References |
Storch et al. (2005), Darras et al. (2021), Peikert et al. (2022b)
|
Darras et al. (2021), Rabe et al. (2021), John et al. (2023)
|
Rabe et al. (2021), Recktenwald et al. (2022a), Reichel et al. (2022)
|
This paper |
Diagnostic power |
Limited (improved in automated 3D classification) |
Good discrimination to controls, specificity still needs to be shown |
Good discrimination to controls, specificity still needs to be shown |
Discrimination at detectable limit, statistics limited to this paper |
Correlation with severeness or disease state |
No evidence |
Unknown |
Unknown |
Unknown |
Blood sample volume |
50 μL |
Typically, 1.5 mL |
5 μL |
200 μL |
Routine devices available |
Blood smear examination at different levels of automation (3D is not routine) |
Several levels of automation available; parameters easy adaptable for manual devices |
Yes (Erysense by Cysmic GmbH, Saarbrücken, Germany) |
Yes (Lorrca by RR Mechatronics, Zwaag, The Netherlands) |
Possibility of multiplexing/ throughput |
Unlikely |
In principle yes, but needs (software) adaptation of existing technologies |
In principle yes, but needs hardware developments of existing technologies |
Challenging |
Implementation in clinical settings |
Difficult, prone to bias, needs repeated training |
Easy, though requires instrument upgrade |
Medium, institution should set standard for diagnostic workup and quality control |
Medium, institution should be regular user of instrument and set standard for diagnostic workup and quality control |