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Volume 19, Number 9—September 2013

Dispatch

Benznidazole Treatment of Chagasic Encephalitis in Pregnant Woman with AIDS

Margarita BisioComments to Author , Jaime Altcheh, Jorge Lattner, Guillermo Moscatelli, Valeria Fink, Juan M. Burgos, Facundo García Bournissen, Alejandro G. Schijman, and Héctor Freilij
Author affiliations: Hospital de Niños Ricardo Gutiérrez, Buenos Aires, Argentina (M. Bisio, J. Altcheh, G. Moscatelli, F. García Bournissen, H. Freilij); Instituto de Investigaciones en Ingeniería Genética y Biología Molecular Dr Héctor N. Torres, Buenos Aires (M. Bisio, A.G. Schijman); Hospital Juan A. Fernández, Buenos Aires (J. Lattner, V. Fink); Facultad de Medicina de la Universidad de Buenos Aires, Buenos Aires (J.M. Burgos)

Suggested citation for this article

Abstract

We report a case of chagasic meningoencephalitis reactivation in a pregnant woman co-infected with Trypanosoma cruzi and HIV that was successfully managed with benznidazole and highly active antiretroviral therapy. Early diagnosis enabled rapid specific treatment that improved the health of the patient and her baby.

Chagas disease, caused by the protozoan Trypanosoma cruzi, is transmitted to humans mainly by triatomine bugs (vector-borne route), through blood transfusions, or from mother to child through the placenta (transplacental route) (1). In patients co-infected with HIV, Chagas disease reactivation generally occurs in persons with CD4 T-cell counts <200 cells/mm3 and results in severe meningoencephalitis or myocarditis (2). Confirmation of central nervous system (CNS) reactivation requires T. cruzi detection in 1) cerebrospinal fluid, 2 brain tissue, or 3) blood, with neurologic manifestations and clinical response to parasiticidal treatment (2). CNS reactivation is associated with a high mortality rate, and management consists of combining anti–T. cruzi drugs (benznidazole or nifurtimox) with highly active antiretroviral therapy (HAART) to favor immune reconstitution (2,3).

Migration by persons from Chagas disease–endemic areas to vector-free urban centers, and changes in the epidemiologic profile of HIV, have led to a large overlap in the geographic distribution of the 2 infections (4). In fact, the prevalence of T. cruzi infection among HIV-seropositive patients from disease-endemic regions was found to be 1.3% in Brazil and 1.9% in Spain (4,5).

Because safety of benznidazole in pregnancy has not been established (6), its use in treating pregnant women is contraindicated (7,8). Prevalence of vertical transmission of T. cruzi infection from immunocompetent women to their fetus varies from 0.1% to 18% among regions (7), and such transmission is strongly associated with the maternal blood-parasite load (7,9). However, patients co-infected with HIV exhibit higher levels of parasitemia and a higher congenital transmission rate (10) than those who are not co-infected. Indeed, in our experience, 6 of 7 co-infected pregnant women transmitted T. cruzi infection (11). We describe a noteworthy case-patient from that series, a woman who experienced reactivation of T. cruzi infection during the third trimester of pregnancy but did not transmit the parasite infection, probably because she received, without delay, treatment with benznidazole and HAART.

The Patient

A 33-year-old woman, who had been infected with HIV for 11 years, started receiving lamivudine, zidovudine, and nevirapine at week 26 of pregnancy. At that time, CD4 cell count was 18 cells/mL. She had begun receiving HAART 1 year before pregnancy but abandoned treatment after a few months. Her compliance with treatment, laboratory tests, and follow-up was poor.

Figure

Thumbnail of Diagnosis, treatment, and prophylaxis monitoring of Trypanosoma cruzi infection in a pregnant woman and her daughter. The mother, who had chagasic encephalitis and AIDS, was treated with benznidazole (Bz). Po, positive; Ng, negative;  Nd, not determined; results of ELISA were considered positive when R was &gt;1.2);  IHA, indirect hemagglutination assay (IHA was considered positive when titers were &gt;16); kDNA-PCR, kinetoplast DNA-PCR; qPCR, quantitative PCR (dynamic range of dete

Figure. . Diagnosis, treatment, and prophylaxis monitoring of Trypanosoma cruzi infection in a pregnant woman and her daughter. The mother, who had chagasic encephalitis and AIDS, was treated with benznidazole (Bz). Results...

At week 32 of pregnancy, she was admitted to the hospital with clinical manifestations of intracranial hypertension and meningoencephalitis (temporospatial disorientation, slurred speech, nausea and vomiting, and hemiparesis). A CNS mass was detected by magnetic resonance imaging (Figure). Results of serologic tests were negative for Toxoplasma gondii, Treponema pallidum, and hepatitis B and C viruses but positive for T. cruzi. Reactivation of Chagas disease was confirmed by a positive microhematocrit measurement (12). PCR targeted to T. cruzi kinetoplast DNA was positive, and quantitative PCR (qPCR) targeted to satellite T. cruzi DNA yielded 308.9 parasite equivalents/mL of blood (13). The parasite genotype (discrete typing unit) detected by PCR strategies was identified as TcV (14). Most probably, this patient acquired the infection by the vector-borne route in a highly disease-endemic province in Argentina where she had lived as a child.

Although data on benznidazole use in pregnancy are lacking, after an in-depth discussion of potential risks and benefits of the treatment, we concluded that, because of her severe clinical condition, treatment with benznidazole could be beneficial. Within 48 hours of the diagnosis, she received benznidazole (5 mg/kg/day, for 84 days) without side effects. The patient showed rapid neurologic and clinical improvement. Parasitic loads, determined by qPCR, dropped rapidly (Figure). During treatment, results of the microhematocrit, PCR, and anti–T. cruzi serologic testing became negative for the parasite. Magnetic resonance images showed substantial reduction of edema and the mass and reconstitution of the interventricular line without evidence of ventricular dilatation (Figure). Seven weeks after treatment initiation, cerebrospinal fluid was negative for T. cruzi by serologic testing, microhematocrit, and PCR.

At week 36 of gestation, the patient gave birth to a girl by elective cesarean section. The baby’s birthweight was low for gestational age (1,700 g, <3rd percentile), and her Apgar score was 7/8. The newborn was hospitalized for 32 days. Microhematocrit and PCR results suggested that she had not acquired T. cruzi infection. This lack of infection was confirmed by means of serologic testing at 1 year of age, per current Chagas disease guidelines (12). Moreover, results of PCR for HIV and p24 antigen tests were negative in 2 different samples, enabling perinatal infection with HIV to be ruled out.

After delivery, the mother continued to receive HAART with benznidazole prophylaxis (5 mg/kg/day 3×/week) for 6 months. A follow-up computed tomographic scan performed 14 months after delivery showed a favorable response. Moreover, serologic, parasitologic, and molecular studies remained negative for T. cruzi (Figure). To date, the patient continues to show erratic compliance with follow-up. As a consequence, immunologic recovery has not yet been achieved.

Conclusions

Benznidazole is traditionally considered contraindicated in pregnancy because data that support its safety to the fetus are lacking (8). Nevertheless, because of the severe clinical picture of the patient, and the known lower risks of fetal toxicity in the second and third trimesters of pregnancy (6), treatment was administered on a compassionate basis. Among patients who have AIDS and Chagas disease reactivation with CNS involvement, early parasiticidal and HAART treatment can improve the poor prognosis (2,3). Cordova et al. (2) reported a mortality rate of 79% in a cohort of 15 patients with co-infection, with a median time of survival of 21 days after hospitalization. However, the researchers associated this high mortality rate with delayed diagnosis, because it took a median of 18 days to recognize the condition. In the patient reported here, the short interval (72 hours) between admission and initiation of benznidazole treatment may have improved the chances of a successful outcome. Moreover, to our knowledge, the patient in this case has longest reported survival time after diagnosis of chagasic reactivation caused by HIV co-infection, with 7 years of follow-up (15).

Microhematocrit and PCR successfully demonstrated the presence and elimination of T. cruzi, and qPCR enabled the decrease in parasitic load to be monitored. T. cruzi TcV detected in peripheral blood was described as prevalent in the population from the Southern Cone (14). Notably, negative serologic results were achieved early after treatment, which is only usually seen in immunocompetent patients at the acute phase of disease or in recent congenital infections. The rapid negative seroconversion observed in this patient is uncommon. The continued seronegative results when her immune system presumably was reconstituted suggests strongly that she had an actual parasitologic cure.

Moreover, the baby’s weight at birth was low for gestational age. Various reasons could explain the low birthweight, including the infectious status of the mother or the severe stress she was experiencing at the time of admission. Also, a potential effect of benznidazole for the baby cannot be fully ruled out. Nonetheless, the benefit to both mother and child clearly outweighed the risk. The baby did not acquire either infection.

This case illustrates that parasiticidal treatment may decrease parasitic load and prevent vertical transmission of T. cruzi, even in co-infected patients among whom a higher incidence of congenital infection and illness of newborns is observed (10). This result reinforces the idea that benznidazole has a role in the prevention of congenital transmission of Chagas disease. Therefore, studies that explore its safety and effectiveness during pregnancy may be warranted.

Dr Bisio has a postdoctoral position in the Parasitology and Chagas Disease Department of the Children´s Hospital “Ricardo Gutiérrez,” Buenos Aires, Argentina. Her work focuses on improving molecular diagnostic tools and their effect on treatments, evaluation, and control of parasitic diseases.

Acknowledgments

We extend our appreciation to the patient who is the subject of this report and her daughter.

This work was partially supported by grants from the National Council of Science and Technology (CONICET) (PIP 112-20081-02915) to A.G.S. J.A. and H.F. are members of the clinical researcher career of the Government of Buenos Aires. A.G.S., J.M.B., and F.G.B. are members of CONICET researcher’s career. M.B. is a research fellow of Bunge y Borne Foundation.

References

  1. Rassi A Jr, Rassi A, Marin-Neto JA. Chagas disease. Lancet. 2010;375:1388402 . DOIPubMed
  2. Cordova E, Boschi A, Ambrosioni J, Cudos C, Corti M. Reactivation of Chagas disease with central nervous system involvement in HIV-infected patients in Argentina, 1992–2007. Int J Infect Dis. 2008;12:58792 . DOIPubMed
  3. Bern C. Chagas disease in the immunosuppressed host. Curr Opin Infect Dis. 2012;25:4507 . DOIPubMed
  4. Almeida EA, Lima JN, Lages-Silva E, Guariento ME, Aoki FH, Torres-Morales AE, Chagas' disease and HIV co-infection in patients without effective antiretroviral therapy: prevalence, clinical presentation and natural history. Trans R Soc Trop Med Hyg. 2010;104:44752 . DOIPubMed
  5. Llenas-Garcia J, Hernando A, Fiorante S, Maseda D, Matarranz M, Salto E, Chagas disease screening among HIV-positive Latin American immigrants: an emerging problem. Eur J Clin Microbiol Infect Dis. 2012;31:19917 . DOIPubMed
  6. World Health Organization. Model prescribing information: drugs used in parasitic diseases. 1995 [cited 2013 Jul 2]. http://apps.who.int/medicinedocs/es/d/Jh2922e/
  7. Carlier Y, Truyens C. Maternal-fetal transmission of Trypanosma cruzi, one hundred years of research. In: Telleria J, Tibayrenc M, editors. American trypanosomiasis: Chagas disease. London: Elsevier; 2010. p. 539–81.
  8. Carlier Y, Torrico F, Sosa-Estani S, Russomando G, Luquetti A, Freilij H, Congenital Chagas disease: recommendations for diagnosis, treatment and control of newborns, siblings and pregnant women. PLoS Negl Trop Dis. 2011;5:e1250 . DOIPubMed
  9. Bern C, Verastegui M, Gilman RH, Lafuente C, Galdos-Cardenas G, Calderon M, Congenital Trypanosoma cruzi transmission in Santa Cruz, Bolivia. Clin Infect Dis. 2009;49:166774 . DOIPubMed
  10. Scapellato PG, Bottaro EG, Rodriguez-Brieschke MT. Mother-child transmission of Chagas disease: could coinfection with human immunodeficiency virus increase the risk? Rev Soc Bras Med Trop. 2009;42:1079 . DOIPubMed
  11. Bisio M, Cura C, Duffy T, Altcheh J, Giganti SO, Begher S, Trypanosoma cruzi discrete typing units in Chagas disease patients with HIV co-infection [cited 2013 Jul 2]. Rev Biomed. 2009;20:166–78. http://www.revbiomed.uady.mx/pdf/rb092033.pdf
  12. Freilij H, Altcheh J. Congenital Chagas' disease: diagnostic and clinical aspects. Clin Infect Dis. 1995;21:5515 . DOIPubMed
  13. Schijman AG, Bisio M, Orellana L, Sued M, Duffy T, Mejia Jaramillo AM, International study to evaluate PCR methods for detection of Trypanosoma cruzi DNA in blood samples from Chagas disease patients. PLoS Negl Trop Dis. 2011;5:e931 . DOIPubMed
  14. Zingales B, Andrade SG, Briones MR, Campbell DA, Chiari E, Fernandes O, A new consensus for Trypanosoma cruzi intraspecific nomenclature: second revision meeting recommends TcI to TcVI. Mem Inst Oswaldo Cruz. 2009;104:10514 . DOIPubMed
  15. Almeida EA, Ramos Junior AN, Correia D, Shikanai-Yasuda MA. Co-infection Trypanosoma cruzi/HIV: systematic review (1980–2010). Rev Soc Bras Med Trop. 2011;44:76270 . DOIPubMed

Figure

Suggested citation for this article: Bisio M, Altcheh J, Lattner J, Moscatelli G, Fink V, Burgos JM, et al. Benznidazole treatment of chagasic encephalitis in pregnant woman with AIDS. Emerg Infect Dis [Internet]. 2013 Sep [date cited]. http://dx.doi.org/10.3201/eid1909.130667

DOI: 10.3201/eid1909.130667

Table of Contents – Volume 19, Number 9—September 2013

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Margarita Bisio, Laboratorio de Parasitología y Enfermedad de Chagas, Hospital Gutiérrez, Gallo 1330, Buenos Aires, Argentina


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