BBC Science Focus

HELEN GLENNY

Electrocon­vulsive therapy has a reputation as a violent – even barbaric – treatment for mental illness.But with clinics gradually closing nationwide, is the UK losing a life-saving therapy?

- by HELEN GLENNY

Electrocon­vulsive therapy is shrouded in controvers­y and misunderst­anding. Science writer Helen explains why it might be time to rethink this potentiall­y life-saving therapy.

On a cold Monday in May 2010, Karen escaped, in a panic, from her room in a Birmingham hospital’s psychiatri­c ward. She arrived at a motorway flyover. Looking down, she watched the traffic, plotting for the perfect time to jump. The flashbacks had become too much. “My only purpose was to end my life,” she recalls. “I did not want to be here.”

Karen’s descent into severe depression had started six months earlier, when her husband had been diagnosed with a life-threatenin­g heart condition and she had dedicated herself to supporting him and their three kids. Her partner recovered and returned to work, but Karen began to struggle psychologi­cally, and in the months that followed she isolated herself from her friends, became anxious and eventually stopped eating. After losing a dangerous amount of weight, Karen saw a psychiatri­st, who admitted her to hospital.

Everyone thought the stress of her husband’s illness was the sole cause of Karen’s downward spiral, but it wasn’t that simple. “Things came back that I’d been burying,” she says. “I wasn’t able to bury them any more.” During an appointmen­t with her psychiatri­st in hospital, Karen spoke for the first time about a traumatic event from her childhood. When she was 14, she had been raped by a stranger on her way home from a friend’s house. “I didn’t tell anybody about it. It was a form of self-protection: if I didn’t

talk about it, it hadn’t happened,” she says. After that revelation, flashbacks plagued her. “It was like going through it all over again, what I could feel, what I could see, what I could hear,” says Karen. A week after that meeting with her psychiatri­st, she took a step up onto the flyover’s protective metal railing, ready to jump. Within seconds, two passing drivers pulled over, got out of their cars, and prevented her from jumping for long enough for the police to arrive and take her back to hospital.

BEYOND THE SHOCK

In the past year, more than 18,000 people have been hospitalis­ed in the UK with depression. Many of those people have a severe, treatment-resistant form of the illness, meaning they haven’t had any success with the usual treatments, like psychother­apy and antidepres­sants.

Some UK psychiatri­sts choose to offer these patients a treatment that’s clouded in stigma and believed by many to be barbaric and

abusive: electrocon­vulsive therapy, or ECT. In 2016-17, around 1,700 people received ECT in England, Ireland, Wales and Northern Ireland. During the treatment, an electric current is passed through a patient’s brain to induce a seizure. Proponents of ECT claim that it is the fastest acting and most effective treatment for severe depression, and argue that the stigma prevents patients from receiving a potentiall­y life-changing therapy. One of those psychiatri­sts was looking after Karen in December 2010, seven months after her first suicide attempt, and saw the possibilit­y of an effective treatment when nothing else she had tried had helped.

A modern ECT session, says Prof George Kirov, a psychiatri­st at Cardiff University’s School of Medicine, goes like this: an anaestheti­st inserts a thin tube in the back of the patient’s hand and administer­s both muscle relaxants and a general anaestheti­c, which puts the patient to sleep. An ECT nurse squeezes conductive gel onto a pair of electrodes and holds one to each of the patient’s temples. Another member of the team then sets the level of the electrical current, and pushes a button. Current pulses briefly through the electrodes, eliciting a seizure that lasts between 15 and 40 seconds. Prof Rupert McShane, a consultant psychiatri­st at Oxford Health NHS Foundation Trust, explains that the muscle relaxants keep the patient mostly still. “Usually you can see some muscle twitching, but we use an electroenc­ephalogram [which monitors brain activity] to see that the patient is having a fit.”

The procedure is surprising­ly quick. The patient wakes up a couple of minutes after their seizure finishes, and they are taken to a supervised recovery room. When they feel up to moving, they are offered a drink and some food. They’ll do this twice a week, for around six weeks.

After Karen’s first session, in December 2010, she woke up to “the worst headache of my life”, she says. Other patients report becoming confused and needing time to remember where they are. During the weeks of treatment, patients often experience memory loss; for the majority, this resolves itself in the months after treatment finishes.

After her fourth session, Karen went back to her ward and asked for a drink. This was a big deal for two reasons. Karen had lost any interest in eating or drinking over the preceding weeks – now she was doing it voluntaril­y. She had also chosen to speak to someone – another rarity. With each session she felt progressiv­ely better, and eventually started eating on her own. “It felt like there wasn’t something heavy on me any more,” she says. Karen stopped after nine sessions, and her psychiatri­st discharged her a few weeks later, in February 2011.

THE SCIENCE

What was going on in Karen’s brain that made her feel better so quickly? No one knows, exactly. What we do know is that the seizure is key: the better the seizure – gauged by certain

qualities on the EEG – the greater the improvemen­t. Researcher­s have found several possible pathways that could be involved (see box, overleaf).

Karen’s rapid response was not unusual, however. In 2004, results from one of the largest ever ECT studies were published in the Journal Of Clinical Psychiatry. The study looked at 253 patients with major depressive disorder, and found that threequart­ers of them reached remission after receiving ECT. In this context, remission can mean that mute patients start speaking, or catatonic patients start moving. Suicidal thoughts might recede, and patients may begin to engage with long-term therapy. McShane says that, for people with severe depression, those rates of improvemen­t are considerab­ly better than for antidepres­sants. But ECT research isn’t without controvers­y.

Clinical psychologi­st Dr John Read at the University of East London points out that no placebo-controlled study of ECT has been published since 1985, and those published before then were of “questionab­le methodolog­ical quality”. Without trustworth­y placebo-controlled studies, he says, any positive ECT results could simply be due to a placebo effect. In contrast, McShane says that the pre-1985 studies have already proved ECT’s effectiven­ess, and cautions against repeating those studies: “It would be unethical to take a group of people with depression and treat half of the sample with an ineffectiv­e, sham treatment.”

Read also has concerns that the effect of ECT doesn’t last, and claims there has never been a long-term follow-up study in which ECT outperform­s a placebo. And indeed, Kirov notes that in his clinic, and in others in the UK, about half of patients become unwell again within a year. This is even with the help of antidepres­sants, psychother­apy and what’s called ‘maintenanc­e ECT’, where the patient continues with ECT, but with decreasing frequency. Kirov says that relapse is ECT’s biggest problem. “They get back into depression. Not necessaril­y to the same level, but they go back.” And if relapse is the main problem with ECT, then side effects are certainly the second.

In 2011, the late actor Carrie Fisher wrote about her experience with ECT in her memoir Shockaholi­c. But her mostly positive account came with a caveat: “the truly negative thing about ECT is that it’s incredibly hungry and the only thing it has a taste for is memory”.

ECT interferes with memory, both anterograd­e (the laying down of new memories), and retrograde (recalling things from the past). Anterograd­e memory problems usually resolve themselves a few months after finishing treatment, but for some individual­s – 13 to 55 per cent of people, depending on which study you read – retrograde memory loss can be permanent. Kirov says that for these people, continuing becomes a personal choice: “Some of them are disturbed by their memory problems and decide to stop.” Karen experience­d retrograde memory loss, though it has improved since finishing treatment. “I couldn’t remember things, like what we did on holiday, and that was quite frustratin­g. But I didn’t like being unwell, so there was a trade-off.”

REPUTATION PROBLEMS

Historical scars also mar ECT’s reputation: early applicatio­ns didn’t use muscle relaxants, so it produced violent seizures where patients occasional­ly broke bones. Ken Kesey’s 1962

“EARLY ECT DIDN’T USE MUSCLE RELAXANTS, SO IT PRODUCED VIOLENT SEIZURES”

book One Flew Over The Cuckoo’s Nest, and the 1975 movie, depicted ECT as a form of behavioura­l control for psychiatri­c patients, perhaps an accurate portrayal of certain hospitals back in the 1950s. And in the 1980s, ECT was used as a ‘treatment’ for homosexual­ity. This practice didn’t last, but it still remains etched in cultural memory.

The use of ECT is declining in the UK, according to the latest report by the ECT Accreditat­ion Service. “Its portrayal in movies has been profoundly stigmatisi­ng, and has misreprese­nted current practice,” says McShane. He argues that a lack of knowledge around severe depression means the costs and benefits of the treatment cannot be accurately weighed up. “That discussion often omits the severity of the illness. ECT causes side effects, but so does chemothera­py.” He says that if the public were more aware of the reality of being severely mentally unwell, they might be more accepting of the treatment – “but those patients often don’t want to talk”.

Stigma can affect doctors as well as patients. According to Kirov, most psychiatri­sts who object to ECT haven’t actually seen it used. To counter misinforma­tion, he encourages every medical student to observe ECT. But he isn’t sure what to do for the public. “It’s hard to change public opinion. People have heard too many bad stories,” he says.

To make matters worse, ECT has become a proxy for a longargued question: is depression a medical problem, or a social one? Read, who’s critical of ECT, argues the social side, saying that ECT is the most extreme example of the over-medicalisa­tion of human distress: “It’s not an appropriat­e response to a social problem.” He calls for more work on population-wide wellness, and improved access to a range of psychologi­cal therapies and social support. McShane insists that ECT patients “are generally either too ill to make use of psychother­apy, or have already tried it without success”.

BRIGHT FUTURE

In the end, Karen needed both ECT and psychother­apy. Her return to health was difficult. She relapsed a few months after her first course of ECT, falling back into severe depression. “I was reliving [the trauma] all the time. I started hearing him constantly talking to me, and I could feel him touching me.” By February 2012 she was back in a psychiatri­c unit, sectioned after another suicide attempt. She spent a year and a half trying various other therapies, before starting her second round of ECT in August 2013. At that time, Karen was too unwell to give consent herself, but her family fought for her to receive it.

After three sessions, Karen became calmer. “I had lots of input from then on,” she says. Karen was assigned a new psychologi­st, who guided her through psychother­apy during her ECT. She continued with the ECT, gradually reducing its frequency, until she was having just one session every three weeks. In September 2014, she was discharged, and in 2015 decided to stop ECT completely. “I’d got to a point with therapy where I was processing what had happened to me,” she says. In 2016, after three years of therapy, Karen decided to stop that too. She doesn’t regularly see doctors any more, and says that life is finally back to normal for her.

What would have happened if ECT wasn’t an option? “I don’t think I’d be here,” she says. She cautions that while ECT certainly isn’t for everyone, “there is a role for it. Banning it would be like removing a lifeline.” by HELEN GLENNY Helen is a freelance science and travel journalist, with a background in neuroscien­ce and physiology.

DISCOVER MORE

Watch short films and read articles about mental health from the BBC Three series Minds Matter. bit.ly/bbc_mind_matters If you have been affected by any issues raised in this article, there is help and advice available here: bit.ly/mental_health_support If you are concerned about the mental health of you or a loved one, please visit your GP.

“THERE IS A ROLE FOR ECT. BANNING IT WOULD BE LIKE REMOVING A LIFELINE”

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