Sickle Cell Disease: Core Concepts for the Emergency Physician and Nurse Acute Chest Syndrome Case Study David M. Cline, MD Wake Forest School of Medicine.

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Presentation transcript:

Sickle Cell Disease: Core Concepts for the Emergency Physician and Nurse Acute Chest Syndrome Case Study David M. Cline, MD Wake Forest School of Medicine

Objectives At the conclusion of the case study discussion, the learner will be able to identify: 1.The recommended antibiotics for SCD patients diagnosed with acute chest syndrome 2.The recommended indications for simple and exchange transfusion in SCD patient admitted with acute chest syndrome.

Pretest Question # 1 What are the recommended antibiotics for SCD patients diagnosed with acute chest syndrome? A. Levofloxacin IV B. 3 rd or 4 th generation cephalosporin, and a macrolide IV. C. Vancomycin plus piperacillin/tazobactam IV D. Doxycyline IV

Pretest Question #2 What are in the indications for simple transfusion in SCD patients with Acute Chest Syndrome? A.Drop in hemoglobin of 1.0 g/dL below baseline B.Drop in hemoglobin of 2.0 g/dL below baseline C.Failure achieve a pulse oximetry reading of greater than 98%. D.Failure achieve a pulse oximetry reading of greater than 95%.

History of the Present Illness 31 year old black male with SS sickle cell disease presents the emergency department with complaint of “pain crisis.” The patient states this episode is identical to his typical pain crisis, where he experiences pain in his chest, his abdomen, and both of his upper lateral thighs. The pain began yesterday, and has not responded to his oral pain medication, Dilaudid 4 mg tabs, 1 every 4 hours as needed for pain.

Past Medical History Additional past medical history includes avascular necrosis of both hips, priapism, NSTEMI, cholecystectomy, and one prior episode of acute chest syndrome. He smokes cigarettes, ¼ pack per day, and drinks beer occasionally. The patient averages 1 visit to the emergency department every month, and he is admitted to the hospital approximately 50% of the time.

Physical Exam Triage vital signs include temperature of 99.6, blood pressure of 113/65 mm Hg, pulse 98 bpm, respirations 20/min, oxygen saturation of 93% on room air. General: he appears acutely in pain. HEENT is within normal limits except for mild icterus of the conjunctiva Lungs clear to auscultation and percussion Heart: heart rate and rhythm regular, no murmurs, no gallop, no rubs.

Physical Exam Continued Abdomen: soft with diffuse tenderness that is similar to what had been described previously in his medical record. Extremities: He is tender over both hips and lateral thigh areas as previously described in the record. His peripheral pulses are intact. Neuro: He is alert and oriented, CN 2-12 intact, sensation 5/5 and motor strength 5/5 through-out.

Emergency Department Course The patient is placed on oxygen and IV fluids. The patient is given several doses of pain medication to relieve his significant pain. Laboratory analysis reveals a white blood cell count of 17,000, with segs of 66.7%, Bands 1.76%, lymphs 25.8%, hemoglobin of 8.9 (at baseline for this patient). Chest X-ray is ordered; shows the following subtle finding:

Chest X-ray Radiology: “Basilar opacity over right base, best seen on the lateral film.

Hospital Course The patient is started on intravenous ceftriaxone, and azithromycin for atypical organisms. 12 hours after admission, the oxygen saturation drops to 89%. In preparation for exchange transfusion, it is noted that the hemoglobin has dropped 1 gram from initial reading. The patient is transferred to ICU, and exchange transfusion is started. He recovers uneventfully.

Discussion The patient has three risk factors for acute chest syndrome: SS disease, currently smoker, and prior history of acute chest syndrome. Because the patient frequently complains of chest pain with his uncomplicated vaso-oclusive crisis, differentiating acute chest from uncomplicated pain crisis is difficult. Because the findings on chest x-ray are often subtle, especially initially, comparing the current film to prior films is essential. Additional red flags: temperature of 99.6°F, SPO2 of 93% on RA, white blood cell count of 17,000. The patient deteriorated after admission as recognized by his dropping oxygen saturations and hemoglobin. This is a common course with acute chest syndrome and therefore admitted patients with sickle cell disease should carefully monitored.

Discussion (continued) Guidelines suggest selection of 3 rd or 4 th generation cephalosporin, and a macrolide IV to treat infection. Guidelines suggest giving simple transfusion (10 mL/kg RBCs) to improve oxygen carrying capacity for patients with symptomatic ACS whose hemoglobin concentration falls 1.0 g/dL or more below baseline. If baseline Hgb is 9 g/dL or greater, simple blood transfusion may not be required. Urgent exchange transfusion is recommended when there is rapid progression of ACS as manifested by oxygen saturation below 90% despite supplemental oxygen, increasing respiratory distress, progressive pulmonary infiltrates, and/or decline in hemoglobin concentration despite simple transfusion. In these cases, consult hematology and/or critical care, and/or apheresis specialists to provide therapy.

References

Post-test Question # 1 What are the recommended antibiotics for SCD patients diagnosed with acute chest syndrome? A. Levofloxacin IV B. A 3 rd or 4 th generation cephalosporin, and a macrolide IV. C. Vancomycin plus piperacillin/tazobactam IV D. Doxycyline IV

Post-test Question #2 What are in the indications for simple transfusion in SCD patients with Acute Chest Syndrome? A.Drop in hemoglobin of 1.0 g/dL below baseline B.Drop in hemoglobin of 2.0 g/dL below baseline C.Failure achieve a pulse oximetry reading of greater than 98%. D.Failure achieve a pulse oximetry reading of greater than 95%.