Cardiovascular Journal of Africa: Vol 24 No 4 (May 2013) - page 37

CARDIOVASCULAR JOURNAL OF AFRICA • Vol 24, No 4, May 2013
AFRICA
135
for intervention, as these factors are documented indicators of
worsening disease progression in PE. The relationship between
proteinuria and the heart need further evaluation, as well as
its relationship to HIV infection. A significant number of our
patients were HIV infected but there were no significant changes
in the BNP or TDI levels, or even in outcome in these subjects.
In our study, seven pre-eclamptic patients required emergency
care post delivery, in keeping with the association between PE
and adverse pregnancy events. Of the seven pre-eclamptics
who required emergency care, two required ICU admission. An
increased rate of Caesarean sections, lower Apgar scores, lower
birth weight and an increased admission rate to neonatal ICU
has been described in PE.
33
Numerous studies have documented
similar pregnancy sequelae in patients with PE.
32-34
Recently, foetal wellbeing by weekly assessment of umbilical
artery Doppler examinations and biophysical profiles were
investigated by Sezik
et
al
. in patients with pre-eclampsia in
their third trimester.
33
It was found that 38% of patients had an
abnormal Doppler on the last evaluation before delivery. In this
group, significantly higher blood pressures and serum uric acid
levels were recorded, lower platelet counts, higher incidence of
IUGR, lower Apgar scores at five minutes, a higher incidence of
perinatal deaths and higher operative delivery rates.
33
We also found umbilical artery velocity to be more practical
in evaluating the foetus in late pregnancy than uterine artery
Doppler studies, which have been used to predict PE and
IUGR.
30-33
Technical difficulties in obtaining access to uterine
Doppler flow readings precluded the use of this measurement
in our study. The increase in the resistance index on umbilical
Doppler velocimetry is well described,
32,33
and abnormal Doppler
umbilical artery waveforms are a strong predictor of perinatal
mortality and are associated with a poor perinatal outome.
32
Previous studies have shown that BNP levels were elevated in
patients with pre-eclampsia but the numbers have been few and
they have not correlated these changes with TDI.
15,17,24
Limitations of the study
BNP is significantly affected by age, gender, renal function and
obesity. Given its correlation with multiple cardiac variables,
BNP has high sensitivity but low specificity for the detection
of elevated left ventricular filling pressures. In our study this
variability was avoided by selecting primiparous patients who
were of similar age and constituted a fairly homogenous group
of black patients, permitting comparisons to be made.
Also, as mentioned above, most of the changes in BNP that
occurred were within normal ranges for our laboratory. It is
likely that BNP activation would be more pronounced in severe
PE. Furthermore, this study was conducted on patients in the
third trimester. Recruitment earlier in pregnancy might have
shown whether or not BNP could be used as a marker of PE.
Conclusion
This study showed that there were significant differences in BNP
levels during PE and this probably reflects the haemodynamic
changes in this condition. Serum BNP levels were significantly
elevated in pregnancies complicated by PE, particularly in those
with more severe disease. This increase was reflected in elevated
tissue Doppler estimations of LV filling pressure (E/E
a
ratio).
References
1.
De Swiet. Maternal mortality: confidential enquiries into maternal
deaths in the United Kingdom.
Am
J
Obstet
Gynaecol
2000;
182
:
760–766.
2.
Waterstone M, Bewley S, Wolfe C. Incidence and predictors of severe
obstetric morbidity: case control study.
Br Med J
2001;
322
: 1089–1093.
3.
Duley, L. Maternal mortality associated with hypertensive disorders
of pregnancy in Africa, Asia, Latin America and the Caribbean.
(Confidential enquiry in maternal mortality).
Br
J
Obstet
Gynaecol
2009;
116
: 247–256.
4.
Panday M, Mantel GD, Moodley J. Audit of severe acute morbidity in
hypertensive pregnancies in a developing country.
J Obstet Gynaecol
2004;
24
(4): 387–391.
5.
Redman CW, Sargent IL. Latest advances in understanding pre-eclamp-
sia.
Science
2005;
308
: 1592–1594.
6.
Sibai B, Dekker G, Kupferminc M. Pre-eclampsia.
Lancet
2005;
365
:
785–799.
7.
Hawfield A, Freedman BI. Pre-eclampsia: the pivot role of the placenta
in its pathophysiology and markers for early detection.
Ther
Adv
Cardiovasc Dis
2009;
3
(1): 65–73.
8.
Carty DM, Delles C, Dominiczak. Novel biomarkers for predicting pre-
eclampsia.
Trends Cardiovasc Med
2008;
18
: 186–194.
9.
FranzMB,AndreasM,Schiessl,
etal.
BNT-proBNPisincreasedinhealthy
pregnancies compared to non-pregnant controls.
Acta Obstet Gynecol
Scand
2009;
88
(2): 234–247. Doi: 10.1080/00016340802596025.
10. Seino Y, Ogawa A. Yamashita T,
et
al
. Application of NT-proBNP and
BNP measurements in cardiac care: a more discerning marker for the
detection and evaluation of heart failure.
Eur
J
Heart
Fail
2004;
6
:
295–300.
11. De Lemos JA, McGuire DK, Drazner MH. B-type natriuretic peptide in
cardiovascular disease.
Lancet
2006;
362
: 316–322.
12. Maisel A. B-type natriuretic peptide levels: diagnostic and prognostic in
CHF what’s next?
Circulation
2002;
105
: 2328–2331.
13. Itoh H, Sagawa N, Mori T,
et al
. Plasma brain natriuretic peptide level in
pregnant women with pregnancy-induced hypertension.
Obstet Gynecol
1993;
82
(1):71–77.
14. Okuno S, Hamada H, Yasuoka M,
et
al
. Brain natriuretic peptide and
cyclic guanosine monophosphate levels in normal pregnancy and pre-
eclampsia.
J Obstet Gynaecol Res
1999; 25(6): 407–410.
15. Kaaja R, Moore M, Yandle T,
et
al
. Blood pressure and vasoactive
hormones in mild pre-eclampsia and normal pregnancy.
Hypertens
Pregnancy
1999;
18
(2): 173–187.
16. Furuhashi N. Brain natriuretic peptide and atrial natriuretic peptide
levels in normal pregnancy and pre-eclampsia.
Gynecol Obstet
Invest
1994;
38
(2): 73–77.
17. Gottdiener JS, Bednarz J, Devereux R,
et
al
. American Society of
Echocardiography recommendations for use of echocardiography in
clinical trials.
J Am
Soc Echocardiogr
2004;
17
(10): 1086
1119.
18. Sohn DW, Chai IH, Lee DJ, Kim HC, Oh BH, Lee MM,
et
al
.
Assessment of mitral annulus velocity by Doppler tissue imaging in
the evaluation of left ventricular diastolic function.
J Am Coll Cardiol
1997;
30
(2): 474
480.
19. Tihtonen KM, Kooobi T, Vuolteenano O,
et
al
. Natriuretic peptides and
haemodynamics in pre-eclampics.
Am
J Obstet Gynecol
2007;
196
(4):
328–335.
20. Kale A, Kale E, Yalinkaya A, Akendeniz N,
et
al
. The comparison of
amino terminal pro-brain natriuretic peptide levels in pre-eclamptic and
normotensive pregnancy.
J Perinat Med
2005;
33
: 121–124.
21. Fleming SM, O’Byrne L, Grimes H,
et
al
. Amino terminal pro brain
natriuretic peptide in normal and hypertensive pregnancy.
Hypertens
Pregnancy
2001;
20
: 169–175.
22. Moghbei N, Srinivas SK, Bastek,
et
al
. Terminal pro-brain natriuretic
peptide as a biomarker for hypertensive disorders of pregnancy.
Br
J
Obstet Gynecol
2010;
27
(4): 313–319.
23. Yurteri-Kaplan L, Shelley Saber, Zamudio S. Brain natriuretic peptide
in term pregnancy.
Repro
Sci
2012;
19
: 520.
24. Resnik J, Hong C, Resnik R,
et
al
. Evaluation of B-type natriuretic
peptide (BNP) levels in normal and pre-eclamptic patients.
Am
J Obstet
Gynecol
2005;
193
; 450–455.
25. Hameed AB, Chan K, Ghamsary M, Uri Elkayam U. Longitudinal
changes in the B-type natriuretic peptide levels in normal pregnancy
1...,27,28,29,30,31,32,33,34,35,36 38,39,40,41,42,43,44,45,46,47,...68
Powered by FlippingBook