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BS EN ISO 23500-1:2019

$215.11

Preparation and quality management of fluids for haemodialysis and related therapies – General requirements

Published By Publication Date Number of Pages
BSI 2019 96
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1.1 General

This document is the base standard for a number of other standards dealing with water treatment equipment, water, dialysis water, concentrates, and dialysis fluid (ISO 23500 series) and provides dialysis practitioners with guidance on the preparation of dialysis fluid for haemodialysis and related therapies and substitution fluid for use in online therapies, such as haemodiafiltration and haemofiltration. As such, this document functions as a recommended practice.

This document does not address clinical issues that might be associated with inappropriate usage of the water, dialysis water, concentrates, or dialysis fluid. Healthcare professionals involved in the provision of treatment for kidney failure should make the final decision regarding the applications with which these fluids are used, for example, haemodialysis, haemodiafiltration, high-flux haemodialysis, and the reprocessing of dialysers, and need to be aware of the issues that the use of inappropriate fluid quality raises in each of the therapies.

The concepts incorporated in this document should not be considered inflexible or static. The recommendations presented here should be reviewed periodically in order to assimilate increased understanding of the role of dialysis fluid purity in patient outcomes and technological developments.

1.2 Inclusions

This document addresses the user’s responsibility for dialysis fluid once the equipment used in its preparation has been delivered and installed.

For the purposes of this document, dialysis fluid includes:

  1. dialysis water (see 3.17 for definition) used for the preparation of dialysis fluid and substitution fluid,

  2. dialysis water used for the preparation of concentrates at the user’s facility,

  3. concentrates,

  4. the final dialysis fluid and substitution fluid.

The scope of this document includes

  1. the quality management of equipment used to treat and distribute water used for the preparation of dialysis fluid and substitution fluid, from the point at which municipal water enters the dialysis facility to the point at which the final dialysis fluid enters the dialyser or the point at which substitution fluid is infused,

  2. equipment used to prepare concentrate from powder or other highly concentrated media at a dialysis facility, and

  3. preparation of the final dialysis fluid or substitution fluid from dialysis water and concentrates.

NOTE Because water used to prepare dialysis fluid can also be used to reprocess dialysers not marked intended for single use, this aspect of water use is also covered by this document.

1.3 Exclusions

This document does not apply to sorbent-based dialysis fluid regeneration systems that regenerate and recirculate small volumes of dialysis fluid, systems for continuous renal replacement therapy that use pre-packaged solutions, and systems and solutions for peritoneal dialysis.

PDF Catalog

PDF Pages PDF Title
2 National foreword
4 European foreword
7 Foreword
8 Introduction
9 1 Scope
1.1 General
1.2 Inclusions
10 1.3 Exclusions
2 Normative references
3 Terms and definitions
17 4 Quality requirements
4.1 General
4.2 Dialysis water
4.2.1 General
4.2.2 Chemical contaminants in dialysis water
19 4.2.3 Organic Carbon, pesticides and other chemicals
4.2.4 Microbiological contaminants in dialysis water
20 4.3 Requirements for concentrate
4.3.1 Chemical and microbiological contaminants in concentrate
4.3.2 Water used to prepare concentrate
4.4 Requirements for dialysis fluid
4.4.1 General
21 4.4.2 Microbiological requirements for standard dialysis fluid
4.4.3 Microbiological requirements for ultrapure dialysis fluid
4.4.4 Microbiological requirements for online-prepared substitution fluid
4.5 Record retention
22 5 Critical aspects of system design
5.1 General
5.2 Technical aspects
23 5.3 Microbiological aspects
24 5.4 Environmental impact
6 Validation of system performance
6.1 General
25 6.2 Validation plan
6.3 Installation and operational qualification
26 6.4 Performance qualification
6.5 Routine surveillance and revalidation
27 7 Quality management
7.1 General
7.2 Surveillance of fluid quality
7.2.1 Surveillance of dialysis water quality
28 7.2.2 Surveillance of concentrate quality
7.2.3 Surveillance of dialysis fluid quality
7.3 Surveillance of water treatment equipment
7.3.1 General
7.3.2 Surveillance of sediment filters
29 7.3.3 Surveillance of cartridge filters
7.3.4 Surveillance of softeners
7.3.5 Surveillance of carbon media
30 7.3.6 Surveillance of chemical injection systems
7.3.7 Surveillance of reverse osmosis
32 7.3.8 Surveillance of deionization
7.3.9 Surveillance of endotoxin-retentive filters
7.4 Surveillance of dialysis water storage and distribution
7.4.1 Surveillance of water storage tanks
7.4.2 Surveillance of the water distribution systems
33 7.4.3 Surveillance of bacterial control devices
7.5 Surveillance of concentrate preparation
7.5.1 Surveillance of mixing systems
34 7.5.2 Surveillance of additives
7.6 Surveillance of concentrate distribution
7.7 Surveillance of dialysis fluid proportioning
8 Strategies for microbiological control
8.1 General
35 8.2 Disinfection
8.2.1 General
8.2.2 Microbiological aspects of fluid system design
36 8.2.3 Disinfection frequency
37 8.3 Microbiological surveillance methods
8.3.1 General
8.3.2 Sample collection
38 8.3.3 Heterotrophic plate count
40 8.3.4 Bacterial endotoxin test
8.3.5 Determination of yeast and mould
9 Location of and access to the water treatment system
10 Personnel
41 Annex A (informative) Rationale for the development and provisions of this document
46 Annex B (informative) Equipment
64 Annex C (informative) Surveillance guidelines for water treatment equipment, distribution systems, and dialysis fluid
69 Annex D (informative) Strategies for microbiological control
76 Annex E (informative) Validation
79 Annex F (informative) Special considerations for home haemodialysis
85 Annex G (informative) Special considerations for acute haemodialysis
90 Bibliography
BS EN ISO 23500-1:2019
$215.11