HC Deb 26 February 2002 vol 380 cc1071-2W
Dr. Murrison

To ask the Secretary of State for Health what assessment he has made of the impact on waiting lists of the implementation of the advice on prion transmission by the Spongiform Encephalopathy Advisory Committee. [32783]

Yvette Cooper

The move to single use instruments for tonsil and adenoid surgery in January 2001 was part of the Department's strategy to reduce the theoretical risk of transmitting variant Creutzfeldt Jakob Disease (vCJD) through surgical instruments. The Spongiform Encephalopathy Advisory Committee (SEAC) advised that single use instruments be considered for tonsil and adenoid surgery as part of this strategy "provided patient safety would not be compromised".

An initial shortage of single-use instruments led to the number of patients waiting for tonsil and adenoid surgery rising between January and June 2001, however the waiting list has fallen each month since June 2001. The number of patients waiting over 18 months for tonsil and adenoid surgery peaked in July 2001 at 206, but this figure had reduced to eight by November 2001.

Following the increase in provision of single use instruments in June 2001 the Medical Devices Agency Adverse Incident Centre received reports of adverse events with their use in tonsil and adenoid surgery. This included an increase in primary and secondary bleeding that required re-hospitalisation, return to theatre and blood transfusion. In the interests of patient safety and taking account of the improvement in central sterile services in hospitals to decontaminate instruments, it was decided to advise surgeons to use reusable instruments. As a result of this action on 14 December 2001, we expect all tonsillectomy and adenoidectomy patients to be treated within the 18 month maximum in-patient waiting time guarantee.