Open AccessCase Report on Sickle Cell Anaemia (SS Pattern)
Author(s) -
Mayur Waghaye,
Sheetal Sakharkar,
Samrudhi Gujar,
Swapna Morey,
Archana Dhengare,
Prerna Sakharwade,
Darshana Kumari,
Pooja Kasturkar,
Madhuri Naik
Publication year - 2021
Publication title -
journal of pharmaceutical research international
Language(s) - English
Resource type - Journals
ISSN - 2456-9119
DOI - 10.9734/jpri/2021/v33i57b34055
Subject(s) - medicine , sickle cell anemia , anemia , hemoglobin , bilirubin , gastroenterology , pediatrics , hemolytic anemia , anxiety , disease , psychiatry
Sickle cell anemia is a kind of hemolytic anemia that is passed down in families. It is a kind of hemolytic anemia caused by inheriting the sickle hemoglobin gene. Africans, as well as individuals from the Middle East, the Mediterranean region, and India's aboriginal tribes, have a lower level of the sickle hemoglobin (HbS) gene. A kind of anemia that affects both children and adults is sickle cell anemia.
Clinical Finding: Since 5 days, A 25-year-old man has been experiencing generalized bodily pain and anxiety.
Examining the Problem: ALT (SGPT)- 97 U/L, AST (SGOT)- 56 U/L, total bilirubin – 5.4 mg percent, bilirubin conjugated – 1.7 mg percent, bilirubin unconjugated – 3.7 mg percent, total RBC count – 3.71 million/cu mm, total WBC count – 22100 cu mm, total platelets count – 6.46 lack/cu.
Ultrasonography: Heterogeneous spleen.
Therapeutic Intervention: Inj. Piptaz 4.5 gm TDS, inj. Levoflox 500 mg, tab. Hydroxyurea 500 mg, tab. Neurobion forte, inj. Pan 40 mg, inj. Tramadol 100 mg.
Outcome: The client's condition has improved as a result of the treatment. He has no longer generalized bodily aches, and his anxiety levels have decreased.
Conclusion: A 25-year-old man was admitted to Acharya Vinoba Bhave Hospital's Medicine ward with a history of sickle cell anaemia and complaints of nonspecific body aches and anxiousness. His condition improved after he received proper therapy.