​ Error Prevention Features of the AQUIOS CL Overview

Specimen Barcodes
Positive Specimen ID (Patient and Specimen) Monitoring
Remote User Alerts
Smart-Track Reagent Monitoring
Scanning Control Assay Ranges
Locked System

Laboratory standards and regulations set forth by governmental bodies such as the Centers for Disease Control (CDC) help to define the procedures that laboratories follow. These procedures are used in an effort to standardize the workflow and are used as safety countermeasures and help to prevent errors. Error prevention, however, is costly and time consuming.

The AQUIOS CL flow cytometer utilizes several error prevention features that are cost effective and in many cases automatically helping to improve safety and reduce the cost and time that often goes hand-in-hand with error prevention methods.

Laboratories follow procedures defined by laboratory standards and regulations set forth by regulatory bodies such as the Centers for Disease Control (CDC) among others. The procedures are in place as safety countermeasures and as error prevention methods. The work behind error prevention can be expensive and time consuming. The AQUIOS CL flow cytometer design has taken this into account in as many areas as possible. The AQUIOS CL flow cytometer has several systems built-in to prevent failures.

The AQUIOS CL flow cytometer has error prevention systems to assist in:
• General workflow
• Startup, cleaning, and worklist generation
• Sample preparation
• Quality control
The sections below provide an overview of each of the error prevention systems in the . . . at a Glance tables at the end  of each section. Each error prevention is then explained in further detail below the table.

Specimen Barcodes 

Unlike traditional flow cytometers, all compatible barcodes on the AQUIOS CL flow cytometer can be automatically read by the tube barcode reader without the need for a handheld barcode scanner, reducing the need to manually scan specimens. Refer to Appendix D, Barcode Specifications in the AQUIOS CL Flow Cytometer Instructions for Use (PN B21496).

Positive Specimen ID (Patient and Specimen) Monitoring

On a traditional flow cytometer, barcode scanners are used to scan both the daughter tube and the specimen into the system. This workflow has the potential for sample misidentification if an operator scans the incorrect daughter tube and/or specimen and places it in the incorrect location in the rack or carousel.

The AQUIOS CL flow cytometer reduces the possibility of sample misidentification by scanning the specimen tube right before aspiration. This form of error prevention, although new to flow cytometry, was borrowed from hematology instruments such as the DxH800.

Remote User Alerts

In current flow cytometry laboratories (1,2), an instrument operator sets up the cytometer and monitors it as the sample is run. This also implies that instruments typically have dedicated operators who need to be available to periodically monitor the instrument.

The AQUIOS CL flow cytometer monitors the sample in real time and, if three consecutive runs are flagged, it can be set up to notify the operator by a text message or an e mail. Once notified, the operator can address the issue right away. This ability allows an operator to run multiple instruments, perform other tasks in the laboratory as samples are being processed and walk away knowing that the flow cytometer can notify the operator of any significant issues. This is unique to the AQUIOS CL flow cytometer and not available on any other flow cytometer.

The AQUIOS CL flow cytometer also tracks a variety of errors throughout the workflow. Refer to Chapter 9, Troubleshooting in the AQUIOS CL Flow Cytometer Instructions for Use for a list of errors and the relevant messages tracked by the system.

Smart-Track Reagent Monitoring

Smart-Track reagent monitoring is not available on traditional sample prep devices. Traditional sample prep systems do not detect if an incorrect antibody bottle was used. Conversely, the AQUIOS system has reagents that use a unique 2D barcode identity for tracking the expiration date, on board expiration, lot, and container numbers and links this information to the sample. The reagent consumption and plate usage are monitored by the system as the samples are processed. Updates of new reagents, plate usage, reagent availability and reagent location are displayed after opening and closing the reagent door.


FLOWC_HIV AQUIOS reagent tracking


NOTE: The AQUIOS CL Flow Cytometer system does not track the AQUIOS Sodium Hypochlorite Solution. You must track the expiration date of the AQUIOS Sodium Hypochlorite Solution upon use.

Consumables maintained on board are automatically read into the system when placed onboard. Barcoded reagents that are not housed onboard can be read into the system by presenting the barcode on the label to the external barcode reader.

Expiration dates and reagent quantity are both measured in real time. The Reagent Status page displays the amount of remaining reagent and the number of tests remaining or the remaining reagent volume (in %). Upon startup, the system displays how many tests remain before replacement is required. When a replacement is required, the system displays one of two warnings: the reagents are either low or depleted.

Scanning Control Assay Ranges

Traditional systems require that control assay ranges be input manually. This is time consuming and there is a risk of data entry errors. Since the AQUIOS CL system monitors and tracks the barcodes in real time by scanning upon loading and scanning before aspiration, samples can be loaded into the cassettes in any order and the cassettes can be loaded onto the system in any order. There is no longer a need to track a complex worklist with multiple tubes for the specimen and the daughter tube. And, there is no need to manually track the location of each daughter tube in the system. This reduces the risk of sample misidentification.

Locked System 

All settings are locked except for the following: ability to adjust gates and regions* and ability to adjust compensation (not done on a regular basis). A locked system prevents user error due to erroneous setting selections or any unintended changes to the settings. A locked system makes it easy to use and allows less experienced operators to be trained to run the system.

FLOWC-HIV-aquios-error prevention startup cleaning - Section 9

AQUIOS CL Flow Cytometer References

  1. Evaluation of a novel automated volumetric flow cytometer for absolute CD4+ T lymphocyte quantitation
    Gossez M, Malcus C, Demaret J, Frater J, Poitevin-Later F, Monneret G
    Cytometry B Clin Cytom. 2017 Nov;92(6):456-464. doi: 10.1002/cyto.b.21360. Epub 2016 Feb 23.
  2. Comparison of methods and TAT assessment: Volumetric AQUIOS CL and bead-based FACS CANTO II cytometers
    Grossi V, Infantino M, Meacci F, Bellio E, Bellio V, Ciotta G, Priami F, Sarzi-Puttini P, Atzeni F, Li Gobbi F, Damiani A, Benucci M, Manfredi M
    Cytometry B Clin Cytom. 2018 Jul;94(4):674-678. doi: 10.1002/cyto.b.21513. Epub 2017 Feb 15.
  3. Performance verification of the new fully automated Aquios flow cytometer PanLeucogate (PLG) platform for CD4-T-lymphocyte enumeration in South Africa
    Coetzee LM, Glencross DK
    PLoS One. 2017; 12(11): e0187456. Published online 2017 Nov 3.  doi: 10.1371/journal.pone.0187456
  4. T lymphocyte immunophenotyping in bronchoalveolar lavage on AQUIOS CL cytometer.
    Humeau C, Darrouzain F, Gouilleux-Gruart V
    J Immunol Methods. 2018 Oct;461:91-99. doi: 10.1016/j.jim.2018.06.022. Epub 2018 Jul 3.
  5. Analytical performance of an automated volumetric flow cytometer for quantitation of T, B and natural killer lymphocytes.
    Degandt S, Peeters B, Jughmans S, Boeckx N, Bossuyt X.
    Clin Chem Lab Med. 2018 Jul 26;56(8):1277-1288. doi: 10.1515/cclm-2017-0638.
  6. Acceptable "Real-Life" Variability for Lymphocyte Counts by Flow Cytometry
    Ticchioni M, Brouzes C, Durrieu F, Lambert C; Association Française de Cytométrie accreditation working group (AFC-AG).
    Cytometry B Clin Cytom. 2018 Dec 7. doi: 10.1002/cyto.b.21751. [Epub ahead of print]
  7. Advantages of the Use of AQUIOS CL Flow Cytometer in Evaluation of CD4 and CD8 in HIV Patients: CMCVAMC Experience
    Patel S, Wolf B, Jhala D
    American Journal of Clinical Pathology, Volume 150, Issue suppl_1, 21 September 2018, Pages S70, https://doi.org/10.1093/ajcp/aqy093.170

Efficiently manage your high

volume routine applications

with AQUIOS CL,  which enables

automation of your most

routine, repetitive tasks.

FLOWC_HIV CD4 London health Sciences AQUIOS - Section 7

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HIV Advanced Disease Management Solutions

HIV Advanced Disease Management Solutions

Monitoring CD4 lymphocyte counts is essential in providing critical information that impacts patient care. CD4 monitoring allows caregivers to know when the disease transforms and stage its progression so they can implement the most appropriate intervention.. 

Error Prevention and Quality Control with AQUIOS CL ​

The AQUIOS CL system employs several features that work to prevent errors during quality control. These prevention methods can be broken down into the following:

Automatically Pause when QC Fails 

QC Checks  - Daily QC (Controls) & Real Time QC (Patient Sample)

Error Prevention and Worklist Generation with AQUIOS CL

The AQUIOS CL system employs several features that work to prevent errors during startup, cleaning, and worklist generation. These prevention methods can be broken down into the following:


Test Requests to and from the LIS

Creating Worklists 

Error Prevention and Sample Preparation with AQUIOS CL ​

The AQUIOS CL system employs several features that work to prevent errors during sample prep. These prevention methods can be broken down into the following:

Flow Cell Clogging Prevention
Reducing Tandem Dye Degradation/ Evaporation/ Condensation
Absolute Counting
Plus others