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Plasma is known as liquid gold, not just because of its colour. (Image: The Spinoff)
Plasma is known as liquid gold, not just because of its colour. (Image: The Spinoff)

SocietyAugust 20, 2024

‘This is what you can do’: Behind the scenes of our dwindling plasma supply

Plasma is known as liquid gold, not just because of its colour. (Image: The Spinoff)
Plasma is known as liquid gold, not just because of its colour. (Image: The Spinoff)

Only around 17,500 people across the country donate plasma regularly. It’s not enough and our needs are growing. Gabi Lardies investigates.

Four people recline on tan leather seats. You could be mistaken for thinking they were enjoying the advanced technology of massage chairs, were it not for the thin tubes taped to the inside of their elbows and threaded through the complicated faces of bulky plastic machines, almost as tall, and wider, than me. 

One man lies back with a book. On his right is a little plate with Squiggles and Toffee Pops biscuits stacked on top of cheese and crackers. A nurse fusses around his elbow. A bag about the size of a palm has filled up with his blood. It’s dark. This is a sort of overflow filter; it catches the first blood to leave the body, which is more likely to have some bacteria from the surface of the skin. This small bag will be used to thoroughly test the blood.

The blood pushes forward, coiling through the tubes and around the machine, making its way to a white cylinder, about the size of a toilet roll. Red soaks through a white filter. Here, it’s divided. Red blood is piped to a plastic container, and plasma – the golden liquid our red blood cells, white blood cells and platelets are suspended in – drips down into a bag. Once that bag reaches a certain weight (related to the man’s size), the red liquid in the plastic container will reverse its journey, returning to the donor.

When the donation is finished, all the tubing, needles and filters will be put into a hazardous waste bin to be incinerated. The donor will rest on a couch nearby for 15 minutes under the watch of a nurse. Then he will be on his way, his body already replenishing the plasma, and in two days his blood will be back to normal.

NZ Blood’s APS machines are less than a year old and make the process of giving plasma easier and faster. (Photo: Getty Images)

This man is one of around 17,500 people across the country who donate plasma regularly. It’s a much smaller figure than the 117,000-odd people on New Zealand Blood Services’ (NZ Blood’s) donor list, and even that is only about 4% of New Zealanders who are eligible to donate. It takes a little longer to donate plasma – an hour and a half all up, instead of an hour for donating blood – and plasma can’t be collected at mobile clinics, because those machines that separate the blood are heavy, delicate, and expensive. The plasma from whole blood donations is separated out later, but not as much can be collected. 

In 2012, New Zealanders were donating enough blood and plasma for our blood service to be completely self-sufficient. Today, we can meet the demand for red blood cells, platelets, and fresh plasma through donations within the country, but we are importing antibody concentrates or immunoglobulin, an important product made from plasma. We need about 250 more plasma donations a week to be self-sufficient again, and the need is growing by about 10% year-on-year. 

“Demand for red is pretty much flat, we kind of peaked about 10, 15 years ago,” says Richard Charlewood, a transfusion medicine specialist at NZ Blood. He’s been giving me a tour around NZ Blood’s Epsom centre, which has more big machines and fast-walking people wearing white lab coats than I’ve ever seen before. “The science came out saying the hospitals were over-transfusing – you don’t need to transfuse so many patients, and so, yeah, the number has eased off.”

Strict traceability procedures are applied to all donations. If something turns up during testing, all donations from a donor are locked down. (Photo: Gabi Lardies)

The opposite is true of plasma: demand is increasing. “Plasma is science-changing medicine,” he says. Over the past few decades, more and more uses have been found for biopharmaceutical products made from plasma. “It doesn’t appear that there’s going to be any sort of let up,” Charlewood adds. 

Plasma can currently be made into 11 treatments for cancer patients, trauma and burns victims, pregnant women (where they have a different blood type to their baby), auto-immune diseases, blood-clotting issues and compromised immune systems. The growing demand is driven by a growing need for immunoglobulins, antibodies made by our immune systems that protect us from bacteria and viruses. They are extracted from a healthy donor’s plasma and given to someone who cannot make their own, either because of disease or other treatments.

“Our favourite customers are the children in Starship’s oncology ward,” says Charlewood. After treatment wipes out the kids’ immune systems, immunoglobulins make up for it. Some patients, like those with auto-immuse disorders, may need immunoglobulins once a week for the rest of their life. Depending on their weight and illness, each dose could require the antibodies from 50 plasma donations.

Something happens when I ask Charlewood about self-sufficiency. He’s a tall man, with greying hair, but it’s like I’ve bought up a happy memory from childhood, a feeling he’s trying to capture again that’s almost in reach. He’d love for us to be self-sufficient again, and compared to other countries, we’re pretty close. He says we’re about 70-80% self-sufficient, while Australia is about 40% self-sufficient, and Canada is trying to get to 20%. 

The small percentage of plasma products we do import doesn’t look anything like the donated bags of plasma hanging from the machines. It’s already been processed into immunoglobulin, a clear liquid packaged in glass bottles in branded boxes. They’ve got the look of Big Pharma. Simple, white with black, sans-serif text, and just a triangle of colour in one corner. One of the products is called Privigen®. When the same product is made from our own plasma, it’s called Privigen® NZ.

We buy these plasma products from CSL Behring, an industrial-scale biopharmaceutical manufacturer in Australia. It’s the kind of place where “you could eat off the floor, but they wouldn’t let you,” says Charlewood, because obviously our mouths are full of nasties. That is also where our plasma goes to be made into Privigen® NZ and other products. 

tiny glass bottle of Normal Immunoglobulin-VF
Normal Immunoglobulin-VF, made from plasma, is given to give protections from of hepatitis A, measles and poliomyelitis for people whose immune systems cannot make their own antibodies. (Photo: Gabi Lardies)

On the day plasma is collected from donors in Aotearoa, it’s put into a big, stainless-steel cube. It’s a freezer that looks a lot like the dish sterilisers that grace almost every hospitality kitchen, and indeed this one was originally designed to freeze cakes at a cheesecake factory. “There’s a lot of repurposing from the food industry,” says Charlewood.

Once frozen, the bags of plasma are kept in a walk-in freezer at minus 30 degrees celsius or colder. When you walk in, you can feel the moistness in your nose get crispy, and glasses have to be taken off, as they’re instantly frosted. The bags accumulate for a month or so, on steel trolleys, until they’re sent to CSL. By that time, there will be about 10 tonnes of plasma. There, it’s pooled into huge vats and fractionated – divided by different processes into different parts. 

The quantities sound massive, but plasma is mostly made up of water, and “that goes out the window,” says Charlewood. The most common protein in plasma is albumin, the same stuff that makes up egg whites. This is bottled and used for burns patients and patients in intensive care to keep their blood pressure up. Then there’s clotting factor concentrates made for people with bleeding disorders (like Willebrand disease) and people on blood thinners who have had an accident. “What people most want,” though, Charlewood says, is the antibody concentrates like Privigen® NZ. For each bag of plasma, “we maybe get three grams, like, not even half a teaspoon” of antibodies, he adds.

Frozen plasma donations waiting to be sent to Australia for processing. (Photo: Gabi Lardies).
Though plasma is donated, processing it is very expensive. In a freezer at the Epson blood centre, plasma donations wait to be sent to Australia for processing. (Photo: Gabi Lardies)

It’s expensive to process plasma into these products. Charlewood says antibody concentrates are, on a gram for gram basis, more expensive than gold. That, along with its colour, is why plasma is known as “liquid gold”. On a per-capita basis, we are not high users of antibody concentrates, says Charlewood, perhaps because of its high cost. They’re administered carefully, only when there’s a high chance they will help someone.

The antibody concentrates that we import, for example Privigen®, are made identically, but with a different source of plasma. “The US collects a vast amount of plasma,” says Charlewood. Some of that is collected by a subsidiary of CSL Behring called CSL Plasma. The US plasma fractionation market was worth 15.64 billion USD in 2022 – considerably more than their natural gas exports, which are in the tens of millions. US plasma is “supporting most of the world, because very few countries are self-sufficient,” says Charlewood. 

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But the US will always support the US first. When less plasma was coming in during the Covid pandemic, Charlewood says suppliers made it very clear that if there wasn’t enough for all, it was “a USA-first policy”. He says that although we’re spending millions each year, we’re a comparatively small country and client – “so we would be dropped so quickly.”

There are plenty of ethical concerns around plasma gathered in the US. Unlike much of the rest of the world, people are paid for their plasma. Collection centres – many with “CSL Plasma” in chunky red lettering on the buildings – are mostly set up in impoverished areas, including on the southern border with Mexico. Payments have been as little as US$10, and at times paid in liquor store vouchers. At the bottom of the billion-dollar industry are “the poorest of the poor,” says Charlewood.

photo of CSL plasma centre in the US
“If you look at where they put the clinic facilities, it isn’t in Bel Air,” says Richard Charlewood. (Photo: CSL Plasma in Davenport, Iowa by Farragutful via Wikipeidia).

On one front it’s working, since the US is providing lifesaving plasma to much of the rest of the world, including us. So should we pay people in New Zealand to encourage more donations here? Charlewood thinks not, because “that introduces more dangers.” Apart from the ethical considerations, when you dangle money in front of poor people for their plasma, they’re less honest about their medical conditions and lifestyle choices, because they need the money.

This is also true of replacement donor systems, where family or friends are required to donate the same quantity of blood that has been given to their loved one. It’s been proven that using plasma from altruistic donors means less diseases and other problems with the plasma. This is important because gathering, checking and processing it all is extremely expensive – and because we want the blood to be safe. 

Another issue is that if you make something a commodity instead of a gift, altruistic donors drop off. While the US may have heaps of plasma, they’re “quite short on fresh stuff,” says Charlewood, meaning whole blood donations. “They really live hand-to-mouth in that area.”

I am one of those bad people who have never given blood. I am not scared of needles. I meet the requirements most of the time. I have no excuses, only that it hasn’t seemed a pressing priority. When I ask friends and colleagues why they don’t donate blood or plasma, that’s the most common answer I hear. People are not opposed to donating, but they just don’t get around to it. We’re the 96% of possible donors who could make our blood service self-sustainable. 

“This is what you can do to help your community,” says Charlewood. “So many charities are always asking for a little bit of this and a little bit of that, and we can’t always help financially, or not everybody can. But this is one thing you probably can do.”

Today, I fail the eligibility test, because I travelled to South America just two months ago. But there’s still something I can do to get a taste of what it’s like to donate, and apparently it’s the worst part: a finger prick. Usually the prick is to make sure the donor has a good amount of haemoglobin, indicating they’ve got plenty of iron. For me, it’s to find out my blood type. 

Richard Charlewood, transfusion medicine specialist at NZ Blood, explains how children can have different blood types to their parents. This can sometimes be a problem during pregnancy.

“It’s not too bad, honestly,” says Sophie, a nurse who has set up a towel, some droppers and a little fan in a room called “Rangitoto”. She lifts a little pink device and a card with three circles on it from a plastic tub. She asks for my finger and places it under the pink thing. “One, two…” and it shoots, like a tiny ear-piercing gun.

“That is often the worst part,” she says. Apparently the inside of the elbow is less sensitive, and once the needle is in, you “really don’t feel it.” Blood beads at the site of the prick, and she suctions it up with the world’s tiniest straw. Then, she dabs the blood on the three circles on the card. 

Next, serum from the three droppers is mixed with the blood in each circle. In the first two circles, my blood mixes smoothly. In the last, it speckles. Speaking in simplified terms, each blood type corresponds to a different combination of speckles and smoothness. Sophie helps me decipher it on a chart. “O Positive,” I exclaim, truly surprised because my mum always told me I was either A or B, so O seems much more exciting. My dreams of blood donation swell. 

“It’s the most common blood type in New Zealand,” says Sophie. I deflate. I thought I was special. Sophie picks up on my disappointment, and quickly soothes me. “It’s the most needed, because about 30% of people in hospital needing blood are your same blood type,” she says. “People always want to be rare, but what we really want most of the time is O Positive.” I feel myself edging closer and closer to the donor list.

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Construction in an L-shaped block of Westmere and Point Chevalier is highly contentious.
Construction in an L-shaped block of Westmere and Point Chevalier is highly contentious.

SocietyAugust 19, 2024

Inside Westmere’s dwindling anti-cycleway movement

Construction in an L-shaped block of Westmere and Point Chevalier is highly contentious.
Construction in an L-shaped block of Westmere and Point Chevalier is highly contentious.

Occupy Garnet Road is still trying to keep its mission alive and kicking in a small pocket of Auckland. Lyric Waiwiri-Smith headed to a community meeting to find out if people still care.

Handmade signs provide little decoration for the Garnet Station theatre where no one under 30 (except me) has come to hear the Westmere community gripes. “Stop AT [Auckland Transport],” one sign reads, beside a sketch of Garnet Road’s four-way roundabout drawn with a sad face in the middle, then “Single lane roundabout maddness.” The spelling error gets a chuckle out of a few attendees. “That’s Lisa’s fault, isn’t it,” emcee Gael Baldock says. “She can’t spell.”

Veteran activist Lisa Prager, of sledgehammer fame, is one of the most vocal Occupy Garnet Road (OGR) members, often to her own detriment. She was arrested in 2018 after bashing a traffic island with a sledgehammer to protest a Grey Lynn cycleway, once chained herself to a digger and has equated her protest against the felling of trees to standing up to the Holocaust. She spearheaded OGR’s mission in 2017, after occupying a roundabout outside of her business in protest of a cycleway. But tonight, personal reasons have kept her at home, so her partner-in-crime Baldock heads the meeting alone at Garnet Station, a cafe owned by Prager and her partner Verity George.

The meeting was called for “Westmere shopkeepers, concerned Westmere locals, Waitematā local board area residents and Meola Road commuters”, but only 11 members of the public have shown up, including this reporter. Baldock chalks the “poor” turnout to the fact that the meeting was only called days ago, and her posters promoting the event were ripped off the streets. No shopkeepers are present, and when asked, Baldock declines to reveal the concerns they had apparently shared with her regarding the works. “I wouldn’t want you to print what I had said for them,” she tells me, despite speaking on their behalf for the entire meeting.

It’s the six-year-long war for Westmere’s roads, a fight boldly undertaken by a very select few against Auckland Transport, the council and anyone else who gets in their way. Tonight’s topics of discussion focus on Westmere and Point Chevalier’s cursed and contentious “L” connecting Meola Road, Garnet Road and Point Chevalier Road, which has been under construction for months, with improved floodplains, foundations, traffic speeds and landscaping promised by Auckland Transport. This particular pocket of Auckland is especially attractive for a new cycleway thanks to the 41% of students at the nearby Western Springs College who walk or cycle to school, a figure higher than most areas of Aotearoa, which may help bump cycling figures in Auckland up to the 17% AT is hoping for.

If you ask OGR and its supporters, the works have provided everything but an improvement to their daily commute. Baldock quotes herself from a New Zealand Herald article published six years ago before the “L” area construction began: “As I was quoted in the Herald, this will be a blood sandwich.”

Construction on Westmere’s Garnet Road.

She thanks her supporters despite the small turnout, telling us we must have been moved to back her after reading her latest column in the local magazine, Ponsonby News (she has copies to share in case we haven’t seen it). It’s a curious publication – somehow, Baldock (and often Prager) has her views published in almost every edition. 

Her recent column focuses on rat running, the practice of using residential streets rather than main roads and motorways to get from A to B, an apparently growing problem that is particularly bad through the nearby “bird streets”: Huia Road, Kiwi Road and Tui Street. It’s not illegal, though highly controversial, and if you ask Baldock, those guilty of it are just as conniving as her enemies at AT.

Unlike Ponsonby News, “The Spinoff” does not get you very far in this area of Westmere. “The Spinoff … they’re big fans of all of this, aren’t they?” One suspicious local at the meeting asks me. In an attempt to ease the tension, I reply: “I don’t think anyone’s a big fan of road works.” He shakes his head. “I mean, a big fan of what this all means.” If only he could spend a day in The Spinoff office listening to the whinging of the staffers who live in the inner west and hate the traffic as well.

What this all means is more cycleways for Westmere, meaning more headaches for these residents. They represent the Nimbys of their neighbourhood, but they do have genuine concerns about the roads here and in neighbouring suburbs. One woman describes the road works as a “nightmare”, another is concerned Meola Road has become too dangerous to use and someone else is sick of cars using her street to avoid congestion. A man from Rock The Vote (which was part of the Brian Tamaki-founded Freedoms New Zealand alliance at the last election), wearing a branded baseball cap, worries AT is becoming “very anti-car” and threatens to put candidates forward for the next local body election to stop them. Another woman in the crowd is unimpressed by his speech: “But what are you actually going to do?”

A picture of Meola Road in its current closed form.
Meola Road construction in January (Photo: Dempsey Wood Civil Limited/Auckland Transport)

Baldock has myriad reasons to oppose cycleways, too. She believes construction could ruin local businesses, the roads are no longer safe, it costs too much and the design is crap because she didn’t make it (she often references her background in “design and architecture”, though she is better known as an artist). To top it off, she’s very sure no one will be using those cycleways anyway. “There’s one group of cyclists that want a cycleway,” Baldock says, “and it’s the people who don’t wear helmets and have normal clothes.”

Baldock tells the crowd she went down to watch the traffic on Meola Road on a Friday afternoon after the final school bell, and was shocked to see that a mere 12 rangatahi were using the cycleways. She says this minuscule number of children is proof that no one really wants or uses the cycle lanes – though if that were true, the numbers at this meeting would suggest that even fewer people care enough to fight them.

Over an hour in and no resolution recognised, a couple get up to leave, and another woman starts filing her nails. I wonder if it would be rude for a reporter to Irish exit a community meeting early – I really want to go to Westmere Roast for dinner before it’s too late. I get up, Baldock announces “the journalist is leaving”, and before I can get out the door, the local with The Spinoff suspicions asks me where I’m based. My cover is blown: I live in Parnell.

Getting up to leave, Baldock asks me not to go before I share my own thoughts on cycleways. It’s not really the function of an objective journalist, but the anti-Spinoff man is watching me with piqued interest. I tell her I recall working in hospitality on Karangahape Road during the cycleways construction in 2019, how the road works impacted foot traffic, and that I understand her concerns that businesses could go under. This sends her off on another spiel, and after standing there and letting her talk at me for a few minutes, I slip out the door.

Westmere is chillingly cold, and Baldock’s last-minute questioning has made me lose my appetite for dinner. Traffic was relatively slow moving along the Garnet Road shops when I was making my way here around 6pm due to cycleway construction, and though it may be slightly annoying, it was smooth sailing the rest of the way, past a blinking road sign advertising that businesses were still open. Now, the streets are almost completely silent, and it takes less than 15 minutes to drive back to Parnell, through a bit of my own neighbourhood construction and traffic. In the grand scheme of things, it could be worse.

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