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Table 1 Institutional health information system

From: Does the health information system in Jordan support equity to improve health outcomes? Assessment and recommendations

Data sources and references

Owners of the data

Data production

Program

data collected

Forms of data

Institutional data

[8, 10, 19, 22, 24, 25, 29,30,31,32]

MoH, RMS, Private sector, University

Routinely

Individual Service and Source Records

Institutional data

Paper based

National electronic registration system

[17, 19, 23, 24, 31, 33, 34]

MoH, RMS, Private sector, University

Routinely

Hakeem

Information gathered from individual cases at the healthcare facility level is compiled and organized at the levels of the healthcare facility, governorate, and nation.

Computerized

National electronic registration system

[19]

MoH

Routinely

Interactive Electronic Reporting System (IERS)

Information gathered from individual cases at the healthcare facility level is compiled and organized at the levels of the healthcare facility, governorate, and nation.

Computerized (tablet based)

Institutional data [17, 19, 23, 24, 31, 33, 34]

Individual institution

Routinely

Individual, service and resource records

Institutional data

Paper and computer based

National registration system [12, 13, 19, 24, 27, 29, 31, 32]

Directorate of NCDs (MoH)

Routinely collected and collated annually

National Renal Disease Registry

Patients are registered upon receiving a confirmed diagnosis at healthcare facilities and specialized hospitals, with their information classified according to three factors: age, sex, and place of residence.

Paper based at Hospital level – Collated and digitized centrally

National registration system

[12, 13, 19, 24, 27, 29, 31, 32]

Directorate of NCDs (MoH)

Routinely collected and collated annually

National Thalassemia Registry

Patients are registered upon receiving a confirmed diagnosis at healthcare facilities and specialized hospitals, with their information classified according to three factors: age, sex, and place of residence.

Paper based at Hospital level – Collated and digitized centrally

National registration system

[12, 13, 24, 27, 29, 31, 32]

Directorate of NCDs (MoH)

Routinely collected and collated annually

National Cancer Registry

Patients are registered upon receiving a confirmed diagnosis at healthcare facilities and specialized hospitals, with their information classified according to three factors: age, sex, and place of residence.

Paper based at Hospital level – Collated and digitized centrally

  1. Source Study data sources