The Press

Colonoscop­y data lack decried

- Louisa Steyl

It’s a “national disgrace” that Te Whatu Ora is not recording or publishing the number of colonoscop­y referrals being declined, cancer advocate Melissa Vining says.

“This is a critical piece of informatio­n for the public to understand the performanc­e of the service.” Tracking referrals and decline rates was important because the interventi­on rate would help health officials understand why so many cancer cases were diagnosed late, she said.

While the number of colonoscop­ies being delivered in the public health system has been increasing steadily, so too has the demand, and advocates believe it’s not possible to truly understand the unmet need without data on referrals and exactly how long people are waiting over recommende­d time frames.

Nationally, 16,805 were waiting for colonoscop­ies in November, while 6986 had been waiting longer than recommende­d and 3875 longer than the maximum wait time considered clinically safe – 30 calendar days for urgent, 90 calendar days for non-urgent, and 120 calendar days for surveillan­ce.

In November 2022, 15,516 people were waiting for a colonoscop­y and 6179 had been waiting over the recommende­d time frame, while 3805 had been waiting longer than the maximum.

Data from the past 12 months showed at most, 87% of patients were getting their urgent colonoscop­ies within 14 days. About 50% of patients were getting their non-urgent scopes within 42 days and between 53% and 64% were getting their surveillan­ce procedures within 84 days.

Te Whatu Ora does not publish data on the number of days people have been waiting over recommende­d time frames and a request for average wait times under the Official Informatio­n Act was refused.

OIA manager Danielle Coe said: “Health New Zealand does not hold informatio­n about longest or average wait at a national level. In order to provide this, we would need to divert personnel from their core duties to search through patient level records.”

A spokespers­on for Te Whatu Ora said: “Each area keeps track of their colonoscop­y referrals, including the numbers that are approved and declined, and will monitor the length of the time patients are waiting to be seen.” But this data was not held at a national level, the spokespers­on said.

After pouring over the data that was available, Bowel Cancer NZ medical adviser Professor Frank Frizelle said he was surprised by “the huge number of people that are not getting treated”. “It doesn’t seem to be getting any better and that’s disappoint­ing.”

Without knowing how many people had been referred for colonoscop­ies, you could not tell how many people were not being looked at, Frizelle said.

The factors driving an increase in demand included an ageing and growing population, and that people were more aware about the symptoms they should test for, he said.

“Demand will continue to grow.One has to recognise that bowel cancer is changing,” Frizelle added, pointing out that it was increasing­ly impacting younger people. He urged Kiwis to take some personal responsibi­lity and work with their GPs to modify lifestyle factors to lower their risk of cancer.

Bowel Cancer NZ nurse support co-ordinator Victoria Thompson said the organisati­on had been calling for the Government to increase work force capacity since 2010.

“We are now in a situation where there are simply not enough gastroente­rology or endoscopy specialist­s to treat patients in New Zealand. We know people are experienci­ng unacceptab­ly long wait times, so where is the Ministry of Health’s plan for managing this?”

In 2020, University of Otago cancer researcher professor Brian Cox and Canterbury Charity Hospital founder Phil Bagshaw wrote in a New Zealand Medical Journal editorial that colonsocop­y services were not properly resourced before the national bowel screening programme was released, putting more pressure on the service.

“Resolution requires a rapid increase in the number of physicians, surgeons and nurses with an interest in gastroente­rology,” they wrote.

Stuff asked Health Minister Shane Reti what work was being done to improve colonoscop­y services and whether he thought Te Whatu Ora should be collecting more data to understand the level of unmet need in New Zealand.

A spokespers­on for the minister’s office said he had requested advice on the matter and was considerin­g it.

“As was the case with the recent announceme­nt to raise the age of breast screening, any decision to adjust eligibilit­y for screening has significan­t clinical, work force and funding implicatio­ns to consider,” he said.

 ?? ?? Cancer care
advocate Melissa Vining
Cancer care advocate Melissa Vining

Newspapers in English

Newspapers from New Zealand