|ORIGINAL ARTICLE: EPIDEMIOLOGY OF CANCER AND CANCER SCREENING
|Year : 2020 | Volume
| Issue : 1 | Page : 13-16
Reliability of conventional Papanicolaou smear in diagnosing bacterial vaginosis among women with clinical genital infection
Kavita Vivek Anand1, Sharmila Anil Pimple1, Gauravi A Mishra1, Rupali V Sahare2, Saleem Pathuthara3, Kedar K Deodhar4, Surendra S Shastri5
1 Department of Preventive Oncology, Tata Memorial Centre, Affliliated to Homi Bhabha National Institute, Mumbai, Maharashtra, India
2 Department of Microbiology, R. N. Cooper General Hospital, Tata Memorial Hospital, Mumbai, Maharashtra, India
3 Department of Cytopathology, Tata Memorial Hospital, Mumbai, Maharashtra, India
4 Department of Pathology, Tata Memorial Hospital, Mumbai, Maharashtra, India
5 Department of Health Disparities Research, Division of Cancer Prevention and Population Science, MD Anderson Cancer Centre, Houston, USA
|Date of Web Publication||26-Dec-2019|
Dr. Sharmila Anil Pimple
Department of Preventive Oncology, Tata Memorial Centre, Affliliated to Homi Bhabha National Institute, Mumbai, Maharashtra
Source of Support: None, Conflict of Interest: None
Objective: Bacterial vaginosis (BV) is a common reproductive tract infection (RTI) reported among Indian women. BV can influence the persistence of high-risk oncogenic human papillomavirus, a causative factor for cervical cancer. BV and cervical cancer are major public health issues in a developing country like India. It becomes important for a resource-constrained country like India with poor healthcare access to implement control measures to screen and treat RTI in an attempt to prevent the risk for cervical cancer. Papanicolaou (Pap) smear is an established screening tool for cervical cancer and the diagnosis of RTIs, forms a part of its evaluation. The present study explores the validity of conventional Pap smear in diagnosing BV. Methodology: Pap smear and Gram stain smear were collected for 254 women with clinically evident cervicitis/cervicovaginitis (genital infection). Using the Nugent score on Gram stain as a gold standard, we determined the sensitivity and specificity of Pap smear to diagnose BV. Results: The overall prevalence of BV in the study population was 44% using the Nugent score. Pap smear showed sensitivity and specificity of 70.9%. (CI- 61.5% - 79.2%) and 56.8% (CI – 48.2%–65.2%), respectively. The positive predictive value of Pap smear to diagnose BV was 56.5% (CI – 47.8%–64.9%), and the negative predictive value was 71.2% (CI – 61.8%–79.4%). Conclusion: In the present study, conventional Pap smear demonstrates good accuracy to detect BV. Pap testing for cervical cancer screening can additionally serve as an effective screening tool for diagnosing BV among women with genital infection in healthcare settings.
Keywords: Bacterial vaginosis, cervicitis, human papillomavirus, Nugent score, Papanicolaou smear
|How to cite this article:|
Anand KV, Pimple SA, Mishra GA, Sahare RV, Pathuthara S, Deodhar KK, Shastri SS. Reliability of conventional Papanicolaou smear in diagnosing bacterial vaginosis among women with clinical genital infection. South Asian J Cancer 2020;9:13-6
|How to cite this URL:|
Anand KV, Pimple SA, Mishra GA, Sahare RV, Pathuthara S, Deodhar KK, Shastri SS. Reliability of conventional Papanicolaou smear in diagnosing bacterial vaginosis among women with clinical genital infection. South Asian J Cancer [serial online] 2020 [cited 2020 Apr 2];9:13-6. Available from: http://journal.sajc.org/text.asp?2020/9/1/13/274067
| Introduction|| |
The midterm report of the National AIDS Control Organization (NACO), India, which was based on a review of published and unpublished population-based studies, reported bacterial vaginosis (BV) to be the most common reproductive tract infections (RTIs) among Indian women. A huge burden of symptomatic/asymptomatic BV is reported worldwide., There is emerging evidence of a strong association between cervicitis and BV.,
BV infection needs to be addressed as it has the potential to cause maternal morbidity due to its association with common conditions such as pelvic inflammatory disease, chorioamnionitis, and preterm labor in women. Due to the change in vaginal microbiological flora and inflammation associated with BV, it may help in acquiring and transmitting human papillomavirus (HPV) infection which is the main cause for cervical cancer. The inflammation of the cervix causes break in the cervical epithelium helping the HPV to gain entry in the actively proliferating basal cells of the cervical epithelium. Inflammation is known to cause DNA damage of the host cell leading to the integration of viral DNA, which leads to gradual progression of HPV infection to microinvasion and invasive cervical cancer. BV may serve as a cofactor for the persistence of high-risk HPV, thus diagnosing and treating BV infection may help to reduce the risk of cervical cancer in women.,,,,
Papanicolaou (Pap) smear beside an established screening test for the detection of cervical precancerous lesions is also posed to diagnose sexually transmitted infections (STI)/reproductive transmitted infections (RTIs). Pap smear has the potential to serve as a cost-effective tool for dual screening of BV and cervical cancer which are the most common cause of morbidity and mortality reported among Indian women., Among the RTIs, the role of Pap smear to diagnose BV has conflicting results reported from several developed and developing countries.,,,,,, There is limited evidence from India about the accuracy of Pap smear in detecting BV. To the best of our knowledge, the only community-based study conducted from India demonstrated encouraging results of Pap smear to diagnose BV infection with sensitivity of 78%. The present study evaluates the accuracy of Pap smear to diagnose BV infection in women with clinically evident genital infection using the Nugent score on Gram-stained smear as the gold standard.,, The microbiology evaluation to diagnose BV infection by the Nugent score done for the women enrolled in the present study is a part of the main study which looks into “Performance of HPV DNA test in the presence of coinfection with common RTIs”.
| Methodology|| |
The study design is a prospective blinded cross-sectional study of women in the reproductive age group who presented for routine cervical cancer screening in a tertiary care institute between August 2016 and August 2018.
The inclusion criteria for the study were nonpregnant women in the age group of 30–50 years and having clinically evident cervicitis/cervicovaginitis (genital infection) on per speculum examination. The case definition of cervicitis was unhealthy cervix with the presence of cervical erythema and inflammation that bleeds on touch with mucopurulent/purulent discharge. Among 3900 women visiting the department of cancer screening during the period from August 2016 to August 2018, 2407 nonpregnant women in the age group of 30–50 years were screened for the eligibility criteria of clinically evident genital infection on per speculum examination. Two hundred and fifty-four women who satisfied the eligibility criteria were consented for recruitment in the study.
The women were then interviewed for sociodemographic data, reproductive history, medical history, and symptoms pertaining to STIs/RTIs such as white discharge per vaginum, lower abdominal pain, burning micturition, dyspareunia, and postcoital bleeding. The information was captured on a prestructured, validated proforma.
Smears of cervicovaginal discharge for Gram stain followed by Pap smear were taken for all the women enrolled in the study. All the women received treatment for genital infection(s).
Conventional Pap smears were obtained using sterilized, moistened cotton-tipped swab sticks, by standardized procedure, as a part of the routine screening test for cervical cancer. The Pap smear was collected from the transformation zone, lateral vaginal wall, and endocervix. The cytopathology department evaluated the Pap smears by the Bethesda system 2014. The cytologist was blinded to the clinical per speculum examination findings and the Nugent score on Gram stain.
Pap smear criteria for diagnosing BV was: “individual squamous cells covered by a layer of coccobacilli that obscure cell membrane, forming the so-called clue cells. The presence of a large number of inflammatory cells representing vaginitis with the conspicuous absence of lactobacilli” [Figure 1].
|Figure 1: Papanicolaou smear showing superficial and intermediate squamous epithelial cells studded with coccobacilli giving the characteristic “Clue cells” appearance diagnostic of bacterial vaginosis (Papanicolaou, ×200)|
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Sterile soft cotton-tipped swab stick was used to collect the discharge for Gram staining. The cervicovaginal swab was collected by inserting the cotton-tipped swab stick in the endocervix and rotated to collect the endocervical discharge, and the vaginal discharge was collected from posterior fornices and lateral vaginal walls for all women enrolled in the study. The discharge was uniformly spread on a glass slide. The smears were heat fixed and transferred to the Microbiology Department of collaborating institute for Gram staining and evaluation. The microbiologist was blinded to Pap smear results and clinical per speculum examination findings.
The gram-stained slides were evaluated for BV using the Nugent scoring system. The slides were read at ×1000 using oil immersion. The Nugent score uses a system of scoring points allotted to number of different bacteria present in the sample, different bacterial morphology, and amount of lactobacillus present. The score ranges from 0 to 10. A total score of 0–3 is considered as normal vaginal flora, a score of 4–6 is classified as intermediate flora, and a score of 7–10 is considered to be consistent with a diagnosis of BV.
The main study was a collaborative study between the Department of Microbiology of Municipal General Hospital and cancer screening department of a tertiary cancer hospital. The study protocol was reviewed and approved by the Institutional Review and Ethics committees of participating centers.
The data were captured and analyzed using the Statistical Package for the Social Sciences (SPSS-v24) for frequency distribution. The test characteristics in terms of sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) of Pap smear were calculated using Stata 13.0.
| Results|| |
A total of 254 women with clinically evident genital infection on per speculum examination were enrolled in the study. The mean age of women was 38 years. Among the women enrolled in the study, 204 (80.3%) women were symptomatic for STIs/RTIs complaints, whereas 50 (19.7%) were asymptomatic. One hundred and twelve (44.1%) women were diagnosed with BV by the Nugent score whereas Pap smear reported BV in 138 (55.4%) women [Table 1].
|Table 1: Prevalence of bacterial vaginosis among women with clinical evident genital infection|
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Among 254 women, five (2%) women had Pap smear reported inadequate for evaluation. Eighty-nine (35%) women had normal/inflammatory smear reported without infection. Overall in the study population (n = 254), Pap smear reported BV infection in 138 (54.3%) women and epithelial cell abnormality in 46 (18.1%) women. Thirty-one (12.2%) women among the study population had BV infection associated with epithelial cell abnormalities reported on Pap smear. Candida infection or trichomoniasis infection was reported in seven (2.8%) women [Table 2].
|Table 2: Distribution of Papanicolaou smear results among women with clinically evident genital infection|
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Using the Nugent score for diagnosing BV as the gold standard, Pap smear showed sensitivity and specificity of 70.9% (confidence interval [CI] – 61.5%–79.2%) and 56.8% (CI – 48.2%–65.2%), respectively. PPV was 56.5% (CI – 47.8%–64.9%) and NPV was 71.2% (CI – 61.8%–79.4%) [Table 3].
|Table 3: Comparison of Papanicolaou smear and Nugent criteria for the diagnosis of bacterial vaginosis|
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| Discussion|| |
As per the NACO 2012 report, the prevalence of BV infection among Indian women varied between 17.8% and 63.7%. In the present study population, the prevalence of BV infection was 44.1% by the Nugent score. About 19.7% of women were asymptomatic, which indicates a possibility of large number of undiagnosed asymptomatic genital infections among Indian women [Table 1]. BV infection has the potential to serve as a cofactor for persistent high-risk HPV in the pathogenesis of cervical precancerous/cancerous lesions. Among the present study population, 18.1% (n = 46/254) women reported epithelial cell abnormalities on the Pap smear [Table 2]. Among 46 epithelial cell abnormalities (ASCUS and above lesions) reported on Pap smear, 67.3% (n = 31/46) of patients were reported to be associated with BV infection demonstrating the need to treat BV infection.
Pap smear is an established screening tool to detect epithelial cell abnormalities associated with cervical precancerous/cancerous lesions. The Amsel criteria and Nugent score are the two most commonly evaluated gold standard methods to diagnose BV infection.,,,,,,, The aim of the present study was to evaluate the test characteristics of Pap smear as a screening tool for diagnosing BV infection using a Nugent score of 7 and above.
The 1991 Bethesda system for reporting cervicovaginal cytology stated predominance of coccobacilli to be consistent with the shift of vaginal flora but was not sufficient to diagnose BV infection. Later, Prey et al. demonstrated that 96% of women showing a predominance of coccobacilli on Pap smear also had reported BV infection on Gram stain. Tokyol et al. in their study reported the sensitivity and specificity of Pap smear in diagnosing BV to be 43.1% and 93.6%, respectively, using the Nugent score as the gold standard. The low sensitivity of Pap smear to diagnose BV infection may be attributed to evaluating cervical swab instead of the vaginal swab for diagnosing BV infection on Gram staining since BV is primarily a vaginal infection.
Compared to other studies,,, the present study reported an improved sensitivity of 70.9% and specificity of 56.8% of Pap smear to diagnose BV infection. The PPV and NPV of Pap smear to diagnose BV was 56.5% and 71.2%, respectively [Table 3].
The higher sensitivity of Pap for detecting BV infection in the present study may be attributed first to the standard procedure of performing Pap smear as per protocol of the institute to include the area of transformation zone, vagina, and endocervix, and hence that Pap smear has both vaginal and cervical components. Second, women enrolled in the study were with a clinically evident genital infection on per speculum examination, and thus, the positivity rates of BV were expected to be high among these women. Third, Pap smear slides were reported by trained cytotechnologist of the tertiary care cancer institute with the National Accreditation Board for Testing and Calibration Laboratories accredited laboratory. The reasons for low specificity of Pap smear to diagnose BV infection may be due to first, the vaginal microbiological flora consists of several types of obligate and facultative anaerobic bacteria that are commensal, including Gardnerella vaginalis, Peptostreptococcus species, and Bacteroides species. Overgrowth of the above-mentioned organisms is the main cause for BV infection among women. The Nugent score on Gram stain has a standard scoring system that takes into consideration different bacterial morphologies of the above-mentioned organisms and their number present in the given high-power field (HPF) along with lactobacilli to distinguish the normal/intermediate vaginal flora from BV infection. Pap smear unlike Nugent score lacks standardized scoring system to identify the number of bacteria and lactobacilli present per HPF, a needed prerequisite for diagnosing BV infection. The standard Pap stain used for Pap smear under good magnification power of objective lenses can identify the morphology of the bacteria (cocci, bacilli, and coccobacilli) but has limitations to comment on Gram-positive/Gram-negative nature of bacteria. Finally, criteria to diagnose BV infection by Pap smear which is consistent with “shift of vaginal flora suggestive of BV” and not “vaginitis” may be due to normal/intermediate vaginal flora due to other obligate and facultative anaerobic bacteria present in vaginal flora that clearly does not prove clinical infection.,
| Conclusion|| |
BV infection is the most common female RTI reported from the Indian subcontinent. Unwillingness on the part of Indian women to attend health care facilities for STI/RTI screening and treatment due to poor access, an inadequate number of laboratory diagnostic facilities in public health program settings makes them prone for lower genital tract infections. Persistent untreated genital tract infections can increase the susceptibility of acquiring HPV infection. Acquisition and persistence of high-risk HPV have significant implications for contributing to cervical carcinogenesis.,
The Pap smear primarily is a screening test for cervical cancer however, the reporting of STIs/RTIs forms a part of evaluation as per the framework provided by the Bethesda system for evaluation of Pap smears. Since the accuracy of diagnosing clinical BV infection varies and the majority of women with BV infection can be asymptomatic, Pap smear may serve as a means of diagnosing BV infection in resource-constrained countries like India. In the present study, Pap smear was found to be a fairly reliable tool for diagnosing BV among women with genital infection without the requirement of additional diagnostic tests or cost of Gram stain, which itself is not routinely done in Indian health-care settings. Thus, facilities of Pap smear where available should be utilized to screen and treat women for BV promptly to reduce associated morbidity with BV infection.
The authors would like to thank Mrs Savita R. Karnad, Scientific Officer Department of Microbiology, Dr. R.N Cooper Hospital and Dr. Kishore Bisure, Prof and Head Department of Microbiology, Dr. R.N. Cooper General Hospital, Mumbai for the technical support to the manuscript. We thank Dr. Pramod Kharade for the support to conduct the study, Mr S.G. Raybhattanavar for management of data accuracy.
Financial support and sponsorship
This study was financially supported by Intramural funding of Research Administration Council, Tata Memorial Centre. Grant No 1671.
Conflicts of interest
There are no conflicts of interest.
| References|| |
Sodhani P, Garg S, Bhalla P, Singh MM, Sharma S, Gupta S. Prevalence of bacterial vaginosis in a community setting and role of the pap smear in its detection. Acta Cytol 2005;49:634-8.
Marrazzo JM, Wiesenfeld HC, Murray PJ, Busse B, Meyn L, Krohn M, et al.
Risk factors for cervicitis among women with bacterial vaginosis. J Infect Dis 2006;193:617-24.
Paavonen J, Critchlow CW, DeRouen T, Stevens CE, Kiviat N, Brunham RC, et al.
Etiology of cervical inflammation. Am J Obstet Gynecol 1986;154:556-64.
Peipert JF, Montagno AB, Cooper AS, Sung CJ. Bacterial vaginosis as a risk factor for upper genital tract infection. Am J Obstet Gynecol 1997;177:1184-7.
Woodman CB, Collins SI, Young LS. The natural history of cervical HPV infection: Unresolved issues. Nat Rev Cancer 2007;7:11-22.
Nam KH, Kim YT, Kim SR, Kim SW, Kim JW, Lee MK, et al.
Association between bacterial vaginosis and cervical intraepithelial neoplasia. J Gynecol Oncol 2009;20:39-43.
Gillet E, Meys JF, Verstraelen H, Verhelst R, De Sutter P, Temmerman M, et al.
Association between bacterial vaginosis and cervical intraepithelial neoplasia: Systematic review and meta-analysis. PLoS One 2012;7:e45201.
Williams VM, Filippova M, Soto U, Duerksen-Hughes PJ. HPV-DNA integration and carcinogenesis: Putative roles for inflammation and oxidative stress. Future Virol 2011;6:45-57.
International Agency for Research on Cancer. Human papillomaviruses. IARC Monographs on the Evaluation of Carcinogenic Risks to Humans. Vol. 64. International Agency for Research on Cancer; 1995.
Walboomers JM, Jacobs MV, Manos MM, Bosch FX, Kummer JA, Shah KV, et al.
Human papillomavirus is a necessary cause of invasive cervical cancer worldwide. J Pathol 1999;189:12-9.
Nayar R, Wilbur DC. The pap test and Bethesda 2014. “The reports of my demise have been greatly exaggerated.” (after a quotation from mark Twain). Acta Cytol 2015;59:121-32.
Prey M. Routine pap smears for the diagnosis of bacterial vaginosis. Diagn Cytopathol 1999;21:10-3.
Eriksson K, Forsum U, Bjørnerem A, Platz-Christensen JJ, Larsson PG. Validation of the use of pap-stained vaginal smears for diagnosis of bacterial vaginosis. APMIS 2007;115:809-13.
Davis JD, Connor EE, Clark P, Wilkinson EJ, Duff P. Correlation between cervical cytologic results and gram stain as diagnostic tests for bacterial vaginosis. Am J Obstet Gynecol 1997;177:532-5.
Tokyol C, Aktepe OC, Cevrioǧlu AS, Altindiş M, Dilek FH. Bacterial vaginosis: Comparison of pap smear and microbiological test results. Mod Pathol 2004;17:857-60.
Karani A, De Vuyst H, Luchters S, Othigo J, Mandaliya K, Chersich MF, et al.
The pap smear for detection of bacterial vaginosis. Int J Gynaecol Obstet 2007;98:20-3.
Greene JF 3rd
, Kuehl TJ, Allen SR. The Papanicolaou smear: Inadequate screening test for bacterial vaginosis during pregnancy. Am J Obstet Gynecol 2000;182:1048-9.
Wang J. Bacterial vaginosis. Prim Care Update Ob Gyns 2000;7:181-5.
Nugent RP, Krohn MA, Hillier SL. Reliability of diagnosing bacterial vaginosis is improved by a standardized method of gram stain interpretation. J Clin Microbiol 1991;29:297-301.
Money D. The laboratory diagnosis of bacterial vaginosis. Can J Infect Dis Med Microbiol 2005;16:77-9.
Platz-Christensen JJ, Larsson PG, Sundström E, Wiqvist N. Detection of bacterial vaginosis in wet mount, Papanicolaou stained vaginal smears and in gram stained smears. Acta Obstet Gynecol Scand 1995;74:67-70.
Vardar E, Maral I, Inal M, Ozgüder O, Tasli F, Postaci H. Comparison of gram stain and pap smear procedures in the diagnosis of bacterial vaginosis. Infect Dis Obstet Gynecol 2002;10:203-7.
Siddig EE, Albari RF, Mohamed MA, Elamin BK, Edris AM. Bacterial vaginosis in Khartoum state, Sudan: Comparison of gram stain with pap test procedures. Afr J Microbiol Res 2017;11:644-8.
Luff RD. The Bethesda system for reporting cervical/vaginal cytologic diagnoses. Report of the 1991 Bethesda workshop. Am J Clin Pathol 1992;98:152-4.
Larsen B, Monif GR. Understanding the bacterial flora of the female genital tract. Clin Infect Dis 2001;32:e69-77.
Giacomini G, Paavonen J, Rilke F. Microbiologic classification of cervicovaginal flora in Papanicolaou smears. Acta Cytol 1989;33:276-8.
Giacomini G, Schnadig VJ. The cervical Papanicolaou smear: Bacterial infection and the Bethesda system. Acta Cytol 1992;36:109-10.
Kharsany AB, Hoosen AA, Moodley J, Bagaratee J, Gouws E. The association between sexually transmitted pathogens and cervical intra-epithelial neoplasia in a developing community. Genitourin Med 1993;69:357-60.
[Table 1], [Table 2], [Table 3]