Can we scientifically identify Low-risk subjects of Preeclampsia?
Not being
high-risk does not necessarily mean one is low-risk. It is well known that
amongst many parameters to identify potential subjects for developing
preeclampsia, nearly all are for identifying high-risk subjects. However there
is hardly any research work published that can guide us to low-risk subjects. These
are the days of not stopping at identifying high-risk but actually identifying
low-risk subjects of preeclampsia.
Why do we need to identify the
low-risk subjects also?
It has been found
in clinical practice long since that not being high-risk does not necessarily
mean one is low-risk. There are majority of subjects who are not high-risk but
are also not necessarily low-risk. As a result we all are over using
prophylactic measures. Also we are scared to stop prophylaxis once a subject is
labelled high-risk and is never tested again. While pregnancy is a dynamic state,
it surely happens that some subjects who may be high risk initially may cease
to be so as pregnancy advances due to multiple reasons. Why then to continue
prescribing them prophylactic measures. Some of them can be very costly and
nearly all can have side effects. This blog shares scientific research
data with you by which you can identify low-risk pregnant subjects for
preeclampsia.
How does it help in preeclampsia
and OVs?
More than three
decades ago our group started working to decode the mysteries of preeclampsia.
In this aspirin emerged as a front-runner for prevention. I first spoke on this
sharing results of my work at AMOGS conference in Meeraj in 1992. Since then
much water has flown under the bridge. I was once asked by the chairman at the
session where I was giving my lecture in Sri Lanka as to whether it will be all
right to start giving Aspirin to all pregnant subjects. This made me respond
“Why to give it to low-risk” subjects. Around this time I was also working on
low-dose heparin in prevention of major OVs. If one is able to identify
low-risk subjects clearly then these preventive medications need not be given.
This makes the management more scientific and focused.
Tools to identify low-risk subjects
Currently the
nearly universal tool used is the tool of default. This means if a subject is
not high-risk, she is low-risk for these conditions. Such a thinking is wrought
with error and fallacy. All of us are familiar with the fact that there always
are subjects who may not be high-risk when prediction methods are used. This is
usually around 12 weeks of pregnancy. But they can still develop preeclampsia
as pregnancy rolls on. No wonder we have a recommendation of using more than
one set of tools for prediction. The most recommended are Colour Doppler and
biochemical markers along with the clinical obstetric history of the subject.
In set-ups like
those where we are working there are many practical and logistical disadvantage
of the combination. The biochemical methods are costly and need an extra
time-consuming visit to the laboratory. We have been able to provide a solution
to this. We use more than one colour Doppler parameters to identify “low-risk”
subjects for preeclampsia and other late OVs.
The reason for
using more than one parameter is to increase the accuracy of the results. This
is precisely the reason why biochemical markers were studied and used in
combination with colour Doppler. Using the same basis, we are using more than
one colour Doppler parameters to identify low-risk subjects with very good
results.
Our Results:
This prospective
longitudinal study was conducted to identify subjects who are at a low-risk for
developing preeclampsia remote from term. Most of the currently popular studies
identify high-risk subjects. Also, they usually use a biochemical parameter.
The present study identifies low-risk subjects only on the basis of two
parameters of uterine artery color Doppler in first-trimester of pregnancy and
did not use any biochemical parameter.
Materials and Methods
All singleton pregnancies that registered in
the first trimester were included for this study. Uterine artery color Doppler
was performed between 11-13+6 weeks. Subjects who showed a
Pulsatility Index (PI) PI≤1.0 and absent Diastolic Notch (DN) in both uterine
arteries were prospectively followed up for development or otherwise of
preeclampsia before 32 weeks of pregnancy. Their outcome was compared with that
of subjects with other groups. Two tools of statistical analysis were used.
Chi-square test for calculating the P-value and sensitivity, specificity,
positive and negative predictive value calculations were done for drawing
accurate conclusions from the results.
Results:
510
pregnant subjects were prospectively followed-up in this study.
TABLE:
Statistical Groups with Distribution of Cases
Uterine
Artery Doppler at 11-13+6 weeks |
Developed
Preeclampsia? |
Number |
PI≤1
and DN Absent |
Did
not develop Preeclampsia |
47 |
PI≤1
and DN Present |
Did
not develop Preeclampsia |
157 |
P>1
and DN Absent |
Did
not develop Preeclampsia |
13 |
P>1
and DN Present |
Did
not develop Preeclampsia |
211 |
PI≤1
and DN Absent |
Developed
Preeclampsia |
7 |
PI≤1
and DN Present |
Developed
Preeclampsia |
24 |
PI>1
and DN Absent |
Developed
Preeclampsia |
3 |
PI>1
and DN Present |
Developed
Preeclampsia |
48 |
TOTAL |
510 |
(Key: PI =
Pulsatility Index, DN = Diastolic Notch)
On statistical
analysis, it was found that subjects with a combination of PI≤1 and absent DN
had a very significantly less likelihood of developing preeclampsia making them
low-risk subjects. On applying one more tool of statistical analysis these
results were found to have a very high sensitivity and negative predictive
value.
Comment:
The
combination of uterine artery PI≤1.0 and an absent diastolic notch at 11-13+6 weeks
USG scan is effective to identify subjects at low-risk of developing
preeclampsia remote from term. This is essentially a one-step method not
relying on any separate biochemical markers for its efficacy. While the
presence of these findings on color Doppler identified low-risk subjects
effectively, the absence of these findings does not automatically indicate a
high-risk subject. This is a statistical limitation of this study. Additional
research can help in confidently using these tools in clinical settings.
Conclusion:
The combination of
uterine artery PI≤1.0 and an absent diastolic notch at 11-13+6 weeks
USG scan is effective to identify subjects at low-risk of developing
preeclampsia remote from term.
Note:
For accessing the full text of this
paper please click on: https://www.drpankajdesai.com/MRP/1.htm
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