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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptHHS Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
 
Sex Transm Dis. Author manuscript; available in PMC 2017 May 1.
Published in final edited form as:
PMCID: PMC4840465
NIHMSID: NIHMS755081

High rate of partner treatment among Chlamydia trachomatis infected pregnant women in Lima, Peru

Minh Nguyen, MS,1 Jeanne Cabeza, MD, MSPH,2 Eddy Segura, MD, MPH,2,3 Patricia J García, MD, PhD,4 and Jeffrey D Klausner, MD, MPH2

Abstract

This was a substudy of sixty Chlamydia trachomatis infected women from a larger study of pregnant women in Lima, Peru. Participants were encouraged to bring their partners in for concurrent patient-partner treatment (CPPT). The alternative partner treatment was expedited partner therapy (EPT). Partner treatment uptake was 91.7%. Twenty one partners (38.2%) received treatment through CPPT, and 34 (61.8%) through EPT. Living with the partner was significantly associated with having the partner treated (p=0.0028).

Keywords: Chlamydia trachomatis, concurrent patient-partner treatment, expedited partner therapy

Chlamydia trachomatis infection during pregnancy has been linked to numerous adverse outcomes. A study in the Netherlands found a strong association between chlamydial infection and preterm delivery before 32 and 35 weeks gestation1, while another study in New South Wales demonstrated a 40% increase in the odds of stillbirth associated with a prior chlamydia notification2. Moreover, infants exposed to the bacteria can develop conjunctivitis, pneumonia as well as asymptomatic rectal and vagina infections3. Because of the compelling evidence for adverse outcomes in pregnancy, CDC has recommended routine screening for Chlamydia trachomatis during the first prenatal visit4. However, screening and prompt treatment alone might not suffice to guarantee a negative test of cure and prevent repeated infection. Acquisition of new partners and failure to treat all partners have been identified as risk factors for reinfection5. Concurrent patient-partner treatment is a method in which patients are instructed to bring their own partners when they return for treatment6. Expedited partner therapy, on the other hand, is the clinical practice of treating the sex partners of patients, in whom sexually transmitted infections are diagnosed, by providing prescriptions or medications to the patient to take to the partner without the health care provider first examining the partner7.

In Peru, a national population-based survey in 2002 found a prevalence rate of chlamydial infection of 6.5% in women aged 18 to 29 years old8. Several studies in Peru also showed a significant role of partners in determining the risk of HIV and other STIs among pregnant women9,10. CPPT and EPT are not offered as a standard of care in Peru and physicians only focus on the syndromic management of sexually transmitted diseases11.

As part of a larger study to determine the acceptability and feasibility of Chlamydia trachomatis screening among pregnant women in Lima, Peru, we found a prevalence of Chlamydia trachomatis of 10%12. The primary objectives of the substudy were to report partner treatment uptake and to examine the associations between partner treatment uptake and whether the women were living with their partners.

Study design and methods were reported previously in the larger study13. All sixty Chlamydia trachomatis infected pregnant women were asked to return to the hospital for treatment and counselling. They were encouraged to bring their partners when they came back for counseling and concurrent patient-partner treatment. Following CDC 2010 guidelines, we instructed participants to bring the partner(s) who had sexual contact with them during the 60 days preceding diagnosis, or the most recent partner if the time of last sexual contact was more than 60 days4. For those who brought their partners in, the couple attended counseling together and then both received directly observed treatment with 1g of oral azithromycin (CPPT). Women whose partners did not come received the same directly observed treatment at the hospital and brought home 1g azithromycin as well as instructions to deliver to the partners themselves (EPT). We also asked participants to come back to the hospital for a test of cure in 3 weeks. Those whose test of cure came back positive were retreated.

Specimens were tested for Chlamydia trachomatis using the Aptima Combo2 system (Hologic, San Diego, California, USA) at the Laboratory of Sexual Health of Cayetano Heredia University in Lima, Peru. HIV and syphilis status of the participants were collected from hospital's medical chart. Data analysis was conducted using SAS 9.3 (SAS Institute, Inc., Cary, NC). Demographics, relationship status, risk behaviors, genital/vaginal symptoms (discharge, wound, ulcer or genital wart) of Chlamydia trachomatis infected pregnant women and their partners, pregnant women's test of cure results as well as partner treatment uptake were analyzed by descriptive statistics. The partner was considered treated with CPPT if he came for treatment with the pregnant woman and was considered treated with EPT if the woman chose to bring home the medication. We then evaluated the associations between living with the partner and partner treatment. Exact p-value was reported, using Fisher's exact test.

The age of infected women ranged from 16 to 42 years old (median age was 23). The majority of those women was less than 25 years of age (60%), among which 38.8% was 19 years old or younger (table 1). Fifty-nine (98.3%) out of 60 infected women came back for treatment. Only one woman said she had got tested elsewhere and did not think she had been infected. Among those who received treatment, 52 (88.1%) returned for a test of cure.

Table 1
Characteristics of Chlamydia infected pregnant women in Lima, Peru (n=60)

Of 60 partners identified, 40 (66.7%) were cohabiting with the patients. Seven (11.7%) were husbands and 33 (55.0%) were live-in partners of the participants. All of the partners were the fathers of the babies the women were going to have. Fifty five partners (91.7%) received treatment, either by direct observation or report of infected index case. Among those partners, 21 (38.2%) came to the hospital with the women to get concurrent patient-partner therapy, and 34 (61.8%) did not come and got treatment through expedited partner therapy. One of the five women whose partners didn't get any treatment did not come to be treated for herself. For the remaining four, the women were not able to, or did not want to contact their partners. Compared to women who did not live with their partners, women who lived with the partners were significantly more likely to get the partners treated (100% vs 75%, p=0.0028) (table 3).

Table 3
Partner treatment, stratified by patient's living with partner status (n=60)

Of 59 treated women, 52 (88.1%) came back for a test of cure. The median time between date of treatment and date of return visit for a test of cure was 22 days (Interquartile range: 21-27 days). Six (11.5%) of those who came back tested positive and after the second treatment, subsequent tests of cure among these women were negative. The proportions of women tested positive were 10.5%, 10.3% and 25.0% among CPPT, EPT and no treatment group, respectively (table 4).

Table 4
Association between partner treatment and a positive test of cure (n=52)

In our substudy of Chlamydia trachomatis infected pregnant women in Peru, we found a very high rate of partner treatment uptake, either by direct observation or by the number of index cases getting medications for the partners. EPT was the more preferable option. A study on partner services in California Family Planning Clinics found that only 34% of the partners of Chlamydia trachomatis infected women had been receiving treatment through either CPPT or EPT13. In another study by Mickiewicz et al, which examined the acceptance rate of EPT among Chlamydia trachomatis and Neisseria gonorrhoeae patients in an urban clinic in Denver, USA, the rates ranged from 20 to 48%, depending on the requirement of complete documentation of EPT in the clinic electronic medical record14. Several reasons might help to explain the discrepancy between other studies’ results and ours. First, pregnant women might take partner notification and treatment more seriously, since not only them but also the babies will suffer from the sequelae of infection. Second, many of the infected women reported sexual symptoms and that might be a reason why they and their partners were motivated to seek treatment. Third, the sample size of this study was much smaller, and the study design did not take into account the barriers concerning EPT in a real-world clinical setting15. Finally each of the partners identified was the father of the baby, therefore he could be more involved in the woman's prenatal care and routine visits, and might be more likely to come for concurrent treatment with the woman. Despite all the reasons above, our results still showed a promising possibility that by offering infected pregnant women both CPPT and EPT, we will be able to treat many more partners, who otherwise would go untreated.

We found a positive association between living with the partner and getting the partner treated. Yu et al reported found that being in a steady relationship had increased the odds of the partner getting treated by seven fold13. Indeed, women who live with the partner or have a steady relationship are more concerned about their partner's sexual health and their own risks of being reinfected. Also, living at the same place makes it easier for the women to bring their partners to the clinic or take home the medications to deliver to them.

Our study was subject to several limitations. First, all of the information on partners was reported by the pregnant women and might suffer from misclassification or recall biases. Our study suffered from the small sample size, with only 60 patients. Furthermore, participants were recruited from two of the largest hospitals in the country, and they might not be representative of Chlamydia trachomatis infected pregnant women from other maternal health clinics.

Despite the limitations, our findings still showed offering EPT as an alternative to CPPT would maximize the proportion of partners receiving treatment. Concurrent patient-partner treatment can be incorporated in routine prenatal visits and if CPPT is not possible, the choice of bringing home one dose of medication is highly acceptable among infected pregnant women. In the US, it is recommended that medical providers offer EPT to heterosexual patients with chlamydia when the provider cannot ensure that all of a patient's sex partners from the prior 60 days will be treated7. However, WHO currently has no guidelines on partner treatment of pregnant women16. Given the importance of treating partners of Chlamydia trachomatis infected pregnant women, we believe that these guidelines should be reviewed to include this essential part of STI management.

Further studies with larger sample sizes, in different maternal care facilities are necessary to examine the rate of partner treatment and its impact on the resolution of Chlamydia trachomatis infection among pregnant women.

Table 2
Characteristics of the partner of last sexual intercourse of Chlamydia infected pregnant women in Lima, Peru (n=60)

Short summary

A study of Chlamydia trachomatis infected pregnant women in Lima, Peru found high partner treatment uptake when participants were offered concurrent patient-partner treatment or expedited partner therapy.

Acknowledgements

We are grateful to Hologic Genprobe, San Diego, CA for donation of the Aptima Combo 2 assay kits used in the study. We are indebted to Dr. Pedro García of Instituto Nacional Materno Perinatal (INMP) and Dr. Francisco Escudero of Hospital Nacional Arzobispo Loayza (HNAL). We are grateful to research midwives Paola Pfluker, Carla Obregón, Vivian Mendoza, and Verónica Dioses and counsellor midwives Nancy Acosta and Soledad Rodriguez at the Instituto Nacional Materno Perinatal and Bertha Zavaleta at Hospital Nacional Arzobispo Loayza, as well as the staff at both hospitals and at Universidad Peruana Cayetano Heredia. Finally, we wish to thank the patients themselves for their participation. This research was supported by a grant (NIH R 25 MHO87222) from the National Institute of Mental Health.

Footnotes

Conflict of interest: None

References

1. Rours GIJG, Duijts L, Moll HA, Arends LR, et al. Chlamydia trachomatis infection during pregnancy associated with preterm delivery: a population-based prospective cohort study. Eur J Epidemiol. 2011 Jun;26(6):493–502. [PMC free article] [PubMed]
2. Liu B, Roberts CL, Clarke M, Jorm L, et al. Chlamydia and gonorrhoea infections and the risk of adverse obstetric outcomes: a retrospective cohort study. Sex Transm Infect. 2013 Dec 1;89(8):672–8. [PubMed]
3. Darville T. Chlamydia trachomatis infections in neonates and young children. Semin Pediatr Infect Dis. 2005 Oct;16(4):235–44. [PubMed]
4. CDC Sexually transmitted diseases treatment guidelines, 2015. MMWR. 2015;64(3):10. [PubMed]
5. Scott LaMontagne D, Baster K, Emmett L, et al. Incidence and reinfection rates of genital chlamydial infection among women aged 16 24 years attending general practice, family planning and genitourinary medicine clinics in England: a prospective cohort study by the Chlamydia Recall Study Advisory Group. Sex Transm Infect. 2007 May 2;83(4):292–303. [PMC free article] [PubMed]
6. Mmeje O, Coleman JS. Concurrent patient-partner treatment in pregnancy: An alternative to expedited partner therapy? Sex Transm Dis. 2012 Sep;39(9):665–70. [PubMed]
7. CDC Sexually transmitted diseases treatment guidelines, 2015. MMWR. 2015;64(3):8.
8. Cárcamo CP, Campos PE, García PJ, et al. Prevalences of sexually transmitted infections in young adults and female sex workers in Peru: a national population-based survey. Lancet Infect Dis. 2012 Oct;12(10):765–73. [PMC free article] [PubMed]
9. Vildózola H, Bazul V, Cambillo E, et al. [Prevalence of Hepatitis B infection and risk factors in two groups of pregnant adolescents related to the number of sexual partners]. Rev Gastroenterol Perú Órgano Of Soc Gastroenterol Perú 2006 Sep;26(3):242–58. [Article in Spanish] [PubMed]
10. Johnson KM, Alarcón J, Watts DM, et al. Sexual networks of pregnant women with and without HIV infection. AIDS Lond Engl. 2003 Mar 7;17(4):605–12. [PubMed]
11. Ministerio de Salud Guias Nacionales de Atencion Integral de Salud Sexual y Reproductiva. 2004
12. Cabeza J, Garcia PJ, Segura E, et al. Feasibility of Chlamydia trachomatis screening and treatment in pregnant women in Lima, Peru: a prospective study in two large urban hospitals. Sex Transm Infect. 2015 Feb 1;91(1):7–10. [PMC free article] [PubMed]
13. Yu Y-Y, Frasure-Williams JA, Dunne EF, et al. Chlamydia partner services for females in California family planning clinics. Sex Transm Dis. 2011 Oct;38(10):913–8. [PubMed]
14. Mickiewicz T, Tayyib A Al-, Thrun M, et al. Implementation and effectiveness of an expedited partner therapy program in an urban clinic. Sex Transm Dis. 2012;39(12):923–9. [PubMed]
15. Committee opinion no. 506: Expedited partner therapy in the management of gonorrhea and chlamydia by obstetrician-gynecologists. Obstet Gynecol. 2011 Sep;118(3):761–6. [PubMed]
16. WHO . Guidelines for the management of sexually transmitted infections. WHO; 2003.