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. 2017 Dec 12;41:e174. doi: 10.26633/RPSP.2017.174

TABLE 2. Characteristics of congenital anomaly surveillance systems in Latin America, and the baseline of microcephaly prevalence before 2015.

Country/Countries

Name of surveillance program

Year started

Legislation/Funding

Mandatory

Sources of ascertainment

Size and coverage

Stillbirth included

Verbatim description of congenital anomalies

Baseline microcephaly per 10 000 births (before 2015)

Argentina

National Registry of Congenital Anomalies of Argentina (RENAC)

2009

Funded by Ministry of Health of Argentina

No

The detection period lasts until discharge from the hospital

300 000 annual births

Yes

Yes

1.90a

Brazil

Live Birth Information System (SINASC)

2001

Financed by Ministry of Health of Brazil; obligatory notification

Yes

Live birth certificate

National

No

No

0.57b

Chile

Regional Register Congenital Malformation of Maule Health Service

2001

Based on ECLAMC and funded by the Maule Health Service

No

Pediatricians and midwives at the delivery units of participating hospitals

Maule Region; 13 500 births annually

Yes

Yes

1.4c

Colombia

Bogota Congenital Malformations Surveillance Program

2006

Based on ECLAMC; founded by District Health Secretary of Bogotá and Pontificia Universidad Javeriana

No

Control-case methods same as the ECLAMC (nurses, gynecologists, neonatologists)

104 700 births annually were monitored in the city of Bogotá

Yes

Yes

2.5d

Costa Rica

Costa Rican Birth Defects Register Center

1986

Founded by Public Health Ministry of Costa Rica; obligatory notification

Yes

Since 2009, the age of obligatory notification was extended to children under 1 year of age

The program is population based

Yes

Yes

4.31e

Cuba

Cuban Register of Congenital Malformation

1985

Financed by Public Health Ministry of Cuba

No

Reports are obtained from hospitals all over Cuba

96% of Cuban births

Yes

Yes

0.22f

Mexico

Mexican Registry and Epidemiological Surveillance of External Congenital Malformations

1978

Research grants

No

Reports are obtained from 21 hospitals in 11 cities of Mexico

3.5% of all births in Mexico

Yes

Yes

2.01f

Uruguay

National Registry of Congenital Defects and Rare Diseases (RNDCER)

2011

Financed by Public Health Ministry of Uruguay; obligatory notification

Yes

Reports are obtained from different health professional and patient organizations

The program is population based

Yes

Yes

0.52g

Various South American countries

Latin American Collaborative Study of Congenital Malformations (ECLAMC)

1968

Research program

No

Collaborating pediatricians at the delivery units of participating hospitals

Approximately 1% of the annual births of the South American countries

Yes

Yes

4.83f

b

Available from SINASC, at: http://www2.datasus.gov.br/DATASUS/index.php?area=060702 Accessed 27 June 2016.

c

Personal communication (Drs. Aurora Canessa and Rosa Fajardo) (Maule Register – ECLAMC).

g

Available from: http://www.msp.gub.uy/marco-normativo/registro-nacional-de-defectos-cong%C3%A9nitos-y-enfermedades-raras Accessed 12 May 2016. (unpublished information: total births, 191 820 (2011-2014), with 10 cases reported).

Source: Prepared by the authors from the study results.