Skip to main content

Advertisement

Log in

The Relation Between Venous Reserve Capacity and Low Plasma Volume

  • Original Article
  • Published:
Reproductive Sciences Aims and scope Submit manuscript

Abstract

Objective: Prepregnant low plasma volume (LPV) is associated with subsequent gestational hypertensive disease. It is unknown to what extent an LPV affects the venous reserve capacity (VRC). We tested the hypothesis that LPV reduces the VRC, as indicated by presyncope or altered cardiovascular changes in response to head-up tilt. Study design: In 52 nonpregnant women with a history of preeclampsia or recurrent miscarriage, the authors assessed plasma volume, stroke volume, and cardiac output and determined blood pressure, heart rate, and autonomic responses to stepwise inflicted head-up tilt. Results: 12 participants had LPV, which related to presyncope when compared with subjects with normal plasma volume (NPV). Women with LPV without presyncope demonstrated a circulatory response comparable to NPV women at the expense of consistently higher heart rate. Conclusion: LPV decreases the capacity to cope with head-up tilt without affecting the response pattern, suggesting reduced VRC.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Sibai B, Dekker G, Kupferminc M. Pre-eclampsia. Lancet. 2005;365:785–799.

    Article  Google Scholar 

  2. Weintraub AY, Sheiner E, Bashiri A, Shoham-Vardi I, Mazor M. Is there a higher prevalence of pregnancy complications in a live-birth preceding the appearance of recurrent abortions? Arch Gynecol Obstet. 2005;271:350–354.

    Article  Google Scholar 

  3. Wilson BJ, Watson MS, Prescott GJ, et al. Hypertensive diseases of pregnancy and risk of hypertension and stroke in later life: results from cohort study. BMJ. 2003;326:845.

    Article  Google Scholar 

  4. Spaanderman ME, Ekhart TH, van Eyck J, Cheriex EC, de Leeuw PW, Peeters LL. Latent hemodynamic abnormalities in symptom-free women with a history of preeclampsia. Am J Obstet Gynecol. 2000;182:101–107.

    Article  CAS  Google Scholar 

  5. Spaanderman ME, Van Beek E, Ekhart TH, et al. Changes in hemodynamic parameters and volume homeostasis with the menstrual cycle among women with a history of preeclampsia. Am J Obstet Gynecol. 2000;182:1127–1134.

    Article  CAS  Google Scholar 

  6. Courtar DA, Spaanderman ME, Aardenburg R, Janssen BJ, Peeters LL. Low plasma volume coincides with sympathetic hyperactivity and reduced baroreflex sensitivity in formerly preeclamptic patients. J Soc Gynecol Investig. 2006;13:48–52.

    Article  Google Scholar 

  7. Bernstein IM, Shapiro RE, Whitsel A, Schonberg AL. Relationship of plasma volume to sympathetic tone in nulliparous women. Am J Obstet Gynecol. 2003;188:938–942.

    Article  Google Scholar 

  8. Aardenburg R, Spaanderman ME, Ekhart TH, van Eijndhoven HW, van der Heijden OW, Peeters LL. Low plasma volume following pregnancy complicated by preeclampsia predisposes for hypertensive disease in a next pregnancy. BJOG. 2003;110:1001–1006.

    Article  Google Scholar 

  9. Aardenburg R, Spaanderman ME, van Eijndhoven HW, de Leeuw PW, Peeters LL. Formerly preeclamptic women with a subnormal plasma volume are unable to maintain a rise in stroke volume during moderate exercise. J Soc Gynecol Investig. 2005;12:599–603.

    Article  Google Scholar 

  10. Fu Q, Witkowski S, Okazaki K, Levine BD. Effects of gender and hypovolemia on sympathetic neural responses to orthostatic stress. Am J Physiol Regul Integr Comp Physiol. 2005;289:R109–R116.

    Article  CAS  Google Scholar 

  11. Kimmerly DS, Shoemaker JK. Hypovolemia and neurovascular control during orthostatic stress. Am J Physiol Heart Circ Physiol. 2002;282:H645–H655.

    Article  CAS  Google Scholar 

  12. Brown MA, Lindheimer MD, de Swiet M, Van Assche A, Moutquin JM. The classification and diagnosis of the hypertensive disorders of pregnancy: statement from the International Society for the Study of Hypertension in Pregnancy (ISSHP). Hypertens Pregnancy. 2001;20:IX–XIV.

    Article  CAS  Google Scholar 

  13. Hasebe Y, Iriki M, Takahasi K. Usefulness of R-R interval and its variability in evaluation of thermal comfort. Int J Biometeorol. 1995;38:116–121.

    Article  CAS  Google Scholar 

  14. Du Bois D, Du Bois EF. A formula to estimate the approximate surface area if height and weight be known. Arch Intern Med. 1916;17:863–871.

    Article  Google Scholar 

  15. Wieling W, van Lieshout JJ, Ten Harkel AD. Dynamics of circulatory adjustments to head-up tilt and tilt-back in healthy and sympathetically denervated subjects. Clin Sci (Lond). 1998;94:347–352.

    Article  CAS  Google Scholar 

  16. Hainsworth R, Al-Shamma YM. Cardiovascular responses to upright tilting in healthy subjects. Clin Sci (Lond). 1988;74:17–22.

    Article  CAS  Google Scholar 

  17. Harms MP, Wesseling KH, Pott F, et al. Continuous stroke volume monitoring by modelling flow from non-invasive measurement of arterial pressure in humans under orthostatic stress. Clin Sci (Lond). 1999;97:291–301.

    Article  CAS  Google Scholar 

  18. Laude D, Elghozi JL, Girard A, et al. Comparison of various techniques used to estimate spontaneous baroreflex sensitivity (the EuroBaVar study). Am J Physiol Regul Integr Comp Physiol. 2004;286:R226–R231.

    Article  CAS  Google Scholar 

  19. Cooke WH, Hoag JB, Crossman AA, Kuusela TA, Tahvanainen KU, Eckberg DL. Human responses to upright tilt: a window on central autonomic integration. J Physiol. 1999;517:617–628.

    Article  CAS  Google Scholar 

  20. Zaidi A, Benitez D, Gaydecki PA, Vohra A, Fitzpatrick AP. Haemodynamic effects of increasing angle of head up tilt. Heart. 2000;83:181–184.

    Article  CAS  Google Scholar 

  21. Aardenburg R, Spaanderman ME, Courtar DA, van Eijndhoven HW, de Leeuw PW, Peeters LL. A subnormal plasma volume in formerly preeclamptic women is associated with a low venous capacitance.J Soc Gynecol Investig. 2005;12:107–111.

    Article  Google Scholar 

  22. Aviado DM, Guevara AD. The Bezold-Jarisch reflex. A historical perspective of cardiopulmonary reflexes. Ann N Y Acad Sci. 2001;940:48–58.

    Article  CAS  Google Scholar 

  23. Barker DJ. Fetal origins of cardiovascular disease. Ann Med. 1999;31(suppl 1):3–6.

    Article  Google Scholar 

  24. Spaanderman M, Ekhart T, van Eyck J, de Leeuw P, Peeters L. Preeclampsia and maladaptation to pregnancy: a role for atrial natriuretic peptide? Kidney Int. 2001;60:1397–1406.

    Article  CAS  Google Scholar 

  25. El-Sayed MS, Ali N, El-Sayed AZ. Haemorheology in exercise and training. Sports Med. 2005;35:649–670.

    Article  Google Scholar 

  26. Julu PO, Cooper, VL Hansen S, Hainsworth R. Cardiovascular regulation in the period preceding vasovagal syncope in conscious humans. J Physiol. 2003;549:299–311.

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Ineke Krabbendam MD.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Krabbendam, I., Janssen, B.J., Van Dijk, A.P.J. et al. The Relation Between Venous Reserve Capacity and Low Plasma Volume. Reprod. Sci. 15, 604–612 (2008). https://doi.org/10.1177/1933719108316983

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1177/1933719108316983

Key words

Navigation