J. Eadie, Brisbane, Australia

M. J. Eadie

Over several centuries, those born in Scotland have often left their homeland because of the perceived lack of opportunity, and then made successful lives in other countries. This behavior was particularly frequent during the so-called Highland clearances of the 18th and 19th centuries. Scottish landowners dispossessed their tenant farmers who had been engaged in small-scale agriculture for generations, to make land available for more profitable sheep rearing. As one consequence, more people of Scottish ancestry now live elsewhere in the world than in Scotland itself. In 1956, there was a Highland clearance on a micro scale, when lack of available consultant positions in the British National Health Service resulted in a trained neurologist of Highlander origin emigrating to Australia.

An outline map of Australia found among John Sutherland’s papers, with dotted latitude lines added to it in his hand. The map includes names of the cities where he studied multiple sclerosis prevalence, and the local prevalence figures per 100,000 of population he obtained, have subsequently been inserted; the figures from his earlier survey in red, and from the later one in purple.

John Sutherland (Fig 1) was born in Caithness, in the extreme northeast of mainland Scotland, in 1919. He was educated in Glasgow, and graduated in medicine from the University of Glasgow in 1943. After service in the wartime Royal Navy, he returned to the Western Infirmary, Glasgow, in 1946 as medical registrar to Douglas Adams, a consultant physician with neurological interests, particularly concerning multiple sclerosis. Adams launched Sutherland into clinical and laboratory research related to the disease, resulting in the addition of a research medical degree (Glasgow) to Sutherland’s existing basic medical qualifications. After his appointment in Glasgow ended, Sutherland went to Inverness, the so-called “capital” of the Scottish highlands, in 1950, as senior medical registrar. He remained there for five years, followed by some months in a similar level position in Aberdeen, a little further south on the east coast of Scotland. In Inverness, though without the formal title, he in effect functioned as neurological consultant for the Scottish Highlands, the Hebridean Islands off the northwest coast of the country, and the Orkney and Shetland Islands north of the mainland. From Inverness he investigated a suspicion that arose out of his multiple sclerosis clinical studies in Glasgow, namely that there might be an uneven distribution in the occurrence of multiple sclerosis between parts of Scotland.

Because of his close professional relationships with medical practitioners in the areas he serviced, he achieved a high multiple sclerosis case ascertainment rate and, after various field expeditions, found that the prevalence of the disease in the shaded areas of the map (Fig 2) covered over in red was approximately twice that in the remaining shaded parts. He realized that the red areas were those where the population was predominantly of Nordic origin, a later-day result of Viking invasions and settlement centuries earlier. The remaining shaded areas had populations largely of Gaelic lineage and who still could understand and employ the Gaelic language. Thus, he obtained persuasive evidence, perhaps the earliest, that genetic and racial factors might play a role in the etiology of multiple sclerosis.

John Sutherland’s map of Scotland. The shaded areas show where he investigated the prevalence of multiple sclerosis, with the original version modified by coloring over in red in the higher prevalence areas.

In the year that this study was published,¹ Sutherland arrived in Australia to take up an academic position in Brisbane, the capital of the state of Queensland that occupies most of the northeast quarter of the continent (Fig 3). After a few years, he commenced consultant neurological practice in that city. In the 1950s, it was generally believed locally that multiple sclerosis rarely occurred in the northern half of Australia, and that native-born Queenslanders never suffered from it. Sutherland soon showed that these ideas resulted from a local medical unfamiliarity with the spectrum of clinical manifestations of the disorder, so that it simply was not being recognized.

Knowing that multiple sclerosis prevalence increased with increasing distance from the equator in the northern hemisphere, and because of his earlier investigation being alert to the possible relationship between geographical and racial factors and disease distribution, Sutherland proceeded to investigate whether a similar disease prevalence distribution in relation to latitude existed in the southern hemisphere. No adequate data were then available. Australia was a peculiarly suitable site for investigating the matter. It possessed a 3000 km -long north-to-south dimension, a uniform and high standard of medical practice throughout, main population centers spaced reasonably evenly along its eastern seaboard, and was populated almost exclusively by those of British and other European stock who spoke English (though some of them may have initially wondered if Sutherland also did, until his broad Scotch accent gradually became somewhat attenuated).

John Sutherland in his 60’s

Sutherland initially carried out a field study of multiple sclerosis prevalence in three tropical Queensland coastal cities (Cairns, Townsville, and Mackay) and in sub-tropical Toowoomba (about 100 km west of Brisbane).² Recognized cases of the disease were found to have a lower prevalence in the tropical than in the sub-tropical population, though the disease prevalence was low relative to that in Northern hemisphere populations.

Spurred on by this finding, he then collaborated with local neurologists and epidemiologists in selected southern cities (Newcastle, Perth and Hobart) to show a higher multiple sclerosis prevalence the further south the matter was studied.³ Later still, in another collaborative study that took in New Zealand, overall closer to the South Pole than the southernmost parts of Australia, further evidence was obtained.⁴ Thus Sutherland’s name became associated with a series of investigations that demonstrated beyond reasonable doubt that multiple sclerosis prevalence increased with greater distance from the equator in the southern as well as in the northern hemisphere.

He also initiated other multiple sclerosis epidemiological investigations in Australia. One study showed that the prevalence of the disease correlated with the notifications of paralytic poliomyelitis in epidemics of that disease at different latitudes in Australia. This finding led to speculation that exposure to some unidentified organism, occurring earlier in childhood in hotter climates, while some residual immunity of maternal origin persisted, might have prevented later clinical disease. However, in cooler climates, exposure to the cause occurred later and resulted in overt disease.⁵ He also drew attention to a correlation between decreasing average annual sunlight exposure in regions of Australia and increasing multiple sclerosis prevalence,⁴ a finding largely forgotten until resurrected by recent interest in the relation between vitamin D and the disease. Additionally, he proposed a speculative hypothesis regarding multiple sclerosis prevalence and the capacity of regional soils to bind molybdenum in preference to copper.⁶

In Australia, Sutherland became a very successful consultant who developed an additional major interest in medico-legal neurology. With the years, his active investigative work into multiple sclerosis diminished, though he retained a watch on the relevant literature until the end, which came in 1995.

Scotland’s inability to provide appropriate professional opportunity for another of its many sons thus provided Australia with one of that country’s pioneer neuroepidemiologists, a man whose investigative endeavors helped awaken ongoing broader interest into multiple sclerosis far from his homeland.

References

1. Sutherland JM (1956) Observations on the prevalence of multiple sclerosis in northern Scotland. Brain 79: 635-654.
2. Sutherland JM, Tyrer JH, Eadie MJ, Casey JH, Kurland LT (1966) The prevalence of multiple sclerosis in Queensland, Australia. Acta Neurologica Scandinavica 42 (Suppl 19): 57-67.
3. McCall MFG, Brereton TLG, Dawson A, Millingen K, Sutherland JM, Acheson ED (1968) Frequency of multiple sclerosis in three Australian cities – Perth, Newcastle and Hobart. Journal of Neurology Neurosurgery and Psychiatry 31:1-9.
4. Sutherland JM, Tyrer JH, Eadie MJ (1962) The prevalence of multiple sclerosis in Australia. Brain; 85:149-164.
5. Eadie MJ, Sutherland JM, Tyrer JH (1965) Multiple sclerosis and poliomyelitis in Australasia. British Medical Journal 1: 1471-1473.
6. Layton W, Sutherland JM (1975) Geochemistry and multiple sclerosis: a hypothesis. Medical Journal of Australia. 1:73-77

Mamta Bhushan Singh, MD, and Michael F. Finkel, MD

Mamta Bhushan Singh, MD

The medical world thinks of the developed and developing societies in terms of diagnostic and treatment differences. However, there are realities that are common to both spheres concerning most medical conditions.

As a medical student, one would read of common disorders that were not being treated. Epilepsy was a striking example. In many rural Indian communities, up to 90 epilepsy patients out of every 100 were not getting treatment. In bureaucratese, this was a treatment gap of 90 percent.

Michael F. Finkel, MD

The treatment of epilepsy has since evolved. Over two-dozen antiepileptic drugs are currently available. Many drugs are off patent and generically manufactured, and available in India and other developing nations at reasonable prices. But the epilepsy treatment gap of up to 90 percent still exists in many rural Indian communities! So, why has nothing changed for the lot of millions of epilepsy patients?

Let us humanize the numbers. By using calculations from an often-quoted epilepsy prevalence figure of 1 percent of the population, at least 12 million Indians are struggling with epilepsy.¹ Large prevalence studies are unavailable, and many experts agree that this number is more likely to be closer to 15 million or even higher. This implies that more than 10 million epilepsy patients in India are untreated. Extrapolating worldwide, there are more than 50 million epilepsy patients and at least 40 million of these reside in developing countries. The estimate is that 75 percent of patients in developing countries are outside the domain of any kind of effective treatment. This implies at least 30 million untreated persons.

Ironically, epilepsy is one of the relatively easily controllable neurological diseases.

Untreated epilepsy with frequent generalized tonic-clonic seizures results in serious injuries and burns. Patients may lose sight, digits, or limb. The visible scars are further stigmatizing for patients who struggle with societal acceptance. Photo credit: Priya Jain.

What is life like with untreated epilepsy? Most persons with epilepsy who do not have any other neurological illness are essentially normal at all times other than during their seizures. A seizure generally lasts for a few minutes during which, amongst other things, the person is unaware of his or her surroundings, and after which the person may remain confused for a variable amount of time or may sleep off the effects. In either case, the individual is back to normal within a few hours, often without even requiring a trip to the doctor’s clinic or the emergency room.

Then what is the great problem about having untreated active epilepsy with an occasional seizure? Imagine having brief episodes of unawareness just once or twice in a month, in six months or even in a year, but not knowing when these would happen. So, you may be driving to work, crossing the street, climbing a tree, in bed with your partner, swimming in the pool, or speaking mid-sentence in that all important meeting. Suddenly, out of the blue, you start convulsing or just fidgeting with your buttons or speaking in an unintelligible jargon or wet your clothes in full public gaze. How would it feel to know that you had done either of these, and then have to go back to the same people in front of whom this had happened? Well, that is assuming that these people agree to work or socialize with you after witnessing a seizure.

The economic impact of untreated epilepsy is formidable in all societies. Many untreated epilepsy patients remain unemployable, especially if local attitudes consider it to be a contagious disease, a mental illness, or a demonic possession. Thus, they are removed as contributors to the economy. Even if they are poor and have minimum wage jobs, this still adds up to a substantial amount of money loss because of the millions affected.

There are other grave consequences of untreated epilepsy. If the patient is of school or college age, they are very likely to have to drop out. This is either due to their parents’ fear that their child may be injured during a seizure, or on the insistence of teachers. With limited scope for education, landing a good job later in life is subsequently reduced. The intrigue and misinformation surrounding epilepsy reduces social acceptance of patients. Any relationship, including a stable marriage, especially for women with epilepsy, is unlikely. Abandonment of women with epilepsy and their children from marital relationships is common. Such women, with little or no education, no skills and sometimes also with small children to take care of, are often left at the mercy of an impoverished community.

So, is epilepsy difficult to treat? No. Epilepsy is a relatively easy disease to treat in most patients. The diagnosis is clinical and based upon eliciting a history of stereotyped episodes during which the patient may behave abnormally, have involuntary movements or jerks, generally become unaware of his surroundings and then recover in a short time. After the clinical diagnosis, a couple of investigations— EEG and brain imaging — may be done. Investigations may help in deciding the best anti-epileptic drug, in prognosticating how long the treatment is likely to be needed, and how responsive to treatment the patient’s epilepsy might be.

However, even if investigations are not available, as is the case in many developing countries, most patients can still be started on treatment based on clinical history and examination alone. Treatment costs are not very high with generic medications. For example, in India, patients who are treated with one antiepileptic drug spend about $2-$5 per month. Many other developing countries face severe shortages of antiepileptic medication and also have to contend with high medication costs. Along with starting antiepileptic drugs, it is necessary to educate and inform patients at the first visit and at every subsequent opportunity, about their disease and it’s treatment. Without backing up drug treatment with education or “epilepsy literacy,” outcomes are unlikely to be good. After starting treatment, regular reviews at least once or twice a year are needed. Patients have to continue treatment for several years. At least 60-70 percent of epilepsy patients will become seizure-free on medication quite easily. The remaining minority have more difficult forms of epilepsy and need further evaluation and treatment at a specialized epilepsy center. Surgery may be an option for some of these difficult patients.

What are the main challenges? Despite the relative simplicity of the process of epilepsy diagnosis and initiating treatment, millions remain untreated in India and the developing world. To our minds, the biggest hurdles are reliance on specialist doctors who are either entirely missing or extremely scarce and located only in a few large metropolitan cities. This produces a lack of organized, credible, and easily accessible primary care throughout these countries.

Hence, we have the current situation in these countries, where effective systems are not in place. For example, even if an epilepsy patient in a rural area is aware that visiting a doctor and getting the condition treated is possible, what can he do? To whom does he or she go? There is no easy track for one to follow. In India, a hierarchy of health centers exists with a scaling up in staff skill and numbers, and improvement in facilities based upon the size of the population being served. However, doctors and services are not reliably available at these facilities. As a result, an epilepsy patient in a village can either spend an entire lifetime untreated and seizing, or, if he or she is feisty, may make a long and expensive journey to a big city for treatment. No patient should have to do that. In India, there are about 638,000 villages with difficult access. Therein lies the problem. Unless treatment is made available within a radius of about 25-50 kilometers of every small village and town, epilepsy patients and the nation’s economy will continue to suffer needlessly.

Some epilepsy is also preventable. Millions of epilepsy patients in India and worldwide have what is best described as “preventable epilepsy.” In other words, their epilepsy should not have even happened in the first place. Tapeworms cause epilepsy associated with neurocysticercosis. It reflects lack of access to clean food and water, poor sanitation and hygiene, and is an illustration of the public health aspect of epilepsy. Accidents, including frequent road traffic accidents, may lead to head injury and posttraumatic epilepsy. This form of epilepsy is notoriously difficult to treat and often requires surgery. Birth injuries and hypoxic brain damage are more likely to occur with unsupervised childbirth at home. This practice is diminishing, but still prevalent in many rural communities in the developing world. Such babies may also have epilepsy in addition to cerebral palsy, mental subnormality, and behavioral abnormalities. Other preventable epilepsies include epilepsy associated with other brain infections, and drug and alcohol abuse.

How can we overcome epilepsy? Clearly, what the medical community and governments have been doing so far has not worked. The International League Against Epilepsy celebrated its centenary in 2009. The WHO has existed for seven decades. Work has definitely been done and some progress made. But it is too little and at a very slow pace. Times have changed, and many newer resources are available. The need of the hour is a paradigm shift in all aspects of epilepsy care.

We need to think about who will shoulder the responsibility of caring for epilepsy patients in communities where there is a shortage of doctors and specialists. Can the epilepsy care workforce be expanded beyond doctors? Can epilepsy only be diagnosed by seating the patient in front of a doctor in a hospital clinic setting, or are there other viable, safe, and acceptable options? Do patients have to be transported to big city hospitals for investigations or can this also be done in heretofore-overlooked settings?² Once started on treatment, can regular patient reviews only be done in clinics, or can they be done remotely by telemedicine? Untreated epilepsy can no longer be considered just another medical condition. It is a public health issue. Lives are being impacted as adults become unemployable and the caretaker is likewise reduced in their workforce role.

If diagnosing and treating epilepsy remains only an epileptologist’s, neurologist’s, or even a general physician’s brief, then in developing countries like India, untreated epilepsy will never go away. Non-specialists such as paramedical personnel, district health workers, and nurse clinicians need to be trained and enlisted to expand the epilepsy workforce. Technology is now becoming available for various aspects of epilepsy care and can be pressed into action. Evidence is accruing that epilepsy diagnosis by non-physicians using a phone application is possible.³ This can at least be used as a screening tool in remote rural communities. Nurse-led epilepsy clinics may be considered.4 Diagnosing and starting treatment using mobile rural outreach clinics and patient follow-up using the ubiquitous mobile phone are all viable options that hold promise.^5,6

Finally, unless efforts at diagnosing and starting treatment are not accompanied by concerted efforts of raising epilepsy literacy amongst patients, caregivers, and laypersons, success will remain elusive. An Epilepsy Resolution approved by the World Health Assembly on the May 26, 2015 is considered a historical landmark. This resolution was overdue and now societies need to push hard to make it work.

Are countries really too poor to bargain for generic drugs for their citizens? The defense budget of India for 2015-16 is $40 billion, and even a 1 percent reduction in this may be enough to treat the currently untreated epilepsy patients for one year. Reducing the country’s nuclear spend marginally or even getting a sliver of funds spent by the Board of Cricket Control in India may be enough for funding epilepsy treatment in untreated patients. Savings can be achieved in developed countries by allowing the treating personnel to use the appropriate generics rather than the cheapest ones, a common conundrum for U.S. physicians, since the cheapest are not always the most effective. This promotes more seizures and more expenses related to caring for the additional seizures and related injuries. A statement has been attributed to former Secretary of State Condoleezza Rice that the U.S. budget for military bands is higher than that for the U.S. State Department. Certainly these funds can be diverted to effective treatments for uninsured U.S. citizens, rather than to ceremony. Even where universal health care exists, there are expenses that can be cut to fund these physician-prescribed needed medications.

References

1. www.who.int/mediacentre/factsheets/fs999/en/
2. www.bostonglobe.com/business/2015/05/21/mobile-health-technology-helps-tackle-epilepsy bhutan/c6vmO7XOznyDegIa4BYSAM/story.html
3. Patterson V. Singh M. Rajbhandari H. Vishnubhatla S. Validation of a phone app for epilepsy diagnosis in India and Nepal. Seizure 30, 2015, 46–49
4. Paul P. Agarwal M. Bhatia R. Vishnubhatla S. Singh MB: Nurse-led epilepsy follow-up clinic in India: is it feasible and acceptable to patients? A pilot study. Seizure; 2014;23(1): 74-6
5. Bigelow J. Singh V. Singh M. Medication adherence in patients with epilepsy after a single neurologist visit in rural India. Epilepsy Behav. 2013 Nov;29(2):412-5

J.Eduardo San Esteban, MD

J.Eduardo San Esteban, MD

From Oct. 29th to Nov. 3rd, 2016, Cancun, Mexico, will host the 14th Pan American Congress of Neurology. This will be the second time for the Pan American Congress to be held in this country. Mexico hosted the fourth Pan American Congress in 1975. There have been more than 50 years of Pan American neurology meetings and maybe the time has come to question ourselves as to whether we have made some progress in this continent in building a real Pan American Neurology and more important, how prepared we are to develop an alliance to help each other in the pursuit of improved care of our patients with neurological illness.

The American continent, with a population of around one billion is marked by inequality in human development. We also have a diversity of geographic, economic, political, and cultural systems. And, of course, we also have different health systems to provide care to an ever more demanding population. The obvious differences between the countries north and south of the Rio Grande have provided the grounds for a multinational effort to increase our cooperation. There are social and economic treaties, cultural and professional agreements, some of them with better results than others, but all of them with the idea of finding an improved quality of life. The cooperation among the Latin American states has been also prolific. Despite some differences, our similarities have prevailed, and in multiple examples we can see the results of intelligent and generous collaborations.

Neurological disease has increased its burden over the world population. Naturally, the Pan American community is no exception. There are some particular situations in different areas— infectious and parasitic disease are still everyday events in some areas, malnutrition and metabolic in others, children with sequelae of difficult pregnancies and deliveries are prevalent in some communities, but the frequent pathologies of the nervous system are similar in all of our countries. Cerebrovascular disease, epilepsy, neurodegenerative disease, developmental difficulties, headaches, and behavioral syndromes have a very similar prevalence. Increases in communication and migration have also contributed to provide a more universal panorama of illness. And, of course the appearance of new threats like Zika virus has swiftly become a multinational preoccupation.

The neurological community has an ideal opportunity to play a significant part in this continental effort. The southern countries have a common language, a very similar cultural background, and a rather equal social, ethnic, and developmental history. We also have a significant increase in technology and communications that have made distances shorter and real-time interaction an everyday occurrence. The northern countries have developed scientific and technological strength that keep them in the frontier of new knowledge. The advance of educational technological facilities have made teleconferences, telemedicine, online courses, and consultations an everyday event.

The question is: Can we, the neurologists of the American continent, build a professional, scientific, social, and educational alliance to help with the possibilities of improving the care of neurological patients around the continent?

What should we do and what can we do to achieve a situation of true and universal cooperation? A north, south, east, and west alliance can be a reality in the fields of education, epidemiology, interchange of information, online consultations, collaborative studies, and so on.

No doubt, the area of neurological education seems the immediate possible goal. There are already multiple programs ongoing. The traditional journey of Latin American professionals to the United States and Canada for an update in the state-of-the-art of neurology, and programs for the neurological subspecialties are a common-day reality. But the extent of these educational efforts hardly meets the needs of a large population of specialists who do not have the opportunities to travel. Well-planned alliances between countries could help to reduce these gaps. Online education is a useful tool. Teleconferences and meetings, and the distribution of information in accordance with a well-planned program that avoids commercialization of information, are all possible ways of collaboration.

The production of human resources for neurological care is another area where alliances can prove beneficial. Based in carefully performed studies that provide information about needs, a combined program of online and onsite education can help to reduce the lack of the most needed professional and technical resources. Even at the level of pre-graduate students, a multinational effort could address the needs of medical schools for a more complete neurological education. Education of first-contact physicians, family and general practitioners, and even paramedical personnel that provide attention in remote areas can be tackled by such an alliance.

Time is short. Population growth is fast, and new challenges wait for us everyday. Maybe the time has come to stop the search for the lost time and start a true alliance of Pan American countries to improve the health of our people who ail from neurological diseases. Maybe, as multinational independent professionals, with no other aims but to help our patients, we can put forth a special effort to develop such an alliance. Maybe we can have a continental Pan American neurology that can help bring the benefits of science, knowledge, and technology to a large population of patients who do not currently have opportunities to enjoy the same care as others. There are more than 30 countries in our continents united by geographical chance, but with the need to be united by more than that.

The forthcoming Pan American Congress in Cancun could be an opportunity to talk about these themes and ideas, and perhaps come up with an incipient program to help us make up the lost time.