1. The patient, a child, presented with symptoms of sickle cell anemia crisis including swelling, fever, jaundice, and cyanosis as reported by the mother.
2. Sickle cell anemia is a hereditary disease that causes red blood cells to become rigid and sickle shaped, clogging small blood vessels and limiting organ perfusion.
3. Over an 8 hour period, the nurse assessed the patient's respiratory status, cardiac function, and pain levels to promote optimal perfusion and prevent complications from the sickle cell anemia crisis.
1. The patient, a child, presented with symptoms of sickle cell anemia crisis including swelling, fever, jaundice, and cyanosis as reported by the mother.
2. Sickle cell anemia is a hereditary disease that causes red blood cells to become rigid and sickle shaped, clogging small blood vessels and limiting organ perfusion.
3. Over an 8 hour period, the nurse assessed the patient's respiratory status, cardiac function, and pain levels to promote optimal perfusion and prevent complications from the sickle cell anemia crisis.
1. The patient, a child, presented with symptoms of sickle cell anemia crisis including swelling, fever, jaundice, and cyanosis as reported by the mother.
2. Sickle cell anemia is a hereditary disease that causes red blood cells to become rigid and sickle shaped, clogging small blood vessels and limiting organ perfusion.
3. Over an 8 hour period, the nurse assessed the patient's respiratory status, cardiac function, and pain levels to promote optimal perfusion and prevent complications from the sickle cell anemia crisis.
1. The patient, a child, presented with symptoms of sickle cell anemia crisis including swelling, fever, jaundice, and cyanosis as reported by the mother.
2. Sickle cell anemia is a hereditary disease that causes red blood cells to become rigid and sickle shaped, clogging small blood vessels and limiting organ perfusion.
3. Over an 8 hour period, the nurse assessed the patient's respiratory status, cardiac function, and pain levels to promote optimal perfusion and prevent complications from the sickle cell anemia crisis.
(Member: St. Paul University System) St. Paul Avenue, 2727 Bantay, Ilocos Sur DEPARTMENT OF NURSING
NOVILYN C. PATARAY BSN – II
SICKLE CELL ANEMIA ASSESSMENT DIAGNOSI PATHOPHYSIOLOG PLANNING INTERVENTION RATIONALE EVALUATION S Y Subjective: “nasakit Risk for A hereditary disease that After 8 hours of nursing 1. Assess 1. During SC After 8 hours of nursing etoy buo nga bagi na deficient fluid destroys red blood cells by intervention, the patient respiratory status. crisis, red intervention, the patient ken marigatan pay volume related causing them to become will manage pain of SC blood cells manages pain of SC crisis, nga umages ken kasla to infarctions rigid and sickle shaped. crisis, promote optimal cannot promoted optimal perfusion lang nabanbannog tas limiting the Occurs mainly in persons perfusion and effectively and prevented the marigatan pay nga kidney’s ability of African descent. prevention of deliver oxygen complications. uminom” as verbalized to concentrate The sickle shaped cells complications. to the tissues by the mother. urine. become clogged in the resulting in small blood vessels poor perfusion Objective: causing obstruction of the 2. Changes in Swelling of circulation. This results in 2. Monitor cardiac respiratory hands/feet damage to the various status. status and Fever tissues. hypoxia may Jaundice lead to Cyanosis arrhythmias. Presence of 3. Clogged sickle cells on 3. Assess for and vessels results histologic manage pain. in damage to exam the tissues and organs.