Literature DB >> 28764173

Clinical and Laboratory Predictors of Frequency of Painful Crises among Sickle Cell Anaemia Patients in Nigeria.

Angela Ogechukwu Ugwu1, Obike Godswill Ibegbulam2, Theresa Ukamaka Nwagha3, Anazoeze Jude Madu3, Sunday Ocheni2, Iheanyi Okpala2.   

Abstract

INTRODUCTION: The severity of Sickle Cell Anaemia (SCA) in terms of frequency of painful Vaso-Occlusive Crises (VOC) may be affected by clinical and haematological parameters amongst others. Elucidation of these factors in a given disease prevalent environment is necessary for prompt and effective management of patients with frequent painful VOC. AIM: This study aimed at determining the clinical and laboratory predictors of frequency of painful VOC among SCA patients in Enugu, Southeastern Nigeria.
MATERIALS AND METHODS: It was a cross-sectional study of 100 consecutive SCA patients receiving care at the University of Nigeria Teaching Hospital, Enugu, Nigeria between May 2012 and February 2014. The eligible patients were categorized into two groups namely; Group A and Group B. Group A/study group (severe disease) comprised SCA patients who had experienced three or more painful crises (≥3 crises) in the last one year preceding the study but, currently in steady state, while Group B/control group (mild-moderate disease), comprised SCA patients matched for age, sex, highest educational status, and occupation but who have had no painful crisis or had only one or two painful crises (0-2 crises) in the last one year preceding the study and currently in steady state.
RESULTS: The overall mean age of the patients was 18.4±12.2 (range=2-52) years. The mean values of the haematological parameters including haemoglobin concentration, white cell count, platelet count, and neutrophil count were significantly higher in those with severe crises than mild-moderate crises (p<0.05). Sickle cell related complications including Avascular Necrosis (AVN) and leg ulcers were significantly higher in the study group than the control group (p<0.05).
CONCLUSION: There was significant association between the frequency of crises and haemogblobin level, platelet and neutrophil counts and some clinical parameters: AVN, nephropathy and stroke. Future preventive interventions for reduction in frequency of crisis amongst patients with SCA could be targeted at controlling the blood levels of the identified haematological parameters.

Entities:  

Keywords:  Clinical parameters; Frequency of crisis; Laboratory parameters

Year:  2017        PMID: 28764173      PMCID: PMC5535366          DOI: 10.7860/JCDR/2017/26446.10042

Source DB:  PubMed          Journal:  J Clin Diagn Res        ISSN: 0973-709X


  16 in total

1.  Frequency of pain crises in sickle cell anemia and its relationship with the sympatho-vagal balance, blood viscosity and inflammation.

Authors:  Danitza Nebor; Andre Bowers; Marie-Dominique Hardy-Dessources; Jennifer Knight-Madden; Marc Romana; Harvey Reid; Jean-Claude Barthélémy; Vanessa Cumming; Olivier Hue; Jacques Elion; Marvin Reid; Philippe Connes
Journal:  Haematologica       Date:  2011-07-12       Impact factor: 9.941

2.  Clinical factors and incidence of acute chest syndrome or pneumonia among children with sickle cell disease presenting with a fever: a 17-year review.

Authors:  Todd P Chang; Worapant Kriengsoontorkij; Linda S Chan; Vincent J Wang
Journal:  Pediatr Emerg Care       Date:  2013-07       Impact factor: 1.454

3.  Markers of severe vaso-occlusive painful episode frequency in children and adolescents with sickle cell anemia.

Authors:  Deepika S Darbari; Onyinye Onyekwere; Mehdi Nouraie; Caterina P Minniti; Lori Luchtman-Jones; Sohail Rana; Craig Sable; Gregory Ensing; Niti Dham; Andrew Campbell; Manuel Arteta; Mark T Gladwin; Oswaldo Castro; James G Taylor; Gregory J Kato; Victor Gordeuk
Journal:  J Pediatr       Date:  2011-09-03       Impact factor: 4.406

4.  Routine screening for sickle cell haemoglobinopathy by electrophoresis in an infant welfare clinic.

Authors:  O O Omotade; C M Kayode; S L Falade; S Ikpeme; A A Adeyemo; F M Akinkugbe
Journal:  West Afr J Med       Date:  1998 Apr-Jun

5.  Definitions of the phenotypic manifestations of sickle cell disease.

Authors:  Samir K Ballas; Susan Lieff; Lennette J Benjamin; Carlton D Dampier; Matthew M Heeney; Carolyn Hoppe; Cage S Johnson; Zora R Rogers; Kim Smith-Whitley; Winfred C Wang; Marilyn J Telen
Journal:  Am J Hematol       Date:  2010-01       Impact factor: 10.047

Review 6.  Beyond the definitions of the phenotypic complications of sickle cell disease: an update on management.

Authors:  Samir K Ballas; Muge R Kesen; Morton F Goldberg; Gerard A Lutty; Carlton Dampier; Ifeyinwa Osunkwo; Winfred C Wang; Carolyn Hoppe; Ward Hagar; Deepika S Darbari; Punam Malik
Journal:  ScientificWorldJournal       Date:  2012-08-01

7.  Coagulation profile of children with sickle cell anemia in steady state and crisis attending the university of Nigeria teaching hospital, Ituku-Ozalla, Enugu.

Authors:  J M Chinawa; I J Emodi; A N Ikefuna; S Ocheni
Journal:  Niger J Clin Pract       Date:  2013 Apr-Jun       Impact factor: 0.968

Review 8.  Pathophysiological insights in sickle cell disease.

Authors:  Marie-Hélène Odièvre; Emmanuelle Verger; Ana Cristina Silva-Pinto; Jacques Elion
Journal:  Indian J Med Res       Date:  2011-10       Impact factor: 2.375

9.  Haematological values in homozygous sickle cell disease in steady state and haemoglobin phenotypes AA controls in Lagos, Nigeria.

Authors:  Akinsegun Akinbami; Adedoyin Dosunmu; Adewumi Adediran; Olajumoke Oshinaike; Phillip Adebola; Olanrewaju Arogundade
Journal:  BMC Res Notes       Date:  2012-08-01

10.  Saudi SCD patients' symptoms and quality of life relative to the number of ED visits.

Authors:  Anwar E Ahmed; Ahmed S Alaskar; Donna K McClish; Yosra Z Ali; Mohammed H Aldughither; Ahmad M Al-Suliman; Hafiz M Malhan
Journal:  BMC Emerg Med       Date:  2016-08-20
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