Cervicitis is a clinical syndrome characterized by inflammation of primarily the columnar epithelium of the uterine endocervix. It can be acute or chronic, with acute having infectious causes, and chronic having mostly non-infectious sources. The clinical spectrum of the disease varies widely, from asymptomatic cases to patients with mucopurulent cervical discharge and systemic signs. Any of these cases has the potential to develop devastating complications like pelvic inflammatory disease (PID), irrespective of the initial presentation. It is, therefore, very important for the clinician to recognize the symptoms, investigate and reach a diagnosis promptly, and initiate effective treatment immediately.[1]
The etiology can be broadly classified into infectious and non-infectious. Infectious agents include Neisseria gonorrhea, Chlamydia trachomatis, and less commonly, herpes simplex, Trichomonas vaginalis, and Mycoplasma genitalium. Neisseria and chlamydia primarily infect the columnar epithelium of endocervix, whereas HSV and trichomonas affect the squamous epithelium of ectocervix.[2][3] Bacterial vaginosis has also been associated with cervicitis.[4]
Non-infectious causes include mechanical and chemical irritants. Surgical instruments or foreign objects like pessaries, condoms, diaphragms, cervical caps, or tampons can cause mechanical trauma. Chemical irritants cause allergic reactions and include soaps, laundry products, spermicides, latex, vaginal douches, and contraceptive creams.[1][5]
Systemic inflammatory diseases like lichen planus and Behcet syndrome have also been implicated in cervicitis. The hypoestrogenic state seen with natural or surgical menopause can mimic cervicitis. This is due to the atrophy of the vaginal and uterine lining.[1] However, the exact etiology cannot be determined in more than half the cases.[6] It is not clinically possible to differentiate the inflammation caused by mechanical or chemical irritants from that caused by infectious etiologies.
The exact prevalence of cervicitis is difficult to determine due to the lack of a standard definition and variation by population. Since sexual activity is the main risk factor for the infectious causes, it may affect about 30%-40% of the patients seen in sexually transmitted infection (STI) clinics.[3][7]
The highest incidence is in sexually active women aged 15 to 24.[8] It is more common in human immunodeficiency virus (HIV) positive women, with an estimate of 7400 per 100,000 women diagnosed with HIV. Mycoplasma is the commonly implicated agent in this population.[9] Chlamydia cervicitis is 4 to 5 times more common than gonococcal cervicitis.[10]
It was demonstrated by Taylor et al. that 61% of women enrolled in a randomized trial were negative for chlamydia, Neisseria, trichomonas, or mycoplasma by nucleic acid amplification testing (NAAT).[6] Many such studies have proven that we are unable to determine the etiological agent for cervicitis in many of the cases.[4][11]
When viewed microscopically, cervical Gram stains with more than 30 white blood cells (WBCs) per high power field (HPF) are labeled as cervicitis.[3] Histopathology and Gram staining have no clinical utility in the diagnostic evaluation of women with physical findings of cervicitis because they show non-specific inflammatory infiltrate.[12]
A thorough medical history is instrumental in the identification of risk factors. Both symptomatic and asymptomatic women who come in for screening should be asked their sexual history in detail with the use of the 5 Ps: partners, practices, prevention of pregnancy, protection from STIs, and previous STIs. Typical symptoms reported include purulent or mucopurulent vaginal discharge and intermenstrual or post-coital bleeding. Dyspareunia has also been reported. An in-depth inquiry should also be carried out for the associated symptoms, i.e., urinary symptoms (for concomitant urethritis), and abdominal pain (for PID or endometritis).
All women with suspicion of cervicitis should undergo pelvic and vaginal examinations. The classic signs include yellow or mucoid discharge from the os and easy bleeding of the endocervix on touching with cotton applicator (also called friability). However, a normal physical exam does not rule out an infection. Additionally, punctate hemorrhages (strawberry vagina) is suggestive of trichomonas, while vesicles and ulcers indicate an HSV infection. Mycoplasma cervicitis is asymptomatic in many patients; therefore, many cases remain undiagnosed.[13]
Upper genital involvement should be suspected in the case of high fever, abdominal or adnexal tenderness, and cervical motion tenderness.
Once a clinical diagnosis has been established after a thorough history and physical exam, the initial investigation is for the identification of the causative organism. The most sensitive and specific test is the nucleic acid amplification testing (NAAT) for the most common organisms, chlamydia, and Neisseria. NAAT can be performed on endocervical, vaginal fluid, or urine samples.[14]
In the case of concurrent vaginal infection, testing for trichomonas, and bacterial vaginosis (BV) should be done. Saline microscopy, amine whiff test, and vaginal pH are performed for BV, whereas NAAT is the preferred test for trichomonas.[2] If these organisms are not identified, NAAT for mycoplasma may be done. Testing for HSV is not recommended unless there is high clinical suspicion.
The resolution of symptoms is dependent on the etiology of cervicitis. According to the CDC guidelines, empiric treatment is recommended for women at higher risk of STIs, which include women <25, those with a new sexual partner, a partner with an STI, or multiple concurrent sexual partners. For these women, antimicrobials to cover for chlamydia and gonorrhea is given. Empiric treatment is also suggested for women with no identifiable pathogen on testing. Treatment can be deferred until the confirmatory tests are available for women at lower risk of STIs. According to the guidelines published by Institut national d’excellence en Sante et en services sociaux (INESSS), the empiric regimens are as follows:
For infectious agents identified by laboratory investigations, the treatment is as follows:
Treatment of sexual partners is also recommended, and sexual activity should be stopped until completion of therapy and resolution of treatment.[2] HIV positive women with cervicitis are given the same treatment as HIV negative. Prompt treatment in these women reduces viral shedding and may reduce the risk of HIV transmission.[16]
Women with cervicitis usually have a high risk of concurrent STIs and should be evaluated for them. If testing for infection is negative, then non-infectious causes are investigated, including tests for contact dermatitis and systemic diseases like lichen planus. In postmenopausal women, genitourinary syndrome of menopause may mimic cervicitis. However, it presents with other symptoms of the syndrome, including atrophic vaginitis.[17]
The overall prognosis of infectious causes cervicitis is good. Recovery is within a week, or two and a test of cure is not required.
In the case of treatment failure and recurrent infection, the first step is to confirm the eradication of the causative organisms by repeat testing. A thorough history is taken for an assessment of re-exposure (e.g., new or untreated sexual partner) and for non-infectious causes (e.g., chemical irritants and systemic diseases). Once the infection has been ruled out, there are no clear options for further management. Persistent antibiotic therapy is also not recommended due to lack of evidence of benefit and concerns for antibiotic resistance.[2]
The term chronic cervicitis is used for women with persistent discharge for three months despite the resolution/exclusion of infection. Usually, it is caused by non-infectious sources, and there is no standard approach to these cases. This cervicitis of unknown etiology may respond to antibiotics, silver nitrate, or loop electrosurgical excision procedure.[18]
Ascension of infection into the upper genital tract and development of pelvic inflammatory disease is the feared complication of this cervicitis. PID can cause inflammation and scarring of the fallopian tubes and can further have both acute and chronic sequelae, which include abscess formation, chronic pain and infection, ectopic pregnancy, and infertility. One study showed that with a delay of care, PID due to chlamydia can increase the risk of infertility by three-fold.[19]
As with all sexually transmitted infections, patient education and preventative medicine is the key to decreasing the prevalence of this disease. The ABC (abstinence, being faithful, condom use) strategy of STI prevention has the potential to curb the spread of this disease as well.[20] It is especially important for women of childbearing age to seek prompt treatment so that the myriad of complications that arise from upper genital tract disease can be avoided.
Cervicitis is primarily a sexually transmitted infection. Therefore, its control requires an interprofessional approach that encompasses preventive medicine at the level of primary care clinicians, as well as effective management of the patients at secondary and tertiary healthcare facilities. The interprofessional team involves clinicians who diagnose and initiate treatment, nurses who monitor the condition of the patient, and pharmacists who tailor the drugs according to each patient.
In complicated cases (e.g., cervicitis complicated by PID), a gynecologic or surgical consultation may be necessary. Sexually transmitted infection clinics also play a vital role in the identification and management of cervicitis. For improved outcomes and better patient care, effective communication between the members of the team as well as with the outpatient and STI clinics is essential. This would provide the clinicians with an in-depth history of the case and enable them to have a patient-centered approach. [Level 1 and 2]
[1] | Wilson JF, In the clinic. Vaginitis and cervicitis. Annals of internal medicine. 2009 Sep 1; [PubMed PMID: 19721016] |
[2] | Workowski KA,Bolan GA, Sexually transmitted diseases treatment guidelines, 2015. MMWR. Recommendations and reports : Morbidity and mortality weekly report. Recommendations and reports. 2015 Jun 5; [PubMed PMID: 26042815] |
[3] | Marrazzo JM,Martin DH, Management of women with cervicitis. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America. 2007 Apr 1; [PubMed PMID: 17342663] |
[4] | Marrazzo JM,Wiesenfeld HC,Murray PJ,Busse B,Meyn L,Krohn M,Hillier SL, Risk factors for cervicitis among women with bacterial vaginosis. The Journal of infectious diseases. 2006 Mar 1; [PubMed PMID: 16453256] |
[5] | Taylor SN, Cervicitis of unknown etiology. Current infectious disease reports. 2014 Jul; [PubMed PMID: 24859465] |
[6] | Taylor SN,Lensing S,Schwebke J,Lillis R,Mena LA,Nelson AL,Rinaldi A,Saylor L,McNeil L,Lee JY, Prevalence and treatment outcome of cervicitis of unknown etiology. Sexually transmitted diseases. 2013 May; [PubMed PMID: 23588127] |
[7] | Manhart LE,Critchlow CW,Holmes KK,Dutro SM,Eschenbach DA,Stevens CE,Totten PA, Mucopurulent cervicitis and Mycoplasma genitalium. The Journal of infectious diseases. 2003 Feb 15; [PubMed PMID: 12599082] |
[8] | Satterwhite CL,Torrone E,Meites E,Dunne EF,Mahajan R,Ocfemia MC,Su J,Xu F,Weinstock H, Sexually transmitted infections among US women and men: prevalence and incidence estimates, 2008. Sexually transmitted diseases. 2013 Mar; [PubMed PMID: 23403598] |
[9] | Dehon PM,Hagensee ME,Sutton KJ,Oddo HE,Nelson N,McGowin CL, Histological Evidence of Chronic Mycoplasma genitalium-Induced Cervicitis in HIV-Infected Women: A Retrospective Cohort Study. The Journal of infectious diseases. 2016 Jun 1; [PubMed PMID: 26783349] |
[10] | Burnett AM,Anderson CP,Zwank MD, Laboratory-confirmed gonorrhea and/or chlamydia rates in clinically diagnosed pelvic inflammatory disease and cervicitis. The American journal of emergency medicine. 2012 Sep; [PubMed PMID: 22030186] |
[11] | Pollett S,Calderon M,Heitzinger K,Solari V,Montano SM,Zunt J, Prevalence and predictors of cervicitis in female sex workers in Peru: an observational study. BMC infectious diseases. 2013 Apr 30; [PubMed PMID: 23631602] |
[12] | Marrazzo JM,Handsfield HH,Whittington WL, Predicting chlamydial and gonococcal cervical infection: implications for management of cervicitis. Obstetrics and gynecology. 2002 Sep; [PubMed PMID: 12220782] |
[13] | Tosh AK,Van Der Pol B,Fortenberry JD,Williams JA,Katz BP,Batteiger BE,Orr DP, Mycoplasma genitalium among adolescent women and their partners. The Journal of adolescent health : official publication of the Society for Adolescent Medicine. 2007 May; [PubMed PMID: 17448398] |
[14] | Recommendations for the laboratory-based detection of Chlamydia trachomatis and Neisseria gonorrhoeae--2014. MMWR. Recommendations and reports : Morbidity and mortality weekly report. Recommendations and reports. 2014 Mar 14; [PubMed PMID: 24622331] |
[15] | Young C,Argáez C, 2017 Sep 21; [PubMed PMID: 30234930] |
[16] | Gitau RW,Graham SM,Masese LN,Overbaugh J,Chohan V,Peshu N,Richardson BA,Jaoko W,Ndinya-Achola JO,McClelland RS, Effect of acquisition and treatment of cervical infections on HIV-1 shedding in women on antiretroviral therapy. AIDS (London, England). 2010 Nov 13; [PubMed PMID: 20871388] |
[17] | Portman DJ,Gass ML, Genitourinary syndrome of menopause: new terminology for vulvovaginal atrophy from the International Society for the Study of Women's Sexual Health and the North American Menopause Society. Menopause (New York, N.Y.). 2014 Oct; [PubMed PMID: 25160739] |
[18] | Mattson SK,Polk JP,Nyirjesy P, Chronic Cervicitis: Presenting Features and Response to Therapy. Journal of lower genital tract disease. 2016 Jul; [PubMed PMID: 27243142] |
[19] | Hillis SD,Joesoef R,Marchbanks PA,Wasserheit JN,Cates W Jr,Westrom L, Delayed care of pelvic inflammatory disease as a risk factor for impaired fertility. American journal of obstetrics and gynecology. 1993 May; [PubMed PMID: 8498436] |
[20] | Shafer CW, STD prevention: why limit ourselves to just an ounce? South Dakota medicine : the journal of the South Dakota State Medical Association. 2015; [PubMed PMID: 25985610] |