Increasing fetal hemoglobin as a possible key for improvement of hypoxia and saving last breath in COVID-19 patient: "postulating a hypothesis"

被引:5
作者
Abdelzaher, Muhamed A. [1 ]
Ibrahim, Ashraf E. S. [2 ]
Negm, Essamedin M. [3 ]
机构
[1] Alahrar Teaching Hosp, Neurosurg Dept, Zagazig, Egypt
[2] Zagazig Univ, Chest Dept, Fac Med, Zagazig, Egypt
[3] Zagazig Univ, Anesthesia & Surg Intens Care Dept, Fac Med, Zagazig, Egypt
关键词
COVID-19; Hypoxia; Fetal hemoglobin; Fetal blood; Hydroxyurea; SICKLE-CELL-ANEMIA; HYDROXYUREA;
D O I
10.1186/s43168-021-00078-7
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: COVID-19 patients normally experience mild cold-like symptoms that progress from the early viral response phase through the lung phase to the hyper-inflammation phase. Acute respiratory distress syndrome (ARDS) characterizes the most critical stage of the illness with progressive respiratory failure. Hypoxemia is the most dangerous and challenging problem. We suggest an inductive study approach to postulate a hypothesis and synthesis of supporting evidence as a trial to resolve hypoxia in patients with COVID-19 by increasing the volume of fetal hemoglobin which has a high affinity for oxygen using methods for hypothesis related research evidence synthesis. Conclusion: We recommend involving umbilical cord fetal blood transfusion or the use of hydroxyl urea as a clinical trial on COVID-19 patients and also for all other types of ARDS to determine its efficacy in correction of hypoxemia, controlling progression of the disease, and increasing survival rate.
引用
收藏
页数:5
相关论文
共 21 条
[1]  
Bhattacharya N., 2001, Clinical and Experimental Obstetrics and Gynecology, V28, P47
[2]  
Charache S, 1997, SEMIN HEMATOL, V34, P15
[3]  
CHARACHE S, 1987, BLOOD, V69, P109
[4]   Hydroxyurea induces fetal hemoglobin by the nitric oxide-dependent activation of soluble guanylyl cyclase [J].
Cokic, VP ;
Smith, RD ;
Beleslin-Cokic, BB ;
Njoroge, JM ;
Miller, JL ;
Gladwin, MT ;
Schechter, AN .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (02) :231-239
[5]  
FIBACH E, 1993, BLOOD, V81, P1630
[6]  
Huang CL, 2020, LANCET, V395, P497, DOI [10.1016/S0140-6736(20)30211-7, 10.1016/S0140-6736(20)30183-5]
[7]  
Linch D, 1998, ENCY IMMUNOLOGY
[8]  
Litwack G, 2018, GLYCOLYSIS GLOCUNEOG
[9]   Hydroxyurea for the treatment of sickle cell anemia [J].
Platt, Orah S. .
NEW ENGLAND JOURNAL OF MEDICINE, 2008, 358 (13) :1362-1369
[10]   HYDROXYUREA ENHANCES FETAL HEMOGLOBIN PRODUCTION IN SICKLE-CELL-ANEMIA [J].
PLATT, OS ;
ORKIN, SH ;
DOVER, G ;
BEARDSLEY, GP ;
MILLER, B ;
NATHAN, DG .
JOURNAL OF CLINICAL INVESTIGATION, 1984, 74 (02) :652-656