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Correlation of Erythrocyte Count and Hemoglobin Levels with Hemoglobin Electrophoresis in Thalasemia Patients

Korelasi Jumlah Eritrosit dan Kadar Hemoglobin dengan Hemoglobin Elektroforesis pada Pasien Thalasemia

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DOI:

https://doi.org/10.21070/ups.11287

Keywords:

thalassemia, hemoglobin levels, erythrocyte, hemoglobin electrophoresis

Abstract

Thalassemia caused by a mutation in the globin gene that causes a decrease in the production of one of the globin chains. This study uses secondary data with a quantitative analysis research design with cross-sectional approach, which aims to determine the correlation between the number of erythrocytes and hemoglobin levels with hemoglobin electrophoresis in thalassemia patients at Dr. Saiful Anwar Regional General Hospital, East Java Province, as many as 50 samples from October 2023 to May 2026. Based on the results of the Spearman correlation analysis, it shows a significant correlation between total Hb levels and HbA (r=0.290), (p=0.020). Hb levels with HbA2 do not show a correlation (r=-0.056), (p=0.351). The number of erythrocytes doesn't show a correlation with Hb A (r=0.032), (p=0.414), but shows positive correlation with Hb A2 (r=0.261), (p=0.034). So the total Hb level is related to HbA, while the number of erythrocytes is related to HbA2.

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References

D. K. Rediyanto, “Deteksi Dini Thalassemia,” Pratista Patol., vol. 8, no. 1, pp. 17–28, 2023, [Online]. Available: http://majalahpratistapatologi.com/p/index.php/journal/article/view/112

Pedoman Nasional Pelayanan Kedokteran Tata Laksana Thalasemia. 2018.

H. R. Ashan and D. E. Putri, “Aspek Klinis Dan Pemeriksaan Laboratorium Talasemia B,” J. Kesehat. Tambusai, vol. 4, no. 2, pp. 2641–2647, 2023, doi: https://doi.org/10.31004/jkt.v4i2.15002.

L. Rujito, Talasemia : Genetik Dasar dan Pengelolaan Terkini. Purwokerto: UNSOED Press, 2019.

S. I. N. Aina, U. H. Fetriyah, and M. Basit, “Asuhan Keperawatan Keluarga Pada Anak Usia Remaja Dengan Thalasemia Di Wilayah Kerja Puskesmas Terminal,” Malahayati Nurs. J., Vol. 6, No. 1, Pp. 315-330 Asuhan, 2024, doi: https://doi.org/10.33024/mnj.v6i1.12384.

D. S. S. Rejeki, N. Nurhayati, S. Supriyanto, and E. Kartikasari, “Studi Epidemiologi Deskriptif Talasemia,” Kesmas Natl. Public Heal. J., vol. 7, no. 3, p. 139, 2012, doi: 10.21109/kesmas.v7i3.61.

P. R. Situmorang, N. Gea, R. Vera, and D. S. Napitupulu, “Skrining Hbe Metode Elektroforesis Gel Sebagai Deteksi Dini Β-Talasemia pada Mahasiswi Sekolah Tinggi Ilmu Kesehatan Santa Elisabeth Medan 2024,” J. Kesehat. Tambusai, vol. 5, no. 3, pp. 7078–7086, 2024.

D. Amnestya and A. Sudrajat, “Gambaran Nilai Hemoglobin Pasien Thalasemia Rumah Sakit Hermina Arcamanik,” J. Heal. Anal. Student, vol. 1, no. 1, pp. 12–17, 2024, [Online]. Available: https://journal.piksi.ac.id/index.php/jhas/article/download/1539/899

Syuhada, D. Fitriani, D. Marlina, and M. Laksmidara, “Perbandingan Hasil Pemeriksaan Hematologi Jumlah Eritrosit Pada Sampel Darah Pasien Thalasemia Dengan Antikoagulan K2EDTA Segera Dan Setelah Ditunda 4 Jam Post Sampling Di RSUD Dr. H. Abdul Moeloek Bandar Lampung,” J. Ilmu Kedokt. dan Kesehat., vol. 10, no. 8, pp. 2549–4864, 2023, [Online]. Available: http://ejurnalmalahayati.ac.id/index.php/kesehatan

I. Z. Sadiq et al., “Thalassemia: Pathophysiology, Diagnosis, and Advances in Treatment,” Thalass. Reports, vol. 14, no. 4, pp. 81–102, 2024, doi: https://doi.org/10.3390/thalassrep14040010.

“Talasemia Penyakit Keturunan, Hindari dengan Deteksi Dini,” Kementerian Kesehatan Republik Indonesia, 2022. [Online]. Available: https://kemkes.go.id/id/talasemia-penyakit-keturunan-hindari-dengan-deteksi-diniengan-deteksi-dini/

H. S. Harefa and P. R. S. R. V. B. Tarigan, “Skrining Gen Hbe Sebagai Deteksi Thalassemia Dengan Metode Elektroforesis Pada Mahasiswi Sekolah Tinggi Ilmu Kesehatan Santa Elisabeth Medan,” MANUJU MALAHAYATI Nurs. J., vol. 7, no. 11, pp. 4662–4671, 2025, doi: 10.33024/mnj.v7i11.22835.

H. Hidayat, F. Ladyani, N. Herlina, and M. Muhammad, “Gambaran Fraksi Hemoglobin Penderita Thalasemia Menggunakan Metode Elektropoesis Kapiler Di Rsud Dr. H. Abdul Moeloek Bandar Lampung Tahun 2022,” SEHAT J. Kesehat. Terpadu, vol. 2, no. 3, pp. 164–172, 2023, doi: 10.31004/sjkt.v2i3.18186.

B. Pratama and I. Kurniati, “Pendekatan Diagnosis Berbasis Molekuler pada Pasien Talasemia The Molecular-Based Diagnostic Approach on Thalassemia Patient,” Medula, vol. 9, no. 2, pp. 339–345, 2019, [Online]. Available: http://juke.kedokteran.unila.ac.id/index.php/medula/article/download/2649/pdf

D. E. Sabath, “The role of molecular diagnostic testing for hemoglobinopathies and thalassemias,” Int. J. Lab. Hematol., vol. 45, no. S2, pp. 71–78, Jun. 2023, doi: 10.1111/ijlh.14089.

I. D. A. N. Canis Paloma, “Talasemia : sebuah Tinjauan Pustaka,” Biocity J. Pharm. Biosci. Clin. Community, vol. 1, no. 2, pp. 89–100, 2023, doi: 10.30812/biocity.v1i2.2525.

A. Novilla, T. N. Clarisa, A. Furqon, and S. Romlah, “Skrining Talasemia Pada Mahasiswa TLM ( D3 ) Fakultas Ilmu Dan Teknologi Kesehatan Universitas Jenderal Achmad Yani Cimahi,” J. Ilm. Kesehat., vol. 16, no. 2, pp. 356–363, 2024, doi: e:ISSN: 2656-1190.

Regar J, “Aspek Genetik Talasemia,” J. Biomedik, vol. 1, no. 3, pp. 151–158, 2009, [Online]. Available: www.usu.ac

Ş. Değermenci and D. Aslan, “HbA2 levels in children with β-thalassemia trait associated with iron deficiency A perspective for pediatricians,” Am. J. Clin. Pathol., vol. 162, no. 6, pp. 544–548, 2024, doi: 10.1093/AJCP/AQAE085.

F. Qoriba, Putu Ristyaning Ayu Sangging, Maulana, and R. Lisiswati, “Fluktuasi Nilai HbA2 pada Carrier β-Thalasemia: Literature Review,” Medula, vol. 14, no. 8, pp. 1668–1672, 2024, doi: https://doi.org/10.53089/medula.v14i8.1306.

Posted

2026-07-15