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Recurrence of hypertensive disorders ofpregnancy: an individual patient
data metaanalysis
Presented by : Dr. R. Bagus Prakoso
Moderator: Prof. Dr. H. A. Kurdi, SpOG (K)
Hypertensive disorders of pregnancy (HDP)
are a common health problem
the second most common cause of
maternal death worldwide
They complicate approximately 2-8%
of all pregnancies
related to intrauterine
growth restrictionA major psychologic
impact on the woman and her
family
counseling on recurrence of a hypertensive disease in a futurepregnancy is important
many studies have focused on the investigation of recurrence rates of HDP
difficult because of many potential sources of bias
The primary goal of this IPD metaanalysis study was to calculate the recurrence risk of HDP. Secondarily, we aimed to show the recurrence of Individual hypertensive syndromes.
MATERIALS AND METHODSSources
literature search in the electronic libraries PubMed (Medline)and Embase.
The search covered all records until August 2012.
The following terms were used: ‘‘preeclampsia”
All studies that described cohorts of women with a history of a hypertensive disorder that resulted in a delivery at any
gestational age were eligible
Two independent reviewers (M.F.vO. and J.L.) screened theidentified articles for eligibility based on title and abstract.
Discrepancies were resolved by a third reviewer (W.G.)
MATERIALS AND METHODS Data collection
@ eligible articles, contact information of author was obtained through Medline, Embase, or the Internet.
Approached the authors by email to inform them about the IPD metaanalysis project and to invite them to share their data
The quality of all studies that were included was evaluated with the Newcastle Ottawa Scale for cohort studies
MATERIALS AND METHODSDefinitions
HDP were defined as GH, preeclampsia,superimposed preeclampsia, or HELLPsyndrome
Chronic hypertension was not an exclusion criterion for the IPD but was in some individual studies
Preeclampsia was defined as hypertension
diastolic blood pressure 90 mm Hg or systolic blood pressure 140 mm Hg on 2 occasions that were 4-5 hours apart
with proteinuria(defined as a positive [0.3 g/L]
proteinuria dipstick test, a protein/ creatinine ratio of 30
mg/mmol in a random sample or an urine protein excretion of 300 mg for
24 hrs)after 20 weeks’ gestation
Mild or severe preeclampsiawas not separately defined,
MATERIALS AND METHODSDefinitions
Women with hypertension at >20 weeks’ gestation without proteinuria or a significant rise in blood pressure (if a woman had
known chronic hypertension).
the presence or a history of preconceptional hypertension or detection of hypertension in the first one-half of the pregnancy
De novo proteinuria or a sudden increase in proteinuria if already present, qualified women with chronic hypertension
hemolysis (elevated lactate dehydrogenase levels [600 U/L], elevated liver enzymes by levels of aspartate transaminase or
alanine transferase 70 U/L, and low platelets <100,000/mm)
GH
Chronic hypertension
superimposed preeclampsia
HELLP syndrome
MATERIALS AND METHODSStatistical analysis
performed 3 post hoc sensitivity analyses:
Statistical analysis was performed with SPSS software (version 20.0; SPSS Inc, Chicago, IL)
and R software (version 3.0.1; The R Foundation for Statistical Computing).
RESULTS Study selection
The combineddatabase
comprised a total of
99,415 women
RESULTS Study selection
RESULTS Subgroup analysis
compared recurrence among multiple and singleton
pregnancies.
516 were multiple 56
98.553 were singleton 20.408
presence of thrombophilia &LMW-heparin use &
recurrence
56 women used prophylactic LMW-heparin 26
141 women didnot use LMW-heparin 56
without thrombophilia &LMW-heparin use &
recurrence
52 women used prophylactic LMW-heparin
244 women did not useLMW-heparin
8
104
10.9%
20.7%
39.7%
46%
15.4%
42.6%
COMMENT Main findings
The recurrence rate of an HDP (any type) is 20.7%
HELLP syndrome or delivery of an SGA child increasesrecurrence of HDP
Decrease gestational age at delivery in the index pregnancy increases both the chance of having
recurrence and the chance to deliver prematurely again
The use of LMW heparin was not protective forrecurrence in our data, but the numbers
are too small to draw conclusions
Women who were normotensive before pregnancy and who experienced recurrence of a hypertensive disorder
had a 4 times increased risk of the development of chronic hypertension after pregnancy.
CONCLUSION
AMONG WOMEN THAT EXPERIENCE HYPERTENSION IN PREGNANCY, RECURRENCE RATE IN NEXT PREGNANCY IS
RELATIVE LOW
COURSE OF DISEASE IS MILDER FOR MOST WOMEN WITH RECURRENT DISEASE
Is the study in paper you’ve read using survei or registration data?
This paper using registration data of samples
Induction vs deduction how this paper explain these ?
This paper using deduction method to reach its conclusion
Variabel scale, explain this papers varables
They are nominal (eq: race, medical hystory), categorical (eq: parous, conception), and interval data (almost all variabel convert into interval data)
Type of Variabel: dependent vs independent, explain what are them in this paper
Dependent: reccurence of hypertensiveIndependent: baseline and demografic characteristic
Type of Data: primer, secunder, tersier, explain about this paper type of data
Using secunder data
Group vs Individual data, explain about this papers type of data
Using group data
Routine vs ad hoc data, explain about this papers type of data
Ad hoc data
Central, variation, position measurement variable, explain about this papers variables
They are using central (mean and median ) and variation measurement
Master table, distribution table, crosstab table. Explain about this papers table data
The table has been explained previously
Graph: hystogram, ogive, stem & leaf, box-plot, bar, line, scatter. Explain about this papers graph
This paper mainly using bar graphic
Explain about this papers Quality data conclusion
It has 95% confidence interval
Bias, explain about this papers bias Metaanalyse data was very subjective.The study used data from the eighties,which caused data to be lost.The data that were obtained from very different study designs, settings, and populations.
Explain about this Papers number of sample for estimation and hypotetical test
They purposively selecting all samples that meet the inclusion criteria from 22 studies
Explain about this paper randomization sampling technique: simple, systematic, stratification, cluster ?
There is no randomisation
Statistic technique used in this paper Binomial regression model for dichotomous outcomes and of a random intercept random/effects linear regression model for continuous outcomes.
Explain about this paper statistical analysis / practice fraud
No statistical analysis fraud founded
Explain wheter there are mistaken in conclude the statistical analysis result
No conclusion mistaken noted
How they presented biostatistic analysis riset or vital registration, naratively / written ?
They present writtenly
Did they used madia to present biostatistic analysis riset?
SPSS and R software
Thank you ….