University study identifies key cancer factors

Professor of Population Health at the University of Waikato Ross Lawrenson. Photo: Supplied

 

The leader of two three-year studies says that New Zealand continues to have poor cancer outcomes compared to other developed countries.

 

“A big factor in our poor performance is that patients with both lung and bowel cancer tend to present with advanced disease,” says Professor of Population Health at the University of Waikato, Ross Lawrenson.

 

Released on Friday, the findings of two University of Waikato health research projects have identified the critical role of primary care in improving outcomes for New Zealanders with cancer.

 

Funded by the Health Research Council, one project looked at how to reduce delays in the diagnosis of colorectal cancer, while the other investigated ways to improve early diagnosis of lung cancer among Maori and rural communities.

 

Both studies have determined access to primary care is a key factor in avoiding late diagnosis, as well as reducing inequities for Maori.

 

“Our research looked at the patient pathway from diagnosis to treatment, to identify and address the barriers to people accessing care," says Lawrenson.

 

Waikato University research identifies crucial role of primary care in improving outcomes for cancer patients.

 

The studies were conducted over three years in the Midland Cancer Region which comprises Waikato, Lakes, Bay of Plenty and Tairawhiti DHBs – although Lawrenson says the findings are applicable at a national level.

 

Research into the late diagnosis of lung cancer among Maori communities identified several barriers preventing Māori from accessing primary care.

 

These include the mounting costs of multiple appointments, symptom ambiguity and the importance of trust and understanding between Māori patients and their GPs.

 

“What became clear is the need for culturally safe care and a workforce that understands the needs of Maori patients and whanau,” says Lawrenson.

 

“Our research also clearly showed the importance of whanau as carers and advocates for Maori lung cancer patients.”

 

Lawrenson said that with lung cancer mortality rates three to four times higher for Maori than non-Maori, intervention was critical. Working with local communities, the research team developed a Ha Ora website for resources and self-help, alongside other interventions including lung cancer awareness videos and a kaiawhina training programme to help upskill health staff.

 

Research into colorectal cancer also identified inequities for Maori, who are more likely to experience greater delays in diagnosis and less likely to receive a colonoscopy than non-Maori.

 

“There needs to be a concentrated effort to ensure equity for Maori in the national bowel screening programme, as well as in general access to diagnosis and treatment,” says Lawrenson.

 

Also among their findings was the need to increase public awareness of symptoms of colorectal cancer.

 

“Bowel cancer can be difficult to diagnose. We need greater awareness of symptoms for both patients and GPs,” says Lawrenson. “If we want to improve outcomes, there needs to be more investment in primary care, and I think we need to take a hard look at our systems to ensure there’s equal access to care for everyone.”

 

The report ‘Reducing delay and increasing access to early diagnosis for colorectal cancer’ was authored by Ross Lawrenson, Tania Blackmore, Chunhuan Lao, Lynne Chepulis, Mark Elwood, Tim Stokes, Jon Emery, David Weller, Jacquie Kidd, Melissa Firth, Christopher Jackson, Rawiri Keenan, Brendan Hokowhitu, Ralph van Dalen, Judith Warren, and Lyn Hunt.

 

The report ‘Hā Ora: Improving access to early diagnosis of lung cancer for Māori and rural communities’ was authored by Ross Lawrenson, Shemana Cassim, Jacquie Kidd, Anna Rolleston, Rawiri Keenan, Brendan Hokowhitu, Melissa Firth, Denise Aitken, Janice Wong, Lynne Chepulis, Chunhuan Lao, Paul Conaglen, Karen Middleton, and Lyn Hunt.

 




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3 Comments

Tom Ranger

Posted on 11-03-2021 13:15 | By Tom Ranger

Well...Public HC is crap imo. Private is the way to go. For most maori especially in rural area’s...They cannot afford private health insurances etc. Good luck to anyone getting up that public waiting list. Maori or not. So it’s not really an even playing field here... When speaking about health...poor people come out worse than full-time workers. Many maori are financially poor. Many others are financially poor as well. They are in the same position.

@Yadick

Posted on 08-03-2021 15:39 | By morepork

You are right, of course. But the problem here is cultural, not physical. There IS a cultural difference between Maori Communities and non-Maori ones. Even though modern Maori can see past it and get treatment when they need it, there are still many Maori (especially older ones who are likely to be in this group) who distrust non-Maori health care, and, in fact, mistrust non-Maori in general. It will take time, but progress is being made. It would be easy for us to say: "Well, they’re shooting themselves in the foot." But that doesn’t help the situation. I agree with you that the word "inequity" was misused in the report; it is a choice that is made, but it is an ill-informed choice. We need to address it with proper information and education.

What Inequities?

Posted on 07-03-2021 12:37 | By Yadick

Research into colorectal cancer also identified inequities for Maori, who are more likely to experience greater delays in diagnosis and less likely to receive a colonoscopy than non-Maori. This has nothing whatsoever to do with Inequities. It is by choice and poor decision making. Maori have exactly the same health care opportunities afforded them as everybody else.

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