Chagas in Colombia

Clinical care guide based on current protocols for the diagnosis, treatment and follow-up of Chagas disease.

Active protocolMinistry of Health and Social Protection of Colombia (MinSalud), with PAHO/WHO
Review2010 (Guía clínica); diagnóstico y vigilancia actualizados por el INS (protocolo v04 2022 y lineamiento PDR 2025)

Diagnosis

Summary

Acute phase

  • Confirm with direct parasitological methods: fresh examination and, after 30 days of symptoms, concentration methods (2010 Guide, pp. 28-29).
  • Document seroconversion at 21 days with simultaneous serology (2010 Guide, p. 34).
  • Do not order IgM: it is not available in the country (2010 Guide, p. 34).

Chronic phase

  • Confirm with two serological tests of different principles (IgG anti-T. cruzi); ELISA is the initial test (2010 Guide, pp. 33 and 36).
  • Consider a positive result an ELISA ≥2 times the cut-off or an IFA ≥1:32, according to the 2010 Guide (p. 33).
  • Perform IFA or Immunoblot as a third test if the first two are discordant (protocol v04 2022, p. 11).

Rapid diagnostic tests

  • 2025 update: in settings without ELISA, use RDTs with verified sensitivity and specificity ≥95 % (RDT guideline 2025, pp. 7, 13-14 and 16).
  • Confirm with a second test (RDT or ELISA) and a third if discordant (pp. 13-14 and 16).
  • Do not use them in suspected acute cases, immunosuppression, children under 10 months or blood banks (p. 14).

Reactivation and immunosuppression

  • Look for the parasite with direct methods in blood, CSF or other fluids, with or without PCR (2010 Guide, p. 36).
Source: Clinical Care Guide for Chagas Disease (MinProtección Social/PAHO, 2010) and current INS documents (protocol v04 2022 and RDT guideline 2025)

Diagnostic algorithm and laboratory

In the chronic phase, the current algorithm is total-antigen ELISA (sensitivity ≥98 %) plus recombinant-antigen or synthetic-peptide ELISA/ChLIA (specificity ≥98 %) (INS 2017, pp. 20 and 24).

Indeterminate values —10-20 % above and below the cut-off— are referred to a reference laboratory (2010 Guide, p. 33).

In the acute phase, direct methods are repeated several times a day for at least a week; in the chronic phase they are not indicated except when reactivation is suspected. Results are reported within 6 working days (2010 Guide, pp. 36-39; INS 2017, pp. 19-25).

Kits must follow INVIMA and MinSalud recommendations (2010 Guide, pp. 38-39).

Treatment

Summary

Who to treat

  • Treat every acute case: it is a medical emergency (2010 Guide, p. 40).
  • Treat congenital infection (p. 40).
  • Treat people under 18 years with chronic infection, regardless of clinical form (p. 40).
  • Treat reactivation due to immunosuppression and accidental exposure (p. 40).
  • In chronic adults the decision is individual; the benefit is greater with less than 15 years of exposure and no severe heart damage (p. 41).

Regimens and doses

  • Benznidazole: 5-10 mg/kg/day in 2-3 doses for 60 days; in adults 5 mg/kg/day is usually sufficient (p. 42).
  • In children doses close to 10 mg/kg/day are tolerated; maximum 300 mg/day (p. 42).
  • Nifurtimox: adults 5-8 mg/kg/day and children 10 mg/kg/day, for 60 days in 2-3 doses (p. 44).
  • Stepwise start: ¼ of the dose on day 1, ½ on days 2-3 and the full dose from day 4 (p. 44).

Contraindications and precautions

  • Do not prescribe during pregnancy: aetiological treatment is contraindicated (p. 45).
  • Contraindicate in severe neurological, hepatic or renal disorders (p. 45).
Source: Clinical Care Guide for Chagas Disease (MinProtección Social/PAHO, 2010) and current INS documents (protocol v04 2022 and RDT guideline 2025)

Special cases

  • Congenital: 5 mg/kg/day increased over 6 days to 10 mg/kg/day for 60 days.
  • Reactivation: 60 days, extendable to 90.
  • Occupational accident: benznidazole 7-10 mg/kg for 10 days (30 days if a high parasite load is suspected); no prophylaxis for minimal risk (p. 46).

Follow-up

Summary

Monitoring during treatment

  • Provide weekly medical follow-up (2010 Guide, p. 42).
  • Request laboratory tests at baseline, at 20 days and at the end: blood count with platelets, AST, ALT, blood urea nitrogen and creatinine (p. 42).

Cure criterion

  • Confirm with serological negativisation in two or more consecutive conventional tests (positive IFA ≥1:16) (p. 47).
  • Repeat checks six-monthly or annually (p. 47).
  • Expect negativisation in 1 year (congenital), 3-5 years (acute), 5-10 years (recent chronic) and more than 20 years (long-standing infection) (p. 47).

Cardiac assessment

  • Perform baseline ECG and chest X-ray for every seropositive person (2010 Guide, pp. 68-69).
  • In the indeterminate form, assess annually with ECG and chest X-ray; if the ECG is abnormal, refer to internal medicine or cardiology (pp. 68-69).
Source: Clinical Care Guide for Chagas Disease (MinProtección Social/PAHO, 2010) and current INS documents (protocol v04 2022 and RDT guideline 2025)

Chronic heart disease

  • Echocardiography identifies systolic dysfunction, the main prognostic factor.
  • Treat ventricular dysfunction with ACE inhibitors and beta-blockers; add spironolactone for symptomatic patients.
  • Use amiodarone for arrhythmias, pacemaker or ICD as indicated, and individualised anticoagulation (2010 Guide, pp. 60-67).

Digestive form

Megaesophagus is managed with dietary and lifestyle measures and sphincter relaxants (nifedipine 10 mg sublingually 45 minutes before eating) as palliative treatment (pp. 67-68).

Pregnancy and Congenital Chagas

Summary

Screening in pregnancy

  • Include serology in routine prenatal tests in at-risk areas (2010 Guide, pp. 71 and 73).
  • Assess every seropositive pregnant woman with an electrocardiogram and Doppler echocardiogram from the first visits, because of the risk of decompensation (p. 71).

Treatment

  • Do not treat during pregnancy: aetiological treatment is contraindicated (pp. 45 and 73).
  • Treat the mother after breastfeeding (p. 73).

Newborn

  • Look for trypomastigotes in cord blood at delivery (2010 Guide, p. 72).
  • Under the current INS protocol: parasitology at birth, repeat at 3 or 6 months and serology at 10 months (v04 2022, p. 10).
  • Bear in mind that the 2010 Guide varies between 6 and 9 months (p. 35) and 6 to 12 months (p. 72).
Source: Clinical Care Guide for Chagas Disease (MinProtección Social/PAHO, 2010) and current INS documents (protocol v04 2022 and RDT guideline 2025)

Congenital form

  • Transmission is possible at any stage of maternal infection.
  • 60-90 % of cases are asymptomatic.
  • Hepatomegaly —and sometimes splenomegaly— is the most important sign; it usually resolves between 6-12 months without treatment (2010 Guide, pp. 20-21).

Confirmation and treatment of the newborn

  • If IgG antibodies persist at 6-12 months, confirm congenital Chagas disease and start treatment immediately (2010 Guide, pp. 72-73).
  • Extend the study to the household (protocol v04 2022, p. 10).

Pediatrics

Summary

Who to treat

  • Treat everyone under 18 years with chronic infection, regardless of clinical form (2010 Guide, p. 40).
  • Children tolerate the drug better: benznidazole up to 10 mg/kg/day and nifurtimox 10 mg/kg/day for 60 days (pp. 42 and 44).

Active detection

  • Prioritise detection of seropositive children with serology campaigns in children under 15 years (pp. 25, 49 and 51-52).
  • In a 20-year series, efficacy was low in those treated after 3 years of age (2010 Guide, p. 48).

Newborn

  • With compatible clinical signs and negative direct tests, use PCR before 6 months (p. 31).
  • Repeat IgG serology at 10 months, under the current INS protocol (v04 2022, p. 10).
Source: Clinical Care Guide for Chagas Disease (MinProtección Social/PAHO, 2010) and current INS documents (protocol v04 2022 and RDT guideline 2025)

Stepwise infant regimen

5 mg/kg/day increased over 6 days to 10 mg/kg/day for 60 days, given after meals, with the same clinical and laboratory follow-up as chronic patients (2010 Guide, p. 45).

Adverse Reactions

Summary

The therapeutic margin is narrow: adverse reactions are expected in all patients, especially adults (2010 Guide, p. 75).

Dermatitis

  • Mild dermatitis, about 20 %, between the 5th and 10th day: continue treatment (pp. 42-43).
  • Treat moderate dermatitis (less than 5 %) with temporary suspension, antihistamines or prednisolone 20 mg/day and reintroduction according to tolerability (pp. 42-43).
  • Stop and hospitalise severe dermatitis (less than 1 %) (pp. 42-43).

Bone marrow depression

  • Monitor neutropenia between the 20th and 30th day (less than 1 %) with leucocyte counts (p. 43).
  • Warn the patient about fever or odynophagia because of the risk of agranulocytosis (p. 43).

Peripheral neuropathy

  • High risk with 8 mg/kg/day for more than 30 days and a total dose above 15 g (p. 44).
  • It may appear up to a week after finishing and leave paraesthesia (p. 44).

Other reactions

  • Stop treatment if ageusia appears (0.5 % of cases) (p. 44).
  • Nifurtimox causes fewer skin effects but worse digestive tolerance and psychiatric disturbances (p. 44).

Pharmacovigilance

  • Notify adverse reactions under INVIMA and MinSalud rules; notification is mandatory for providers (2010 Guide, pp. 45 and 75).
Source: Clinical Care Guide for Chagas Disease (MinProtección Social/PAHO, 2010) and current INS documents (protocol v04 2022 and RDT guideline 2025)

Symptomatic management

Pruritus, dehydration and scaling: corticosteroid ointments and moisturising lotions twice a day (2010 Guide, p. 43).

Surveillance

Summary

Notification

  • Notify Chagas disease to SIVIGILA (2010 Guide, p. 73).
  • Notify immediately and individually every probable or confirmed acute case (protocol v04 2022, pp. 12 and 15).
  • Notify chronic cases weekly, only in priority populations: pregnant women, people under 18 years, Indigenous populations and women of childbearing age (15-49 years) (p. 15).

Operational definitions

  • Probable or confirmed acute: includes congenital transmission and outbreaks from oral transmission (protocol v04 2022, pp. 10-11).
  • Probable chronic: one reactive ELISA/CLIA; confirmed chronic: two tests of different antigenic principles (pp. 10-11).
  • If discordant, perform IFA or Immunoblot (pp. 10-11).

Targets and indicators

  • Perform a direct parasitological test in 100 % of acute cases (protocol v04 2022, pp. 22-23).
  • Perform a focus study in 100 % of outbreaks and isolated cases (pp. 22-23).
  • Meet the 100 % target for the lethality indicator (pp. 22-23).

Laboratory

  • Repeat direct parasitological tests serially, at least 3 times, in the acute phase (v04 2022, p. 20).
  • Take part in annual external performance assessments with the network (LNR/INS, LSPD and local laboratories) (INS 2017, pp. 32-33).
Source: Clinical Care Guide for Chagas Disease (MinProtección Social/PAHO, 2010) and current INS documents (protocol v04 2022 and RDT guideline 2025)

Early detection

Screening protocol for T. cruzi in every prolonged fever from an endemic area; testing for T. cruzi during routine thick smear reading where malaria coexists; active detection of seropositive children and screening of pregnant women (2010 Guide, pp. 24-26 and 74).

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