38 results
treatment hematology hivaids opportunistic prevention comparison differential syndrome adultonset anemia aplastic blood causes classification hemophagocytic hlh lung lymphohistiocytosis medications mycobacterium
Suspected catheter-related bloodstream infection - Management Algorithm • Temperature 37.8 C • Rigors
Antibiotic Management ... Hemodynamically stable ... Antibiotic Management ... • Persistent fever ... #CRBSI #diagnosis
Campylobacter Clinical • Fever • Abdominal pain • Diarrhea (bloody stools) • Vomiting
Clinical • Fever ... • Supportive (infection ... self-limited) • Antibiotics ... for severe disease ... Campylobacter #Diagnosis
IDSA 2017 CDiff Guidelines - Table 7. Potential Treatment Agents for Treatment of the Primary Clostridium difficile
IDSA 2017 CDiff ... Guidelines - Table ... Clostridium difficile infection ... Episode #Pharmacology ... #Management #CDiff
Lung Abscess - Diagnosis and Management Summary Lung Abscess Etiology: • Necrosis of lung parenchyma by a
and Management ... polymicrobial infection ... decubitus - air fluid level ... Lung Abscess Management ... once stable -
Adult-Onset Still's Disease Clinical triad: Fever, Arthralgia/arthritis, Skin rash ± odynophagia + Biological inflammation: Increased neutrophils, Hyperferritinemia, decreased
Clinical triad: Fever ... Differential Diaqnoses ... : • Infectious ... #diagnosis #management ... #treatment #rheumatology
Common Variable Immunodeficiency (CVID) What? CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
late adulthood • Diagnosis ... • Liver diseases ... Low serum IgG level ... and M panel Management ... #diagnosis #management
Kawasaki Disease (KD) - Diagnosis and Management Summary Kawasaki Disease (KD) is the most common vasculitis of
Kawasaki Disease ... (KD) - Diagnosis ... and Management ... cæxist with other infections ... KD #vasculitis #rheumatology
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
, ↓ Fibrinogen level ... • Autoimmune diseases ... Adult-onset Still disease ... #management #treatment ... #summary #rheumatology
Summary of Coagulation Deficiencies Inherited: • Hemophilia A - Deficiency of Factor VIII • Hemophilia B -
malnutrition, Antibiotics ... ) • Advanced Liver ... Disease - Alcohol ... Deficiencies #Summary #table ... #comparison #diagnosis
Hemophagocytic Lymphohistiocytosis (HLH) Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
age, however the disease ... can mimic common infections ... rapidly, and empiric antibiotic ... #management #treatment ... #hematology
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