1 The Perinatal Periods of Risk CityMatCH
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11
The Perinatal Periods of RiskThe Perinatal Periods of Risk
CityMatCH http://www.citymatch.org/
22
PPOR PPOR MapsMaps Fetal & Infant Fetal & Infant Deaths Deaths
500-1499 g
1500+ g
Fetal Death Neonatal
Post- neonatal
Maternal Health/ Prematurity
Maternal Care
Newborn Care
Infant Health
Birth
weig
ht
Age at Death
33
PPOR analytic methodsPPOR analytic methods Analytic Preparation Analytic Preparation
http://www.citymatch.org/PPOR/HowTo/Content/AnalyticReadinessWKSHOhttp://www.citymatch.org/PPOR/HowTo/Content/AnalyticReadinessWKSHOP.pptP.ppt
Acquire access to three required Acquire access to three required vital records computer filesvital records computer files
Prepare vital records files and Prepare vital records files and required data elementsrequired data elements
Assess data qualityAssess data quality Assess study sample sizeAssess study sample size
44
PPOR analytic methodsPPOR analytic methodsPhase I:THE MAPSPhase I:THE MAPS
http://www.citymatch.org/PPOR/HowTo/HowToDo.http://www.citymatch.org/PPOR/HowTo/HowToDo.htmhtm Define study populationDefine study population
Restrict study population by Restrict study population by birthweight and gestational agebirthweight and gestational age
Calculate numbers and rates for Calculate numbers and rates for the feto-infant mortality mapthe feto-infant mortality map
Compare different time periods, Compare different time periods, subpopulations and geographic subpopulations and geographic areasareas
55
PPOR analytic methodsPPOR analytic methodsPhase I, continued: THE GAPSPhase I, continued: THE GAPS
Select reference populationSelect reference population Calculate excess mortality rates Calculate excess mortality rates
and numbers of deathsand numbers of deaths Identify excess mortality gapsIdentify excess mortality gaps
66
PPOR Analytic MethodsPPOR Analytic Methods——
Phase 2 AnalysisPhase 2 Analysis Explains Explains whywhy the excess deaths the excess deaths
occurred so that appropriate occurred so that appropriate action can be taken.action can be taken.
77
PPOR is aboutPPOR is about ACTIONACTIONMaternal Health/
Prematurity
Maternal Care
Newborn Care
Infant Health
Preconception Health Health Behaviors Perinatal Care
Prenatal Care High Risk Referral Obstetric Care
Perinatal Management Neonatal Care Pediatric Surgery
Sleep Position Breast Feeding Injury Prevention
88
Three Phase 2 DirectionsThree Phase 2 Directions Community health and health Community health and health
systems assessmentsystems assessment Fetal Infant Mortality Reviews Fetal Infant Mortality Reviews
(FIMR)(FIMR) Further epidemiologic studyFurther epidemiologic study
PPOR Analytic Methods PPOR Analytic Methods ——
99
PPOR Analytic MethodsPPOR Analytic Methods——
Phase 2 AnalysisPhase 2 Analysis
The third direction is the focus of The third direction is the focus of this presentation:this presentation:
Epidemiologically investigate Epidemiologically investigate the reasons for excess the reasons for excess mortalitymortality
1010
PPOR Analytic MethodsPPOR Analytic Methods——
Steps of Phase 2 Analysis : Steps of Phase 2 Analysis :
Identify Identify causal pathwayscausal pathways or or biologic mechanisms for biologic mechanisms for excess mortalityexcess mortality
Estimate Estimate prevalenceprevalence of risk and of risk and preventive factors by type of preventive factors by type of mechanismmechanism
Estimate the Estimate the impactimpact of the risk of the risk and preventive factors.and preventive factors.
1111
PPOR Phase 2 AnalysesPPOR Phase 2 AnalysesLimitationsLimitations
Large number of deaths neededLarge number of deaths needed to obtain to obtain statistically significant because models are statistically significant because models are complex and effect sizes are small.complex and effect sizes are small.
Unlikely to identify new causesUnlikely to identify new causes because an because an observational study using vital records and observational study using vital records and existing data. existing data.
Unlikely to find a single cause for excess Unlikely to find a single cause for excess mortalitymortality because the feto-infant mortality it because the feto-infant mortality it is a multifactorial problemis a multifactorial problem
1212
How can we most How can we most effectively determine effectively determine the likely causes of the likely causes of excess deaths in our excess deaths in our
community?community?
1313
PPOR Phase 2 AnalysesPPOR Phase 2 Analyses StrategyStrategy
Eliminate factors unlikely to be Eliminate factors unlikely to be contributingcontributing
Find and target factors likely to be Find and target factors likely to be contributingcontributing
1414
PPOR Phase 2 AnalysesPPOR Phase 2 Analyses StrategyStrategy
A factor is a likely contributor if:A factor is a likely contributor if:
1.1. KNOWNKNOWN cause of death based on cause of death based on scientific literature.scientific literature.
2.2. MORE PREVALENTMORE PREVALENT among the among the population with excess deathspopulation with excess deaths
Impact analysis helps prioritize among Impact analysis helps prioritize among likely contributorslikely contributors
1515
Phase 2 Analysis PlanPhase 2 Analysis Plan
Depends on:Depends on:
Phase 1 Analysis resultsPhase 1 Analysis results
Availability of dataAvailability of data
Community prioritiesCommunity priorities
1616
Phase 2 Analysis PlanPhase 2 Analysis Plan
Guidelines Developed for :Guidelines Developed for :
Infant HealthInfant Health
Maternal Health/PrematurityMaternal Health/Prematurity
Recommendations for :Recommendations for :
Maternal CareMaternal Care
1717
Phase 2 Analyses Phase 2 Analyses Preparation Preparation
The The DEATH CERTIFICATEDEATH CERTIFICATE is the source of is the source of Age at deathAge at death Cause of deathCause of deathThe The BIRTH CERTIFICATEBIRTH CERTIFICATE is the source for is the source for Maternal characteristics & risk factorsMaternal characteristics & risk factors Circumstances of the birthCircumstances of the birth Infant risk factors & conditionsInfant risk factors & conditions Geo-coding (mother’s residence)Geo-coding (mother’s residence)
1818
Phase 2 Analyses Phase 2 Analyses Preparation of data for impact Preparation of data for impact
estimationestimation
o Use a birth cohort file of live births and Use a birth cohort file of live births and fetal deaths with linked deaths. fetal deaths with linked deaths.
o Convert death cohort files to a single Convert death cohort files to a single birth cohort file Combine linkedbirth cohort file Combine linked
o Add fetal deaths for the same year with Add fetal deaths for the same year with a variable indicating the outcome.a variable indicating the outcome.
1919
Preparation of data for impact estimationPreparation of data for impact estimation Converting 2000 and 2001 Converting 2000 and 2001 Period Files to a 2000 Birth Period Files to a 2000 Birth
Cohort FileCohort File Linked Linked FileFile
Year Year BornBorn
Year DiedYear Died ActionAction
20002000 19991999 20002000 OmitOmit
20002000 20002000 20002000 KeepKeep
20012001 20002000 20012001 KeepKeep
20012001 20012001 20012001 OmitOmit
2020
Data Source>Data Source> Birth/Fetal Birth/Fetal CertificateCertificate
Death Cert.Death Cert.
IDID OutcomeOutcome Birth-Birth-weightweight
Maternal Maternal AgeAge
Cause of Cause of DeathDeath
Fet01Fet01 Fetal Fetal DeathDeath
798798 1717 InfectionInfection
Fet02Fet02 Fetal Fetal DeathDeath
25372537 3434 Cong. Cong. AnomalyAnomaly
LB01LB01 SurviveSurvive 35113511 2222
LB02LB02 Infant Infant DeathDeath
23142314 2525 SIDSSIDS
LB03LB03 SurviveSurvive 12931293 2121
LB04LB04 Infant Infant DeathDeath
631631 2626 InfectionInfection
Preparation of data for impact Preparation of data for impact
estimationestimation Portion of birth cohort data Portion of birth cohort data
filefile
2121
Phase 2 Data Phase 2 Data PreparationPreparation
o Other files can be also now be linked to Other files can be also now be linked to the combined study filethe combined study file
o If geocoded according to street If geocoded according to street address, census tract or zip code (e.g.), address, census tract or zip code (e.g.), GIS analysis including neighborhood GIS analysis including neighborhood and community factors, census, crime, and community factors, census, crime, housing, etc. housing, etc.
2222
Phase 2 Analyses Phase 2 Analyses Preparation Preparation
OTHER DATA SETSOTHER DATA SETS to consider: to consider: Hospital discharge systemHospital discharge system PRAMSPRAMS Birth defects surveillanceBirth defects surveillance Pregnancy/Pediatric Nutrition Surveillance Pregnancy/Pediatric Nutrition Surveillance Injury surveillanceInjury surveillance STD reportsSTD reports Child abuse reporting systemsChild abuse reporting systems Program files (Medicaid, WIC, etc)Program files (Medicaid, WIC, etc) Linked program filesLinked program files
2323
When linked to birth certificates,other datasets can be used to estimate the impact of risk factors on mortality.
2424
INFANT HEALTH INFANT HEALTH PERIODPERIOD
Protocol is on the web atProtocol is on the web at http://www.citymatch.org/PPOR/HowTo/Content/PHAS2IH.dochttp://www.citymatch.org/PPOR/HowTo/Content/PHAS2IH.doc
2525
Phase 2 Analyses-Infant Health Phase 2 Analyses-Infant Health PeriodPeriod Identify causal pathways or Identify causal pathways or
biologic mechanisms for excess biologic mechanisms for excess mortalitymortality
Use Underlying Cause of Death Use Underlying Cause of Death
Categorize by CDC’s Postneonatal Categorize by CDC’s Postneonatal Mortality Surveillance System Mortality Surveillance System
birth defectsbirth defects infectionsinfections injuriesinjuries perinatal conditionsperinatal conditions SIDSSIDS other causesother causes
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Infant HealthInfant Health
SIDS
Injury
Infection
Anomalies
Each category has its
own set of risk
factorsPerinatal
Phase 2 Analyses-Infant Health Phase 2 Analyses-Infant Health PeriodPeriod
Identify causal pathways or biologic Identify causal pathways or biologic mechanisms for excess mortalitymechanisms for excess mortality
2727
Cause-specific mortality rate (CSMR)Cause-specific mortality rate (CSMR)
the number of deaths in each category the number of deaths in each category
number of live births>=1500gnumber of live births>=1500g
ExcessExcess Cause-specific mortality rate Cause-specific mortality rate
= Study Pop. CSMR – Ref. Pop. CSMR= Study Pop. CSMR – Ref. Pop. CSMR
Phase 2 Analyses-Infant Health Phase 2 Analyses-Infant Health PeriodPeriod Identify causal pathways or Identify causal pathways or
biologic mechanisms for excess biologic mechanisms for excess mortalitymortality
2828
Example City
Number of IH
Deaths
IH Death Rate
Ref. IH Death
RateExcess CSMR
Congenital Anomaly 11 0.179 0.16 0.019
Infection 13 0.211 0.14 0.071
SIDS 75 1.219 0.84 0.379
Perinatal Conditions 31 0.504 0.25 0.254
Other/Undefined 16 0.260 0.27 -0.010
total IH 146 2.372 1.66 0.712
Live Births >= 1500g 61,540
Phase 2 Analyses-Infant Health Phase 2 Analyses-Infant Health PeriodPeriod Identify causal pathways or Identify causal pathways or
biologic mechanisms for excess biologic mechanisms for excess mortalitymortality
2929
Cause-Specific Contribution to Excess Infant Health Deaths
Congenital Anomaly
3%
SIDS52%
Perinatal Conditions
35%
Infection10%
Example CityExample City
Excess Infant Health Mortality Rate=0.712 per 1000 live births
3030
Passive smokePassive smoke Sleep positionSleep position Breast-feedingBreast-feeding BeddingBedding Co-sleepCo-sleep Maternal ageMaternal age Death scene Death scene
investigationinvestigation
Folic acid intakeFolic acid intake Alpha-feto Alpha-feto
proteinprotein AlcoholAlcohol Drug abuseDrug abuse DiabetesDiabetes UltrasoundUltrasound Delivery siteDelivery site
SIDS Anomalies
Phase 2 Analyses-Infant Health Phase 2 Analyses-Infant Health PeriodPeriod Estimate prevalence of risk and Estimate prevalence of risk and
preventive factors by type of mechanismpreventive factors by type of mechanism
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Medical homeMedical home ImmunizationsImmunizations Breast-feedingBreast-feeding Passive smokePassive smoke Prenatal carePrenatal care Maternal ageMaternal age Infection typeInfection type
BeddingBedding SupervisionSupervision EnvironmentEnvironment Injury typeInjury type
InjuryInfection
Phase 2 Analyses-Infant Health Phase 2 Analyses-Infant Health PeriodPeriod Estimate prevalence of risk and Estimate prevalence of risk and
preventive factors by type of mechanismpreventive factors by type of mechanism
3232
SIDS—major contributor to excess SIDS—major contributor to excess deathsdeaths
Examine risk factor disparity for SIDSExamine risk factor disparity for SIDS Compare prevalence between study Compare prevalence between study
population to reference populationpopulation to reference population Denominator is all live birthsDenominator is all live births
Estimate prevalence of risk and Estimate prevalence of risk and preventive factors by type of mechanismpreventive factors by type of mechanism
3333
Phase 2 Analyses-Infant Health Phase 2 Analyses-Infant Health PeriodPeriod OTHER DATA SETSOTHER DATA SETS to consider: to consider:
Hospital discharge systemHospital discharge system PRAMSPRAMS Birth defects surveillanceBirth defects surveillance Pregnancy/Pediatric Nutrition Surveillance Pregnancy/Pediatric Nutrition Surveillance Injury surveillanceInjury surveillance STD reportsSTD reports Child abuse reporting systemsChild abuse reporting systems Program files (Medicaid, WIC, etc)Program files (Medicaid, WIC, etc) Linked program filesLinked program files
3434
Phase 2 Analyses-Infant Health PeriodPhase 2 Analyses-Infant Health Period
Example CityExample CityPrevalence of SIDS Risk Factors Among Live Prevalence of SIDS Risk Factors Among Live Births Study versus Reference PopulationsBirths Study versus Reference Populations
20.4
15.4
8
11.2 10.1 10
0
5
10
15
20
25
TeenMothers
Sleepingon
Stomach
Smoking
Study PopReference Pop
3535
Phase 2 Analyses-Infant Health Phase 2 Analyses-Infant Health PeriodPeriod Estimate the impact of the risk Estimate the impact of the risk
and preventive factorsand preventive factors
Risk Ratio or Relative RiskRisk Ratio or Relative Risk Probability of disease Probability of disease
in the exposed in the exposed population divided by population divided by the probability of the probability of disease in the disease in the unexposed unexposed populationpopulation
A/(A+B)A/(A+B)RR= RR=
C/(C+D)C/(C+D)
OutcomOutcome Yese Yes
OutcomOutcomee
NoNo
Risk Risk FactorFactor
YesYes
AA BB
Risk Risk Factor Factor NoNo
CC DD
3636
Population Attributable Risk Population Attributable Risk PercentPercent
Compares the rate for the whole population Compares the rate for the whole population to the rate for those WITHOUT the risk factorto the rate for those WITHOUT the risk factor
Based on the relative risk and the prevalence Based on the relative risk and the prevalence of the exposure for the whole population.of the exposure for the whole population.
Has a meaningful interpretation: Has a meaningful interpretation: “Percent of “Percent of the population that would be prevented from the population that would be prevented from the poor outcome if the risk factor were the poor outcome if the risk factor were eliminated from the entire population.”eliminated from the entire population.”
Relevant to overall impact and cost.Relevant to overall impact and cost.
Phase 2 Analyses-Infant Health Phase 2 Analyses-Infant Health PeriodPeriod
Estimate the impact of the risk and preventive factorsEstimate the impact of the risk and preventive factors
3737
Population Attributable RiskPopulation Attributable RiskDeb Rosenberg recommends using the formulaDeb Rosenberg recommends using the formula
PAR = PPAR = P0 0 – P– P22
Where Where PP00 is the proportion of the whole population that have the bad is the proportion of the whole population that have the bad
outcomeoutcomePP2 2 is the proportion of those without the risk factor that have the bad is the proportion of those without the risk factor that have the bad
outcome.outcome.
The difference is interpreted as the proportion of bad outcomes that The difference is interpreted as the proportion of bad outcomes that would be eliminated if no-one in the population had the risk would be eliminated if no-one in the population had the risk factor. This is the proportion of bad outcomes that can be factor. This is the proportion of bad outcomes that can be “attributed” to the factor.“attributed” to the factor.
Phase 2 Analyses-Infant Health Phase 2 Analyses-Infant Health PeriodPeriod
Estimate the impact of the risk and preventive factorsEstimate the impact of the risk and preventive factors
3838
Population Attributable Risk Percent Population Attributable Risk Percent (PAR%)(PAR%)
PAR% = {P (RR-1) /1+P (RR-1)} x 100PAR% = {P (RR-1) /1+P (RR-1)} x 100
WhereWhere P P = proportion of the population with a = proportion of the population with a particular risk factor, and particular risk factor, and
RRRR = Risk Ratio = Risk Ratio (can substitute Adjusted Odds Ratio or (can substitute Adjusted Odds Ratio or RR from logistic regression or published literature)RR from logistic regression or published literature)
Phase 2 Analyses-Infant Health Phase 2 Analyses-Infant Health PeriodPeriod
Estimate the impact of the risk and preventive factorsEstimate the impact of the risk and preventive factors
3939
PAR ResourcesPAR Resources
http://www.soph.uab.edu/mch-imrm/stats.htm,
LEVIN 1953, Fleiss 1981 p76 Calculator at : http://
www.urmc.rochester.edu/cpm/education/mach/PARC.xls
4040
Phase 2 Analyses-Infant Health PeriodPhase 2 Analyses-Infant Health Period PAR% EXAMPLE: PAR% EXAMPLE: EXAMPLEEXAMPLE INFANT INFANT MORTALITY ATTRIBUTABLE TO TEEN MORTALITY ATTRIBUTABLE TO TEEN
MATERNAL AGEMATERNAL AGE Example:Example: RR=1.998RR=1.998 PAR%=8.94PAR%=8.94
Maternal Age
Infant Deaths
Infants Surviving
<=19 35 3082
>=20 159 27897
If no teen births occurred, 8.94% fewer babies If no teen births occurred, 8.94% fewer babies would die in Example. This translates to 17 fewer would die in Example. This translates to 17 fewer deaths, or a reduction in IMR from 6.2 to 5.7 per deaths, or a reduction in IMR from 6.2 to 5.7 per thousand live births.thousand live births.
4141
MATERNAL HEALTH / MATERNAL HEALTH / PREMATURITY PREMATURITY
PERIODPERIODProtocol is on the web atProtocol is on the web at
http://www.citymatch.org/PPOR/HowTo/Content/PHAS2MH.dhttp://www.citymatch.org/PPOR/HowTo/Content/PHAS2MH.dococ
4242
Causes for 500-1,499g areCauses for 500-1,499g are MultifactorialMultifactorial ComplexComplex InconsistentInconsistent Varies by trainingVaries by training
Phase 2 Analyses-Mat. Phase 2 Analyses-Mat. Health/Prem.Health/Prem.
Identify causal pathways or biologic Identify causal pathways or biologic mechanisms for excess mortalitymechanisms for excess mortality
4343
Kitagawa’sKitagawa’s formula algebraically formula algebraically partitions excess mortality into 2 partitions excess mortality into 2 stratastrata
portion to portion to birthweight distributionbirthweight distribution portion to portion to birthweight specific birthweight specific
mortalitymortality
Phase 2 Analyses-Mat. Phase 2 Analyses-Mat. Health/Prem.Health/Prem.
Identify causal pathways or biologic Identify causal pathways or biologic mechanisms for excess mortalitymechanisms for excess mortality
4444
KitagawaKitagawa
Phase 2 Analyses-Mat. Phase 2 Analyses-Mat. Health/Prem.Health/Prem.
Identify causal pathways or biologic Identify causal pathways or biologic mechanisms for excess mortalitymechanisms for excess mortality
Maternal Health/ Maternal Health/ PrematurityPrematurity
Birthweight Distribution
Birthweight- Specific Mortality
4545
n
nnnn
nnnn PP
MMMM
PP1 21
2121
21 )(2
)()(
2
)(
Phase 2 Analyses-Mat. Phase 2 Analyses-Mat. Health/Prem.Health/Prem.
Identify causal pathways or biologic Identify causal pathways or biologic mechanisms for excess mortalitymechanisms for excess mortality
The Kitagawa FormulaThe Kitagawa Formula
Where “P” stands for birthweight distribution (proportion of births in stratum n)
And “M” stands for specific mortality (the mortality rate in stratum n)
http://www.citymatch.org/PPOR/HowTo/Content/kitgawa_updated_98_00.xls
(save the spreadsheet on your own computer)
4646
Contribution to Mortality Contribution to Mortality DifferenceDifference
Birth Birth weightweight
Bwt Bwt Dist.Dist.
Mort. Mort. RateRate
Bwt Bwt Dist.Dist.
Mort.Mort.
RateRate
500-749500-749 0.4%0.4% 612.5612.5 0.2%0.2% 573.5573.5
750-999750-999 0.4%0.4% 205.5205.5 0.2%0.2% 244.3244.3
1000-12491000-1249 0.3%0.3% 166.7166.7 0.2%0.2% 134.6134.6
1250-14991250-1499 0.5%0.5% 117.0117.0 0.3%0.3% 98.098.0
1500-19991500-1999 1.9%1.9% 66.966.9 1.1%1.1% 50.450.4
2000-24992000-2499 4.9%4.9% 20.120.1 3.4%3.4% 19.919.9
2500+2500+ 91.691.6 3.63.6 94.5%94.5% 2.72.7
TotalTotal 100%100% 10.010.0 100%100% 6.06.0
Pinellas County National Reference Group
4747
Contribution to Mortality Contribution to Mortality DifferenceDifference
Pinellas County vs National Reference GroupPinellas County vs National Reference Group
Birth Birth WeightWeight
Birthweight Birthweight DistributionDistribution
MortalitMortality Ratey Rate
CombinedCombined
500-749500-749 1.41.4 0.10.1 1.51.5
750-999750-999 0.40.4 -0.1-0.1 0.30.3
1000-12491000-1249 0.10.1 0.10.1 0.20.2
1250-14991250-1499 0.20.2 0.10.1 0.30.3
1500-19991500-1999 0.40.4 0.20.2 0.70.7
2000-24992000-2499 0.30.3 0.00.0 0.30.3
2500+2500+ -0.1-0.1 0.80.8 0.70.7
TotalTotal 2.82.8 1.21.2 4.04.0
4848
Feto-Infant Mortality Feto-Infant Mortality Contribution to MortalityContribution to Mortality
Pinellas County vs National Reference Pinellas County vs National Reference GroupGroup
70%
30%
91%
9%
Distribution Mortality Rates
Total Fetal Infant Mortality
Maternal Health/ Prematurity
Mortality
4949
Presenting kitagawa resultsPresenting kitagawa resultsKitagawa: Most Common Kitagawa: Most Common
ConclusionConclusion ““The predominant cause of death for VLBW The predominant cause of death for VLBW
babies is birthweight distribution: too many babies is birthweight distribution: too many babies are born at very low weights. Our babies are born at very low weights. Our community will benefit most by preventing community will benefit most by preventing prematurity”prematurity”
““Birthweight-specific mortality nearly Birthweight-specific mortality nearly matches that of the reference group. Babies matches that of the reference group. Babies born too small are surviving nearly as well as born too small are surviving nearly as well as babies in the reference group.”babies in the reference group.”
5050
Presenting kitagawa resultsPresenting kitagawa resultsKitagawa: Some cities have up to 40% Kitagawa: Some cities have up to 40% of excess deaths in the MH/P period of of excess deaths in the MH/P period of
risk due to birthweight specific risk due to birthweight specific mortality.mortality.
““Birthweight-specific mortality in our Birthweight-specific mortality in our target group is not as good as it is in the target group is not as good as it is in the reference group. Babies in that group reference group. Babies in that group that are born too small are not surviving that are born too small are not surviving as well as can be expected.”as well as can be expected.”
5151
SmokingSmoking Prenatal carePrenatal care RaceRace Maternal ageMaternal age ParityParity STD/Bacterial Vag.STD/Bacterial Vag. Multiple Preg.Multiple Preg. SES/EducationSES/Education Birth IntervalBirth Interval Maternal HTN/DiabetesMaternal HTN/Diabetes
Gestational ageGestational age Referral systemReferral system Perinatal carePerinatal care Mat. complicationsMat. complications Neonatal conditionsNeonatal conditions Pay sourcePay source
Birthweight Distribution (VLBW Births)
Birthweight- Specific Mortality
Phase 2 Analyses-Mat. Phase 2 Analyses-Mat. Health/Prem.Health/Prem.
Estimate prevalence of risk and Estimate prevalence of risk and preventive factors by type of preventive factors by type of
mechanismmechanism
5252
Maternal Health/ Maternal Health/ PrematurityPrematurity
Birthweight Distribution
Birthweight- Specific Mortality
Percent VLBW
VLBW Births and Fetal Deaths
All Births And Fetal
Deaths
Mortality Rate
OUTCOME DENOMINATOR
Phase 2 Analyses-Mat. Phase 2 Analyses-Mat. Health/Prem. Health/Prem. Estimate prevalence of Estimate prevalence of risk and preventive factors by type of risk and preventive factors by type of
mechanismmechanism
5353
Prematurity—major contributor to Prematurity—major contributor to excess deathsexcess deaths
Examine risk factor disparity for Examine risk factor disparity for prematurityprematurity
Compare prevalence between study Compare prevalence between study population to reference populationpopulation to reference population
Denominator is all live birthsDenominator is all live births
Phase 2 Analyses-Mat. Phase 2 Analyses-Mat. Health/Prem.Health/Prem. Estimate prevalence of Estimate prevalence of
risk and preventive factors by type of risk and preventive factors by type of mechanismmechanism
5454
Phase 2 Analyses-Mat. Health/Prem.Phase 2 Analyses-Mat. Health/Prem.
Estimate prevalence of risk and preventive Estimate prevalence of risk and preventive factorsfactors
OTHER DATA SETSOTHER DATA SETS to consider: to consider: Hospital discharge systemHospital discharge system PRAMSPRAMS Birth defects surveillanceBirth defects surveillance Pregnancy/Pediatric Nutrition Surveillance Pregnancy/Pediatric Nutrition Surveillance Injury surveillanceInjury surveillance STD reportsSTD reports Child abuse reporting systemsChild abuse reporting systems Program files (Medicaid, WIC, etc)Program files (Medicaid, WIC, etc) Linked program filesLinked program files
5555
Should fetal deaths be Should fetal deaths be included in study of VLBW included in study of VLBW
Births?Births? Risk factor information on fetal deaths is Risk factor information on fetal deaths is
more frequently missing.more frequently missing.
Excluding fetal deaths will have little Excluding fetal deaths will have little impact because they make up less than impact because they make up less than 1% of all births in most communities. 1% of all births in most communities.
5656
Example CityExample CityPrevalence of Prematurity Risk FactorsPrevalence of Prematurity Risk Factors
Non-Hispanic White versus Ref. Non-Hispanic White versus Ref. PopulationPopulation
153022
75
020406080
100
Smoking DuringPregnancy
Satisfaction withPrenatal Care
Per
cen
t o
f A
ll L
ive
Bir
ths
Reference Population White, Non-Hispanic
5757
70
5
3010
0
20
40
60
80
100
Teenage Mothers Multiple Births
Per
cen
t o
f al
l li
ve b
irth
s
Black, Non-Hispanic Reference Population
Example CityExample CityPrevalence of Prematurity Risk FactorsPrevalence of Prematurity Risk Factors
Non-Hispanic Black versus Ref. Non-Hispanic Black versus Ref. PopulationPopulation
5858
PluralityPlurality
PPOR analyses are not restricted to PPOR analyses are not restricted to singleton live births. Multiple births singleton live births. Multiple births contribute to a community’s feto-infant contribute to a community’s feto-infant mortality rate and may contribute to mortality rate and may contribute to an increasing rate or population an increasing rate or population disparity. These births should be disparity. These births should be include in Phase 1 Analysis and further include in Phase 1 Analysis and further studied as part of the Phase 2 Analysis studied as part of the Phase 2 Analysis
5959
Plurality—bill’s slidePlurality—bill’s slide
Multiple births can contribute to a Multiple births can contribute to a community’s feto-infant mortality community’s feto-infant mortality rate, increasing trend or population rate, increasing trend or population disparity. disparity.
Phase 1 Analysis is not restricted to Phase 1 Analysis is not restricted to singleton live births. singleton live births.
Plurality studied separately as part of Plurality studied separately as part of Phase 2 Analyses.Phase 2 Analyses.
6060
PluralityPlurality
PPOR analyses are not restricted to PPOR analyses are not restricted to singleton live births. Multiple births singleton live births. Multiple births contribute to a community’s feto-infant contribute to a community’s feto-infant mortality rate and may contribute to mortality rate and may contribute to an increasing rate or population an increasing rate or population disparity. These births should be disparity. These births should be include in Phase 1 Analysis and further include in Phase 1 Analysis and further studied as part of the Phase 2 Analysis studied as part of the Phase 2 Analysis
6161
Map of Fetal-Infant Mortality Map of Fetal-Infant Mortality RatesRates by Pluralityby Plurality
Baltimore City 1997–99Baltimore City 1997–99
61.8 (52)61.8 (52)
0.00.0
(0)(0)
34.434.4
(29)(29)
28.528.5
(24)(24)
Total Rate = 124.7 per 1000
Multiple Gestation
Excess Deaths = 95
5.4 (151)5.4 (151)
3.33.3
(92)(92)
1.01.0
(29)(29)
2.22.2
(62)(62)
Total Rate = 11.9 per 1000
Singleton
6262
Map of Map of ExcessExcess Fetal-Infant Fetal-Infant DeathsDeaths
Baltimore City, 1997 – 1999Baltimore City, 1997 – 1999Multiple Gestation to Singleton Multiple Gestation to Singleton
PregnancyPregnancy
50%0%
-3%
23%Maternal Health/PrematurityMaternal Care
Newborn Care
Infant Health
6363
FIMR RecommendationsFIMR RecommendationsMultiple Gestation Multiple Gestation
PregnancyPregnancy Baltimore City, 1997 – 1999Baltimore City, 1997 – 1999
Increase awareness of the increased Increase awareness of the increased risk associated with multiple risk associated with multiple gestation pregnancy in the gestation pregnancy in the community.community.
Improve case management of Improve case management of multiple gestation pregnancy.multiple gestation pregnancy. Educate the provider communityEducate the provider community Modify the Prenatal Risk Assessment Modify the Prenatal Risk Assessment
protocol to include multiple gestation as protocol to include multiple gestation as a risk factor for referral to the Maternal a risk factor for referral to the Maternal and Infant nursing program.and Infant nursing program.
6464
•Relative risk•Population attributable risk•Logistic regression for adjusted odds ratios
Phase 2 Analyses-Mat. Phase 2 Analyses-Mat. Health/Prem.Health/Prem. Estimate the impact of Estimate the impact of
the risk and preventive factorsthe risk and preventive factors
6565
Impact of Risk Factors for Orange County 1999
Comparison Adjusted Odds-Ratio
95% Confidence Interval
White Hispanics vs. Non-Whites Hispanics
1.105 0.896-1.362
Black Non-Hispanic vs. White Non-Hispanics
1.667 1.364-2.038
Odds Ratio adjusting for: Age, Marital Status, Number of Pre-natal visits, weight gain, mother’s education, mother’s tobacco use and mother’s alcohol use.
Phase 2 Analyses-Mat. Phase 2 Analyses-Mat. Health/Prem.Health/Prem. Estimate the impact of Estimate the impact of
the risk and preventive factorsthe risk and preventive factors
6666
LNP Healthy Start – Pop. Attributable Risk for LNP Healthy Start – Pop. Attributable Risk for VLBWVLBW
FactorFactor PARPAR RR RR
(95% CI)(95% CI)
Previous Preterm DeliveryPrevious Preterm Delivery 16.0%16.0% 136.9136.9
(59.0-341.7)(59.0-341.7)
Pregnancy Related HypertensionPregnancy Related Hypertension 11.8%11.8% 4.84.8
(3.1-7.3)(3.1-7.3)
Inadequate PNC and Eclampsia or Inadequate PNC and Eclampsia or Hypertension (Chronic or Hypertension (Chronic or pregnancy induced) pregnancy induced)
8.3%8.3% 3.7 3.7
(1.6-7.6)(1.6-7.6)
Chronic HypertensionChronic Hypertension 6.7%6.7% 3.33.3
(1.5-6.5)(1.5-6.5)
Med Risk Factors and Inadequate Med Risk Factors and Inadequate PNCPNC
3.3%3.3% 2.5 2.5
(1.5-4.0)(1.5-4.0)
High ParityHigh Parity 1.7%1.7% 1.8 1.8
(1.3-2.5)(1.3-2.5)
SmokingSmoking 0.4%0.4% 1.2 1.2
(.79-1.7)(.79-1.7)
Inadequate PNCInadequate PNC 0%0% 1.01.0
(.7-1.4)(.7-1.4)
PAR results help focus discussions on specific interventions for reduction of VLBW in Lower North HS area
6767
PPOR Phase II AnalysisPPOR Phase II AnalysisUseful Epidemiological ToolsUseful Epidemiological Tools
•KitagawaKitagawa•Relative RiskRelative Risk•Odds RatioOdds Ratio•Population Attributable RiskPopulation Attributable Risk•Logistic RegressionLogistic Regression•Poisson RegressionPoisson Regression•Multi-level ModelingMulti-level Modeling
6868
MATERNAL MATERNAL CARE PERIODCARE PERIOD
6969
Phase 2 Analyses-Maternal Care Phase 2 Analyses-Maternal Care PeriodPeriod
The epidemiology of fetal deaths is The epidemiology of fetal deaths is less knownless known
Fetal Deaths have more missing Fetal Deaths have more missing informationinformation
Causal pathways such as Causal pathways such as chromosomal abnormalities, severe chromosomal abnormalities, severe congenital anomalies, and placental congenital anomalies, and placental vascular abnormalities not captured vascular abnormalities not captured on vital records on vital records
7070
Phase 2 Analyses-Maternal Care Phase 2 Analyses-Maternal Care PeriodPeriod
Risk Factors that are more reliably Risk Factors that are more reliably collected on fetal death certificates includecollected on fetal death certificates include Birthweight and Gestational ageBirthweight and Gestational age Maternal age and raceMaternal age and race Parity and previous fetal lossParity and previous fetal loss SmokingSmoking Education/socioeconomicEducation/socioeconomic Inter-pregnancy intervalInter-pregnancy interval Multiple gestationMultiple gestation
7171
Phase 2 Analyses-Maternal Care Phase 2 Analyses-Maternal Care PeriodPeriod
Risk Factors from other data sourcesRisk Factors from other data sources BMIBMI Weight gained during pregnancy adjusted for BMIWeight gained during pregnancy adjusted for BMI DiabetesDiabetes HypertensionHypertension RH diseaseRH disease
FIMR can be used to examine larger fetal FIMR can be used to examine larger fetal deathsdeaths
7272
USE OF FIMRUSE OF FIMR
7373
Integrating PPOR & FIMRIntegrating PPOR & FIMR
•PPOR and FIMR have complementary strengths.
•PPOR and FIMR use similar community-oriented processes.
•An existing FIMR Community Action Team might include the community stakeholders that the PPOR approach requires, and vice-versa.
7474
Integrating PPOR & FIMRIntegrating PPOR & FIMR
•FIMR data can help in Phase 2 of PPOR Analysis, as a way to better understand the reasons for excess deaths.
•PPOR can help an existing FIMR team by providing a context or framework for their case reviews and community action teams.
•PPOR can help a community focus their FIMR reviews on cases that will most benefit the community.
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Integrating FIMR & PPORIntegrating FIMR & PPORthe Magnolia Project in Jacksonville, FLthe Magnolia Project in Jacksonville, FL
Annual Annual update of contributing update of contributing factorsfactors using PPOR framework using PPOR framework
Case selectionCase selection to gain info on PPOR to gain info on PPOR areas of concernareas of concern
2000-YTD 2003 case reviews: 2000-YTD 2003 case reviews: maternal health, black outcomes, maternal health, black outcomes, target area (n=99)target area (n=99)
7676
Integrating PPOR & FIMRIntegrating PPOR & FIMRthe Magnolia Project in Jacksonville, FL, the Magnolia Project in Jacksonville, FL,
1995-19991995-1999
MATERNAL HEALTHMATERNAL HEALTH
(n=28)(n=28) 85%–Preterm labor or premature 85%–Preterm labor or premature
rupture of membranesrupture of membranes 46%–Sexually transmitted diseases46%–Sexually transmitted diseases 36%–Maternal age less than 21 years or 36%–Maternal age less than 21 years or
more than 35 yearsmore than 35 years 36%–No, late or inconsistent prenatal 36%–No, late or inconsistent prenatal
carecare 32%–Infant infection32%–Infant infection 29%–Pre-existing medical condition29%–Pre-existing medical condition 29%–Substance use (alcohol, tobacco or 29%–Substance use (alcohol, tobacco or
drugs)drugs) 25%–Maternal obesity25%–Maternal obesity 25%–History of previous adverse 25%–History of previous adverse
pregnancy outcomepregnancy outcome 21%–Family planning issues21%–Family planning issues
MATERNAL CAREMATERNAL CARE
(n= 15)(n= 15) 67%–Sexually transmitted 67%–Sexually transmitted
diseasesdiseases 47%–Lack of patient 47%–Lack of patient
educationeducation 33%–Maternal obesity 33%–Maternal obesity 33%–No, late or 33%–No, late or
inconsistent prenatal careinconsistent prenatal care 33%–Substance use 33%–Substance use
(alcohol, tobacco or drugs)(alcohol, tobacco or drugs)
7777
NEWBORN CARENEWBORN CARE
(n=29)(n=29) 55%–Pre-existing infant medical condition55%–Pre-existing infant medical condition 45%–No, late or inconsistent prenatal care45%–No, late or inconsistent prenatal care 34%–Maternal age less than 21 years or 34%–Maternal age less than 21 years or
more than 35 yearsmore than 35 years 31%–No Healthy Start screening 31%–No Healthy Start screening
completedcompleted 28%–History of previous adverse 28%–History of previous adverse
pregnancy outcomepregnancy outcome 21%–Family planning issues21%–Family planning issues 21%–Lack of support systems21%–Lack of support systems 21%–Preterm labor or premature rupture 21%–Preterm labor or premature rupture
of membranesof membranes 21%–Sexually transmitted diseases21%–Sexually transmitted diseases 21%–Substance use (alcohol, tobacco or 21%–Substance use (alcohol, tobacco or
drugs)drugs)
INFANT HEALTHINFANT HEALTH
(n=44)(n=44) 52%–Sexually transmitted 52%–Sexually transmitted
diseasesdiseases 48%–No, late or inconsistent 48%–No, late or inconsistent
prenatal careprenatal care 41%–Need for SIDS education41%–Need for SIDS education 36%–Maternal age less than 21 36%–Maternal age less than 21
years or more than 35 yearsyears or more than 35 years 25%–Pre-existing infant medical 25%–Pre-existing infant medical
conditioncondition 25%–Maternal obesity25%–Maternal obesity 23%–Lack of preventive and 23%–Lack of preventive and
medical follow upmedical follow up
Integrating PPOR & FIMRIntegrating PPOR & FIMRthe Magnolia Project in Jacksonville, FL, the Magnolia Project in Jacksonville, FL,
1995-19991995-1999
7878
Role of FIMRRole of FIMRthe Magnolia Project in Jacksonville, FLthe Magnolia Project in Jacksonville, FL
Aggregate info on contributing factors Aggregate info on contributing factors can help can help identify specific needs, risksidentify specific needs, risks
FIMR info can be used to formulate, FIMR info can be used to formulate, tailor tailor interventionsinterventions
FIMR findings can be used to FIMR findings can be used to monitor monitor impactimpact of new interventions of new interventions
PPOR questions can guide PPOR questions can guide case case selectionselection process process
7979
USE OF USE OF GISGIS
8080
PPOR rates by Neighborhood (red=higher than city rate Philadelphia, PAPhiladelphia, PA)
Maternal Maternal Health/ Health/ Prematurity Prematurity
Maternal Maternal CareCare
Newborn Newborn CareCare
Infant Infant HealthHealth
TotalTotal
All All PhiladelphiaPhiladelphia
5.1 5.1 3.0 3.0 1.5 1.5 2.7 2.7 12.3 12.3
SouthSouth 5.2 5.2 1.6 1.6 1.7 1.7 2.1 2.1 10.6 10.6
SouthwestSouthwest 4.6 4.6 3.7 3.7 1.6 1.6 3.6 3.6 13.513.5
WestWest 6.8 6.8 3.0 3.0 1.8 1.8 2.8 2.8 14.4 14.4
Lower NorthLower North 9.5 9.5 3.5 3.5 2.2 2.2 3.5 3.5 18.7 18.7
Upper NorthUpper North 6.6 6.6 4.0 4.0 1.8 1.8 4.1 4.1 16.5 16.5
Bridesburg/Bridesburg/Kensington/Kensington/RichmondRichmond
4.3 4.3 3.8 3.8 1.7 1.7 2.6 2.6 12.4 12.4
Olney/oak Olney/oak LaneLane
4.2 4.2 2.7 2.7 0.7 0.7 3.93.9 11.5 11.5
Lower NELower NE 3.5 3.5 2.4 2.4 1.3 1.3 1.3 1.3 8.5 8.5
Upper NEUpper NE 3.2 3.2 3.8 3.8 1.4 1.4 0.7 0.7 9.1 9.1
8181
Very Low Birth Weight Births Very Low Birth Weight Births 1998-2000 Density Analysis1998-2000 Density Analysis
Philadelphia, PAPhiladelphia, PA
8282
The Magnolia ProjectThe Magnolia Project Project area:Project area: Five zip codesFive zip codes in in NW NW
JacksonvilleJacksonville Account for Account for more more than than halfhalf of the Black infant mortality of the Black infant mortality in the cityin the city
About About 25,000 women25,000 women age 15-44 age 15-44 years oldyears old live in the project area live in the project area
85%85% African-AmericanAfrican-American
8383