient with HIV infection
who is diagnosed with a gonorrheal or chlamydial infection. (A2)
Sample Collection & Testing Methods
Exposure Site
Sample
Collection Method [a] Comments
Urethra First-catch urine for NAAT [b] • In males, for ease of collection, first-catch urine [c] is recommended over urethral
swab. Some studies have demonstrated equal specificity but lower sensitivity with
urethral swab compared with urine for NAAT. However, additional data are needed
to establish the relative effectiveness of these collection methods.
Vagina/cervix Vaginal or cervical swab
(recommended) or first-catch urine
(alternative) NAAT
• The recommended sample collection method is a vaginal swab for testing with an
FDA-approved assay; this method is equivalent to cervical swab.
• First-catch urine testing, which is inferior to swab, may be used as an alternative.
• Some NAAT assays are approved for self-collected vaginal samples and perform as
well as NAAT for other specimens.
Rectum Males and females: Rectal swab for
NAAT [b]
• Culture is not sufficiently sensitive for detection of rectal C. trachomatis.
Pharynx Males and females: Pharyngeal swab
for NAAT [b]
• Culture is not sufficiently sensitive for detection of pharyngeal C. trachomatis.
• The incidence of pharyngeal chlamydial infection is lower than pharyngeal
gonorrheal infection, and data on the clinical benefit of treating patients with
asymptomatic pharyngeal infection are limited.
• To reduce the risk of transmission, this Committee recommends treatment for
pharyngeal chlamydial infection, even if the pharynx is the only site of infection.
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
Notes:
Sample Collection & Testing Methods
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
a. Handling of specimens: Conditions for collection and transport of samples for laboratory
testing for C. trachomatis and N. gonorrhoeae may greatly affect the sensitivity of culture
because the organisms can degrade easily during transport. Guidance regarding sample
collection with either direct plating or the use of specialized transport media for culture should
be obtained from the clinician’s laboratory. After collection, culture samples should be stored
in the referring laboratory’s recommended transport media and transported at ≤4°C to the
laboratory within 24 hours.
b. NAAT testing is more sensitive than culture for the detection of gonococcal or chlamydial
infections. Although NAAT has not yet received FDA approval for rectal or pharyngeal
specimens, NAAT performed by a laboratory with a Clinical Laboratory Evaluation Program-
specified protocol is recommended for detecting both rectal and pharyngeal C. trachomatis
and N. gonorrhoeae. If NAAT is not available, then culture should be obtained according to the
protocols of the clinician’s institution.
c. For urine screening, clinicians should provide patients with clear instructions for obtaining a
first-catch sample.
Reporting: New York State Requirements
• Clinicians must report within 24 hours from the time a case is first seen all suspected or
confirmed gonorrhea and chlamydia diagnoses to the local health department of the
area where the patient resides.
• For more information, see the following:
 NYSDOH Communicable Disease Reporting:
https://www.health.ny.gov/forms/instructions/doh-389_instructions.pdf
 NYCDOHMH Reporting Diseases and Conditions:
https://www1.nyc.gov/site/doh/providers/reporting-and-services/notifiable-
diseases-andconditions-reporting-central.page
 NYS Local Health Department Contact List:
https://www.health.ny.gov/prevention/prevention_agenda/contact_list.htm
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
Recommendations:
Treatment of Uncomplicated Gonorrhea
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
 Clinicians should treat uncomplicated gonococcal infections of the cervix, urethra, rectum,
or pharynx as follows:
• Preferred: Ceftriaxone 250 mg IM injection in a single dose plus azithromycin 1 g by
mouth in a single dose. (A2)
• Alternative, for patients who are allergic to azithromycin: Ceftriaxone 250 mg IM in a
single dose plus doxycycline 100 mg by mouth twice daily for 7 days. (A2)
• Alternative, if ceftriaxone is not available: Cefixime 400 mg by mouth in a single dose
plus azithromycin 1 g by mouth in a single dose. This regimen is not recommended for
treatment of pharyngeal infection. (A2)
 Clinicians should instruct patients to abstain from sexual activity for at least 7 days after
starting treatment, and to continue to abstain until symptoms resolve and all sex partners
are treated. (A2)
Key Points: Gonorrhea Treatment
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
 Directly observed treatment provided on-site
maximizes adherence.
 N. gonorrhoeae has developed resistance to nearly
all previously effective antimicrobials, leaving
cephalosporins as the only available class of drugs
recommended for treatment of gonococcal
infections.
 Cephalosporin-resistant N. gonorrhoeae has been
reported outside of the U.S., and reduced
susceptibility to cephalosporins has been observed
with isolates of N. gonorrhoeae from residents of
NYC.
 Combination treatment with two antimicrobials with
different mechanisms of action is recommended to
slow further emergence of resistance.
 People infected with N. gonorrhoeae are
frequently coinfected with C. trachomatis.
 In the U.S., in 2016, 26.9% of N. gonorrhoeae
isolates were quinolone-resistant
 Because of fluoroquinolone-resistant N.
gonorrhoeae in the U.S., fluoroquinolones other
than gemifloxacin should not be used to
empirically treat proven or suspected gonococcal
infections; however, if fluoroquinolones are being
considered, then clinicians should perform
fluoroquinolone susceptibility testing before
initiating treatment.
Recommendations: Treatment of
Gonorrhea in Penicillin-Allergic Patients
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
 For patients without prior severe allergic responses to penicillin, clinicians should treat
gonococcal infection with a cephalosporin-containing regimen, as recommended above,
and monitor carefully for adverse effects. (A2)
• Reactions considered severe include the following: severe IgE-mediated response,
such as anaphylaxis or urticaria with pruritic rash, or a severe non-IgE-mediated
response, such as Stevens-Johnson syndrome, toxic epidermal necrolysis, or drug-
induced hypersensitivity with inflammation of internal organs.
 For patients with prior severe allergic responses to penicillin, clinicians should treat
gonococcal infection with a single dose of azithromycin 2 g by mouth plus a single dose
of either gentamicin 240 mg IM or gemifloxacin 320 mg by mouth. (A2)
Recommendations: Treatment
of Uncomplicated Chlamydia and LGV
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
 Clinicians should treat uncomplicated chlamydial infection of
the cervix, urethra, rectum, or pharynx as indicated: (A2)
 Recommended:
• Azithromycin 1 g by mouth as a single dose OR doxycycline
100 mg by mouth twice daily for 7 days.
• Alternatives (NOT recommended for pharyngeal infection):
 Erythromycin base 500 mg by mouth 4 times per day for
7 days OR
 Erythromycin ethylsuccinate 800 mg by mouth 4 times
per day for 7 days OR
 Levofloxacin 500 mg by mouth once daily for 7 days OR
 Ofloxacin 300 mg by mouth 2 times per day for 7 days.
Note: Treat asymptomatic pharyngeal infection even if it is
the only site of infection.
 Clinicians should treat symptomatic chlamydial
proctitis with a medication regimen sufficient to
treat LGV. (A3)
 Recommended:
• Doxycycline 100 mg by mouth twice daily for 21
days OR azithromycin* 1 g by mouth as a single
dose once weekly for 3 weeks.
• Presumptively treat for LGV (see the NYSDOH AI
guideline on LGV); if LGV is excluded by testing,
then patients should complete the standard
seven-day regimen for uncomplicated chlamydial
infection.
*Added June 13, 2019.
Recommendations:
Post-Treatment Follow-Up
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
 Clinicians should follow up with patients who have completed
treatment for gonococcal and chlamydial infections as detailed
in the guideline. (A3)
 Clinicians should rescreen patients who had confirmed
gonococcal or chlamydial infection at 3 months post-
treatment for evidence of reinfection. (A2)
Recommended Follow-Up*
Clinical Circumstance Recommended Clinician Follow-Up
Patient is asymptomatic after treatment with
recommended regimen:
• Urogenital or rectal infection treated with
preferred or appropriate alternative regimens.
• Pharyngeal gonorrhea treated with preferred
regimen.
 Retest at 3 months (or as close to 3 months as possible) post-
treatment to assess for reinfection.
 If lab test is positive for N. gonorrhoeae, assess for re-exposure and
partner treatment, and re-treat with recommended regimen.
Patients is asymptomatic after possibly ineffective
course of treatment:
• Urogenital or rectal infection treated with regimen
other than preferred or alternative regimens.
• Pharyngeal infection treated with an alternative
regimen.
• Suspected nonadherence to full course of
treatment
 Assess for re-exposure and partner treatment.
 Perform a test of cure at site of infection with N. gonorrhoeae NAAT
14 days after completion of treatment.
 If test of cure is positive, perform culture and susceptibility testing
before retreatment and retreat with recommended regimen if
possible.
 If recommended regimen cannot be used, retreat with an alternative
regimen or according to susceptibility test results.
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
*Adapted from CDC 2015 STD Treatment Guideline
Recommended Follow-Up,* continued
Clinical Circumstance Recommended Clinician Follow-Up
Patient is symptomatic post-
treatment: Persistent symptoms
post-treatment; infection at any site.
 Assess for re-exposure and partner treatment.
 Assess patient adherence and use of preferred or appropriate alternative
regimen.
 Swab symptomatic site(s) for N. gonorrhoeae culture and antibiotic
susceptibility testing ≥72 h after treatment. NAAT may be obtained in addition
to culture ≥7 days after treatment.
 Re-treat for suspected treatment failure.
 Assess for STIs that may cause persistent or recurrent symptoms. (Other STIs
may include M. genitalium, T. vaginalis, herpes simplex virus, adenovirus, and
enteric bacteria.)
 For persistent or recurrent urethritis negative for N. gonorrhoeae and C.
trachomatis, treat empirically for M. genitalium and/or T. vaginalis according
to CDC recommendations.
 Assess for non-STI etiologies as part of the differential diagnosis if a patient is
repeatedly symptomatic.
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
*Adapted from CDC 2015 STD Treatment Guideline
Recommended Follow-Up,* continued
Clinical Circumstance Recommended Clinician Follow-Up
Patient is asymptomatic after
treatment with preferred or
alternative regimen.
 Retest at 3 months (or as close to 3 months as possible) post-treatment to
assess for reinfection.
 If laboratory test is positive for C. trachomatis, assess for re-exposure and
partner treatment and re-treat with recommended regimen.
Patient is symptomatic post-
treatment: Persistent symptoms
post-treatment; infection at any site.
 Perform a test of cure at site of infection with C. trachomatis NAAT 3 weeks
after treatment.
 If test of cure is positive, assess for re-exposure and partner treatment, and
re-treat with recommended treatment regimen using azithromycin or
doxycycline. Azithromycin is preferred to maximize adherence.
 If test of cure is negative, consider other STIs that may cause persistent or
recurrent symptoms (other STIs may include M. genitalium, T. vaginalis,
herpes simplex virus, adenovirus, and enteric bacteria).
 Consider non-STI etiologies as part of the differential diagnosis when the
patient is repeatedly symptomatic.
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
*Adapted from CDC 2015 STD Treatment Guideline
Recommendations:
Retreatment of Uncomplicated Gonorrhea
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
 Clinicians should re-treat cases of uncomplicated gonococcal infection following
suspected treatment failure according to recommendations. (AIII)
 NYS Requirement: Clinicians must report cases of suspected gonorrhea treatment
failure that are not due to reinfection:
• New York State: Report suspected treatment failures to the local health department
within 24 hours.
• New York City: Call 866-692-3641 to notify the health department of suspected
treatment failures.
Key Point: Gonococcal and chlamydial reinfection rates are high among people who have
been successfully treated.
Recommended Regimens for Retreatment
Clinical Circumstance Recommended Treatment*
Possible reinfection (most cases).  Ceftriaxone 250 mg by mouth in a single dose plus
azithromycin 1 g by mouth in a single dose.
Low reinfection risk; initial treatment was
incomplete or regimen administered was not
preferred or alternative.
 Ceftriaxone 250 mg by mouth in a single dose plus
azithromycin 1 g by mouth in a single dose.
Low reinfection risk; initial treatment
with cefixime and azithromycin.
 Ceftriaxone 250 mg by mouth in a single dose plus
azithromycin 2 g by mouth in a single dose.
Low reinfection risk; initial treatment with
ceftriaxone 250 mg IM and azithromycin
1 g by mouth.
 Gentamicin 240 mg IM or gemifloxacin 320 mg by
mouth plus azithromycin 2 g by mouth in a single dose.
Reduced susceptibility to relevant antibiotics
on antimicrobial susceptibility testing.
 Consult local health department.
Patient cannot use above regimens due
to allergies.
 Obtain clinical consultation with infectious disease
specialist.
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
*Adapted from CDC 2015 STD Treatment Guideline
Recommendations and Requirements:
Sex Partner Exposure to HIV
 Clinicians should educate patients with partners who do not have HIV infection or
partners of unknown HIV status to be vigilant for any post-exposure acute HIV symptoms
in their partners, such as febrile illness accompanied by rash, lymphadenopathy,
myalgias, and/or sore throat. (A3)
 Partners who present within 36 hours of an HIV exposure should be evaluated as soon as
possible for initiation of PEP. (A2)
 NYS Public Health Law mandates that medical providers do the following:
• Report all suspected or confirmed HIV, gonorrhea, and chlamydia diagnoses to the
local health department in the area where the patient resides.
• Talk with individuals with HIV infection about their options for informing their sexual
partners that they may have been exposed to HIV.
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
Recommendations:
Sex Partner Exposure to Gonorrhea/Chlamydia
 Clinicians should advise their patients that sex partners who were exposed up to 60 days
before the source case’s onset of symptoms or diagnosis of gonococcal or chlamydial
infection should seek evaluation and treatment and HIV testing. (A3)
 When a patient with HIV infection is diagnosed with gonorrhea or chlamydia, clinicians
should advise the patient to encourage sex partners to seek medical care for possible
exposure to HIV and gonorrhea and chlamydia and should inform the patient that
NYSDOH Partner Services offers free, confidential partner notification assistance. (A3)
 NYS Public Health Law allows expedited partner therapy (EPT) for the treatment of
exposure to chlamydial infection. It cannot be used to treat other STIs or for patients
also infected with gonorrhea, syphilis and/or HIV.
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
Patient Education
• When a patient with HIV infection is diagnosed with gonococcal or chlamydial infection,
the clinician should inform the patient about the implications of the diagnosis for his/her
sex partner(s):
 A new STI diagnosis signals that the patient was engaging in sexual behaviors that
place any sex partner at increased risk of acquiring HIV infection, and sex partners
should be tested for HIV.
 A sex partner also may have been exposed to gonorrhea or chlamydia and should be
tested and evaluated for treatment.
 A local health department may contact sex partners confidentially about the
potential exposure and treatment options.
• Clinicians should provide patients with information and counseling about risk reduction
and safer sex practices.
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
Need Help?
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
Access the Guideline
 www.hivguidelines.org > STI Care > Management of
Gonorrhea and Chlamydia in Patients with HIV
 Also available: Printable pocket guide; printable PDF
GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org

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NYSDOH AI Management of Gonorrhea and Chlamydia in Patients with HIV

  • 1. Management of Gonorrhea and Chlamydia in Patients with HIV www.hivguidelines.org
  • 2. Purpose of the Guideline • Increase the numbers of NYS residents with HIV and gonococcal or chlamydial coinfection who are identified and treated with effective interventions. • Reduce gonorrhea and chlamydia rates in support of the NYSDOH Prevention Agenda 2013-2018 goals. • Reduce the growing burden of morbidity associated with gonococcal and chlamydial infections. • Integrate current evidence-based clinical recommendations into the healthcare-related implementation strategies of the Ending the Epidemic initiative, which seeks to end the AIDS epidemic in NYS by the end of 2020. GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
  • 3. Recommendations: Transmission and Prevention  Clinicians should inform patients with HIV infection about the risk of acquiring or transmitting chlamydia, gonorrhea, and other STIs from close physical contact with all sites of possible exposure, including the penis, vagina, mouth, or anus. (A3)  When patients with HIV infection are diagnosed with gonococcal or chlamydial infections, clinicians should educate patients about the following: risk-reduction strategies, including the value of correct condom use (A2); the potential for oral transmission of gonorrhea and chlamydia (A3); the benefits of identifying STIs early (A3); and the need for prompt evaluation and treatment of partners (A3). GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
  • 4. Description of Risk Status for Sexual Exposure to Gonorrhea and Chlamydia Risk Level Description No/Low Risk Patient reports no sexual activity or sex only within a mutually monogamous relationship within the year prior Moderate Risk Patient reports a new sex partner within the year prior High Risk Patient self-identifies as being at high risk of sexually transmitted infections (STIs) and/or reports any of the following for self or sex partner(s): • Multiple or anonymous sex partners • Bacterial STI diagnosed since last STI screening • Participation in sex parties or sex in other high-risk venues • Participation in any type of transactional sex • Use of recreational substances during sex GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
  • 5. Recommendation: Obtaining a Sexual History  Clinicians should ask all patients about sexual behaviors and new sex partners at each routine monitoring visit to assess for risk behaviors that require repeat or ongoing screening. GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
  • 6. Who to Screen? • All patients with HIV infection should be serologically screened for gonorrhea and chlamydia at least once per year. • MSM who engage, or whose partners may engage, in continued high-risk behavior should be serologically screened for gonorrhea and chlamydia at least every 3 months. • The diagnosis of another bacterial STI in a patient with HIV infection or a patient’s sex partner should prompt a clinician to perform gonorrhea and chlamydia screening tests and to consider more frequent screening for gonorrhea and chlamydia. • Pregnant patients with HIV infection should be serologically screened for gonorrhea and chlamydia at the first prenatal visit. GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
  • 7. Recommendations: Screening Frequency  For MSM and transgender women who have sex with men, clinicians should perform 3-site screening (genital, pharyngeal, rectal) at the following intervals: • At first visit and annually thereafter if the patient is at low risk of infection. (A2) • At first visit and every 3 months thereafter if the patient is at high risk of infection. (A2)  For all other patients, clinicians should perform genital screening (urine/urethra, vagina/cervix) and extragenital screening (pharyngeal and/or rectal) at sites of contact at the following intervals: • At first visit and annually thereafter if the patient is at low risk of infection. (A2) • At first visit and every 3 months thereafter if the patient is at high risk of infection. (A2)  Clinicians should serologically screen pregnant patients with HIV infection for gonococcal and chlamydial infections at the first prenatal visit. (A2) GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
  • 8. Key Points: Screening Frequency  Because most gonorrheal and chlamydial infections are asymptomatic, regular screening is essential to protect patients’ health and prevent the spread of STIs. This is an essential component of patient education.  Gonococcal and chlamydial screening at least every 3 months is recommended for all individuals at high risk of exposure, including those who: • Have, or whose partners may have, multiple or anonymous sex partners • Engage, or whose partners may engage, in sexual activity at sex parties or other high-risk venues • Are, or whose partners may be, involved in transactional sex (i.e., sex workers and their clients) • Have been diagnosed with a bacterial STI in the previous 12 months • Report recreational substance use during sexual activity • Self-identify as at high risk for STIs GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
  • 9. When to Consider 3-Site Screening • This Committee supports routine 3-site (urine, pharyngeal, and rectal) screening in sexually active MSM and MtF transgender women who have sex with men. • Screening at 3 sites (i.e., genital, pharyngeal, and rectal) is recommended for patients who are included in recognized high-risk groups and for those who report exposure at extragenital sites. GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org • Information about the patient’s sexual behaviors informs decisions about the frequency and type (genital only or 3-site) of screening and points clinicians to key areas to address in risk- reduction counseling. • The recommendation for extragenital (3-site) screening should be discussed with the patient. For individuals who opt out of 3-site screening, testing based on the patient’s reported sites of anatomical exposure should be performed and documented in the medical record.
  • 10. Recommendations: Presentation of Symptomatic Infection GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org  When patients with HIV present with symptoms suggestive of gonococcal or chlamydial infection, clinicians should perform diagnostic testing as recommended in the guideline. (A1)  Clinicians should include lymphogranuloma venereum (LGV) infection in the differential diagnosis for patients who test positive for rectal chlamydial infection or who present with such symptoms as rectal pain, tenesmus, bloody rectal discharge, or isolated, atypical perianal ulcerative lesions and adenopathy. (A2) Key Point: Although LGV occurs only sporadically in the U.S., outbreaks of LGV proctocolitis have been reported among MSM in New York and other U.S. cities, and many of these cases occurred in individuals with HIV.
  • 11. Recommendations: Laboratory-Based Diagnosis GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org  Clinicians should obtain NAAT (preferred) on samples collected from genital and extragenital sites (A1); if NAAT is not available, then clinicians should: • Send alternative samples for culture in accordance with the protocols of the laboratory performing the analysis, with the understanding that culture is significantly less sensitive than NAAT. (A1)  If a patient has a known exposure to a cephalosporin-resistant strain, clinicians should obtain samples for both culture/susceptibility and NAAT testing from the patient and his/her sex partner(s). (A3)  Clinicians should perform syphilis testing for any patient with HIV infection who is diagnosed with a gonorrheal or chlamydial infection. (A2)
  • 12. Sample Collection & Testing Methods Exposure Site Sample Collection Method [a] Comments Urethra First-catch urine for NAAT [b] • In males, for ease of collection, first-catch urine [c] is recommended over urethral swab. Some studies have demonstrated equal specificity but lower sensitivity with urethral swab compared with urine for NAAT. However, additional data are needed to establish the relative effectiveness of these collection methods. Vagina/cervix Vaginal or cervical swab (recommended) or first-catch urine (alternative) NAAT • The recommended sample collection method is a vaginal swab for testing with an FDA-approved assay; this method is equivalent to cervical swab. • First-catch urine testing, which is inferior to swab, may be used as an alternative. • Some NAAT assays are approved for self-collected vaginal samples and perform as well as NAAT for other specimens. Rectum Males and females: Rectal swab for NAAT [b] • Culture is not sufficiently sensitive for detection of rectal C. trachomatis. Pharynx Males and females: Pharyngeal swab for NAAT [b] • Culture is not sufficiently sensitive for detection of pharyngeal C. trachomatis. • The incidence of pharyngeal chlamydial infection is lower than pharyngeal gonorrheal infection, and data on the clinical benefit of treating patients with asymptomatic pharyngeal infection are limited. • To reduce the risk of transmission, this Committee recommends treatment for pharyngeal chlamydial infection, even if the pharynx is the only site of infection. GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
  • 13. Notes: Sample Collection & Testing Methods GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org a. Handling of specimens: Conditions for collection and transport of samples for laboratory testing for C. trachomatis and N. gonorrhoeae may greatly affect the sensitivity of culture because the organisms can degrade easily during transport. Guidance regarding sample collection with either direct plating or the use of specialized transport media for culture should be obtained from the clinician’s laboratory. After collection, culture samples should be stored in the referring laboratory’s recommended transport media and transported at ≤4°C to the laboratory within 24 hours. b. NAAT testing is more sensitive than culture for the detection of gonococcal or chlamydial infections. Although NAAT has not yet received FDA approval for rectal or pharyngeal specimens, NAAT performed by a laboratory with a Clinical Laboratory Evaluation Program- specified protocol is recommended for detecting both rectal and pharyngeal C. trachomatis and N. gonorrhoeae. If NAAT is not available, then culture should be obtained according to the protocols of the clinician’s institution. c. For urine screening, clinicians should provide patients with clear instructions for obtaining a first-catch sample.
  • 14. Reporting: New York State Requirements • Clinicians must report within 24 hours from the time a case is first seen all suspected or confirmed gonorrhea and chlamydia diagnoses to the local health department of the area where the patient resides. • For more information, see the following:  NYSDOH Communicable Disease Reporting: https://www.health.ny.gov/forms/instructions/doh-389_instructions.pdf  NYCDOHMH Reporting Diseases and Conditions: https://www1.nyc.gov/site/doh/providers/reporting-and-services/notifiable- diseases-andconditions-reporting-central.page  NYS Local Health Department Contact List: https://www.health.ny.gov/prevention/prevention_agenda/contact_list.htm GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
  • 15. Recommendations: Treatment of Uncomplicated Gonorrhea GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org  Clinicians should treat uncomplicated gonococcal infections of the cervix, urethra, rectum, or pharynx as follows: • Preferred: Ceftriaxone 250 mg IM injection in a single dose plus azithromycin 1 g by mouth in a single dose. (A2) • Alternative, for patients who are allergic to azithromycin: Ceftriaxone 250 mg IM in a single dose plus doxycycline 100 mg by mouth twice daily for 7 days. (A2) • Alternative, if ceftriaxone is not available: Cefixime 400 mg by mouth in a single dose plus azithromycin 1 g by mouth in a single dose. This regimen is not recommended for treatment of pharyngeal infection. (A2)  Clinicians should instruct patients to abstain from sexual activity for at least 7 days after starting treatment, and to continue to abstain until symptoms resolve and all sex partners are treated. (A2)
  • 16. Key Points: Gonorrhea Treatment GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org  Directly observed treatment provided on-site maximizes adherence.  N. gonorrhoeae has developed resistance to nearly all previously effective antimicrobials, leaving cephalosporins as the only available class of drugs recommended for treatment of gonococcal infections.  Cephalosporin-resistant N. gonorrhoeae has been reported outside of the U.S., and reduced susceptibility to cephalosporins has been observed with isolates of N. gonorrhoeae from residents of NYC.  Combination treatment with two antimicrobials with different mechanisms of action is recommended to slow further emergence of resistance.  People infected with N. gonorrhoeae are frequently coinfected with C. trachomatis.  In the U.S., in 2016, 26.9% of N. gonorrhoeae isolates were quinolone-resistant  Because of fluoroquinolone-resistant N. gonorrhoeae in the U.S., fluoroquinolones other than gemifloxacin should not be used to empirically treat proven or suspected gonococcal infections; however, if fluoroquinolones are being considered, then clinicians should perform fluoroquinolone susceptibility testing before initiating treatment.
  • 17. Recommendations: Treatment of Gonorrhea in Penicillin-Allergic Patients GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org  For patients without prior severe allergic responses to penicillin, clinicians should treat gonococcal infection with a cephalosporin-containing regimen, as recommended above, and monitor carefully for adverse effects. (A2) • Reactions considered severe include the following: severe IgE-mediated response, such as anaphylaxis or urticaria with pruritic rash, or a severe non-IgE-mediated response, such as Stevens-Johnson syndrome, toxic epidermal necrolysis, or drug- induced hypersensitivity with inflammation of internal organs.  For patients with prior severe allergic responses to penicillin, clinicians should treat gonococcal infection with a single dose of azithromycin 2 g by mouth plus a single dose of either gentamicin 240 mg IM or gemifloxacin 320 mg by mouth. (A2)
  • 18. Recommendations: Treatment of Uncomplicated Chlamydia and LGV GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org  Clinicians should treat uncomplicated chlamydial infection of the cervix, urethra, rectum, or pharynx as indicated: (A2)  Recommended: • Azithromycin 1 g by mouth as a single dose OR doxycycline 100 mg by mouth twice daily for 7 days. • Alternatives (NOT recommended for pharyngeal infection):  Erythromycin base 500 mg by mouth 4 times per day for 7 days OR  Erythromycin ethylsuccinate 800 mg by mouth 4 times per day for 7 days OR  Levofloxacin 500 mg by mouth once daily for 7 days OR  Ofloxacin 300 mg by mouth 2 times per day for 7 days. Note: Treat asymptomatic pharyngeal infection even if it is the only site of infection.  Clinicians should treat symptomatic chlamydial proctitis with a medication regimen sufficient to treat LGV. (A3)  Recommended: • Doxycycline 100 mg by mouth twice daily for 21 days OR azithromycin* 1 g by mouth as a single dose once weekly for 3 weeks. • Presumptively treat for LGV (see the NYSDOH AI guideline on LGV); if LGV is excluded by testing, then patients should complete the standard seven-day regimen for uncomplicated chlamydial infection. *Added June 13, 2019.
  • 19. Recommendations: Post-Treatment Follow-Up GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org  Clinicians should follow up with patients who have completed treatment for gonococcal and chlamydial infections as detailed in the guideline. (A3)  Clinicians should rescreen patients who had confirmed gonococcal or chlamydial infection at 3 months post- treatment for evidence of reinfection. (A2)
  • 20. Recommended Follow-Up* Clinical Circumstance Recommended Clinician Follow-Up Patient is asymptomatic after treatment with recommended regimen: • Urogenital or rectal infection treated with preferred or appropriate alternative regimens. • Pharyngeal gonorrhea treated with preferred regimen.  Retest at 3 months (or as close to 3 months as possible) post- treatment to assess for reinfection.  If lab test is positive for N. gonorrhoeae, assess for re-exposure and partner treatment, and re-treat with recommended regimen. Patients is asymptomatic after possibly ineffective course of treatment: • Urogenital or rectal infection treated with regimen other than preferred or alternative regimens. • Pharyngeal infection treated with an alternative regimen. • Suspected nonadherence to full course of treatment  Assess for re-exposure and partner treatment.  Perform a test of cure at site of infection with N. gonorrhoeae NAAT 14 days after completion of treatment.  If test of cure is positive, perform culture and susceptibility testing before retreatment and retreat with recommended regimen if possible.  If recommended regimen cannot be used, retreat with an alternative regimen or according to susceptibility test results. GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org *Adapted from CDC 2015 STD Treatment Guideline
  • 21. Recommended Follow-Up,* continued Clinical Circumstance Recommended Clinician Follow-Up Patient is symptomatic post- treatment: Persistent symptoms post-treatment; infection at any site.  Assess for re-exposure and partner treatment.  Assess patient adherence and use of preferred or appropriate alternative regimen.  Swab symptomatic site(s) for N. gonorrhoeae culture and antibiotic susceptibility testing ≥72 h after treatment. NAAT may be obtained in addition to culture ≥7 days after treatment.  Re-treat for suspected treatment failure.  Assess for STIs that may cause persistent or recurrent symptoms. (Other STIs may include M. genitalium, T. vaginalis, herpes simplex virus, adenovirus, and enteric bacteria.)  For persistent or recurrent urethritis negative for N. gonorrhoeae and C. trachomatis, treat empirically for M. genitalium and/or T. vaginalis according to CDC recommendations.  Assess for non-STI etiologies as part of the differential diagnosis if a patient is repeatedly symptomatic. GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org *Adapted from CDC 2015 STD Treatment Guideline
  • 22. Recommended Follow-Up,* continued Clinical Circumstance Recommended Clinician Follow-Up Patient is asymptomatic after treatment with preferred or alternative regimen.  Retest at 3 months (or as close to 3 months as possible) post-treatment to assess for reinfection.  If laboratory test is positive for C. trachomatis, assess for re-exposure and partner treatment and re-treat with recommended regimen. Patient is symptomatic post- treatment: Persistent symptoms post-treatment; infection at any site.  Perform a test of cure at site of infection with C. trachomatis NAAT 3 weeks after treatment.  If test of cure is positive, assess for re-exposure and partner treatment, and re-treat with recommended treatment regimen using azithromycin or doxycycline. Azithromycin is preferred to maximize adherence.  If test of cure is negative, consider other STIs that may cause persistent or recurrent symptoms (other STIs may include M. genitalium, T. vaginalis, herpes simplex virus, adenovirus, and enteric bacteria).  Consider non-STI etiologies as part of the differential diagnosis when the patient is repeatedly symptomatic. GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org *Adapted from CDC 2015 STD Treatment Guideline
  • 23. Recommendations: Retreatment of Uncomplicated Gonorrhea GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org  Clinicians should re-treat cases of uncomplicated gonococcal infection following suspected treatment failure according to recommendations. (AIII)  NYS Requirement: Clinicians must report cases of suspected gonorrhea treatment failure that are not due to reinfection: • New York State: Report suspected treatment failures to the local health department within 24 hours. • New York City: Call 866-692-3641 to notify the health department of suspected treatment failures. Key Point: Gonococcal and chlamydial reinfection rates are high among people who have been successfully treated.
  • 24. Recommended Regimens for Retreatment Clinical Circumstance Recommended Treatment* Possible reinfection (most cases).  Ceftriaxone 250 mg by mouth in a single dose plus azithromycin 1 g by mouth in a single dose. Low reinfection risk; initial treatment was incomplete or regimen administered was not preferred or alternative.  Ceftriaxone 250 mg by mouth in a single dose plus azithromycin 1 g by mouth in a single dose. Low reinfection risk; initial treatment with cefixime and azithromycin.  Ceftriaxone 250 mg by mouth in a single dose plus azithromycin 2 g by mouth in a single dose. Low reinfection risk; initial treatment with ceftriaxone 250 mg IM and azithromycin 1 g by mouth.  Gentamicin 240 mg IM or gemifloxacin 320 mg by mouth plus azithromycin 2 g by mouth in a single dose. Reduced susceptibility to relevant antibiotics on antimicrobial susceptibility testing.  Consult local health department. Patient cannot use above regimens due to allergies.  Obtain clinical consultation with infectious disease specialist. GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org *Adapted from CDC 2015 STD Treatment Guideline
  • 25. Recommendations and Requirements: Sex Partner Exposure to HIV  Clinicians should educate patients with partners who do not have HIV infection or partners of unknown HIV status to be vigilant for any post-exposure acute HIV symptoms in their partners, such as febrile illness accompanied by rash, lymphadenopathy, myalgias, and/or sore throat. (A3)  Partners who present within 36 hours of an HIV exposure should be evaluated as soon as possible for initiation of PEP. (A2)  NYS Public Health Law mandates that medical providers do the following: • Report all suspected or confirmed HIV, gonorrhea, and chlamydia diagnoses to the local health department in the area where the patient resides. • Talk with individuals with HIV infection about their options for informing their sexual partners that they may have been exposed to HIV. GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
  • 26. Recommendations: Sex Partner Exposure to Gonorrhea/Chlamydia  Clinicians should advise their patients that sex partners who were exposed up to 60 days before the source case’s onset of symptoms or diagnosis of gonococcal or chlamydial infection should seek evaluation and treatment and HIV testing. (A3)  When a patient with HIV infection is diagnosed with gonorrhea or chlamydia, clinicians should advise the patient to encourage sex partners to seek medical care for possible exposure to HIV and gonorrhea and chlamydia and should inform the patient that NYSDOH Partner Services offers free, confidential partner notification assistance. (A3)  NYS Public Health Law allows expedited partner therapy (EPT) for the treatment of exposure to chlamydial infection. It cannot be used to treat other STIs or for patients also infected with gonorrhea, syphilis and/or HIV. GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
  • 27. Patient Education • When a patient with HIV infection is diagnosed with gonococcal or chlamydial infection, the clinician should inform the patient about the implications of the diagnosis for his/her sex partner(s):  A new STI diagnosis signals that the patient was engaging in sexual behaviors that place any sex partner at increased risk of acquiring HIV infection, and sex partners should be tested for HIV.  A sex partner also may have been exposed to gonorrhea or chlamydia and should be tested and evaluated for treatment.  A local health department may contact sex partners confidentially about the potential exposure and treatment options. • Clinicians should provide patients with information and counseling about risk reduction and safer sex practices. GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
  • 28. Need Help? GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org
  • 29. Access the Guideline  www.hivguidelines.org > STI Care > Management of Gonorrhea and Chlamydia in Patients with HIV  Also available: Printable pocket guide; printable PDF GC/CT 2/28/19 NYSDOH AIDS Institute Clinical Guidelines Program www.hivguidelines.org