Gisborne Hospital Report - Health and Disability Commissioner
Gisborne Hospital Report - Health and Disability Commissioner
Gisborne Hospital Report - Health and Disability Commissioner
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<strong>Gisborne</strong> <strong>Hospital</strong> 1999 – 2000<br />
PSA Testing Procedures<br />
to allow more in-depth review of laboratory st<strong>and</strong>ards, <strong>and</strong> a closer monitoring<br />
of claimed improvements by the provider in the quest for re-registration.<br />
Communication<br />
8.12 Communication between all levels of management <strong>and</strong> technical staff must be<br />
improved. This is perhaps the key recommendation to ensure that the<br />
biochemistry section of the laboratory provides a reliable service on an<br />
ongoing basis. Problems will recur if there is a continuation of the<br />
dysfunctional relationship evident in the past.<br />
Reagent / Calibrator / Control Supplies<br />
8.13 Reagent suppliers (not just Abbott Industries) should put checking systems in<br />
place that ensure that calibrators being sent to a laboratory match the type of<br />
reagent kitset normally supplied to that laboratory. Questions should be asked<br />
if it is not obvious from the order form why the laboratory is deviating from its<br />
normal ordering pattern.<br />
8.14 The laboratory also needs to put a checking system in place so that all<br />
reagents, calibrators <strong>and</strong> controls are confirmed <strong>and</strong> signed off by a senior<br />
technologist as being the correct items before they are made available for use<br />
in the laboratory.<br />
Response to recommendations<br />
8.15 Tairawhiti District <strong>Health</strong> has accepted all the above recommendations <strong>and</strong> has<br />
either already implemented them or is in the process of doing so. The<br />
exception is recommendation 8.13 as Tairawhiti District <strong>Health</strong> believes it is<br />
“an impractical requirement for a reagent supplier <strong>and</strong> that systems should be<br />
in place in laboratories that would make such a procedure unnecessary”.<br />
IANZ<br />
8.16 THL viewed IANZ as the “primary watchdog for community safety” through<br />
its accreditation <strong>and</strong> assessment processes. I believe this view would be<br />
shared by other public hospitals <strong>and</strong> by many in the health sector, including<br />
government agencies. It has become clear in the course of my investigation<br />
that, in light of IANZ’s limited statutory role, this confidence may be<br />
misplaced. I recommend that the Minister of <strong>Health</strong> review the current<br />
regulatory framework (including the Testing Laboratory Registration Act<br />
1972) in order to ensure that consumers are adequately protected.<br />
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