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Technology
Pochi-3 part, XP-300-3 part, XS-1000 AL, 5 part, XN-1000 BPR, 7 part,
10-30 CBC’s/Day 30-75 CBC’s/Day
1-10 CBC’s/Day 10-20 CBC’s/Day
XN-3000 DI-60
• Declining availability
of medical technologists
• Labor intensive
• Not standardized
• Difficult to train
• No historical images
• Limited consultation
• Connectivity between
providers
The Future YOU!!!
XN-3000 DI-60
Automation
Technology
88 μL Sample Volume
MONO
IG
LYMPH
NEUT+BASO
Debris
EO
Reportable Immature Granulocytes
Multiple Myeloma with IG’s
Multiple Myeloma with IG’s
IG – XN DIFF Abstract
Solution:
Automated Immature Granulocyte Count
• May be a useful complement to current infection surveillance program
even when other tests are negative
• With other information may help physicians identify patients with
C infection sooner
FSC
BASO
NRBC
WBC
Debris
SFL
WNR Channel
Reference
Ranges:
IPF 0.9–11.2 %
AML – Initial Run
AML – Reflex Run
AML
Solution: Immature Platelet Fraction
BEFORE AFTER
AC
P
IG, RET He, IPF
SUMMARY
Automation vs Non-Automation
Technology Benefits