השוואת שיטות

	ציון וולס לפקקת ורידים עמוקים (DVT)	ציון חומרת דלקת ריאות CURB-65	מדד qSOFA
תחום	הערכה קלינית	הערכה קלינית	הערכה קלינית
משפחה	Process / pipeline	Process / pipeline	Process / pipeline
שנת המקור	1994	2003	2016
הוגה השיטה	Philip S. Wells	W. Staniford Lim, et al.	Sepsis-3 Taskforce
סוג	Venous thromboembolism risk stratification	Community-acquired pneumonia severity assessment	Rapid sepsis screening
מקור מכונן	Wells, P. S., Hirsh, J., Anderson, D. R., et al. (1994). A simple clinical model for the diagnosis of deep-vein thrombosis combined with impedance plethysmography. Archives of Internal Medicine, 154(13), 1541-1546.	Lim, W. S., van der Eerden, M. M., Laing, R., et al. (2003). Defining community acquired pneumonia severity on presentation to hospital: an international derivation and validation study. Thorax, 58(5), 377-382.	Singer, M., Deutschman, C. S., Seymour, C. W., et al. (2016). The Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3). JAMA, 315(8), 801-810.
כינויים	Wells DVT Score, DVT Wells	CURB-65, Pneumonia severity	Quick SOFA, qSOFA
קשורות	3	3	3
תקציר	The Wells score, developed by Wells et al. in 1994, is a clinical prediction rule that stratifies patients into low, intermediate, or high pretest probability of deep vein thrombosis (DVT). It combines seven clinical features to guide diagnostic testing decisions and reduce unnecessary imaging in suspected DVT patients.	CURB-65, derived and validated by Lim et al. in 2003, is a 5-point severity of illness score for community-acquired pneumonia (CAP). It assesses confusion, urea nitrogen, respiratory rate, blood pressure, and age ≥65 years to stratify mortality risk and guide admission and treatment decisions.	The Quick Sequential Organ Failure Assessment (qSOFA) score, introduced by the Sepsis-3 taskforce in 2016, is a rapid 3-variable bedside screening tool for identifying non-ICU patients at high risk of sepsis-related mortality. It uses altered mentation, systolic hypotension, and tachypnea to quickly stratify patients without requiring laboratory testing.