Abstract INTRODUCTION: Benznidazole (BZL) and Nifurtimox (NFX) are the pharmacological treatment for acute phase Chagas Disease (CD); however, therapy resistance and residual mortality development remain important unresolved issues. Posaconazole (POS) has shown a trypanocidal effect in vivo and in vitro. Thus, this study aimed at comparing the T. Cruzi parasitic load-reducing effect of the combination of BZL+POS against that of monotherapy with either, during acute phase CD, in an experimental murine model. METHODS Nineteen Wistar rats were randomly allocated to four groups and inoculated with the trypomastigotes of T. cruzi strain´s JChVcl1. The rats were administered anti-parasites from day 20-29 post-infection. The Pizzi and Brener method was used for parasitemia measurement. Longitudinal data analysis for the continuous outcome of repeated measures was performed using parasitemia as the outcome measured at days 20, 22, 24, 27, and 29 post-infection. RESULTS All four groups had similar parasitic loads (p=0.143) prior to therapy initiation. Among the three treatment groups, the BZL+POS (n=5) group showed the highest mean parasitic load reduction (p=0.000) compared with the control group. Likewise, the BZL+POS group rats showed an earlier therapeutic effect and were the only ones without parasites in their myocardial samples. CONCLUSIONS: Treatment of acute phase CD with BZL+POS was more efficacious at parasitemia and myocardial injury reduction, compared with monotherapy with either.

A 22-year-old pregnant woman was seen at 14 weeks of pregnancy for infective endocarditis with a vegetation of 15 mm and wide mobility, which affected the native mitral valve accompanied by severe valvular insufficiency. Antibiotic treatment was given for 4 weeks despite the embolism risk. Due to persistence of vegetation size and after considering the fetal and maternal risk, the surgical procedure was favored. We decided to perform valvuloplasty and removal of lesion at 18 weeks of pregnancy. Fetal protection techniques were used and a bioprosthesis was placed before attempting a repair. The postoperative follow-up was satisfactory, achieving a successful birth by cesarean section at 30 weeks.

Presentamos el caso de una paciente de 22 años de edad con embarazo de 14 semanas y endocarditis infecciosa de válvula mitral nativa con una vegetación de 15 mm con amplia movilidad, acompañada de insuficiencia valvular severa. Inicialmente, y pese al riesgo embolígeno, se dio tratamiento antibiótico durante 4 semanas. Por persistencia del tamaño de la vegetación se decide llevar a cirugía para reparación mitral y remoción de la lesión en la semana 18 de gestación, considerando que el balance entre el riesgo fetal y materno estaba a favor del procedimiento quirúrgico. Se usaron técnicas de protección fetal intraoperatoria y se colocó una prótesis biológica previo intento de reparación. La evolución postintervención fue satisfactoria, lográndose parto por cesárea a las 30 semanas.

El trasplante de órganos es una alternativa terapéutica cada vez más frecuente en nuestro medio y con ello las complicaciones y efectos de las medicaciones inmunosupresoras que afectan el sistema nervioso central (SNC). El síndrome de encefalopatía posterior reversible (SEPR) es un trastorno caracterizado por manifestaciones neurológicas potencialmente reversibles, asociadas a cambios en las neuroimágenes, en estrecha asociación con factores precipitantes, dentro de los cuales, se destacan el uso de medicamentos inmunosupresores, quimioterapéuticos y algunas condiciones médicas como hipertensión arterial y enfermedades renales. Las características clinico-radiológicas de este trastorno usualmente revierten con la suspensión de los factores precipitantes; sin embargo el diagnóstico tardío puede llevar a un desenlace fatal. Se presenta un caso de SEPR en una paciente joven a quien se le realizó trasplante cardiaco de urgencia. Durante su manejo post-operatorio recibió tacrolimus como parte del tratamiento del paciente trasplantado. En la cuarta semana de post-operatorio y quinto día de tratamiento con tacrolimus desarrolló cefalea asociada a cifras tensionales elevadas, deterioro de la conciencia y episodios convulsivos tónico-clónicos generalizados; las manifestaciones neurológicas revirtieron en las 48 horas siguientes al retiro del tacrolimus, al igual que los cambios en las neuroimagenes que resolvieron un mes después de las manifestaciones iniciales.

The organ transplantation is a therapeutic alternative increasingly common in our country, thus, the complications and effects of immunosuppressive medications that affect the Central Nervous System (CNS). The Posterior Reversible Encephalopathy Syndrome (PRES) is characterized by neurological manifestations associated with changes in neuroimaging, together with precipitating factors, among which the use of immunosuppressive, chemotherapy and certain medical conditions such as hypertension and kidney diseases stand out. The clinical radiological features of this disorder are usually reversible with discontinuation of the precipitating factors; however a delayed diagnosis may lead to a fatal outcome. A case of PRES on a young patient who underwent an emergency heart transplant occurred in our institution. During his post operative care received tacrolimus as part of the transplant management. In the fourth week of post operative treatment and the fifth day of the use of tacrolimus, the patient presented headache associated with high pressure values, impaired consciousness and episodes of generalized tonic-clonic seizure, the neurological symptoms reversed within 48 hours after the withdrawal of tacrolimus, as well as changes in neuroimaging who decided one month after the initial manifestations.

The aim of this study was to test the possible implication of toll-like receptor 2 (TLR2) and TLR4 gene polymorphisms in determining the susceptibility to Chagas' disease. Genotypes were determined by polymerase chain reaction-restriction fragment length polymorphism in 475 individuals from Colombia, 143 seropositive with chagasic cardiomyopathy, 132 seropositive asymptomatic and 200 seronegative. The TLR2 arginine to glutamine substitution at residue 753(Arg753Gln) polymorphism was absent in the groups analyzed. The TLR4 Asp299Gly and Thr399Ile polymorphisms are in linkage disequilibrium and we observed a very low frequency of these polymorphisms in our study population (2.6% and 1.8% respectively). The overall TLR2 and TLR4 alleles and genotype distribution in seronegative and seropositive were not significantly different. We compared the frequencies between asymptomatic patients and those with chagasic cardiomyopathy and we did not observe any significant differences in the distribution of alleles or genotypes. In summary, this study corroborates the low frequency of TLR2 and TLR4 polymorphisms observed in other populations and suggest that these do not play an important role in Chagas' disease. The validation of these findings in independent cohorts is needed to firmly establish a role for TLR2 and TLR4 variants in Chagas' disease.