Araştırma Makalesi

THE ROLE OF COMPLETE BLOOD COUNT IN PATIENTS WITH HETEROZYGOUS BETA THALASSEMIA

Cilt: 22 Sayı: 6 18 Ekim 2021
PDF İndir
EN TR

THE ROLE OF COMPLETE BLOOD COUNT IN PATIENTS WITH HETEROZYGOUS BETA THALASSEMIA

Öz

OBJECTIVE: The goal of this study was to compare the Mean Platelet Volume (MPV), Platelet Lymphocyte ratio, and Neutrophil Lymphocyte ratio by evaluating the parameters of Complete Blood Count in healthy children and patients with heterozygous Beta-thalassemia (HBT).
MATERIAL AND METHODS: Between July 2016 and September 2019, 60 patients admitted to the pediatric hematology-oncology outpatient clinic diagnosed with HBT and 60 healthy control subjects of similar age and sex were analyzed retrospectively. Children over one year old, whose hemoglobin A2 levels were above 3.5% were included in the study population.
RESULTS: A total of 120 subjects were enrolled in this study. The HBT group included 60 subjects (32 males and 28 females) and the control group included 60 (36 males and 24 females). There were no significant differences between the two groups in terms of age and gender (p=0.29 and p=0.27). Platelet count, MPV, lymphocyte, and ferritin were significantly higher in the HBT group, whereas hemoglobin was significantly lower in the HBT group as compared with the control group.
CONCLUSIONS: Increased MPV and platelets in healthy HBT patients may cause hypercoagulability and may play a role with other risk factors in the predisposition of thrombosis in adult cases. There are very few studies on the incidence of thromboembolic events in cases with HBT. It is necessary to monitor adult HBT cases especially in terms of thromboembolic events, and to study with more cases.

Anahtar Kelimeler

Kaynakça

  1. 1. Somervaille T. Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management. J R Soc Med. 2001;94(11):602‐3.
  2. 2. Taher A.T, Weatherall D.J, Cappellini M.D. Thalassemia. Lancet. 2018;391(10116):155-67.
  3. 3. Cappellini M.D, Poggiali E, Taher A.T, et al. Hypercoagulability in β-thalassemia: A statusquo. Expert Rev. Hematol. 2012;5: 505–11.
  4. 4. Taher A.T, Musallam K.M. Coagulation and thrombotic risk in thalassemia intermedia. Thalassemia Reports 2011; 1(2):15.
  5. 5. Angchaisuksiri P, Atichartakarn V, Aryurachai K, et al. Hemostatic and thrombotic markers in patients with hemoglobin E/beta-thalassemia disease. Am J Hematol. 2007;82(11):1001-4.
  6. 6. Farah R, Nseir W, Kagansky D, et al. The role of neutrophil-lymphocyte ratio, and mean platelet volume in detecting patients with acute venous thromboembolism. J Clin Lab Anal. 2020;34(1):23010.
  7. 7. Tokgoz S, Kayrak M, Akpinar Z, et al. Neutrophil lymphocyte ratio as a predictor of stroke. J Stroke Cerebrovasc Dis. 2013;22: 1169-74.
  8. 8. Çiçek G, Açıkgoz SK, Bozbay M, et al. Neutrophil lymphocyte ratio and platelet-lymphocyte ratio combination can predict prognosis in patients with ST-segment elevation myocardial infarction undergoing primary percutaneous coronary intervention. Angiology. 2015;66: 441-7.

Ayrıntılar

Birincil Dil

İngilizce

Konular

Klinik Tıp Bilimleri

Bölüm

Araştırma Makalesi

Yayımlanma Tarihi

18 Ekim 2021

Gönderilme Tarihi

20 Nisan 2020

Kabul Tarihi

21 Aralık 2020

Yayımlandığı Sayı

Yıl 2021 Cilt: 22 Sayı: 6

Kaynak Göster

APA
Vural, Ö., Susam Şen, H., & Eker, İ. (2021). THE ROLE OF COMPLETE BLOOD COUNT IN PATIENTS WITH HETEROZYGOUS BETA THALASSEMIA. Kocatepe Tıp Dergisi, 22(6), 457-460. https://doi.org/10.18229/kocatepetip.723959
AMA
1.Vural Ö, Susam Şen H, Eker İ. THE ROLE OF COMPLETE BLOOD COUNT IN PATIENTS WITH HETEROZYGOUS BETA THALASSEMIA. KTD. 2021;22(6):457-460. doi:10.18229/kocatepetip.723959
Chicago
Vural, Özge, Hilal Susam Şen, ve İbrahim Eker. 2021. “THE ROLE OF COMPLETE BLOOD COUNT IN PATIENTS WITH HETEROZYGOUS BETA THALASSEMIA”. Kocatepe Tıp Dergisi 22 (6): 457-60. https://doi.org/10.18229/kocatepetip.723959.
EndNote
Vural Ö, Susam Şen H, Eker İ (01 Ekim 2021) THE ROLE OF COMPLETE BLOOD COUNT IN PATIENTS WITH HETEROZYGOUS BETA THALASSEMIA. Kocatepe Tıp Dergisi 22 6 457–460.
IEEE
[1]Ö. Vural, H. Susam Şen, ve İ. Eker, “THE ROLE OF COMPLETE BLOOD COUNT IN PATIENTS WITH HETEROZYGOUS BETA THALASSEMIA”, KTD, c. 22, sy 6, ss. 457–460, Eki. 2021, doi: 10.18229/kocatepetip.723959.
ISNAD
Vural, Özge - Susam Şen, Hilal - Eker, İbrahim. “THE ROLE OF COMPLETE BLOOD COUNT IN PATIENTS WITH HETEROZYGOUS BETA THALASSEMIA”. Kocatepe Tıp Dergisi 22/6 (01 Ekim 2021): 457-460. https://doi.org/10.18229/kocatepetip.723959.
JAMA
1.Vural Ö, Susam Şen H, Eker İ. THE ROLE OF COMPLETE BLOOD COUNT IN PATIENTS WITH HETEROZYGOUS BETA THALASSEMIA. KTD. 2021;22:457–460.
MLA
Vural, Özge, vd. “THE ROLE OF COMPLETE BLOOD COUNT IN PATIENTS WITH HETEROZYGOUS BETA THALASSEMIA”. Kocatepe Tıp Dergisi, c. 22, sy 6, Ekim 2021, ss. 457-60, doi:10.18229/kocatepetip.723959.
Vancouver
1.Özge Vural, Hilal Susam Şen, İbrahim Eker. THE ROLE OF COMPLETE BLOOD COUNT IN PATIENTS WITH HETEROZYGOUS BETA THALASSEMIA. KTD. 01 Ekim 2021;22(6):457-60. doi:10.18229/kocatepetip.723959

88x31.png
Bu Dergi Creative Commons Atıf-GayriTicari-AynıLisanslaPaylaş 4.0 Uluslararası Lisansı ile lisanslanmıştır.