FROM THE OUTSET, an intended purpose of the Workshop on Vital Data for National Needs was to provide information on the range of uses of the current vital statistics data and to suggest important uses on the immediate horizon. Given the tight time constraints of a 1-day session, the workshop zeroed in on two major classes of current uses: public health research and the development of population estimates and projections.
With regard to health policy and health research, summarized in Section 2–A, workshop presentations focused on two major demographic phenomena of long-standing interest: disparities or inequities in health across different racial and ethnic subgroups and gender differences in mortality. This session of the workshop also contrasted these academic perspectives on the uses of vital statistics data with the use of the data for program and planning purposes by the Maternal and Child Health Bureau (MCHB) in the U.S. Department of Health and Human Services. In Section 2–B, we summarize workshop presentations and discussion on the development of population projections and estimates by the Census Bureau and the Social Security Administration; in the latter case, the decades-long projections of population composition based on vital statistics play a key role in the major policy debates on the long-run viability of Social Security entitlements. In terms of future directions, Section 2–C summarizes the workshop’s session that focused on the emerging field of biosurveillance—monitoring of disease and mortality with fine spatial and temporal precision in order to rapidly detect major disease outbreaks or, perhaps, terrorist attacks using biological agents.
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–2–
Uses of Vital Statistics Data
F
ROM THE OUTSET, an intended purpose of the Workshop on Vital
Data for National Needs was to provide information on the range
of uses of the current vital statistics data and to suggest important
uses on the immediate horizon. Given the tight time constraints of a 1-
day session, the workshop zeroed in on two major classes of current uses:
public health research and the development of population estimates and
projections.
With regard to health policy and health research, summarized in Sec-
tion 2–A, workshop presentations focused on two major demographic phe-
nomena of long-standing interest: disparities or inequities in health across
different racial and ethnic subgroups and gender differences in mortality.
This session of the workshop also contrasted these academic perspectives
on the uses of vital statistics data with the use of the data for program and
planning purposes by the Maternal and Child Health Bureau (MCHB) in
the U.S. Department of Health and Human Services. In Section 2–B, we
summarize workshop presentations and discussion on the development of
population projections and estimates by the Census Bureau and the Social
Security Administration; in the latter case, the decades-long projections of
population composition based on vital statistics play a key role in the major
policy debates on the long-run viability of Social Security entitlements. In
terms of future directions, Section 2–C summarizes the workshop’s session
that focused on the emerging field of biosurveillance—monitoring of disease
and mortality with fine spatial and temporal precision in order to rapidly
detect major disease outbreaks or, perhaps, terrorist attacks using biological
agents.
9
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10 VITAL STATISTICS
2–A USES IN HEALTH POLICY AND HEALTH RESEARCH
2–A.1 Social Inequalities in Health
Nancy Krieger (Harvard School of Public Health) spoke on the use of
vital statistics and related data to monitor health inequities in the United
States—studies of trends in health and health care as they are related to
socioeconomic position, ethnicity, and gender. Her remarks summarized
findings from her Public Health Disparities Geocoding Project. Detailed
information on the project and related publications are available online at
http://www.hsph.harvard.edu/thegeocodingproject (April 2009).
The project’s objective is to augment data in public health surveillance
systems, including the birth and death certificate data, with additional so-
cioeconomic covariate information; the resulting constructs are termed area-
based socioeconomic measures (ABSMs). The methodology links geocoded
vital statistics and U.S. census data at the block group, census tract, and ZIP
code tabulation area levels of geography. Ultimately, the intended goal is to
develop a valid, robust, easy-to-construct, and easy-to-interpret ABSM that
can be readily used by any U.S. state health department or health researcher
for public health monitoring and for studying any health outcome from birth
to death for any age, gender, or racial or ethnic group. The project started
in 1998, making use of data from the Massachusetts Department of Public
Health and the Rhode Island Department of Health; the data were for a set
of years centered around the 1990 census, and the socioeconomic data in
the ABSMs made use of information from that census.
To test robustly whether choice of ABSM and geographic level matters,
Krieger said that she focused on a wide variety of health outcomes, including
mortality (all cause and cause specific), birth (specifically, low birth weight)
and also cancer incidence (all sites and site specific), childhood lead poi-
soning, sexually transmitted infections, tuberculosis, and nonfatal weapons-
related injuries. Each outcome was analyzed in relation to 19 different AB-
SMs, capturing diverse aspects of socioeconomic position. Eleven of the
measures were single-variable measures (e.g., percent working class, percent
crowded household) and eight were composites (e.g., deprivation indices de-
veloped in previous research). Analyses were performed for the total popu-
lation and also stratified by race, ethnicity, and gender.
Krieger summarized four key findings from the geocoding project. First,
measures of economic deprivation were most sensitive to the expected so-
cioeconomic gradients in health. Second, census-tract-level analyses yielded
the most consistent results, with maximal geocoding, compared to the block
group and ZIP code data. Third, these findings held for separate analy-
ses conducted for white, black, and Hispanic men and women; they also
held for those outcomes that could be meaningfully analyzed among the
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USES OF VITAL STATISTICS DATA 11
smaller Asian, Pacific Islander, and American Indian populations. Fourth, the
single-variable measure of percentage of persons below poverty performed
as well as more complex composite measures of economic deprivation, in-
cluding the Townsend index.1 The research suggested that socioeconomic
inequalities in health are best monitored with a census-tract poverty mea-
sure; Krieger said that one advantage of this approach is that the measure
can be applied to all persons, regardless of age, gender, current individual-
level educational status, or current employment status.
Krieger presented socioeconomic gradients for several health outcome
measures to illustrate that the technique provides a way for routine docu-
mentation and monitoring of trends using existing vital statistics and pub-
lic health surveillance data. Specifically, her graphic displays divided cen-
sus tracts into categories based on percentage of the population below the
poverty level (e.g., less than 5 percent, 20 percent or greater). The figures
suggested clear poverty gradients in terms of
• low birth weight, the risk of which was two times higher among births
occurring in the most versus least impoverished tracts, that is, 7.5 per-
cent versus 3.6 percent;
• children with elevated lead levels, with a seven-fold excess among those
living in the most versus least impoverished census tracts (33 versus 5
percent);
• syphilis, with excess risk for the most impoverished tracts being 17
times higher than for the least impoverished tracts;
• cervical cancer, the incidence of which was twice as high for the most
impoverished areas (18 versus 9 per 100,000 population);
• nonfatal gunshot injury, with an 11-fold increase (22 versus 2 per
100,000 population); and
• heart disease mortality, with a 1.4-fold excess risk found, resulting in
an excess of nearly 100 deaths per 100,000 population.
Moving to analysis of racial, ethnic, and gender health disparities,
Krieger presented 1989–1991 data on premature mortality (death before
age 65). As context, the data indicated that fully half of the black and His-
panic populations lived in census tracts with 20 percent or more of the pop-
ulation below the poverty level whereas, by contrast, almost 50 percent of
white men and women live in census tracts with less than 5 percent below
poverty. Against this demographic backdrop, the researchers found evidence
1 The Townsend index (Townsend, 1987; Townsend et al., 1988) is a composite index score
based on four area-based census measures: percentage of households with no car, percent-
age of households not owner-occupied, percentage of persons unemployed, and percentage of
households overcrowded.
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12 VITAL STATISTICS
of marked socioeconomic disparities in premature mortality, with the esti-
mated relative risks ranging from 1.6 to 2.8. Within each economic stratum,
an excess of premature mortality remained apparent among the black popu-
lation. Looking a decade later (1999–2001 data), the same trends persisted:
for white non-Hispanic, black, and Hispanic men, higher levels of census-
tract poverty were associated with an elevated risk of dying prematurely,
with black and Hispanic populations most likely to live in the most impov-
erished census tracts.
Krieger noted similar trends in heart disease mortality data from the
period 2000–2005 for Massachusetts. Without disaggregation by poverty
level, age-standardized heart disease rates among men and women show a
basic distinction, with blacks at higher risk than whites. However, stratify-
ing by census-tract poverty level shows more complex gradients: the poorest
census tracts have consistently higher risk levels than the least poor, with
particularly pronounced gaps for white and black men living in the poorer
census tracts. Similar findings follow from an analysis using 2004–2005
Massachusetts birth outcome data involving low birth weight and smoking
during pregnancy. The analysis suggests that racial and ethnic disparities
again exist within each socioeconomic stratum, with blacks doing worse for
low birth weight and whites doing worse in terms of smoking. There are
also marked socioeconomic gradients within each racial or ethnic group.
Analysis of these data is ongoing, with the final report slated to include data
on prenatal care, breast feeding, caesarian sections, preterm deliveries, and
infant mortality.
Krieger said that sharing data, methods, and publications on the project
website is an important part of the project’s goal to enhance the data re-
ported by U.S. state health departments. Project researchers have conducted
training sessions of personnel at health departments, and the techniques have
been used in special reports issued by several states, including Washington
and Maryland. The intent for the project is to expand the state health de-
partments’ use of geographic analysis in analyzing vital statistics.
Krieger noted recent work done in collaboration with the Boston Pub-
lic Health Commission and the Massachusetts Department of Public Health
to extend the work to city-defined neighborhoods and to portray socioeco-
nomic and health data on a consistent set of maps. The system developed
by the researchers concentrates on premature mortality as the outcome mea-
sure; the analysis system is built on modeling premature mortality as a func-
tion of fixed and random effects, allowing for statistical smoothing in the
estimation of small-area rates, estimation of variance at each of the speci-
fied levels, and adjustment for multiple covariates. A particularly interesting
finding from this work was based on mapping the population-based propor-
tion of premature deaths that would not have occurred if residents in every
census tract enjoyed the same age-specific mortality rates as residents of the
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USES OF VITAL STATISTICS DATA 13
least impoverished tracts. Krieger said that this proportion exceeded 20
percent for 8 of Boston’s 60 neighborhoods and 68 percent of the city’s cen-
sus tracts. In two of Boston’s poorest neighborhoods—Roxbury and North
Dorchester—the high excess fractions suggest that, in more than half their
census tracts, some 25–30 of every 100 deaths among people under age 75
would not have happened if people in those neighborhoods had, at each and
every age, the same lower risk of dying as people in the richer areas.
Recently, the project considered U.S. national trends and inequities in
premature mortality from 1960 through 2002. County-level mortality data
from the National Center for Health Statistics (NCHS) were linked to
county-level population and median family income data from the Census
Bureau. These data were used to calculate and compare premature mortality
and infant death rates by county income quintile for the entire study period.
The study found that, even as premature mortality declined in all county
income quintiles, the gap between the lowest and highest income quintiles
persisted over the entire period and it was relatively greatest for prema-
ture mortality in 2000. The greatest progress in reducing these income gaps
occurred between 1965 and 1980, especially for populations of color; there-
after, the health inequities widened. The same pattern held for infant deaths.
The researchers also used an approach similar to that in the Boston neigh-
borhood study, considering excess premature deaths that would not have
occurred if the rates in the least impoverished areas were the same as those
for the most impoverished areas. Under these assumptions, Krieger said
that the research showed that, had everyone experienced the same yearly
age-specific mortality rates as whites in the highest-income-county quintile
between 1960 and 2002, 14 percent of white and 30 percent of nonwhite
premature deaths would have been averted.
Going forward, a challenge will be working with a new data source.
Unlike the 1990 and 2000 censuses, the 2010 decennial census will not in-
clude a long-form sample that obtains additional social and demographic
information (including questions used to calculate census-tract-level poverty
estimates). Instead, that information is now covered in the Census Bureau’s
American Community Survey (ACS). The ACS provides the same data items
as the old long form but, because it is collected on a continuous basis (spread-
ing the sample out over several years), the data are in a new format: rolling
averages based on 1, 3, or—for small areas such as tracts—5 years of data.
Krieger indicated that project researchers are beginning work to explore
how best to develop the tract-level characteristics based on ACS data.
Krieger concluded that vital statistics are critical for understanding cur-
rent and changing U.S. patterns of health and health inequities and the story
they tell is compelling. Krieger noted that some of these themes were ex-
pressed in a 2008 PBS documentary, Unnatural Causes: Is Inequality Making
Us Sick? The basic data of vital events are core to these public education ef-
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14 VITAL STATISTICS
forts, because they alone can reveal whether population health and health
inequities are getting better or worse.
2–A.2 Trends in Mortality
Richard Rogers (University of Colorado) began his remarks by comment-
ing that there was a period, in the 1970s and 1980s, when it was generally
thought that the important questions related to the study of mortality had
already been asked and that the set of factors influencing mortality were well
understood. Thirty years of subsequent research demonstrates that the study
of mortality remains one of critical importance to understanding health in
the United States. As illustrated by Krieger’s presentation, widespread dis-
parities in health and longevity are one important reason for further study
of mortality trends. Rogers said that mortality studies are also important
because mortality affects a variety of different, broader factors, including
social relationships and social institutions; it can have a profound influence
on individuals, on families, on communities. It is important to social policies
and population forecasting; in thinking of health care financing in the long
run, mortality studies are of central importance for administration of Social
Security and Medicare.
International comparisons are a major emerging motivating factor for
studies of mortality. Specifically, Rogers noted a study by Banks et al. (2006)
that found a fairly large disparity between the American and English pop-
ulations. Rogers summarized the study as having two major findings: first,
that prevalence rates for disease were generally higher for Americans than
for the English and, second, that the socioeconomic health status gradient
is a real construct and is evident in both countries. Generally, Rogers said
that the fact that the United States is not at the top of the world in terms
of life expectancy—there are at least 22 other countries with longer life
expectancies—is a basic motivational factor for further study of basic ques-
tions: Why are Americans sick and why does the U.S. life expectancy lag
behind that of other countries?
Because of time constraints, Rogers centered his remarks on sex differ-
ences in life expectancy. The data used in his research include mortality
data from the vital statistics, particularly a linked mortality file combining
records from the National Death Index with survey data from NCHS’s Na-
tional Health and Nutrition Examination Survey (NHANES). The research
also uses data from NCHS’s National Health Interview Survey.
Analysis of estimated life expectancy at birth from 1900 to the present
shows generally increasing life expectancies for both males and females,
though expectancies for males are consistently lower than those for females.
Shifts in the data show the effects of infection for several periods, especially
the influenza epidemic in 1918. After greater control for infectious diseases,
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USES OF VITAL STATISTICS DATA 15
mortality becomes less volatile from the 1940s onward. However, the data
also show a slow convergence of the male and female trend lines as the
gender difference in life expectancy narrows. After peaking at a 7.8-year
difference in 1975 (Arias, 2007), the difference between men and women
in estimated life expectancy has steadily declined: by 2005, the gap was 5.2
years.
Rogers noted that many studies have looked at the differences around the
1978 peak, but fewer studies have examined the motivating factors for the
subsequent decline in the gap. He briefly suggested a range of possible fac-
tors that contribute to sex differences in mortality: biological factors, health
behaviors (smoking, drinking, unsafe driving, exercise), environmental risks,
social relations (marriage, family composition), and socioeconomic status
(education, employment, income, poverty). Rogers suggested that some as-
yet-underresearched possibilities include composite measures that may be
difficult to pick up in national data sets. One is addressing the concepts and
assumptions of “masculinity” and “femininity”—for instance, the extent to
which “masculine” traits of a high pain threshold, reluctance to seek medical
help (absent a life-threatening condition), and failure to get regular health
checkups affect health outcomes. The differential life expectancy by sex
still shows up when mortality rates are disaggregated by age. The biggest
age gap between males and females manifests itself in late teens and early
adolescence, what Rogers said has been described as the “accident peak” or
“testosterone spike.”
Cigarette smoking patterns are one variable that seems to be a central
contributor to sex differences in mortality, but those patterns have changed
over time. Historically, males have tended to smoke in higher proportions
than females—about 53 percent of adult men smoked in 1955, compared
with 25 percent of adult women. However, over time, rates of smoking
have decreased for both sex groups although females have drawn closer to
males (an estimated 24 percent of adult men reported smoking in 2004,
compared with 18 percent of adult women). Rogers cited previous research
in concluding that smoking contributes to some of the sex differences in
mortality and life expectancy. Retherford (1972) attributed 47 percent of the
sex gap in life expectancy in 1972 to cigarette smoking; Rogers’ own work
with colleagues (Hummer et al., 1998; Rogers et al., 2000) suggests that
smoking contributed to about 25 percent of the gap as measured in 1990–
1995. These estimates are consistent with an overall decline in smoking and
a convergence between males and females in their smoking patterns.
Rogers summarized work with hazard ratios derived from NHANES data
for 1988–2000. Though the original intent of the work was to try to explain
away of the sex difference in mortality, the results actually suggest more ex-
planations for a widening of the gap than a narrowing. Relative to males,
females in this period had less education, had lower incomes, and were less
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16 VITAL STATISTICS
likely to be employed—that is, they were disadvantaged on a number of so-
cioeconomic status measures. Once these factors are controlled, the hazard
ratio expands and the gap in mortality widens. Controlling for marital sta-
tus also widens the gap; this finding can be explained by males’ tendency
to marry younger women but die at earlier ages, meaning that females end
up living longer in a widowed status. Rogers also noted that religious atten-
dance has some influence on the sex differential (reducing the gap), because
females are more religious and attend services more frequently. Physical ac-
tivity tends to widen the gap, as does disability (as measured by a question
on difficulty in walking).
Examining causes of death—looking at sex differences in mortality asso-
ciated with specific causes rather than overall—provides additional insight
about the sex gap. Rogers noted that the gap is particularly wide for deaths
due to circulatory disease and cardiovascular disease, while cerebrovascular
diseases have less role in explaining the differences between males and fe-
males. The significant sex differences in terms of deaths due to cancer are
mostly a result of cigarette smoking; the major difference (higher rates of
lung cancer mortality among men) disappears when smoking is considered.
Respiratory diseases do not have a significant difference between the gen-
ders, but deaths due to external causes (accidents, homicides, and suicides)
do; because of small sample sizes, these effects are hard to examine in detail.
Rogers concluded that part of his results are based on specific periods,
specific durations, and specific follow-up time periods. Period effects are
important—researchers get different results in explaining sex differences in
longevity and mortality in the 2000s than were estimated in the 1970s and
1980s. Still, it is important to think about other covariates and, specifically,
what other covariates might be important that are not regularly collected
in current national surveys and national data sets. Such covariates could
include geographic information; they could include better measures of re-
ligiosity or religious attendance; and they could also include such factors
as altruism, genetics, biology, stress, and refined quantification of socioeco-
nomic status.
In discussion, Rogers noted that the existing interview data from the Na-
tional Health Interview Survey and NHANES are generally restricted to the
noninstitutional population: understanding the degree to which these survey
measures are conservative estimates (because they exclude major segments of
older persons in nursing facilities and younger persons in correctional facili-
ties) is an important consideration for future research. It was also noted that
deaths of U.S. citizens overseas—and, particularly, military deaths—are not
included in standard vital statistics (and, hence, not in general assessments
of health inequities that use those data). Rogers concluded that health dis-
parities are important and reducing them is a critical national objective for
the United States; he said that we need more information to more fully un-
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USES OF VITAL STATISTICS DATA 17
derstand some of the differences, by sex, by age, by race and ethnicity, and
by socioeconomic status.
2–A.3 Uses of Vital Statistics by the Maternal and Child Health Bureau
Peter van Dyck (MCHB, Health Resources and Services Administration,
U.S. Department of Health and Human Services) described the various ways
in which vital statistics are used by MCHB:
• as the basis for both assessing eligibility for and monitoring perfor-
mance of targeted public health grants;
• as input to regular publications and policy standards; and
• as a way of evaluating an agency’s progress toward general objectives.
He also commented on MCHB’s role in issuing grants to help states reengi-
neer their vital statistics and child health information systems.
Pursuant to Title V of the Social Security Act of 1935, the MCHB is
responsible for providing a variety of grant and coordination services. The
bureau’s responsibilities make it the oldest continuing health program re-
lated to mothers and children in the nation. Each year, MCHB administers
about $1 billion in grants, most of which—about $600 million—is provided
as block grant allocations to the states and territories. The block grant funds
are allocated using a formula based on a state’s percentage of children living
in poverty as a share of the national total; the funds support the operation
of state-level maternal and child health offices and programs. Van Dyck said
that the states are required to provide matching funds (at least $3 in state
funds for every $4 in federal funds), which the states usually generate by
billing Medicaid or private insurance for the services they deliver to ma-
ternal and child health clients. Some counties also provide funds or staff
support. In this way, the $600 million in federal money for maternal and
child health grants is leveraged to yield a total effort of $5 billion to 6 billion.
To qualify for and obtain the MCHB Title V block grants, state appli-
cants must annually report on a series of 18 specific performance measures;
see Box 2-1. Van Dyck noted that vital statistics are essential to this perfor-
mance and evaluation effort, because several of the performance measures
are obtained directly from vital records data (as indicated in italics in the
box). State grantees are also directed to provide regular information on a
set of six national performance outcome measures, also shown in the box;
all of these are directly computed from vital statistics.
The Title V block grant program also makes use of a set of “health sys-
tem capacity indicators” (HSCIs) and “health status indicators” (HSIs) in
program evaluation, several of which are keyed directly to vital statistics:
• HSCI #04: Percentage of women ages 15–44 with a live birth during
the reporting year for whom the ratio of observed to expected prenatal
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18 VITAL STATISTICS
Box 2-1 Performance and Outcome Measures for the Maternal and Child
Health Bureau Block Grant Program
Performance Measures
1. Percent of screen positive newborns who received timely follow-up to definitive
diagnosis and clinical management for condition(s) mandated by their state-
sponsored newborn screening programs
2. Percent of children with special health care needs age 0–18 whose families part-
ner in decision making at all levels and are satisfied with the services they receive
3. Percent of children with special health care needs age 0–18 who receive coordi-
nated, ongoing, comprehensive care within a medical home
4. Percent of children with special health care needs age 0–18 whose families have
adequate private and/or public insurance to pay for the services they need
5. Percent of children with special health care needs age 0–18 whose families report
the community-based service systems are organized so they can use them easily
6. Percent of youth with special health care needs who received the services nec-
essary to make transitions to all aspects of adult life, including adult health care,
work, and independence
7. Percent of 19–35-month olds who have received full schedule of age appropri-
ate immunizations against measles, mumps, rubella, polio, diphtheria, tetanus,
pertussis, haemophilus influenza, and hepatitis B
8. Rate of birth (per 1,000) for teenagers ages 15–17 years
9. Percent of third-grade children who have received protective sealants on at least
one permanent molar tooth
10. Rate of deaths to children ages 14 years and younger caused by motor vehicle
crashes per 100,000 children
11. Percent of mothers who breast-feed their infants at 6 months of age
12. Percent of newborns who have been screened for hearing before hospital dis-
charge
13. Percent of children without health insurance
14. Percent of children, ages 2–5 years, receiving WIC services that have a Body Mass
Index (BMI) at or above the 85th percentile
15. Percent of women who smoke in the last 3 months of pregnancy
16. Rate (per 100,000) of suicide deaths among youths 15–19
17. Percent of very-low-birth-weight infants delivered at facilities for high-risk deliver-
ies and neonates
18. Percent of infants born to pregnant women receiving prenatal care beginning in
the first trimester
Outcome Measures
1. Infant mortality rate per 1,000 live births
2. Ratio of the black infant mortality rate to the white infant mortality rate
3. Neonatal mortality rate per 1,000 live births
4. Postneonatal mortality rate per 1,000 live births
5. Perinatal mortality rate per 1,000 live births plus fetal deaths
6. Child death rate per 100,000 children ages 1–14
NOTE: Italics indicate that the measure is derived from vital statistics data.
SOURCE: Workshop presentation by Van Dyck; http://mchb.hrsa.gov/training/
performance_measures.asp (April 2009).
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USES OF VITAL STATISTICS DATA 19
visits is greater than or equal to 80 percent on the Kotelchuck Index
(which is related to the mother’s age at time of prenatal care entrance
and the birth weight of the baby if the baby is born early)
• HSCI #05: Comparison of infant deaths between Medicaid and non-
Medicaid recipients, using information associated with prenatal care,
low birth weight, and infant mortality. (Van Dyck added that the
MCHB’s website, which posts these indicators for all grant recipients,
is the only ongoing data site that provides the rate of infant deaths for
Medicaid clients compared with the infant deaths for non-Medicaid
clients.)
• HSCI #09A and B: Self-scores by the states on their data capacity for
implementing four types of data linkages:
– annual linkage of infant birth and infant death certificates
– annual linkage of birth certificates and Medicaid eligibility or
paid claims files
– annual linkage of birth certificates and WIC eligibility files
– annual linkage of birth certificates and newborn screening files
• HSI #01A: Percent of live births weighing less than 2,500 grams
• HSI #01B: Percent of live singleton births weighing less than 2,500
grams
• HSI #02A: Percent of live births weighing less than 1,500 grams
• HSI #02B: Percent of live singleton births weighing less than 1,500
grams
• HSI #03A: Death rate per 100,000 due to unintentional injuries
among children ages 14 years and younger
• HSI #03B: Death rate per 100,000 for unintentional injuries among
children ages 14 years and younger due to motor vehicle crashes
• HSI #03C: Death rate per 100,000 for unintentional injuries for youth
ages 15 through 24 years due to motor vehicle crashes
MCHB also administers the $100+ million, county-based Healthy Start
program, which is intended to reduce infant mortality rates in vulnerable or
poor communities. The program is intended to facilitate service delivery in
selected areas, including easing access to prenatal health care and promot-
ing positive prenatal health behaviors. As with the block grants, Healthy
Start administrators depend on vital statistics—in this case, detailed disag-
gregation of infant mortality rates—to target program activities and eval-
uate progress. Looking at county-level plots of infant mortality rates is a
particularly important diagnostic tool for Healthy Start, allowing MCHB to
pinpoint areas in the nation that might be eligible to apply for grants (grant
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24 VITAL STATISTICS
for women in their 20s but increasing rates for women in their 30s—part of
a longer-term trend toward higher average maternal age at birth. Goss said
that OCA understood that much of the 1965–1990 decline in the fertility
rate was likely attributable to this transition to birth at higher ages and, con-
sequently, not one that would continue to drop forever. Hence, Goss said
that OCA has never assumed birth rates lower than 1.9 for the total fertility
rate. Though some European countries do project a continued decline in
fertility rates, OCA generally assumes a steady, average fertility rate of 2.0
for the U.S. population into the future.
Clearly, Goss said, the cost implications of shifts in birth rates for Social
Security are substantial. The range of OCA’s current projections at the end
of 75 years—a total fertility rate estimated at 2.0, within an interval of 1.7
to 2.3—maps to a estimated cumulative effect of about 15.5–19.8 percent
of payroll. That is, Social Security would require somewhere between 15.5–
19.8 percent of total payroll earnings in order to pay all of its scheduled
benefits. Goss demonstrated that changing fertility assumptions even slightly
can have major effects on the estimates (and on the uncertainty relative to
those estimates) of Social Security’s funding needs.
Goss noted that OCA acquires its birth data from the NCHS-compiled
vital statistics. In terms of data quality, Goss said that OCA is always con-
cerned about the potential for underreporting, given the potential for dis-
tortion of the basic fertility rate that underlies so much of Social Security’s
fiscal projections.
Immigration and Emigration
Goss said that OCA resolves migration into four basic components and
draws its data from a variety of sources.
• Legal immigration: OCA uses data from the U.S. Department of
Homeland Security (DHS) on legally admitted immigrants by age and
sex. OCA typically bases its assumptions on averages of these data over
the past 10 fiscal years. Though most of the categories of legal immi-
grants are numerically limited or capped by law, one category that is
not numerically limited is new immigrants who are immediate relatives
of citizens. From its discussion with DHS staff, OCA has concluded
that this category has been growing. Reconciling this information with
some shifts in other categories (e.g., an increased tendency for persons
acquiring legal permanent resident status to be people adjusting their
immigration status rather than new entrants), OCA raised its standard
assumption of 800,000 gross legal immigrants per year to 1,000,000.
• Legal emigration: OCA uses historical estimates of legal emigration
produced by the Census Bureau, which have ranged from 20 to 30
percent of the level of legal immigration. OCA’s current assumption
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USES OF VITAL STATISTICS DATA 25
for this category is 25 percent of the level of immigration. However,
OCA does make some adjustments to this working rule. In particu-
lar, people can leave the borders of the United States but retain their
insured status for Social Security benefits; hence, for purposes of pro-
jecting Social Security needs, OCA needs to recognize this group in
its calculations. Accordingly, OCA lowers its assumed number of em-
igrants at older ages—effectively treating them as non-emigrants for
estimation purposes.
• Other immigration (undocumented and temporary): Historically, OCA
relied on estimates of net immigration of U.S. residents. However,
starting in 2008, OCA began working with separate estimation of both
inflows and outflows in undocumented and temporary residents, with
separate age structures. OCA’s new calculations are based on analysis
of 2000 census data, combined with estimates generated by DHS in
2006; the age distribution at entry (and exit) is based on unpublished
Census Bureau tabulations for the net “other immigrant” count for
1975–1980. On the basis of this work, OCA’s current annual assump-
tion is about 1.5 million new other immigrants per year.
• Other emigration: On the basis of OCA’s analysis, the office assumes
that about 0.5 million of the 1.5 million other immigrants each year
become legal permanent residents within 5 years. The other 1 million
either stay (in undocumented or temporary status) or emigrate; OCA
currently assumes that about 700,000 of that 1 million eventually exit
the country.
In discussion at the workshop, Goss noted that, in making its projections
of undocumented immigrants, OCA has to make assumptions about the ex-
tent to which the undocumented immigrants work for wages and, if they
do, whether they pay taxes. OCA’s current projections are that about half of
new undocumented immigrants do pay into the system (Social Security and
other taxes) but that the fraction will decline over time. In part, Goss said,
this is due to the increased documentation requirements to obtain a Social
Security card. OCA currently projects that only a relatively small fraction
(10–20 percent) of undocumented individuals will go through the process
of acquiring legal residence and actually receive benefits.
Goss commented that the implications of immigration for Social Security
projection are relatively modest, with only about a 1 percentage point swing
in the Social Security cost rate over the 75-year projection period being at-
tributable to immigration.
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26 VITAL STATISTICS
Disability
Though not commonly thought of as a vital event in the usual sense, Goss
noted that disability is certainly an important and life-changing factor—with
real implications for the cost of Social Security—and so is incorporated into
the fiscal projections. In the absence of firm national data on disabilities, the
Social Security Administration draws its data and assumptions on disability
from its internal data. Specifically, OCA draws on Social Security data on in-
cidence (based on entitlements and awards) and reported medical and work
terminations.
Deaths
For data on deaths, OCA augments NCHS-compiled vital statistics with
Medicare data. For deaths of persons under age 65, the vital statistics of
death by cause are the exclusive source, with Census Bureau population es-
timates as the denominator. For persons age 65 and over, Goss said that
OCA tends to work with its own statistics, based on Medicare enrollments;
although these data are limited to those people who are fully insured in the
Social Security system, OCA has concluded that this approach gives it con-
sistency in the numerator and denominator used in death rates and, more-
over, helps minimize misstatement of age at time of death (as is a lingering
concern with death certificate data). However, the vital statistics mortality
data for persons age 65 and older are still an important input through their
information on the distribution of death by cause.
Goss observed that OCA’s death rates are projections by specific causes of
death. To make such projections, Goss said that OCA pays careful attention
to historical trends in mortality, but its final assumptions may reflect slightly
differing expectations. Though mortality has historically declined rather
rapidly at young ages and not very much at older ages, OCA tends to assume
more rapid acceleration of mortality for the oldest ages (85 and above) than
some figures would suggest.
Goss indicated that the cost sensitivity of its fiscal projections to assump-
tions on mortality is very significant—about a 3 percent swing over the 75-
year projection period between its low- and high-end projections. However,
fertility measures remain the most sensitive part of OCA’s overall projec-
tions.
Marriage and Divorce
Marriage and divorce are critical to consider because of their effects on
both benefits and employments. Though NCHS no longer compiles mar-
riage and divorce data in the national vital statistics, OCA continues to
base it assumptions on age distributions from the last available national
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USES OF VITAL STATISTICS DATA 27
numbers—1995 for marriages and 1988 for divorce. OCA believes that
it has a reasonably good handle on the total number of marriages and di-
vorces, and its projections for both marriage and divorce are effectively flat,
constant trends. Still, Goss said that OCA would clearly benefit from more
recent and detailed data of the form that used to be compiled in the national
vital statistics program.
2–B.2 Population Estimates and Projections at the Census Bureau
Victoria Velkoff and Fred Hollmann (both of the U.S. Census Bureau)
addressed the workshop on the use of vital statistics data in the Census Bu-
reau’s intercensal population estimates and its projections of U.S. population
trends.
By law (13 USC §181), the Census Bureau is required to produce basic
estimates of population and demographic characteristics between decennial
censuses:
During the intervals between each census of population . . . the Sec-
retary, to the extent feasible, should annually produce and publish for
each State, county, and local unit of general purpose government which
has a population of fifty thousand or more, current data on total popu-
lation and population characteristics. . . .
Velkoff commented that the population estimates are used to allocate over
$300 billion in federal funds each year, and they are also used by some states
in their funding formulas. The Census Bureau also uses the intercensal pop-
ulation estimates as controls or weights in major household surveys such
as the Current Population Survey, ACS, the Survey of Income and Program
Participation, and the American Housing Survey. The Bureau of Economic
Analysis uses the population estimates in its estimates of per capita income,
and they play significantly into calculations by other federal agencies. At
the workshop, Kenneth Prewitt (Columbia University) pointed out one par-
ticular federal use that illustrates the circularity and feedback loops in the
broader statistical system: because vital statistics on births and deaths are
a critical component of the population estimates, vital statistics drive both
the numerator (incident counts) and denominator (population) of NCHS’s
calculated birth and death rates.
As the Census Bureau’s system has evolved, national- and state-level pop-
ulation estimates are released by the end of the reference (estimate) year.
Estimates disaggregated by demographic groups and for smaller geographic
areas are rolled out over the course of the year; Velkoff noted in particular
that the Bureau’s nation and state demographic estimates for specific demo-
graphic categories for 2007 were slated for release the day after the April
30, 2008, workshop.
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28 VITAL STATISTICS
The Census Bureau’s population estimates program generates on an an-
nual basis:
• national-level estimates, total and disaggregated by age, sex, race, and
Hispanic origin categories;
• state-level estimates, total and disaggregated by age, sex, race, and
Hispanic origin categories;
• estimates for the 3,141 counties (or county-level equivalents), total
and disaggregated by age, sex, race, and Hispanic origin;
• estimates for about 39,000 incorporated places (cities and towns) and
minor civil divisions (county subdivisions), total population only; and
• estimates for Puerto Rico and its county-level municipios, by age and
sex.
Consistent with the U.S. Office of Management and Budget (OMB) guide-
lines, the full disaggregation by race and Hispanic origin involves 62 cat-
egories: the 31 combinations of the five race categories crossed with two
Hispanic origin categories (Hispanic or not Hispanic).
Velkoff described the basic cohort component method used to generate
Census Bureau estimates: updating the most recent decennial census count
by adding births, subtracting deaths, and adding an estimate of net interna-
tional migration. The Census Bureau generally relies on matches of Internal
Revenue Service records from year to year to estimate domestic migration
(supplemented by Social Security and Medicare data) and the Bureau’s own
ACS for estimating international migration rates. The NCHS vital statistics
data are the basis for the estimates of births and deaths used in the cohort
method.
The Census Bureau also periodically releases long-term population pro-
jections to describe the demographic character of the future U.S. popula-
tion. Hollmann said that these projections are used by states and localities
for specific planning objectives, such as assessing demand for roads, schools,
and other infrastructure improvements. Among federal users, the Bureau
of Labor Statistics uses the population projections as the basis for its own
projections of the future labor force, and the National Center for Education
Statistics uses them to plan education estimates.
The population projections program does not approach the level of
geographic detail of the population estimates program; it produces only
national- and state-level projections (though Hollmann noted that projec-
tions for metropolitan areas are sometimes discussed as a future improve-
ment). Like the full suite of population estimates, the release of population
projections is also staggered over time (albeit a longer time range than the
annual estimates): At the time of the April 2008 workshop, Hollmann in-
dicated that the most recent (interim) national projections were released in
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USES OF VITAL STATISTICS DATA 29
2004, the most recent projections of total state populations dated to 2005,
and national estimates disaggregated fully by race and Hispanic origin cate-
gories was slated for release in summer 2008.
Until recently, the Census Bureau’s population projections were particu-
larly dependent on input from vital statistics because they relied on an essen-
tially census-independent population base. The projections program relied
on the so-called demographic analysis population based on historical vital
statistics and estimates of international migration. However, Hollmann said
that the Census Bureau abandoned that practice in 2000 as a result of com-
fort with the smaller level of aggregate undercount in the census. Hence,
the Census Bureau is using a census base for its rates and projections rather
than a purely demographic basis.
Still, the Census Bureau’s population estimates and projections both
hinge on the NCHS-compiled vital statistics to provide birth and death com-
ponents in various formulas. Velkoff and Hollmann both commented on the
experience of using the vital statistics data and analyses:
• Velkoff noted that the time lag in the availability of final vital statistics
raises some concerns for the Census Bureau’s work. Given the Bu-
reau’s internal timeline of producing some national estimates by the
end of the target year, the Census Bureau typically finds itself in the
position of “projecting” vital events for about a year and a half. Al-
though Velkoff indicated that the Census Bureau has adjusted to this
situation and that these internal projections typically turn out to be of
acceptable quality, there are some instances in which they do not—the
significant population shifts due to Hurricane Katrina in 2005 being
a prominent example. For the purposes of computing the estimates,
Velkoff said that the Census Bureau makes the assumption that local
reporting of births and deaths is 100 percent complete; however, Cen-
sus Bureau researchers who develop the Bureau’s demographic analy-
sis estimates have conducted studies that relax the assumption of con-
stant, complete reporting. The Census Bureau has also recently be-
come concerned with the quality of data on reported age at death,
particularly at the oldest ages, and is conducting work to evaluate its
internal model for mortality at the oldest ages.
• Citing Census Bureau research on the components of change within
the national population projections (Mulder, 2002), Hollmann com-
mented that the Bureau has found that, historically, the largest source
of error in its projections comes from projecting fertility. He noted
that this is not to say that the Bureau has made the largest-magnitude
errors in projecting fertility rate, but rather that variability in the birth
component tends to have the largest effect on the final estimates. Over
the long term, Census Bureau projections both overprojected fertility
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30 VITAL STATISTICS
(e.g., in the late 1960s and 1970s on the back side of the baby boom)
and conservatively underprojected fertility (in later years). Errors have
tended to be less acute in projecting death and international migration
(even though the Census Bureau generally projects the latter as a con-
stant, and thus is almost certainly consistently low).
Both Velkoff and Hollmann commented on the challenge of using vital
statistics data in their current methodologies, given current variation among
registration areas in the format of race and Hispanic origin data; this specific
methodological discussion is summarized in Section 4–B.
Discussion at the workshop centered on the trends projected for the His-
panic population and, in particular, on research on differential trends in
mortality and general health among Hispanics by generation. Nancy Krieger
(Harvard School of Public Health) asked whether nativity in the United
States, versus foreign-born, is factored into the projections. Hollmann indi-
cated that neither nativity nor specific type of Hispanic origin (e.g., Mexican
or Cuban) is directly factored into the models but that it is picked up to the
extent that the projections are based on a historical series driven in part by
such differential trends. Session moderator Samuel Preston (University of
Pennsylvania) commented that lower mortality rates among Hispanics are
evident in Social Security Administration data, which may be less immune to
data reporting effects in the vital statistics data (i.e., without birth and death
certificates playing such a major role in both the numerator and denominator
of calculated rates).
Since the early 1970s, the Census Bureau has worked with a network of
state agency contacts to assist in the production of the annual estimates; later
in the decade, this Federal-State Cooperative Program for Population Esti-
mates (FSCPE) was joined by a companion Federal-State Cooperative Pro-
gram for Population Projections (FSCPP). Under both programs, the states
designate an agency as their representative. In some cases, Velkoff noted, the
state FSCPE contacts directly provide vital statistics to the Census Bureau
(particularly inasmuch as some states’ designated FSCPE or FSCPP agency is
also its participant in the Vital Statistics Cooperative Program).
2–B.3 Discussion
In discussion of this session of the workshop, moderator Samuel Preston
(University of Pennsylvania) commented that one of the values of vital statis-
tics, as they are produced for analysis of fertility and mortality, is that they
can be arrayed by birth cohort. Cohort analysis suggests interesting pat-
terns in both fertility and mortality that are not possible to observe by just
considering period behavior. For births and fertility, no individual cohort
was as extreme in magnitude as the peak in the (period-based) total fertility
rate would suggest, and the cohort-level trends have less variability than in
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USES OF VITAL STATISTICS DATA 31
period behavior. For deaths and mortality, cohort mortality patterns raise
interesting findings looking as far back as the 1930s and the first studies of
cohort mortality patterns. In particular, when sex differentials in mortal-
ity are arrayed on a cohort rather than a period basis, the sex differential
peaks for the cohort born around 1905—exactly the cohort for which sex
differences in smoking behaviors also reached a peak.
Goss concurred that this suggests that vital statistics—and cohort anal-
yses of them—provide great opportunities for investigation of patterns in
mortality and fertility. Goss said that significant work had been done inter-
nationally on this, particularly in the United Kingdom. Goss said that OCA
had also compared its data with counterparts in Canada; Canada has not
seen the same broad improvement in its national rate of mortality as in the
United States, but further analysis of trends could be useful.
2–C GROWING AND EMERGING USES: VITAL STATISTICS AND
BIOSURVEILLANCE
A workshop session moderated by Kenneth Prewitt (Columbia Univer-
sity) considered important applications of vital statistics beyond the health
care planning domain. Michael Stoto (Georgetown University) spoke of
his recent work in health surveillance for national security, also known as
syndromic surveillance or biosurveillance. Although originally focused on
the detection of terrorist attacks using biological agents, Stoto argued that
biosurveillance has come to be interpreted more broadly, as a means for situ-
ational awareness for public health emergencies. In either event, Stoto noted
that the data systems he was discussing have a much more exacting standard
for timeliness than the current vital statistics collections—timeliness mea-
sured in weeks and days, and sometimes hours, rather than years. Indeed,
the basic point of near-real-time acquisition and use of prediagnostic health
data is that waiting until people are diagnosed with diseases or, in the case
of vital statistics, die from them would be too late to inform possible inter-
ventions. Still, he said, there are important linkages between biosurveillance
and the current vital statistics.
The central statistical challenges in biosurveillance are, first, obtaining
and integrating accurate data from a variety of sources in a timely way and,
second, determining whether something is “unusual.” The latter task is com-
plicated by high variability in the background and a possible unstable process
generating the data; it involves making critical trade-offs among sensitivity
(i.e., false negatives), specificity (i.e., false positives), and timeliness.
Current work in biosurveillance has sought to build on existing data sys-
tems in the health care world—such as emergency department reports, sales
of over-the-counter medication, and absenteeism from work and school.
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32 VITAL STATISTICS
These data are usually electronically gathered and highly networked. Us-
ing these data, statistical analyses can detect sudden changes that might sug-
gests a disease outbreak or maybe a covert bioterrorist attack. As an exam-
ple, Stoto described analysis of emergency room data for seven Washington,
DC–area hospitals during winter 2003; for those data, detection algorithms
suggested certain excesses of gastrointestinal diseases at several hospitals at
several points (e.g., early February, early March, mid-April). Though not
definitive—Stoto said that there is no way to know whether, for example,
the early February increase is a sudden escalation due to random chance or
the beginning of something big, that all that is known is that there are dif-
ferences from what happened before February 1—the work provides clues
to follow in ferreting out causes.
Biosurveillance research also involves dealing with a number of practical
issues. These include privacy concerns about the patients to whom the data
refer, as embodied in the Health Insurance Portability and Accountability Act
Privacy Rule and related state laws. Other practical challenges include pro-
prietary concerns (who owns the data and with whom can they be shared),
concerns and possible prohibitions on secondary use of the data, and oper-
ational costs for personnel and information technology. These formidable
practical challenges have partially contributed to the recent shift to cast bio-
surveillance more broadly as a “situational awareness” technique, Stoto said.
Though the purely statistical questions of detecting significant increases in
activity continue to draw attention, interest has shifted toward public health
activities such as “case finding”: making it easier for physicians and other
health care providers to report individual cases that might be of concern
and when and where something might be going on, as well as ways to aid
outbreak investigations and monitor outbreaks.
Given the emphasis on timeliness that is central to biosurveillance sys-
tems, Stoto asked what kind of contributions vital statistics—and the prin-
ciples and practices of vital statistics systems—can bring to bear. Mortality
due to pneumonia and influenza is an instructive example to consider for a
number of reasons, among them a lengthy history of analysis of such data,
experience with the challenge of distinguishing between routine seasonal in-
fluenza and wider pandemic outbreaks, and the fact that exposure to many
biological agents that could be used in a terrorist attack would initially cause
flu-like symptoms. Stoto began by noting recent work by Mills et al. (2004)
analyzing data concerning the 1918 Spanish influenza epidemic in the United
States. That research found big differences from city to city in terms of the
timing and extent of excess influenza deaths. Stoto said that having such data
available during an epidemic would certainly have been useful. Close analy-
sis of data (Collins et al., 1930) suggests further insights on public response
to the disease outbreak. Stoto noted that a classic example that has been
raised from the data is the difference in response by two cities—Philadelphia,
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USES OF VITAL STATISTICS DATA 33
which did relatively little in response, and St. Louis, which was much more
interventionist in terms of closing schools and reducing public activities.
Pneumonia and influenza mortality data for 122 cities that have relatively
rapid vital statistics reporting are still a key component of public health in-
fluenza surveillance. Like the historical data, these data provide useful in-
sight on the timing and extent of flu in one year relative to previous years.
Timeliness, however, is a problem: Data downloaded on one Saturday refer
to deaths in the week ending the previous Saturday. Yet death from influenza
is the end point of a process that typically runs from 1 to 2 weeks, and so
even with the most timely data, insight on the time and nature of infection
is limited by an effective 3-week lag.
The example of influenza monitoring raises the question of how modern
information technology—such as electronic vital records collection and elec-
tronic death records—might make mortality data more useful for near-real-
time monitoring. Vital statistics may never achieve the near-hourly temporal
resolution that is needed for outbreak detection, but Stoto suggested that
there is still a great deal of value in being able to frame assessments based
on what is going on in cause-specific mortality data on a monthly or weekly
basis. The question of geographic representation is an important issue: the
flu surveillance data from which Stoto drew in his example is based on the
cities that, more than a decade ago, were at the forefront in being able to
gather electronic death records; more development, and assessment of the
coverage represented by such cities and areas, is essential.
Stoto closed by noting that vital events reporting had advanced
technologically—going beyond the postcards used for reporting in the
19th century to data compilation by fax, phone, and the Internet. However,
in its basic character, the collection of information on vital events and
disease has not progressed much from the old postcard system. He argued
that there is great benefit in the basic structure of the current vital statistics
system, which leaves “ownership” of case reports with the state and local
authorities, but which provides for federal ownership of the system for
gathering vital records and compiling them. Stoto urged that the nation
consider a notifiable diseases cooperative program, akin to but broader in
scope than the existing vital statistics cooperative program.
Ed Hunter’s presentation (Centers for Disease Control and Prevention)
focused principally on the demands on birth certificates and the issuance
process due to antiterrorism legislation (see Section 3–A), but he concurred
with key parts of Stoto’s presentation. Hunter said that it is still unclear
whether birth certificate requirements will be the final major impetus for a
fully electronic, rapid, standardized vital registration system for births and
deaths (given legally mandated matches of birth and death records). If it is,
however, Hunter said that the system improvements required by the secu-
rity provisions will do all the things that Stoto mentioned were necessary for
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34 VITAL STATISTICS
situational awareness and surveillance, including rapid availability of vital
records data and, ideally, marked decreases in the time lags to issuance of
birth and death data. This development would also have a variety of ben-
eficial spillover effects for the general study of health information. Hunter
concurred in the usefulness of pandemic influenza as an initial study and
development area; he said that the pandemic funding stream is another op-
portunity to build on the state electronic registration systems and to try to
advance their timeliness.