Literature DB >> 25568514

Clinical characteristics of aerobic vaginitis and its association to vaginal candidiasis, trichomonas vaginitis and bacterial vaginosis.

Mahira Jahic1, Mirsada Mulavdic2, Jasmina Nurkic3, Elmir Jahic4, Midhat Nurkic4.   

Abstract

AIM OF THE WORK: Examine clinical characteristics of aerobic vaginitis and mixed infection for the purpose of better diagnostic accuracy and treatment efficiency.
MATERIALS AND METHODS: Prospective research has been conducted at Clinic for Gynecology and Obstetrics, Department for Microbiology and Pathology at Polyclinic for laboratory diagnostic and Gynecology and Obstetrics Department at Health Center Sapna. Examination included 100 examinees with the signs of vaginitis. EXAMINATION CONSISTED OF: anamnesis, clinical, gynecological and microbiological examination of vaginal smear.
RESULTS: The average age of the examinees was 32,62±2,6. Examining vaginal smears of the examinees with signs of vaginitis in 96% (N-96) different microorganisms have been isolated, while in 4% (N-4) findings were normal. AV has been found in 51% (N-51) of the examinees, Candida albicans in 17% (N-17), BV in 15% (N-15), Trichomonas vaginalis in 13% (N-13). In 21% (N-21) AV was diagnosed alone while associated with other agents in 30% (N-30). Most common causes of AV are E. coli (N-55) and E. faecalis (N-52). AV and Candida albicanis have been found in (13/30, 43%), Trichomonas vaginalis in (9/30, 30%) and BV (8/30, 26%). Vaginal secretion is in 70,05% (N-36) yellow coloured, red vagina wall is recorded in 31,13% (N-16) and pruritus in 72,54% (N-37). Increased pH value of vagina found in 94,10% (N-48). The average pH value of vaginal environment was 5,15±0,54 and in associated presence of AV and VVC, TV and BV was 5,29±0,56 which is higher value considering presence of AV alone but that is not statistically significant difference (p>0,05). Amino-odor test was positive in 29,94% (N-15) of associated infections. Lactobacilli are absent, while leukocytes are increased in 100% (N-51) of the examinees with AV.
CONCLUSION: AV is vaginal infection similar to other vaginal infections. It is important to be careful while diagnosing because the treatment of AV differentiates from treatment of other vaginitis.

Entities:  

Keywords:  Aerobic vaginitis; diagnosis; vaginal infections

Mesh:

Year:  2013        PMID: 25568514      PMCID: PMC4272474          DOI: 10.5455/medarh.2013.67.428-430

Source DB:  PubMed          Journal:  Med Arch        ISSN: 0350-199X


1. INTRODUCTION

Ecosystem of vagina is a complex and dynamic system of flora of various microorganisms in different quantity and ratio. Clinical future and treatment of some of the vaginitis, such as trichomonas vaginitis (TV), vulvovaginal candidiasis (VVC) and bacterial vaginosis (BV) are well defined, while other abnormal vaginal conditions are yet to be defined. In 2002, Donders and ass. (1) suggested term aerobic vaginitis (AV) based on bacteriological, immunological and clinical characteristics. This study has been conducted for better understanding of frequency and clinical characteristics of AV, where symptoms, signs and laboratoty tests (pH and amino-odor test) have been analyzed in patients diagnosed with one or mixed infections. These results should help in clinical determination of the causes for vaginal symptoms and more accurate diagnosis and treatment of AV.

2. AIM OF THE WORK

Examine clinical characteristics of aerobic vaginitis and mixed infection for the purpose of better diagnostic accuracy and treatment efficiency.

3. MATERIALS AND METHODS

Prospective research has been conducted at Clinic for Gynecology and Obstetricity, Department for microbiology and pathology at Polyclinic for laboratory diagnostic and Gynecology and Obstetricity Department at Health Center Sapna in period from May 2007 till January 2008. The study included 100 examinees aged 18 to 45. The examinees with clinical signs of vaginitis had some of the stated symptoms (increased vaginal secretion, changed colour of secretion, changed colour of vaginal walls, subjective problems, changed pH value of vaginal environment and positive amino-odor test). Examination programme consisted of three parts: taking anamnesis data (interview) clinical gynecological examination microbiological examination of vaginal and cervical smear Interview consisted of the following data:age of the examinee, marital status, number of deliveries, number of miscarriages and symptoms which indicated presence or absence of vaginitis. Gynecological examination was performed by gynecologist in gynecological clinic. Gynecological examination was performed with speculum and bimanualy. Speculum examination showed clinical characteristics of vaginal wall: redness, presence of vaginal secretion and change in its quality. Presence of 3 or more clinical characteristics are considered to be positive for diagnosis of vaginitis. Gynecological examination also determined pH value of vaginal environment in all of the examinees. Determination of pH value of vaginal environment was performed with indicator tape with span from 0 to 14. Colour indicator tape was put on lateral arch of vagina and results showed on the tape within 30-60 seconds. pH value above 4,0 was considered significant in vaginitis diagnosis. After determining pH value of vaginal environment, all the examinees had amino-odor test. Test included putting vaginal secretion on the glass and pouring 2-3 drops of 10% KOH. Release of fish-like smell was recorded as positive result. After that, vaginal and cervical smears were taken for microbiological analysis of aerobic and anaerobic microorganisms and antibiogram. Smear that was taken for the microbiolgical analysis has been examined with standard microbiological methods: examination of the preparation coloured by Gram and cultivated on standard microbiological bases such as blood and endo agar and identification of increase with biochemical methods. Examination to resistence has been done by disc-difuse method on Müler-Hinton base. Analysis of vaginal flora was performed under the microscope with 400 times magnification where presence and absence of lactobacili, change of flora considering presence of coccus bacterial flora or short curved sticks and combinations, presence of clue cells and presence of parasites and fungi were recorded. Leukocyte finding was graded by number of leukocytes found under the 400 times magnification in the field of view: result with less than 10 leukocytes in the field of view and result with more than 10 leukocytes in the field of view. BV is defined with findings that have 3 out of 4 possible criterion:liquid homogenous grey secretion, presence of clue cells, pH value higher than 4,0 and positive aminoodor test. AV was determined based on criterion by Donders: enhanced yellow secretion, pH value ≥ 5, negative aminoodor test, increased number of leukocytes >10, absence of lactobacilli and microbiologically isolated microorganisms: Escerichia coli (E. coli), Staphylococcus aureus, group B streptococcus and enterococci. Findings were processed by methods of descriptive statistics, student t-test, X² test. Differences for values p<0,05 were considered statistically significant and differences for values p<0,01 statistically highly significant.

4. RESULTS

The examined group of women N-100 were in reproductive period with average age of 32,62±2,6, and married in 85% (N-85). Examining vaginal smears of the examinees with signs of vaginitis in 96% (N-96) different microorganisms which belong to aerobic and anaerobic bacteria, protozoa and fungi have been isolated, while in 4% (N-4) findings were normal. AV has been found in 51% (N-51) of the examinees, Candida albicans in 17% (N-17), BV in 15% (N-15), Trichomonas vaginalis in 13% (N-13) and 4% (N-4) of the examinees didn’t have microbiological cause of vaginitis. In 21% (N-21) of the examinees AV was diagnosed alone while associated with other agents in 30% (N-30). Most common causes of AV are E. coli (N-55) and E. faecalis (N-52). AV and Candida albicanis have been found in (13/30, 43%), Trichomonas vaginalis in (9/30, 30%) and BV (8/30, 26%). Examining clinical characteristics of AV and associated infections of AV and VVC, TV and BV, enhanced secretion has been recorded in 100% (N-51) of the examinees with different characteristics of vaginal secretion (Table 1.) Vaginal secretion is in 70,05% (N-36) yellow coloured, secretion of thick consistency is in 61,53% (N-31) and changed smell of secretion is in 29,94% (N-15) of the examinees with AV. Colour of vagina wall changed into red is recorded in 31,13% (N-16) and pruritis or itching in genital area had 72,54% (N-37) of the examinees with AV. Increased pH value of vagina has been found in 94,10% (N-48) and normal in 5,88% (N-3). pH value 5 in 72,54% (N-37) and pH value 6 in 21,56% (N-11).
Table 1

Characteristics of the examinees with the signs of vaginitis. Legend: a-arithmetic mean + standard tolerance

Characteristics of the examinees with the signs of vaginitis. Legend: a-arithmetic mean + standard tolerance Traits of vaginal secretion, clinical and biochemical characteristics of the examinees with signs of AV Results of microbiological examination of the examinees with signs of vaginitis Most of the examinees had pH value 5. The average pH value of vaginal environment in the examinees with AV was 5,15±0,54 and in associated presence of AV and VVC, TV and BV was 5,29±0,56 which is higher value considering presence of AV alone but that is not statistically significant difference (p>0,05). Amino-odor test was negative in the examinees with AV, while with associated infections it was positive in 29,94% (N-15). Microbiological examination hasn’t recorded presence of lactobacili in vaginal secretion while leukocytes have been elevated in all of the examinees with AV in 100% (N-51).

5. DISCUSSION

In 1990 Helen McDonald warned that women with the risk of preterm labor had two types of abnormal vaginal secretion, first is BV and second are other aerobic microorganisms such as E.coli and Klebsiella (2,3). In 80-90% of cases enhanced vaginal secretion is associated with microbiological cause which can be identified and most of the vaginal infections are consequence of the infection with synergistic bacteria (bacterial vaginosis and nonspecific vaginitis), fungi (vulvovaginal candidiasis) and protozoa (trichomoniasis). It is considered that approximately 50% of infections are caused by bacteria and 50% by fungi and parasite (4). In this research aerobic bacteria play significant role in ethiology of vaginitis and they are often associated with two or more causes which indicates to polymicrobe ethiology of vaginitis (5). AV has been found in 51% (N-51), alone in 21% (N-21) and associated in 30% (N-30). It is most commonly associated with Candida albicans in (13/30, 43%), Trichomonas vaginalis in (9/30, 30%) and BV in (8/30, 26%). In similar studies of AV Fan founds AV as the main cause of vaginitis in one study in 14,7% and in other in 23,74%. In 58% AV is mixed with another causes such as VVC in 30%, TV in 25% and BV in 45% (6,7). Percentage of representation of AV in our research is higher in relation to the quoted one but the percentage of association with other types is the same. Although many studies state that the frequency of AV is still unknown (8), the frequency in pregnant women is in 25%. AV is mostly caused by E.coli and E.faecalis while other causes haven’t been found in this research, although Donders states that causes of AV are: E. coli, enterococi, Staphylococcus sp. and group B of streptococcus (9). E.coli is cited as one of the most common causes of this vaginitis and sometimes is isolated alone. The role of E.coli in vaginitis is very contraversial and this microorganism is one of the main causes of neonatal sepsis and chorioamnionitis (10). Enhanced and changed vaginal secretion has been found in all of the examinees with AV, that is with yellow coloured secretion in 70,05% (N-36) which is similar to Fan research who found yellow vaginal secretion in 63% of the examinees with AV. Thick consistence of secretion was in 61,53% (N-31). Red colour of vagina walls has been recorded in 31,13% (N-16) and pruritus or itching in 72,54% (N-37) of the examinees with AV. Elevated pH value of vaginal environment has been found in 94,10% (N-48), while in similar study pH higher than 4,5 has been found in 84% of the examinees with AV (10). The absence of lactobacilli (11) is a characteristic of AV and in this study lactobacilli haven’t been found in the examinees with AV. Donders also, in several of his studies, records abnormal status of lactobacilli, that is, their absence, which is a negative factor and enables development of infection, especially in pregnancy (11, 12, 13, 14, 15). Enhanced number of leukocytes has been found in 100% (N-51) of the examinees. The other studies also confirm abnormal vaginal flora in women with the risk for preterm labor and presence of E.coli with or without signs of inflamation and increased number of leukocytes in secretion (16, 17, 18). AV is frequent infection of lower genital system and it doesn’t differentiate from other vaginal infections by its clinical characteristics. In high percentage it is associated with other infections. It is very important to pay attention to presence of AV as mixed infection or special entity when dignosing vaginitis, especially in pregnancy. Therapeutic treatment of AV differentiates from other types of vaginitis and wrong diagnose can lead to wrong treatment and complications.
Table 2

Traits of vaginal secretion, clinical and biochemical characteristics of the examinees with signs of AV

  13 in total

1.  Definition of a type of abnormal vaginal flora that is distinct from bacterial vaginosis: aerobic vaginitis.

Authors:  Gilbert G G Donders; Annie Vereecken; Eugene Bosmans; Alfons Dekeersmaecker; Geert Salembier; Bernard Spitz
Journal:  BJOG       Date:  2002-01       Impact factor: 6.531

2.  Vaginal infection and preterm labour.

Authors:  H M McDonald; J A O'Loughlin; P Jolley; R Vigneswaran; P J McDonald
Journal:  Br J Obstet Gynaecol       Date:  1991-05

Review 3.  The life and times of the Enterococcus.

Authors:  B E Murray
Journal:  Clin Microbiol Rev       Date:  1990-01       Impact factor: 26.132

Review 4.  Aerobic vaginitis in pregnancy.

Authors:  Ggg Donders; G Bellen; D Rezeberga
Journal:  BJOG       Date:  2011-06-14       Impact factor: 6.531

5.  Is a change in the vaginal flora associated with an increased risk of preterm birth?

Authors:  J Christopher Carey; Mark A Klebanoff
Journal:  Am J Obstet Gynecol       Date:  2005-04       Impact factor: 8.661

6.  Aerobic vaginitis and mixed infections: comparison of clinical and laboratory findings.

Authors:  Aiping Fan; Yingli Yue; Nv Geng; Huiying Zhang; Yingmei Wang; Fengxia Xue
Journal:  Arch Gynecol Obstet       Date:  2012-09-27       Impact factor: 2.344

7.  [Clinical characteristics of aerobic vaginitis and its mixed infections].

Authors:  Ai-Ping Fan; Feng-Xia Xue
Journal:  Zhonghua Fu Chan Ke Za Zhi       Date:  2010-12

8.  Predictive value for preterm birth of abnormal vaginal flora, bacterial vaginosis and aerobic vaginitis during the first trimester of pregnancy.

Authors:  G G Donders; K Van Calsteren; G Bellen; R Reybrouck; T Van den Bosch; I Riphagen; S Van Lierde
Journal:  BJOG       Date:  2009-06-17       Impact factor: 6.531

9.  Lactobacilli in Papanicolaou smears, genital infections, and pregnancy.

Authors:  G Donders; H G De Wet; P Hooft; J Desmyter
Journal:  Am J Perinatol       Date:  1993-09       Impact factor: 1.862

10.  Association between abnormal vaginal flora and cervical length as risk factors for preterm birth.

Authors:  Gilbert G Donders; Christel Van Calsteren; Gert Bellen; Reinhilde Reybrouck; Thierry Van den Bosch; Ine Riphagen; Stephan Van Lierde
Journal:  Ultrasound Obstet Gynecol       Date:  2010-01-26       Impact factor: 7.299

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Authors:  Gebrehiwet Tesfay Yalew; Saravanan Muthupandian; Kiflom Hagos; Letemichael Negash; Gopinath Venkatraman; Yemane Mengsteab Hagos; Hadush Negash Meles; Hagos Haileslasie Weldehaweriat; Hussein O M Al-Dahmoshi; Morteza Saki
Journal:  PLoS One       Date:  2022-02-25       Impact factor: 3.240

2.  Vaginal Infections' Etiologies in South-Eastern Gabon - An Overview.

Authors:  Michelle Bignoumba; Kelly H Mbombe Moghoa; Jean Ulrich Muandze-Nzambe; Roland Fabrice Kassa Kassa; Yann Mouanga Ndzime; Amahani Gafou; Neil Michel Longo Pendy; Richard Onanga; Brice Serge Kumulungui
Journal:  Int J Womens Health       Date:  2022-04-12

3.  Vaginal Microbiota Evaluation and Lactobacilli Quantification by qPCR in Pregnant and Non-pregnant Women: A Pilot Study.

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Journal:  Front Cell Infect Microbiol       Date:  2020-06-19       Impact factor: 5.293

4.  Characteristics of aerobic vaginitis among women in Xi'an district: a hospital-based study.

Authors:  Taohong Zhang; Yan Xue; Ting Yue; Lili Xiong; Xiaowei Wang; Weihong Wang; Ying Liu; Ruifang An
Journal:  BMC Womens Health       Date:  2020-06-30       Impact factor: 2.809

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Authors:  Elisabetta Caselli; Maria D'Accolti; Erica Santi; Irene Soffritti; Sara Conzadori; Sante Mazzacane; Pantaleo Greco; Carlo Contini; Gloria Bonaccorsi
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6.  Characterization of cervico-vaginal microbiota in women developing persistent high-risk Human Papillomavirus infection.

Authors:  Monica Di Paola; Cristina Sani; Ann Maria Clemente; Anna Iossa; Eloisa Perissi; Giuseppe Castronovo; Michele Tanturli; Damariz Rivero; Federico Cozzolino; Duccio Cavalieri; Francesca Carozzi; Carlotta De Filippo; Maria Gabriella Torcia
Journal:  Sci Rep       Date:  2017-08-31       Impact factor: 4.379

Review 7.  Warding Off Recurrent Yeast and Bacterial Vaginal Infections: Lactoferrin and Lactobacilli.

Authors:  Fabiana Superti; Francesco De Seta
Journal:  Microorganisms       Date:  2020-01-17

8.  Vaginal microbiota evaluation and prevalence of key pathogens in ecuadorian women: an epidemiologic analysis.

Authors:  Ana María Salinas; Verónica Gabriela Osorio; David Pacha-Herrera; Juan S Vivanco; Ana Francisca Trueba; António Machado
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