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Sickle Cell Disease: Pain & Fever

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Presentation on theme: "Sickle Cell Disease: Pain & Fever"— Presentation transcript:

1 Sickle Cell Disease: Pain & Fever
John Cheng, MD PEM Fellows’ Conference July 19, 2006

2 Sickle Cell Disease Hemoglobin S Various types:
Glu  Val at 6 position of β hemoglobin Various types: SS SC Sβ-thalessemia Others

3 Sickle Cell Issues Vaso-Occlusive Crisis Immunocompromise
Sickling and subsequent ischemia Immunocompromise Splenic infarction Encapsulated organisms: H. influenzae, S. pneumonia Salmonella

4 Vaso-Occlusive Crisis (VOC)
Usual type of pain? Concerns: Abdominal pain: splenic sequestration, gallstones Hip pain: avascular necrosis Headache: stroke Chest pain: acute chest syndrome Eye pain: optic artery ischemia Groin pain (male): priapism Extremity pain: dactylitis, osteomyelitis Other pain: possible abscess

5 VOC--Labs CBC with diff Reticulocyte count Blood cultures if h/o fever
Consider electrolytes BMP if dehydrated LFTs if RUQ or epigastric abd pain Consider U/A and Ucx if abd/flank pain Consider Type and Screen

6 VOC--Diagnostics CXR if respiratory symptoms Ultrasound--abdominal
CT scan--head

7 VOC--Treatment Oxygen Hypotonic fluids (D5 1/4NS) Blood transfusion
Keep SaO2 ≥ 92% May be hypoxic at baseline Hypotonic fluids (D5 1/4NS) Reverse sickling Dehydration: 10 cc/kg NS bolus vs 1.5 maintenance BEWARE fluid overload Blood transfusion If neeed, try to get leukocyte-depleted and, if available, C, E, Kell-compatible and sickle neg RBCs

8 VOC--Meds Pain meds Other meds: NSAIDs: Ketorolac 0.5 mg/kg, max 30 mg
Opiates: Morphine mg/kg q min PRN Dilaudid mg/kg Mixed Opiate Agonist/Antagonist: Nubain mg/kg q3h PRN Other meds: Benadryl 1.25 mg/kg PO (NOT IV) q6 PRN

9 VOC--Disposition Admission if not able to control pain OR significant drop in Hgb and/or retic Ask if they think they can manage at home. Home meds: Ibuprofen 10 mg/kg q6-8h x 2d, then PRN Tylenol #3 1 mg/kg q4-6h PRN breakthrough pain Consider Lortab, Oxycodone, Morphine IR Follow up with Sickle Cell clinic in 1-2 days by phone or in clinic Call sickle cell consult.

10 Fever Defined as temp ≥ 38.3°C Immunocompromise Splenic infarction
Usually on Penicillin until 5 y/o Usually have PCV7 and Pneumovax Remember to treat concurrent pain

11 Fever--Labs & Diagnostics
CBC with diff Reticulocyte count Blood cultures Consider CRP and Type & Screen Consider urine or CSF as warranted Chest XRay if respiratory symptoms

12 Fever--Meds No source: If source found: treat as usual after IV Abx
GOAL: 30 minutes from door to antibiotics Rocephin mg/kg, max 2 gm IV/IM If cephalosporin allergy: Meropenem 20 mg/kg IV, max 1 gm If source found: treat as usual after IV Abx If Acute Chest Syndrome: Oxygen, pain meds Consider adding Zithromax, nebulizers, and steroids

13 Fever--Disposition Consider admission for observation if:
Age < 1 y/o Previous bacteremia/sepsis T > 40°C WBC > 30 or < 5, plts < 100 Received Meropenem or Vancomycin Infiltrate on CXR Unable to comply with follow up Other problems: pain, aplastic crisis, splenic sequestration, ACS, stroke, priapism

14 Fever--Disposition If labs unremarkable and well appearing, d/c home and f/u in 24 hours in sickle cell clinic for re-check and 2nd dose of Rocephin. Call sickle cell consult.

15 CAVEAT Read notes from previous visits.
There are some frequent flyers who are supposed to have pain plans in place with hematology.


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