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Arquivos de Neuro-Psiquiatria

Print version ISSN 0004-282X

Arq. Neuro-Psiquiatr. vol.71 no.6 São Paulo June 2013

https://doi.org/10.1590/0004-282X20130040 

Articles

Care of patients with Huntington's disease in South America: a survey

Cuidado de pacientes com doença de Huntington na América do Sul: um inquérito

Ricardo Oliveira Horta Maciel1 

Francisco Eduardo Costa Cardoso1 

Pedro Chaná-Cuevas2 

Carlos Cosentino3 

William Fernández4 

Carlos R. M. Rieder5 

Marcos Serrano-Dueñas6 

Roberto Weiser7 

1Movement Disorders Clinic, Department of Neurology, UFMG, Belo Horizonte MG, Brazil

2Centro de Trastornos del Movimiento (CETRAM), Facultad de Ciencias Médicas, Universidad de Santiago de Chile, Santiago, Chile

3Movement Disorders Unit, Instituto Nacional de Ciencias Neurológicas, Lima, Peru

4Universidad Nacional de Colombia, Institute of Genetics, Bogotá, Colombia

5Universidade Federal Ciências da Saúde Porto Alegre (UFCSPA), Porto Alegre RS, Brazil

6Movement Disorder and Biostatistics Units, Neurological Service, Carlos Andrade Marín Hospital and Medicine Faculty, Pontifical Universidad Católica del Ecuador, Quito, Ecuador

7Department of Neurology, Instituto de Clínicas, Tamanaco, Caracas, Venezuela


ABSTRACT

Huntington's disease (HD) is a rare neurodegenerative disease with a multitude of symptoms, which requires access to specialized multidisciplinary care for adequate management. The aim of this study was to survey the characteristics of care in various HD centers in South America (SA).

Methods

A questionnaire was sent to 24 centers involved in the care for HD patients in SA.

Results

Of the total 24 centers, 19 (79.2%) are academic units. The majority of centers (62.5%) are general movement disorders clinics. Multidisciplinary care is available in 19 (79.2%) centers and in 20 (83.3%) care is provided free of charge. Genetic testing and counseling are available in 25 and 66.6% of centers, respectively. The majority of centers (83.3%) have no institutional support for end-stage care.

Conclusions

Although HD centers in SA are committed to providing multidisciplinary care, access to genetic counseling and end-stage care are lacking in most centers.

Key words: Huntington disease; comprehensive health care; genetic counseling

RESUMO

A doença de Huntington (DH) é uma doença neurodegenerativa rara que requer tratamento multidisciplinar especializado para manejo adequado. O objetivo do presente trabalho foi pesquisar as características da assistência à saúde em centros de DH na América do Sul (AS).

Métodos

Um questionário foi enviado para 24 centros envolvidos no cuidado de pacientes com DH na AS.

Resultados

Dos 24 centros, 19 (79,2%) são unidades acadêmicas. A maioria (62,5%) são clínicas de distúrbios dos movimentos. Cuidado multidisciplinar é disponível em 19 (79,2%) dos centros e em 20 (83,3%), o tratamento é gratuito. O teste e o aconselhamento genético estão disponíveis em 25 e 66,6% dos centros, respectivamente. Não há suporte institucional para cuidado terminal em 83,3% dos centros.

Conclusões

Apesar dos centros de DH na AS terem compromisso com o provimento de cuidados multidisciplinares, o acesso a aconselhamento genético e a tratamento na fase terminal são falhos na maioria dos centros.

Palavras-Chave: doença de Huntington; assistência integral à saúde; aconselhamento genético

Huntington's disease (HD) is a rare autosomal dominant neurodegenerative disease characterized by movement disorders, cognitive decline and psychiatric symptoms 1 . No current efficacious treatment exists, and due to its relentless progression, patients face increasing disability due to a combination of motor impairment and cognitive decline, leading to loss of ambulation, dysphagia and dementia. Loss of autonomy becomes a constant feature as the disease progresses and patients frequently require round-the-clock care in the final stages of disease 2,3 .

Management of patients with HD often requires the involvement of diverse health care professionals including nurses, physiotherapists, speech therapists, psychologists, occupational therapists, and genetic counselors, who have important roles in improving the quality of life and managing the disabilities of HD patients 4 . Moreover, in the latter stages of disease, nursing home facilities and end-stage palliative care are often required, as caregiver burden and quality of life become major concerns 5 .

The availability and quality of care for patients with HD living in South America (SA) has not been reported in the literature. The purpose of this study was to survey the characteristics of care provided in various centers involved in the management of HD patients throughout SA.

METHODS

Questionnaires were sent to 24 centers involved in the care of HD patients in various countries of SA with reputable expertise in the field and active participation in regional Movement Disorders forums. This survey included questions on the clinics' profile and institutional status, staff composition, clinical scales used for patient evaluation, access to neuroimaging, genetic testing and counseling, and end-stage care support.

RESULTS

Of the 24 centers evaluated, 14 were located in Brazil, 4 in Argentina, 2 in Chile and 1 in Colombia, Ecuador, Peru, and Venezuela, each. The combined population of the cities where the centers are located is of 80 million people, comprising 20.7% of the total population of SA or 21.7% of the population of their respective countries.

Profile of centers

The majority of centers, 19 (79.2%), are affiliated with an academic institution, and all are specialized clinics, either of general movement disorders (15/24 or 62.5%), HD-only clinics (6/24 or 25%) or neurogenetics clinics (3/24 or 12.5%). Most clinics are open once a week (22/24 or 91.6%) one (4.2%) is open twice a week, and another (4.2%) five times a week.

Multidisciplinary care is available in 19 of the 24 (79.2%) centers; composition of the teams is summarized in Table 1. Most centers (20/24 or 83.3%) provide care free of charge to patients.

Table 1. Health care professionals composition of Huntington's disease clinics. 

Health profession Absolute frequency Relative frequency (%)
Neurologists 24 100
Physiotherapists 13 54.2
Geneticists 12 50
Speech therapists 11 45.8
Nurses 10 41.6
Psychologists 10 41.6
Occupational therapists 7 29.2
Dentists 6 25
Psychiatrists 4 16.6

Patient assessment

Clinical assessment protocols adopted and neuroimaging tests available in the various centers are reported in Table 2. Genetic testing is available in 6 clinics (25%) and in other 14 (58.3%) it is available elsewhere.

Table 2. Clinical assessment tools and diagnostic neuroimaging used in Huntington's disease centers. 

Absolute frequency Relative frequency (%)
Rating Scales
 MMSE 15 62.5
 UHDRS 13 54.4
 FAB 2 8.3
 MoCA 2 8.3
Neuroimaging
 CT Scan 19 79.2
 MRI 16 66.6
 SPECT 5 20.8
 PET 1 4.2

MMSE: mini-mental state examination, UHDRS: Unified Huntington Disease Rating Scale; FAB: Frontal Assessment Battery, MoCA: Montreal Cognitive Assessment; CT Scan: computed tomography scan; MRI: magnetic resonance image; SPECT: single photon emission computed tomography; PET: positron emission tomography.

End-stage care

Most centers (20/2 or 83.3%) have no institutional support for end-stage care. In other 2 (8.3%) it is accessible via a public institution, or covered by health insurance in other 2 (8.3%) centers.

DISCUSSION

Patients with HD and other neurodegenerative diseases often require coordinated multidisciplinary care to cater for different needs during the course of disease. Different levels of care are required as the disease progresses, from symptomatic therapy, psychological support to patients and caregivers, to genetic counseling to family members and, ultimately, to palliative care 68 .

This study shows that centers responsible for managing patients with HD throughout SA are committed to providing, mostly in free-of-cost settings, the best level of care possible, as attested by the fact that most institutions have multidisciplinary teams capable of tailoring treatment strategies to individual patient needs.

However, a number of weaknesses in this current model need to be addressed. First, the number of centers capable of caring for HD patients is insufficient to cover to the demand in the various countries in relation to the estimated prevalence of the disease in SA. Additionally, few centers have psychiatrists and geneticists in staff to address major patient and caregiver concerns 5 regarding psychiatric and genetic counseling. Genetic testing is available only in a minority of centers, and most patients have to resort to externally provided testing, which can often be expensive, far from their hometowns, and performed without adherence to international recommendations. Finally, the inexistence of structured end-stage disease care and institutionalized support are major obstacles to proper care 9,10 . This needs to be improved as the burden of care can become overwhelming in the final stages of disease, especially in families with multiple persons affected and/or in poor socioeconomic settings.

One limitation of this study is the disproportionate amount of Brazilian centers evaluated in relation to other countries of SA. Although we have made an effort to reach out for as many centers specializing in the care of HD patients as possible, units that may exist in other areas were not included in this study. Even if this is the case, it is fair to conclude that half of the population of SA, perhaps even more in some areas of the continent, cannot access centers capable of delivering specialized care for HD patients.

The European HD Network (EHDN) is a multicenter, multi-national initiative to facilitate HD care and research throughout Europe, including, but not limited to, management of large observational studies, interventional trials, and working groups focused on developing evidence-based guidelines for best-practice standards of care in HD. The creation of the EHDN, has contributed to achieving the goals of multidisciplinary, patient-centered and individualized care as the standards of care for HD patients in Europe, as patients tend to rely on the availability of primary or community care services for adequate management of their condition 11 . The institution of the Latin American HD Network in the models of the EHDN will hopefully aid in improving treatment for SA patients in a similar manner.

Acknowledgements

We thank Katherine Bazley RN for her secretarial assistance.

References

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Received: December 12, 2012; Received: December 17, 2012; Accepted: December 27, 2012

Correspondence: Francisco Cardoso; Avenida Pasteur 89 / 1.107; 30150-290 Belo Horizonte MG - Brasil; E-mail: cardosofe@terra.com.br

Conflict of interest: Francisco Cardoso is Secretary-Elect of the Movement Disorders Society; Brazilian Academy of Neurology Delegate to WFN; Vice-President of the Latin American Huntington Disease Network; honoraria from Roche and Moksha8. Pedro Chana-Cuevas has been a participant in the speaker's bureaus of UCB Pharma, Ipsen, GSK, and Boehringer-Ingelheim. Carlos Rieder is Member of the Education Committee of the Movement Disorders Society/Pan American Section; honoraria from Roche, Boehringer Ingelheim, Moksha8. Carlos Cosentino is President of the Peruvian Neurological Society.

Movement Disorders Clinic, Department of Neurology, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte MG, Brazil.

Creative Commons License This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.