Australia invented surf life saving, pavlova, rotary clothes hoists, plastic bank notes and black box flight recorders. But now I want to concentrate on cochlear implants.
Bill and his identical twin were born (in 1944) in the British city of Devon, into a family of doctors. Their father was still fighting the war in France! Bill Gibson eventually decided he wanted to be a doctor, moving to study in London in the 1960s. Later, as a medical graduate, he specialised in London in otology-ear surgery. Gibson was eventually one of the top Ears, Nose and Throat consultants in the UK.
There was already a primitive version of the bionic ear available in Britain but it provided only a dot-dash sort of sound. Developing this into a multi-channel device that could convert sounds into electronic impulses that the brain could hear was progress.
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Bill knew about Australia’s Prof Graeme Clark's research into cochlear implants, work that was largely dismissed in the UK. In particular, Prof Graeme Clark and his team in Melbourne University’s Otolaryngology Department swere examining ways of using new technology to help deaf people. They focused on the cochlea, the part of the ear that passed sounds to the brain.
Understanding the potential of the Melbourne work, Gibson saw the opportunity to join his surgical skills to the device. The Gibson family emigrated to Australia. It was great that Prof Graeme Clark was very supportive of the recent British arrivals and it was great that Bill’s twin brother had already married an Australian.
In Australia, Julia Patrick noted, the Melbourne ENT hierarchy regarded Prof Clark as eccentric and his work futile; apparently they considered the idea of following speech without lip reading and signing to be silly. Fortunately the University of Sydney was open to individual research, so Gibson applied for, and accepted the first Professorship of Otolaryngology/ENT at Sydney University.
Encouraged by a small group of perceptive supporters at Sydney’s Royal Prince Alfred Hospital (spouse’s alma mater), Gibson received the green light to go ahead: two patients successfully received the first cochlear implants in 1984.
Surgically inserted in the ear of these two patients, the implants did not actually cure deafness; it was a prosthetic substitute for hearing that did the work of the damaged hair cells of the inner ear, the cochlea, to send sound signals to the brain. When it worked, there was a great excitement, seeing the joy on the face of deaf patients when they realised they were part of a hearing world.
There were inevitable failures as the medical teams learned more about distinguishing between patients who were suitable for implants and those who were not, but the profession noted clear progress. The device became compact and Gibson developed a way to implant it.
The first generation of recipients were people who had lost their hearing in adulthood, because they understood the concept of spoken communication. Gibson believed that while restoring hearing to adults was important, the focus should be on youngsters who had been deaf from birth and had never learned to speak. By the age of 7, their speech organs would have effectively atrophied.
By 1986 the cochlear team in Sydney had successfully carried out 20 implants for adults and Gibson was ready, willing and able to perform the surgery on congenitally deaf children. If they received an implant from 9-18 months of age, speech would naturally follow hearing. Gibson chose a four-year-old girl for an implant in 1987, which involved convincing medical regulators that the process was ethical and practical. She was the first paediatric recipient of the Australian-designed bionic ear in the world. This brave little girl learned to both understand and use speech.
When Dr Gibson controversially decided to implant cochlear devices in children, he received many letters criticising the plan. One group in particular, The Signing Deaf Group, believed that congenital deafness should not be seen as a disease to be cured. Instead the focus should be on signing, itself a valid alternative language.
Gibson’s goal was now to identify babies born deaf, allowing them to have an implant. With Gibson’s persuasion, NSW initiated a successful early-detection programme, now Australia-wide. With a cochlear implant, children born congenitally deaf could go to a regular school and lead the life of a normal child. Between 1984 and 2014, he performed the bionic ear operation 2000+ times!
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More recent progress
Dr Gibson helped establish Cochlear Implant Club and Advisory Association, a group that enabled implant recipients to meet regularly, providing support to each other and feedback to doctors. And to obtain funding for specialist facilities and post-op therapy.
The vital personal accounts of 40 of Professor Gibson’s patients are included in the Australian chapters of the biography. The book also considered the issues Dr Gibson experienced in establishing a top class cochlear implant programme, known today as the Sydney Cochlear Implant Centre. The twelve branches of the Centre were one of the many legacies of his career. Another success was the small incision he developed for cochlear implant surgery, to reduce wound breakdown to practically zero. Plus he advised a NSW Ministerial Committee on the best screening test to be used in hospital on new-born infants.
Prof Gibson is now overseeing research into the cause and cure for the debilitating Menière’s Disease. This condition of the ear has resisted medical knowledge since the condition was first identified in France in 1861 by Prosper Menière. Sydney now has the first laboratory in the world dedicated solely to Menière’s Disease Research.
How did the deaf communicate? Before the French priest Michel de l’Epée devised sign language in the C18th, the deaf were written off as useless citizens. For the first time, the priest had demonstrated that deaf people were no less intelligent than their peers. The C19th saw the creation of the world’s first hearing aids, based on Alexander Bell’s telephone. They were clumsy, and although there have been enormous improvements with time, hearing aids could not reproduce high frequencies - they could only amplify residual hearing. The result was that many deaf people continued to use sign language, combined with lip reading.
This was the situation until the early 1980s when Dr William Gibson became aware of the cochlear experiments. Now we need to read Bill Gibson: Pioneering Bionic Ear Surgeon written by Tina Allen, 2017.
This was the situation until the early 1980s when Dr William Gibson became aware of the cochlear experiments. Now we need to read Bill Gibson: Pioneering Bionic Ear Surgeon written by Tina Allen, 2017.
Bill and his identical twin were born (in 1944) in the British city of Devon, into a family of doctors. Their father was still fighting the war in France! Bill Gibson eventually decided he wanted to be a doctor, moving to study in London in the 1960s. Later, as a medical graduate, he specialised in London in otology-ear surgery. Gibson was eventually one of the top Ears, Nose and Throat consultants in the UK.
There was already a primitive version of the bionic ear available in Britain but it provided only a dot-dash sort of sound. Developing this into a multi-channel device that could convert sounds into electronic impulses that the brain could hear was progress.
Cochlear implant in a young child
photo credit: SCIC Cochlear Implant Programme, NSW
Bill knew about Australia’s Prof Graeme Clark's research into cochlear implants, work that was largely dismissed in the UK. In particular, Prof Graeme Clark and his team in Melbourne University’s Otolaryngology Department swere examining ways of using new technology to help deaf people. They focused on the cochlea, the part of the ear that passed sounds to the brain.
Understanding the potential of the Melbourne work, Gibson saw the opportunity to join his surgical skills to the device. The Gibson family emigrated to Australia. It was great that Prof Graeme Clark was very supportive of the recent British arrivals and it was great that Bill’s twin brother had already married an Australian.
In Australia, Julia Patrick noted, the Melbourne ENT hierarchy regarded Prof Clark as eccentric and his work futile; apparently they considered the idea of following speech without lip reading and signing to be silly. Fortunately the University of Sydney was open to individual research, so Gibson applied for, and accepted the first Professorship of Otolaryngology/ENT at Sydney University.
Encouraged by a small group of perceptive supporters at Sydney’s Royal Prince Alfred Hospital (spouse’s alma mater), Gibson received the green light to go ahead: two patients successfully received the first cochlear implants in 1984.
Surgically inserted in the ear of these two patients, the implants did not actually cure deafness; it was a prosthetic substitute for hearing that did the work of the damaged hair cells of the inner ear, the cochlea, to send sound signals to the brain. When it worked, there was a great excitement, seeing the joy on the face of deaf patients when they realised they were part of a hearing world.
There were inevitable failures as the medical teams learned more about distinguishing between patients who were suitable for implants and those who were not, but the profession noted clear progress. The device became compact and Gibson developed a way to implant it.
The first generation of recipients were people who had lost their hearing in adulthood, because they understood the concept of spoken communication. Gibson believed that while restoring hearing to adults was important, the focus should be on youngsters who had been deaf from birth and had never learned to speak. By the age of 7, their speech organs would have effectively atrophied.
By 1986 the cochlear team in Sydney had successfully carried out 20 implants for adults and Gibson was ready, willing and able to perform the surgery on congenitally deaf children. If they received an implant from 9-18 months of age, speech would naturally follow hearing. Gibson chose a four-year-old girl for an implant in 1987, which involved convincing medical regulators that the process was ethical and practical. She was the first paediatric recipient of the Australian-designed bionic ear in the world. This brave little girl learned to both understand and use speech.
When Dr Gibson controversially decided to implant cochlear devices in children, he received many letters criticising the plan. One group in particular, The Signing Deaf Group, believed that congenital deafness should not be seen as a disease to be cured. Instead the focus should be on signing, itself a valid alternative language.
Gibson’s goal was now to identify babies born deaf, allowing them to have an implant. With Gibson’s persuasion, NSW initiated a successful early-detection programme, now Australia-wide. With a cochlear implant, children born congenitally deaf could go to a regular school and lead the life of a normal child. Between 1984 and 2014, he performed the bionic ear operation 2000+ times!
Bill Gibson: Pioneering Bionic Ear Surgeon
written by Tina Allen,
published by NewSouth Publishing in 2017.
More recent progress
Dr Gibson helped establish Cochlear Implant Club and Advisory Association, a group that enabled implant recipients to meet regularly, providing support to each other and feedback to doctors. And to obtain funding for specialist facilities and post-op therapy.
The vital personal accounts of 40 of Professor Gibson’s patients are included in the Australian chapters of the biography. The book also considered the issues Dr Gibson experienced in establishing a top class cochlear implant programme, known today as the Sydney Cochlear Implant Centre. The twelve branches of the Centre were one of the many legacies of his career. Another success was the small incision he developed for cochlear implant surgery, to reduce wound breakdown to practically zero. Plus he advised a NSW Ministerial Committee on the best screening test to be used in hospital on new-born infants.
Prof Gibson is now overseeing research into the cause and cure for the debilitating Menière’s Disease. This condition of the ear has resisted medical knowledge since the condition was first identified in France in 1861 by Prosper Menière. Sydney now has the first laboratory in the world dedicated solely to Menière’s Disease Research.