A Case Report on Sickle Cell Crisis In A 24-Years-Old

Abstract

Sickle cell illness is an autosomal passive blood issue that can prompt weakness. It is brought about by a transformation in the hemoglobin quality, which prompts distortion of red platelets. Distorted red platelets can deter little vessels and they are inclined to annihilation. Sickle cell pallor (SCA) was first depicted in the Western writing over 100 years prior. Explanation of its atomic premise provoked various biochemical and hereditary examinations that have added to a superior comprehension of its pathophysiology.

Patient History: A 24 years old female was admitted in HDU Acharya Vinoba Bhave hospital on dated 27^TH July 2021 with chief complaint of severe body ache since 3days, Tingling sensation over lower lip and chin area since 10 days. After physical examination and investigation doctor diagnosed as sickle cell crisis. Patient had history of sickle cell disease (ss pattern).  She is taking Tab. Folic acid 5mg OD daily. No history of cough, cold and fever.

The Main Diagnosis, Therapeutic Intervention, And Outcome: After physical examination and investigation doctor diagnosed this case of sickle cell crisis. Patient was treated with IV. Fluids-NS, RL, DNS, calcium supplements, antibiotics, analgesic, antiemetic medication and also given inj. Optineuron.  Her General condition was moderate. Nursing Management: Administered IV fluid, monitor vital sign 6 hourly. Administered medication doctor’s order

Conclusion: Timely treatment and management of sickle cell crisis.