From: Mortality and cause-of-death reporting and analysis systems in seven pacific island countries
Category | Strengths | Weaknesses |
---|---|---|
Societal Issues | Social incentives for registration | Private land burials without official approval |
Administrative Environment | Existing legal framework | Inadequate/inconsistent implementation of laws |
Health systems involvement in Civil registration and vital statistics operations | Passive registration i.e. onus to report on citizen | |
Registration process for “off-island” deaths unclear | ||
National statistics committees | Complex statistical reporting requirements | |
System Issues – Administration | Community nurses formally tasked to notify vital events | Improper emphasis on community nurses to report cause of death |
Routine compilation of mortality data by different health departments | Need for better coordination to generate one reconciled mortality dataset from the health system | |
Private health intuitions rarely integrated adequately into reporting systems | ||
No clear delineation of responsibility across institutions, leading to task duplication | ||
Personnel lack authority to query/clarify data | ||
System Issues – Technical | Standard international medical death certificate (except Nauru) | Lay reporting of cause for deaths outside facilities in some countries |
Medical certificates of death not routinely tabulated in all countries | ||
Trained ICD coders | High turnover of trained staff | |
Key personnel adequately skilled for data management at national level | Statistical analysis limited to ten leading causes of death | |
Insufficient data quality assessment and control | ||
Initiatives to set data standards for health information | Dysfunctional/outdated software programs not amenable to modification or upgrade | |
System Issues – Ownership | Strong ownership of systems/interest at national levels that has contributed substantially to ongoing survival of the systems | Generally poor feedback to local level staff |
Many systems are highly dependent on one or two key individuals with a strong interest in providing health data |