Rheological changes in the prodromal and established phases of sickle cell vaso-occlusive crisis
- PMID: 1390248
- DOI: 10.1111/j.1365-2141.1992.tb02998.x
Rheological changes in the prodromal and established phases of sickle cell vaso-occlusive crisis
Abstract
A rheological study has been made in 20 patients with sickle cell anaemia in the steady state and in the prodromal and established phases of 12 vaso-occlusive crises. Rheology of sickle cells was studied by discontinuous density gradient fractionation and by filtration through pores of 5 microns diameter. The prodromal phase of crisis (day 1), when compared with mean steady state values, was associated with the development of a sub-population of poorly deformable dense cells. This sub-population appeared 1 or more days before the acute-phase rise in C-reactive protein, orosomucoid, fibrinogen, plasma viscosity and leucocytes, and before the rise in serum lactate dehydrogenase. As crisis evolved, the sub-population decreased to steady-state values, or below, by days 6-7. Identification of the prodromal phase of sickle cell crisis has allowed the detection of rheological changes of potential aetiological significance.
Similar articles
-
Subclinical ischaemic episodes during the steady state of sickle cell anaemia.J Clin Pathol. 1992 Oct;45(10):902-6. doi: 10.1136/jcp.45.10.902. J Clin Pathol. 1992. PMID: 1385483 Free PMC article.
-
Erythrocyte deformability in sickle-cell crisis.Br J Haematol. 1981 Sep;49(1):103-9. doi: 10.1111/j.1365-2141.1981.tb07202.x. Br J Haematol. 1981. PMID: 7272221
-
Monitoring the acute phase response to vaso-occlusive crisis in sickle cell disease.J Clin Pathol. 1994 Feb;47(2):166-9. doi: 10.1136/jcp.47.2.166. J Clin Pathol. 1994. PMID: 7510726 Free PMC article.
-
Rheology of the sickle cell disorders.Baillieres Clin Haematol. 1987 Sep;1(3):747-75. doi: 10.1016/s0950-3536(87)80023-9. Baillieres Clin Haematol. 1987. PMID: 3327564 Review.
-
The role of blood rheology in sickle cell disease.Blood Rev. 2016 Mar;30(2):111-8. doi: 10.1016/j.blre.2015.08.005. Epub 2015 Aug 28. Blood Rev. 2016. PMID: 26341565 Free PMC article. Review.
Cited by
-
Health-related stigma in young adults with sickle cell disease.J Natl Med Assoc. 2010 Nov;102(11):1050-5. doi: 10.1016/s0027-9684(15)30732-x. J Natl Med Assoc. 2010. PMID: 21141294 Free PMC article.
-
The Role of RBC Oxidative Stress in Sickle Cell Disease: From the Molecular Basis to Pathologic Implications.Antioxidants (Basel). 2021 Oct 13;10(10):1608. doi: 10.3390/antiox10101608. Antioxidants (Basel). 2021. PMID: 34679742 Free PMC article. Review.
-
Inpatient Management of Pain Episodes in Children with Sickle Cell Disease: A Review.Children (Basel). 2024 Sep 10;11(9):1106. doi: 10.3390/children11091106. Children (Basel). 2024. PMID: 39334638 Free PMC article. Review.
-
Flickering analysis of erythrocyte mechanical properties: dependence on oxygenation level, cell shape, and hydration level.Biophys J. 2009 Sep 16;97(6):1606-15. doi: 10.1016/j.bpj.2009.06.028. Biophys J. 2009. PMID: 19751665 Free PMC article.
-
Apolipoprotein A-I and serum amyloid A plasma levels are biomarkers of acute painful episodes in patients with sickle cell disease.Haematologica. 2010 Sep;95(9):1467-72. doi: 10.3324/haematol.2009.018044. Epub 2010 Apr 7. Haematologica. 2010. PMID: 20378559 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Research Materials