3 research outputs found

    Prevalence and Incidence of Parkinson\u27s Disease in Latin America: A Meta-Analysis

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    \ua9 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society. Background: Parkinson\u27s disease (PD) is a rapidly growing neurodegenerative disorder, but up-to-date epidemiological data are lacking in Latin America. We sought to estimate the prevalence and incidence of PD and parkinsonism in Latin America. Methods: We searched Medline, Embase, Scopus, Web of Science, Scientific Electronic Library Online, and Literatura Latino-Americana e do Caribe em Ci\ueancias da Sa\ufade or the Latin American and Caribbean Health Science Literature databases for epidemiological studies reporting the prevalence or incidence of PD or parkinsonism in Latin America from their inception to 2022. Quality of studies was assessed using the Joanna Briggs Institute (JBI) Critical Appraisal Checklist. Data were pooled via random-effects meta-analysis and analyzed by data source (cohort studies or administrative databases), sex, and age group. Significant differences between groups were determined by meta-regression. Results: Eighteen studies from 13 Latin American countries were included in the review. Meta-analyses of 17 studies (nearly 4 million participants) found a prevalence of 472 (95% CI, 271–820) per 100,000 and three studies an incidence of 31 (95% CI, 23–40) per 100,000 person-years for PD; and seven studies found a prevalence of 4300 (95% CI, 1863–9613) per 100,000 for parkinsonism. The prevalence of PD differed by data source (cohort studies, 733 [95% CI, 427–1255] vs. administrative databases. 114 [95% CI, 63–209] per 100,000, P < 0.01), age group (P < 0.01), but not sex (P = 0.73). PD prevalence in β‰₯60 years also differed significantly by data source (cohort studies. 1229 [95% CI, 741–2032] vs. administrative databases, 593 [95% CI, 480–733] per 100,000, P < 0.01). Similar patterns were observed for parkinsonism. Conclusions: The overall prevalence and incidence of PD in Latin America were estimated. PD prevalence differed significantly by the data source and age, but not sex. \ua9 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society

    Global, regional, and national burden of epilepsy, 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016

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    Background Seizures and their consequences contribute to the burden of epilepsy because they can cause health loss (premature mortality and residual disability). Data on the burden of epilepsy are needed for health-care planning and resource allocation. The aim of this study was to quantify health loss due to epilepsy by age, sex, year, and location using data from the Global Burden of Diseases, Injuries, and Risk Factors Study. Methods We assessed the burden of epilepsy in 195 countries and territories from 1990 to 2016. Burden was measured as deaths, prevalence, and disability-adjusted life-years (DALYs; a summary measure of health loss defined by the sum of years of life lost [YLLs] for premature mortality and years lived with disability), by age, sex, year, location, and Socio-demographic Index (SDI; a compound measure of income per capita, education, and fertility). Vital registrations and verbal autopsies provided information about deaths, and data on the prevalence and severity of epilepsy largely came from population representative surveys. All estimates were calculated with 95% uncertainty intervals (UIs). Findings In 2016, there were 45Β·9 million (95% UI 39Β·9–54Β·6) patients with all-active epilepsy (both idiopathic and secondary epilepsy globally; age-standardised prevalence 621Β·5 per 100β€ˆ000 population; 540Β·1–737Β·0). Of these patients, 24Β·0 million (20Β·4–27Β·7) had active idiopathic epilepsy (prevalence 326Β·7 per 100β€ˆ000 population; 278Β·4–378Β·1). Prevalence of active epilepsy increased with age, with peaks at 5–9 years (374Β·8 [280Β·1–490Β·0]) and at older than 80 years of age (545Β·1 [444Β·2–652Β·0]). Age-standardised prevalence of active idiopathic epilepsy was 329Β·3 per 100β€ˆ000 population (280Β·3–381Β·2) in men and 318Β·9 per 100β€ˆ000 population (271Β·1–369Β·4) in women, and was similar among SDI quintiles. Global age-standardised mortality rates of idiopathic epilepsy were 1Β·74 per 100β€ˆ000 population (1Β·64–1Β·87; 1Β·40 per 100β€ˆ000 population [1Β·23–1Β·54] for women and 2Β·09 per 100β€ˆ000 population [1Β·96–2Β·25] for men). Age-standardised DALYs were 182Β·6 per 100β€ˆ000 population (149Β·0–223Β·5; 163Β·6 per 100β€ˆ000 population [130Β·6–204Β·3] for women and 201Β·2 per 100β€ˆ000 population [166Β·9–241Β·4] for men). The higher DALY rates in men were due to higher YLL rates compared with women. Between 1990 and 2016, there was a non-significant 6Β·0% (βˆ’4Β·0 to 16Β·7) change in the age-standardised prevalence of idiopathic epilepsy, but a significant decrease in age-standardised mortality rates (24Β·5% [10Β·8 to 31Β·8]) and age-standardised DALY rates (19Β·4% [9Β·0 to 27Β·6]). A third of the difference in age-standardised DALY rates between low and high SDI quintile countries was due to the greater severity of epilepsy in low-income settings, and two-thirds were due to a higher YLL rate in low SDI countries. Interpretation Despite the decrease in the disease burden from 1990 to 2016, epilepsy is still an important cause of disability and mortality. Standardised collection of data on epilepsy in population representative surveys will strengthen the estimates, particularly in countries for which we currently have no or sparse data and if additional data is collected on severity, causes, and treatment. Sizeable gains in reducing the burden of epilepsy might be expected from improved access to existing treatments in low-income countries and from the development of new effective drugs worldwide

    Global, regional, and national burden of meningitis, 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016

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    Background Acute meningitis has a high case-fatality rate and survivors can have severe lifelong disability. We aimed to provide a comprehensive assessment of the levels and trends of global meningitis burden that could help to guide introduction, continuation, and ongoing development of vaccines and treatment programmes. Methods The Global Burden of Diseases, Injuries, and Risk Factors (GBD) 2016 study estimated meningitis burden due to one of four types of cause: pneumococcal, meningococcal, Haemophilus influenzae type b, and a residual category of other causes. Cause-specific mortality estimates were generated via cause of death ensemble modelling of vital registration and verbal autopsy data that were subject to standardised data processing algorithms. Deaths were multiplied by the GBD standard life expectancy at age of death to estimate years of life lost, the mortality component of disability-adjusted life-years (DALYs). A systematic analysis of relevant publications and hospital and claims data was used to estimate meningitis incidence via a Bayesian meta-regression tool. Meningitis deaths and cases were split between causes with meta-regressions of aetiological proportions of mortality and incidence, respectively. Probabilities of long-term impairment by cause of meningitis were applied to survivors and used to estimate years of life lived with disability (YLDs). We assessed the relationship between burden metrics and Socio-demographic Index (SDI), a composite measure of development based on fertility, income, and education. Findings Global meningitis deaths decreased by 21Β·0% from 1990 to 2016, from 403β€ˆ012 (95% uncertainty interval [UI] 319β€ˆ426–458β€ˆ514) to 318β€ˆ400 (265β€ˆ218–408β€ˆ705). Incident cases globally increased from 2Β·50 million (95% UI 2Β·19–2Β·91) in 1990 to 2Β·82 million (2Β·46–3Β·31) in 2016. Meningitis mortality and incidence were closely related to SDI. The highest mortality rates and incidence rates were found in the peri-Sahelian countries that comprise the African meningitis belt, with six of the ten countries with the largest number of cases and deaths being located within this region. Haemophilus influenzae type b was the most common cause of incident meningitis in 1990, at 780β€ˆ070 cases (95% UI 613β€ˆ585–978β€ˆ219) globally, but decreased the most (–49Β·1%) to become the least common cause in 2016, with 397β€ˆ297 cases (291β€ˆ076–533β€ˆ662). Meningococcus was the leading cause of meningitis mortality in 1990 (192β€ˆ833 deaths [95% UI 153β€ˆ358–221β€ˆ503] globally), whereas other meningitis was the leading cause for both deaths (136β€ˆ423 [112β€ˆ682–178β€ˆ022]) and incident cases (1Β·25 million [1Β·06–1Β·49]) in 2016. Pneumococcus caused the largest number of YLDs (634β€ˆ458 [444β€ˆ787–839β€ˆ749]) in 2016, owing to its more severe long-term effects on survivors. Globally in 2016, 1Β·48 million (1Β·04β€”1Β·96) YLDs were due to meningitis compared with 21Β·87 million (18Β·20β€”28Β·28) DALYs, indicating that the contribution of mortality to meningitis burden is far greater than the contribution of disabling outcomes. Interpretation Meningitis burden remains high and progress lags substantially behind that of other vaccine-preventable diseases. Particular attention should be given to developing vaccines with broader coverage against the causes of meningitis, making these vaccines affordable in the most affected countries, improving vaccine uptake, improving access to low-cost diagnostics and therapeutics, and improving support for disabled survivors. Substantial uncertainty remains around pathogenic causes and risk factors for meningitis. Ongoing, active cause-specific surveillance of meningitis is crucial to continue and to improve monitoring of meningitis burdens and trends throughout the world
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