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. Author manuscript; available in PMC: 2016 Oct 28.
Published in final edited form as: Neuroepidemiology. 2015 Oct 28;45(3):161–176. doi: 10.1159/000441085

UPDATE ON THE GLOBAL BURDEN OF ISCHAEMIC AND HAEMORRHAGIC STROKE IN 1990–2013: THE GBD 2013 STUDY

Valery L Feigin 1, Rita Krishnamurthi 2, Priya Parmar 3, Bo Norrving 4, George A Mensah 5, Derrick A Bennett 6, Suzanne Barker-Collo 7, Andrew Moran 8, Ralph L Sacco 9, Thomas Truelsen 10, Stephen Davis 11, Jeyaraj Durai Pandian 12, Mohsen Naghavi 13, Mohammad H Forouzanfar 14, Grant Nguyen 15, Catherine O Johnson 16, Theo Vos 17, Atte Meretoja 18, Christopher Murray 19, Gregory A Roth 20, Amanda Thrift 21, Amitava Banerjee 22, Andre Pascal Kengne 23, Awoke Misganaw 24, Brett M Kissela 25, Charles Wolfe 26, Chuanhua Yu 27, Craig Anderson 28, Daniel Kim 29, David Rojas-Rueda 30, David Tanne 31, David Lawrence Tirschwell 32, Devina Nand 33, Dhruv S Kazi 34, Farshad Pourmalek 35, Ferrán Catalá-López 36, Foad Abd-Allah 37, Fortuné Gankpé 38, Gabrielle deVeber 39, Geoffrey Donnan 40, Graeme J Hankey 41, Hanne K Christensen 42, Ismael Campos-Nonato 43, Ivy Shiue 44, Jefferson G Fernandes 45, Jost B Jonas 46, Kevin Sheth 47, Yunjin Kim 48, Klara Dokova 49, Konstantinos Stroumpoulis 50, Luciano A Sposato 51, Maria Cecilia Bahit 52, Johanna M Geleijnse 53, Mark T Mackay 54, Man Mohan Mehndiratta 55, Matthias Endres 56, Maurice Giroud 57, Michael Brainin 58, Michael Kravchenko 59, Michael Piradov 60, Michael Soljak 61, Ming Liu 62, Myles Connor 63, Narayanaswamy Venketasubramanian 64, Natan Bornstein 65, Nikolay Shamalov 66, Nobhojit Roy 67, Norberto Cabral 68, Norman J Beauchamp 69, Pablo M Lavados 70, Panniyammakal Jeemon 71, Paulo A Lotufo 72, Rajiv Chowdhury 73, Ramesh Sahathevan 74, Randah R Hamadeh 75, Reza Malekzadeh 76, Richard Gillium 77, Ronny Westerman 78, Rufus Olusola Akinyemi 79, Rustam Al-Shahi Salman 80, Samath D Dharmaratne 81, Sanjay Basu 82, Semaw Ferede Abera 83, Soewarta Kosen 84, Uchechukwu K A Sampson 85, Valeria Caso 86, Vasiliy Vlassov 87, Yohannes Adama Melaku 88, Yoshiohiro Kokubo 89, Yukito Shinohara 90, Yuri Varakin 91, Wenzhi Wang 92, on behalf of the GBD 2013 Stroke Experts Panel
PMCID: PMC4633282  NIHMSID: NIHMS726280  PMID: 26505981

Abstract

Background

Global stroke epidemiology is changing rapidly. Although age-standardised rates of stroke mortality have decreased worldwide in the past two decades, the absolute numbers of people who have a stroke every year, live with the consequences of stroke, and die from their stroke are increasing. Regular updates on the current level of stroke burden are important for advancing our knowledge on stroke epidemiology and facilitate organization and planning of evidence-based stroke care.

Objectives

To estimate incidence, prevalence, mortality, disability-adjusted life-years (DALYs) and years lived with disability (YLDs), and their trends for ischaemic stroke (IS) and haemorrhagic stroke (HS) for 188 countries from 1990–2013.

Methodology

Stroke incidence, prevalence, mortality, DALYs and YLDs were estimated using all available data on mortality and stroke incidence, prevalence and excess mortality. Statistical models and country-level covariate data were employed and all rates were age-standardised to a global population. All estimated were produced with 95% uncertainty intervals (UI).

Results

In 2013, there were globally almost 25.7 million stroke survivors (71% with IS), 6.5 million deaths from stroke (51% died from IS), 113 million DALYs due to stroke (58% due to IS), and 10.3 million new strokes (67% IS). Over the 1990–2013 period, there was a significant increase in the absolute number of DALYs due to IS, and of deaths from IS and HS, survivors and incident events for both IS and HS. The preponderance of the burden of stroke continued to reside in developing countries, comprising 75.2% of deaths from stroke and 81.0% of stroke-related DALYs. Globally, the proportional contribution of stroke-related DALYs and deaths due to stroke compared to all diseases increased from 1990 (3.54% [95% UI 3.11–4.00%] and 9.66% [95% UI 8.47–10.70%]) to 2013 (4.62% [95% UI 4.01–5.30%] and 11.75% [95% UI 10.45–13.31%], respectively), but there was a diverging trend in developed and developing countries with a significant increase in DALYs and deaths in developing countries, and no measurable change in the proportional contribution of DALYs and deaths from stroke in developed countries.

Conclusion

Global stroke burden continues to increase globally. More efficient stroke prevention and management strategies are urgently needed to halt and eventually reverse the stroke pandemic, while universal access to organized stroke services should be a priority.

Keywords: stroke, ischaemic stroke, haemorrhagic stroke, global burden, GBD 2013

Introduction

Stroke remains a major global health problem[1,2] and its significance is likely to increase in the future due to ongoing demographic changes, including ageing of the population and health transitions observed in developing countries.[3] The Global Burden of Disease (GBD) 2010 Study showed that while age-standardised rates of stroke mortality have decreased worldwide in the past two decades, the absolute number of people who have a stroke every year, live with the consequences of stroke, and die from their stroke is increasing. New epidemiological papers on stroke published since 2010 and updated death records are now included in the GBD 2013 Study dataset. Important advances and refinements have been made to the methodology for deriving the GBD estimates. Therefore, this updated report on the current level of stroke burden is important for advancing our knowledge on stroke epidemiology and planning for adequate evidence-based stroke systems of care. In the GBD 2013 study, we use new DisMod[4,5] methodology in order to provide new estimates of incidence, prevalence, disability-adjusted life-years (DALYs) and years lived with disability (YLDs) for ischaemic strokes (IS) and haemorrhagic and other non-ischaemic strokes combined (HS) separately for 1990 and 2013 at regional and global levels.

Methodology

Methods to estimate all-cause mortality and cause-specific mortality been previously described.[6] Stroke modeling and methodology used to estimate GBD 2013 stroke burden (including an updated list of publications included in this analysis) has also been described in detail.[7] In brief, we used all available estimates of stroke incidence, prevalence and case fatality from systematic reviews of the scientific literature, population surveys, and stroke registries. Stroke was defined based on the WHO clinical criteria.[8] All available national mortality data were compiled. Non-specific cause codes were redistributed based on expert opinion and statistical methods.[7] The total for all cause-specific deaths was fitted within an envelope for all-cause mortality. Deaths were compiled into 240 causes, including IS and HS. For stroke death estimates, GBD defined stroke ICD-10 codes as IS, HS, or nonspecific as to type. The parent category of cerebrovascular disease was based on the mapping of the detailed causes. Deaths coded as due to G45 (transient ischaemic attack) were coded as IS and deaths coded as due to nonruptured aneurysms (ICD code I67.0) were coded as HS. Nonspecific codes, including I64, I67.9, I68.8, I69.4–I69.9, were redistributed to IS or HS using a regression model.

An ensemble model was used to estimate a continuous time-series for mortality by age, sex, country (developed or developing), and year. Country-level covariates associated with stroke were used in the model and out-of-sample validity testing was used to assess model performance. 95% uncertainty intervals (UI) were estimated using 1000 draws from the posterior distribution for each age-sex-country group. Disease prevalence was estimated using DisMod state-transition disease modeling software[9] and Bayesian staistical models. IS and HS were modelled separately. Adjustments were made to account for incidence estimates specifying first-ever or any stroke. Disability due to acute stroke was considered to last for 28–30 days and for chronic stroke from 31st day until death. Five disability weights derived from large-scale studies while SF-12 scores from the U.S. Medical Expenditures Panel Survey for stroke patients supplied the distribution of these severity levels plus the proportion asymptomatic.[10] YLDs were calculated as the product of a disability weight and prevalent cases of stroke. DALYs were calculated as the sum of years of life lost prematurely, based on maximum observed global longevity, and YLDs. Countries were stratified into two groups (developed countries [high-income countries] and developing countries [low- and middle-income countries]). We report age-standardised incidence and mortality rates per 100 000 person-years, and prevalence and DALYs estimates per 100 000 people with the direct method of standardisation and GBD estimates of population as a reference.

Results

Globally from 1990 to 2013 there were statistically significant reductions in the incidence, mortality and DALY rates of IS. For HS there were statistically non-significant increases in the incidence and prevalence, and decreases in the mortality and DALY rates (Fig. 1, Table 1). In 2013, the DALYs and mortality rates of IS and HS combined in developing countries (2,189/100,000 per year [95% UI 1,995–2,416/100,000 per year] and 137/100,000 per year [95% UI 125–150/100,000 per year], respectively) were statistically significantly greater than that in developed countries (1,022/100,000 [95% UI 941–1,159/100,000] and 67/100,000 [95% UI 62–78/100,000], respectively) due to the higher rate for HS (Table 1), while the absolute number of people affected by both IS and HS in the world over that time period had increased significantly (Table 2). While mortality rates from IS and HS combined in developed countries were almost halved from 1990 to 2013 (112.9/100,000 and 67.2/100,000), in developing countries IS and HS mortality rates were reduced by only approximately 15% (from 160.9/100,000 in 1990 to 136.9/100,000 in 2013). As shown in Table 2, in 2013 there were almost 25.7 million stroke survivors (71% with IS), 6.5 million deaths from stroke (51% died from IS), 113 million DALYs due to stroke (58% due to IS), and 10.3 million new strokes (67% were IS). Over the 1990 to 2013 period, there was a statistically significant increase in the absolute number of DALYs due to IS, and deaths from, survivors and incident events of both IS and HS. The prevalence nearly doubled for both IS and HS from 1990 to 2013. Globally, from 1990 to 2013 there was a statistically non-significant increase in the prevalence rates of IS (statistically significant increase in the prevalence of IS from 1990 to 2005 was followed by statistically significant decrease from 2005 to 2013; Figure 1) and a statistically significant increase in HS prevalence rates (Figure 1). However, in developed countries the increase in the prevalence rates was statistically significant for both IS and HS (Table 3).

Figure 1.

Figure 1

Age-adjusted DALYs, mortality, incidence and prevalence rates of ischaemic and haemorrhagic strokes per 100,000 people (with 95% uncertainty intervals [UI]) in 1990, 2005 and 2013

Table 1.

Age-adjusted DALYs and mortality rates of ischaemic and haemorrhagic strokes combined per 100,000 people (with 95% uncertainty intervals [UI]) in developed and developing countries in 1990 and 2013

Year and stroke type Metric Developed countries Developing countries Globally
1990: ischaemic and haemorrhagic strokes combined DALYs 1,721.4 (1,564.3–1,866.5) 2,818.2 (2,578.3–3,064.0) 2,430.8 (2,224.0–2,631.4)
Mortality 112.9 (100.6–121.8) 160.9 (146.8–174.8) 141.6 (128.5–153.9)
Ischaemic stroke DALYs 1,023.7 (906.4–1,120.3) 950.6 (807.6–1,096.6) 1,004 (877.6–1,222.4)
Mortality 76.8 (67.3–84.1) 63.7 (54.9–73.8) 71.3 (63.0–79.3)
Haemorrhagic stroke DALYs 697.7 (598.4–789.4) 1,867.6 (1,657.9–2,069.3) 1,426.0 (1,269.9–1,579.9)
Mortality 36.1 (30.1–41.2) 97.2 (84.8–108.6) 70.3 (61.2–77.9)
Mortality 27.9 (25.1–33.2) 80.9 (72.5–93.0) 59.5 (53.5–68.1)
2013: ischaemic and haemorrhagic strokes combined DALYs 1,022.2 (940.9–1,158.6) 2,189.3 (1,995.4–2,416.0) 1,806.9 (1,667.4–1,991.7)
Mortality 67.2 (61.9–78.2) 136.9 (125.2–150.4) 110.1 (101.8–122.2)
Ischaemic stroke DALYs 609.8 (553.0–707.1) 889.4 (718.1–989.8) 791.3 (678.0–868.8)
Mortality 44.9 (40.9–53.5) 65.1 (52.1–72.0) 57.3 (49.3–62.9)
Haemorrhagic stroke DALYs 412.4 (369.1–473.3) 1,299.9 (1,178.2–1,495.9) 1,015.6 (923.2–1,163.2)
Mortality 22.2 (19.6–26.1) 71.8 (64.6–85.6) 52.8 (48.0–62.3)

Table 2.

Absolute number of DALYs, deaths, incident and prevalent cases of ischaemic and haemorrhagic stroke (with 95% uncertainty intervals [UI]) in the world in 1990 and 2013

Metric 1990 2013
Ischaemic stroke DALYs 34,155,606 (29,592,196 – 38,325,866) 47,424,681 (40,537,540 – 52,211,800)
Deaths 2,182,865 (1,923,290 – 2,430,872) 3,272,924 (2,812,654 – 3,592,562)
Incidence 4,309,356 (4,118,103 – 4,531,909) 6,892,857 (6,549,814 – 7,352,226)
Prevalence 10,045,202 (9,643,525 – 10,453,439) 18,305,491 (17,767,372 – 18,920,736)
Haemorrhagic stroke DALYs 55,953,376 (49,881,127 – 62,161,971) 65,454,194 (59,497,415 – 74,654,738)
Deaths 2,401,930.40 (2,109,380.2 – 2,669,117.5) 3,173,951 (2,885,717 – 3,719,684)
Incidence 1,886,345 (1,816,991 – 1,976,659) 3,366,175 (3,199,978 – 3,543,213)
Prevalence 3,891,158 (3,769,541 – 4,019,014) 7,363,457 (7,139,691 – 7,616,146)

Table 3.

Age-adjusted prevalence rates of ischaemic and haemorrhagic strokes per 100,000 people and median percentage change with 95% uncertainty intervals (UI) in developed and developing countries in 1990 and 2013

Years Ischaemic stroke Haemorrhagic stroke
Rate (95% UI) Median % change 1990–2013 (95% UI) Rate (95% UI) Median % change 1990–2013 (95% UI)
Developing countries 1990 155.4 (148.6–161.5) 0.001 (−0.051; 0.065) 113.8 (110.0–117.8) 0.003 (−0.040; 0.049)
2013 156.0 (149.3–164.6) 114.3 (110.3–118.0)
Developed countries 1990 472.7 (446.0–500.1) 0.214 (0.140; 0.317) 93.3 (86.4–99.7) 0.372 (0.253; 0.521)
2013 577.6 (558.7–600.4) 128.3 (121.1–135.9)
Globally 1990 291.2 (278.7–303.8) 0.024 (−0.028; 0.091) 105.6 (102.0–109.2) 0.102 (0.054; 0.161)
2013 299.1 (290.2–309.2) 116.6 (113.1–120.5)

Analysis of age-specific patterns of incidence, prevalence and mortality rates by country development status in 2013 (Figures 2 and 3) showed that IS incidence and prevalence rates in developed countries were statistically significantly greater and demonstrated a steeper increase with age than that in developing countries after the age of 49 and 39 years respectively. However, IS mortality rates after the age of 49 years were greater in developing countries. The age-related patterns of increase in IS mortality rates were similar in developed and developing countries. Age-specific incidence and mortality rates of HS were statistically significantly greater in developing countries after the age of 39 (Figure 3). There was no statistically significant difference in the age-specific prevalence rates between developed and developing countries after age 54 (Figure 3). However, the prevalence rates of HS in younger age groups were significantly greater in developed countries.

Figure 2.

Figure 2

Figure 2

Age-specific incidence, prevalence and mortality rates of ischaemic stroke per 100,000 people per year by country development status in 2013 (shadowed area around solid lines represents 95% uncertainty intervals).

Figure 3.

Figure 3

Figure 3

Age-specific incidence, prevalence and mortality rates of haemorrhagic stroke per 100,000 people per year by country development status in 2013 (shadowed area around solid lines represents 95% uncertainty intervals).

Analysis of the percentage contribution of IS and HS to all diseases (Table 4) showed that the relative burden of strokes in the world increased from 1990 to 2013, particularly for the burden due to IS in which the increase in DALYs and in deaths reached a statistically significant level. In developing countries, statistically significant increases in DALYs and deaths due to stroke were present for both IS and HS, while there was little change in YLDs. In developed countries, we observed a decrease in the proportional contribution of DALYs and deaths from IS and HS to all diseases but an increase in the proportional contribution of YLDs due to stroke. In comparison to other causes of DALYs in the world (Figure 4), stroke was the second largest contributor after ischaemic heart disease globally and in developing countries, and the third largest contributor to DALYs in developed countries (after ischaemic heart disease and lower back and neck pain), with significant regional variation in disease burden across both developed and low to middle-income countries.

Table 4.

Proportional (%) contribution of ischaemic and haemorrhagic strokes burden (with 95% uncertainty intervals [UI]) to all health conditions by year and country development status

Metrics Developing countries
1990 2013
Ischaemic stroke DALYs 0.90 (0.75 – 1.04) 1.65 (1.32 – 1.87)
Deaths 2.97 (2.55 – 3.42) 5.19 (4.20 – 5.72)
YLDs 0.13 (0.10 – 0.16) 0.16 (0.12 – 0.21)
Haemorrhagic stroke DALYs 2.14 (1.90 – 2.40) 2.79 (2.48 – 3.25)
Deaths 5.22 (4.62 – 5.76) 6.40 (5.82 – 7.53)
YLDs 0.10 (0.08 – 0.13) 0.13 (0.10 – 0.16)
Metrics Developed countries
1990 2013
Ischaemic stroke DALYs 3.96 (3.42 – 4.48) 3.49 (3.06 – 4.12)
Deaths 9.87 (8.64 – 10.82) 8.42 (7.65 – 10.03)
YLDs 0.67 (0.51 – 0.84) 0.97 (0.75 – 1.22)
Haemorrhagic stroke DALYs 2.59 (2.17 – 3.05) 2.07 (1.79 – 2.49)
Deaths 4.55 (3.79 – 5.21) 3.82 (3.33 – 4.53)
YLDs 0.13 (0.10 – 0.17) 0.21 (0.16 – 0.26)
Metrics Globally
1990 2013
Ischaemic stroke DALYs 1.34 (1.16 – 1.52) 1.94 (1.64 – 2.18)
Deaths 4.60 (4.02 – 5.12) 5.97 (5.16 – 6.52)
YLDs 0.27 (0.20 – 0.34) 0.35 (0.26 – 0.44)
Haemorrhagic stroke DALYs 2.20 (1.95 – 2.48) 2.68 (2.37 – 3.12)
Deaths 5.06 (4.45 – 5.58) 5.78 (5.29 – 6.79)
YLDs 0.11 (0.08 – 0.14) 0.14 (0.11 – 0.18)

Figure 4.

Figure 4

Figure 4

Proportion contribution (%) of age–standardised DALYs from stroke in comparison to 10 other leading causes of DALYs, Global, 2013

There were large inter- and intra-regional variations in IS and HS age-adjusted incidence, prevalence and mortality rates (Figures 5 and 6; Supplementary Tables). The highest prevalence rate of IS (1,015–1,184/100,000) was shown in developed countries (particularly USA), the lowest (up to 339/100,000) in overall developing countries. The highest IS mortality rates (124–174/100,000 person-years) were observed in Russia and Kazakhstan, and the lowest (at or below 25/100,000) in – Western Europe, North and Central America, Turkmenistan and Papua New Guinea. Prevalence rates of HS were highest (232–270/100,000) in the USA, and lowest (up to 78/100,000) in Latin America, Africa, Middle East, France, Eastern Europe, Northern part of Asia and Russia. HS mortality rates were highest (159–222/100,000 person-years) in Mongolia and Madagascar, and lowest (up to 32/100,000) in North America, most parts of Western Europe, Russia, Iran, Saudi Arabia, Morocco, Japan, Australia and New Zealand (Figure 6).

Figure 5.

Figure 5

Age-standardised prevalence and mortality of ischaemic stroke per 100,000 person-years in various regions in 2013

Figure 6.

Figure 6

Age-standardised prevalence and mortality of haemorrhagic stroke per 100,000 person-years in various regions in 2013

Discussion

The GBD 2013 stroke study supersedes all previous GBD stroke estimates. These new data confirm the previous GBD observations[1] about the significant increase in stroke burden in the world over the last two decades and substantial geographical differences in stroke burden and the directions of the changes by country income level.[1,11] We observed a greater than 3-fold increase in burden due to stroke with 4.85 million stroke deaths and 91.4 million DALYs in developing countries compared with 1.6 million deaths and 21.5 million DALYs in high- income countries. We demonstrated that in 2013 there were almost 25.7 million stroke survivors (71% with IS), 6.5 million deaths from stroke (51% died from IS), 113 million DALYs due to stroke (58% due to IS), and 10.3 million of people with new strokes (67% were IS). Over the 23 years study period (1990–2013), there was a much greater reduction in stroke mortality rates in developed countries than that in developing countries, thus further deepening the disparities in the global stroke burden.

We showed that the HS incidence and mortality are very high in developing countries. The YLD did not change due to HS mainly because of high mortality rate in developing countries. We demonstrated that globally, from 1990 to 2013, there was a statistically significant increase in HS prevalence rates and in developed countries the increase in the prevalence rates was statistically significant for both IS and HS, although the prevalence of IS after 2005 decreased. While the increase in the prevalence of HS in developing countries may be related to the high rate of undetected and/or poorly controlled arterial hypertension,[1215] stroke incidence increase[11] or even better detection of stroke in those countries, the increase in the prevalence of IS and HS in developed countries could be related to the improvements in acute stroke care, or more effective secondary prevention and greater identification of minor stroke cases (including wider use of advanced neuroimaging),[16] which is highly dependent on universal access to primary care.[17,18]

We also found that proportional contribution of DALYs and deaths due to stroke to all diseases has increased from 1990 (3.54% [95% UI 3.11–4.00] and 9.66% [95% UI 8.47–10.70%]) to 2013 (4.62% [95% UI 4.01–5.30] and 11.75% [95% UI 10.45–13.31%], respectively) with a diverging trend in developed and developing countries: a statistically significant increase of the proportional contribution of stroke-related DALYs and stroke-related deaths in developing countries, and a trend, though not statistically significant, towards reduction of the proportional contribution of stroke-related DALYs and stroke-related deaths in developed countries. Apart from health transition in developing nations, this may also be explained by the widening gap in stroke prevention and management between developed and developing countries.[1921] It may emphasize the pressing need for improving stroke prevention and treatment across the world.[22] The results of GBD 2013 showed the rise in the number of people with multi-morbidity and sequelae driven by longevity. Multi-morbidity has major implications for health systems and research, including stroke community.[23,24]

Although this research was based on the most comprehensive stroke epidemiological data relevant to the 1990–2013 study period and utilised the latest advances in DISMOD-MR stroke modeling techniques, it was not free from some limitations. Because death data were not available for all countries, mortality estimates relied on geospatial statistical models based on country-specific information. There was still lack of sufficient epidemiological data on stroke in most countries of the world, particularly in developing nations. To address this limitation, we used country-level covariate data and applied out-of-sample validity testing to assess mortality model performance. Statistical models of stroke incidence and prevalence also relied on Bayesian methods and all available data on incidence and prevalence for each type of stroke. In particular, data from subnational regions were often assumed to represent an entire country. Although data were borrowed across time which may blunt actual trends in disease epidemiology, the initial findings were reviewed by a global network of stroke experts to assess plausibility and then subsequent refinements were made to data sources and modeling strategies based on their comments and suggestions. It should also be noted that current estimates combine intracerebral haemorrhage with other more rare stroke types (such as subarachnoid haemorrhage) to better reflect the burden due to HS. To accurately reflect total disease burden, analysis was not limited to first-ever-in-a-lifetime strokes but also reflects all recurrent events. We were not able to report country-level incidence data because modeling at this level of detail is still under development. The GBD 2015 Study estimates will also include estimates of total stroke incidence (IS and HS combined) that we were not able to provide for this paper. Strengths of the study include the utilisation of the latest advances in DisMod stroke modeling techniques and a more comprehensive dataset available for the analysis after 2010.

Stroke is currently the second largest contributor to DALYs after ischaemic heart disease globally in developing countries, and it is third largest contributor to DALYs in developed countries (after ischaemic heart disease and low back and neck pain). This emphasizes the importance of stroke as a leading global health problem that requires urgent and sustained attention from governments, health care policy makers, international agencies, clinicians, public health specialists and individual citizens. If the current trend in stroke burden continues, the UN Global Targets to reduce premature mortality from NCDs[22] (including stroke) by 25% by 2025 will not be met. More efficient stroke prevention strategies and improved organization of stroke systems of care are urgently needed to halt and eventually reverse the stroke pandemic. Although there were improvements in the rates of DALYs, mortality and incidence rates from 1990 to 2013, the magnitude of the differences between these changes in developed and developing countries increased over time, suggesting disparities in the access to and quality of primary and secondary prevention and acute care between these countries. Therefore, there is an urgent need for action to negate these disparities.

Supplementary Material

Acknowledgments

This work was undertaken as a part of the Global Burden of Diseases, Injuries, and Risk Factors (GBD 2013) study. The results in this paper are prepared independently of the final estimates of the GBD 2010 study. We thank Sarah Safranek, University of Washington Health Sciences Library, for her help in developing the systematic review literature search strategies; Michael F. MacIntyre, Brittany Wurtz, Caitlyn Steiner and Summer Ohno, University of Washington Institute for Health Metrics and Evaluation, for research coordination; Ryan M. Barber, University of Washington Institute for Health Metrics and Evaluation, for creating figures and tables for the paper; Hannah Gardener, University of Miami, for helping reviewing some studies; and Helen McDonald, AUT University National Institute for Stroke And Applied Neurosciences, for organising teleconferences and secretarial support. The authors alone are responsible for the views expressed in this publication.

Role of the funding source

Funded by the Bill and Melinda Gates Foundation. The sponsor of the study had no role in the study design, data collection, data analysis, data interpretation, or writing of the report. The Writing and GBD 2013 Global Analysis Group had access to all data sources and has responsibility for the content of the report and the decision to submit for publication.

GBD Stroke Expert Panel members (in alphabetical order by country)

Argentina (Maria Cecilia Bahit); Australia (Amanda Thrift, Atte Meretoja, Bill Stavreski, Craig Anderson, Edwin Pearse, Geoffrey Donnan, Graeme Hankey, Mark T. Mackay, Stephen Davis, Zanfina Ademi; Austria (Michael Brainin); Azerbaijan (Tural Guliyev); Bahrain (Randah R. Hamadeh); Barbados (Heather Harewood, Karen Springer); Brazil (Iuri da Costa Leite, Jefferson Gomes Fernandes, Norberto Cabral, Paulo Lotufo); Bulgaria (Klara Dokova); Canada (Farshad Pourmalek, Luciano A. Sposato, M. Patrice Lindsay, Patricia Riccio); Chile (Pablo M. Lavados); China (Bin Li, Chuanhua Yu, Guohong Jiang, Jixiang Ma, Maigeng Zhou, Ming Liu, Shankuan Zhu, Wenzhi Wang, Xiaofeng Liang, XXX Deji, Yong Zhang); Colombia (Gabriel Alcalá-Cerra, Gabrielle DeVeber), Denmark (Hanne Christensen, Thomas Truelsen); Egypt (Foad Abd-Allah); Ethiopia (Awoke Temesgen, Berhe Weldearegawi Sahle, Semaw Abera, Yohannes Adama Melaku), Fiji (Devina Nand); France (Maurice Giroud); Germany (Jost B. Jonas, Matthias Endres, Ronny Westerman); Greece (Konstantinos Stroumpoulis); India (Dorairaj Prabhakaran, Jeyaraj Durai Pandian, Man Mohan Mehndiratta, Nobhojit Roy, Panniyammakal Jeemon, Rajeev Gupta, Vasanthan Rajagopalan); Indonesia (Soewarta Kosen, Tati Suryati Warouw); Iran (Reza Malekzadeh); Ireland (Martin O’Donnell); Israel (David Tanne, Natan Bornstein); Italy (Stefano Ricci, Valeria Caso); Japan (Yoshihiro Kokubo, Yukito Shinohara); Jordan (Majed Asad); Kenya (Vitalis Kizito Bwire); Korea (Sun Ha Jee, Young-Ho Khang); Malaysia (Kim Yunjin, Ramesh Sahathevan); Morocco (Fortune Gankpe); Myanmar (Chaw Yin Myint); New Zealand (Priya Parmar, Rita Krishnamurthi, Suzanne Barker-Collo, Valery Feigin); Nigeria (Rufus Olusola Akinyemi); Norway (Ole Norheim); Qatar (Shams Eldin Khalifa); Russia (Michael Kravchenko, Michael Piradov, Nicolay Shalamov, Vasiliy Vlassov, Yuri Varakin); Rwanda (Jean De Dieu Ngirabega, Jean Pierre Nyemazi, Marie Aimee Muhimpundu); Saudi Arabia (Mohammad Saeedi, Neeraj Bedi); Singapore (Narayanaswamy Venketasubramanian); South Africa (Andre Pascal Kengne); Spain (David Rojas-Rueda, Ferrán Catalá-López); Sri Lanka (Samath Dharmaratne); Sweden (Bo Norrving, Rasmus Havmoeller); The Netherlands (Johanna M. Geleijnse); Uganda (Leo Atwine); United Kingdom (Amitava Banerjee, Charles Wolfe, Derrick Bennett, Finbar O’Callaghan, Ivy Shiue, Julia Critchley, Majid Ezzati, Michael Soljak, Myles Connor, Peter Rothwell, Rajiv Chowdhury, Rustam Al-Shahi Salman, William Whiteley, Zhengming Chen); Uruguay (Mercedes Colomar); USA (Adnan Durrani, Anand Dayama, Andrew Moran, Awoke Misganaw, Brett Kissela, Catherine Amlie-Lefond, Catherine O. Johnson, Cheng Huang, Chugh Sumeet, Daniel Kim, David Cundiff, David Lawrence Tirschwell, Dhruv Kazi, Dima Qato, Edmond Kabagambe, Eric Ding, Gene Bukhman, Gene Kwan, George Mensah, George Thurston, Grant Nguyen, Gregory A. Roth, Ismael Campos-Nonato, Josef Coresh, Kate Lefondulq, Kevin Sheth, Matthew Corriere, Mohammad H. Forouzanfar, Mohsen Naghavi, Nana Mainoo, Norman Beauchamp, Ralph Sacco, Richard Gillum, Sanjay Basu, Stephen Schwartz, Sumeet Chugh, Teresa Fung, Tim Byers, Uchechukwu K.A. Sampson, Walter Rocca, Warren Lo).

Footnotes

Contributions

VLF, GAR and CM developed the study concept and oversaw the research. VLF, RK, GAR undertook reviews of studies. MHF, MN and PP provided statistical analysis of the data and produced graphs. VLF wrote the first draft of the report. MHF, MN and CM developed the statistical model and wrote a section on statistical analysis. All authors contributed to the critical revision of the manuscript for important intellectual content.

Conflict of interest

All the authors declare that they have no conflict of interest.

Disclaimer:

The views expressed in this article are those of the authors and do not necessarily represent the views of the National Heart, Lung, and Blood Institute, National Institute of Mental Health, National Institutes of Health, or the U.S. Department of Health and Human Services.

Contributor Information

Valery L. Feigin, National Institute for Stroke & Applied Neurosciences, Auckland University of Technology, Auckland, New Zealand.

Rita Krishnamurthi, National Institute for Stroke & Applied Neurosciences, Auckland University of Technology, Auckland, New Zealand.

Priya Parmar, National Institute for Stroke & Applied Neurosciences, Auckland University of Technology, Auckland, New Zealand.

Bo Norrving, Department of Clinical Sciences, Neurology, Lund University, Sweden.

George A. Mensah, Center for Translation Research and Implementation Science (CTRIS), National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.

Derrick A. Bennett, Clinical Trial Service Unit and Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.

Suzanne Barker-Collo, Clinical Training Programme, School of Psychology, The University of Auckland, Auckland, New Zealand.

Andrew Moran, Division of General Medicine, Columbia University, New York, USA.

Ralph L. Sacco, Department of Neurology, University of Miami Miller School of Medicine, Miami, Florida, USA.

Thomas Truelsen, Department of Neurology, Rigshospitalet, University of Copenhagen, Denmark.

Stephen Davis, Professor of Translational Neuroscience, University of Melbourne, Parkville, Australia.

Jeyaraj Durai Pandian, Department of Neurology, Christian Medical College, Ludhiana, Punjab, India.

Mohsen Naghavi, Department of Global Health, School of Medicine and Public Health, University of Washington, Seattle, USA.

Mohammad H. Forouzanfar, Department of Global Health, School of Medicine and Public Health, University of Washington, Seattle, USA.

Grant Nguyen, Institute for Health Metrics and Evaluation. University of Washington, Seattle, USA.

Catherine O. Johnson, Institute for Health Metrics and Evaluation. University of Washington, Seattle, USA.

Theo Vos, Department of Global Health, School of Medicine and Public Health, University of Washington, Seattle, USA.

Atte Meretoja, University of Melbourne, The Royal Melbourne Hospital L4C, Parkville, Vic., Australia.

Christopher Murray, Department of Global Health, School of Medicine and Public Health, University of Washington, Seattle, Washington, USA.

Gregory A. Roth, Institute for Health Metrics and Evaluation and the Division of Cardiology, School of Medicine, University of Washington, Seattle, Washington, USA.

Amanda Thrift, Stroke and Ageing Research (STARC), Department of Medicine, School of Clinical Sciences at Monash Health, Monash University, Clayton, Vic., Australia.

Amitava Banerjee, Farr Institute of Health Informatics Research, University College London, London, UK.

Andre Pascal Kengne, South African Medical Research Council, Parrow Valley, Cape Town, South Africa.

Awoke Misganaw, Institute for Health Metrics and Evaluation, University of Washington, Seattle, USA.

Brett M. Kissela, Department of Neurology and Rehabilitation Medicine, University of Cincinnati, Ohio, USA.

Charles Wolfe, Division of Health and Social Care Research, King’s College London, London, United Kingdom; and National Institute for Health Research Comprehensive Biomedical Research Centre, Guy’s & St. Thomas’ NHS Foundation Trust and King’s College London, London, UK.

Chuanhua Yu, Prof. of Biostatistics, Wuhan University, Wuhan, P.R. China.

Craig Anderson, The George Institute for Global Health, The University of Sydney, Royal Prince Alfred Hospital, Sydney, Australia.

Daniel Kim, Department of Health Sciences, Northeastern University, Boston, USA.

David Rojas-Rueda, Centre for Research in Environmental Epidemiology, ISGlobal, Barcelona, Spain.

David Tanne, Chaim Sheba Medical Center and Tel Aviv University, Tel Aviv, Israel.

David Lawrence Tirschwell, University of Washington School of Medicine, UW Medicine Comprehensive Stroke Center, Harborview Medical Center, Seattle, WA, USA.

Devina Nand, Health Information Unit, Dinem House, Toorak, Suva, Republic of Fiji.

Dhruv S. Kazi, UCSF School of Medicine, University of California, San Francisco, CA, USA.

Farshad Pourmalek, School of Population and Public Health, University of British Columbia, Vancouver, Canada.

Ferrán Catalá-López, Department of Medicine, University of Valencia, CIBERSAM/INCLIVA, Valencia, Spain.

Foad Abd-Allah, Department of Neurology, Cairo University, Cairo, Egypt.

Fortuné Gankpé, CHU Hassan II, Fez, Morocco.

Gabrielle deVeber, University of Toronto, Childlren’s Stroke Program, Division of Neurology, and the Research Institute, Hospital for Sick Children, Toronto, Canada.

Geoffrey Donnan, The Florey Institute of Neuroscience and Mental Health and School of Neurology. University of Melbourne, Austin Hospital campus, Parkville, VIC, Australia.

Graeme J. Hankey, School of Medicine and Pharmacology, The University of Western Australia, Crawley, and Western Aiustralian Neuroscience Research Institute, Nedlands, WA, Australia.

Hanne K. Christensen, University of Copenhagen and Bispebjerg Hospital, Copenhagen, Denmark.

Ismael Campos-Nonato, Harvard School of Public Health, Nutrition Department, Boston, MA, USA.

Ivy Shiue, Faculty of Health and Life Sciences, Northumbria University, Newcastle upon Tyne, UK.

Jefferson G. Fernandes, School of Health Education and Sciences, German Hospital Oswaldo Cruz, São Paulo, Brazil.

Jost B. Jonas, Department of Ophthalmology, Medical Faculty Mannheim of the University of Heidelberg, Germany.

Kevin Sheth, Division of Neurocritical Care and Emergency Department of Neurology Neurosciences Intensive Care Unit, Yale School of Medicine & Yale New Haven Hospital, USA.

Yunjin Kim, Faculty of Chinese Medicine Southern Malaysia, Southern University College, Johor, Malaysia.

Klara Dokova, Department of Social Medicine and Health Care Organization, Faculty of Public Health, Medical University of Varna, Bulgaria.

Konstantinos Stroumpoulis, Anesthesiology Department, Alexandra General Hospital of Athens Greece.

Luciano A. Sposato, Department of Clinical Neurological Sciences. London Health Sciences Centre, Western University, London, ON. Canada.

Maria Cecilia Bahit, Cardiology Department, INECO Neurociencias Rosario, Rosario, Sante Fe, Argentina.

Johanna M. Geleijnse, Division of Human Nutrition / Epidemiology, Wageningen University, The Netherlands.

Mark T. Mackay, Department of Neurology, Royal Children’s Hospital Melbourne and Murdoch Childrens Research Institute, Parkville, Australia.

Man Mohan Mehndiratta, Department of Neurology, Janakpuri Super Speciality Hospital, New Delhi, India.

Matthias Endres, Klinik und Hochschulambulanz für Neurologie, Charité Universitätsmedizin Berlin, Berlin, Germany.

Maurice Giroud, Dijon Stroke Registry, Service de Neurologie, Dijon, France.

Michael Brainin, Department of Clinical Neurology, Danube University Krems and Karl Landsteiner University, Krems, Austria.

Michael Kravchenko, Scientific Neurological Center, Moscow, Russia.

Michael Piradov, Scientific Neurological Center, Moscow, Russia.

Michael Soljak, School of Public Health, Imperial College, London, England.

Ming Liu, Professor of Neurology, Center of Cerebrovascular Diseases, Department of Neurology, West China Hospital, Sichuan University, Chengdu, China.

Myles Connor, Centre for Clinical Brain Sciences, The University of Edinburgh, Edinburgh, Scotland.

Narayanaswamy Venketasubramanian, Raffles Neuroscience Centre, Raffles Hospital, Singapore.

Natan Bornstein, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.

Nikolay Shamalov, Meditsinskiy Tsentr Gbou VPO Rnimu im. N.I. Pirogova Minzdrava Rossii, Moscow, Russia.

Nobhojit Roy, Environmental Health Resource Hub, School of Habitat Studies, Tata Institute of Social sciences, Mumbai, India.

Norberto Cabral, Joinville Stroke Registry, Clinica Neurológica de Joinville, University of Joinville Region, Brazil.

Norman J. Beauchamp, Department of Radiology, University of Washington, Seattle, WA, USA.

Pablo M. Lavados, Servicio de Neurología, Departamento de Medicina, Clínica Alemana de Santiago-Universidad del Desarrollo and Universidad de Chile, Santiago, Chile.

Panniyammakal Jeemon, Centre for Control of Chronic Conditions, Public Health Foundation of India and Centre for Chronic Disease Control, New Delhi, India.

Paulo A. Lotufo, Universidade de São Paulo Medical School and Centre for Clinical and Epidemiological Research, University of Sao Paulo, Brazil.

Rajiv Chowdhury, Department of Public Health and Primary Care, School of Clinical Medicine, University of Cambridge, Cambridge, UK.

Ramesh Sahathevan, UKM Medical Centre, Kuala Lumpur, Malaysia; and Calvary Healthcare, Bruce, ACT, Australia.

Randah R. Hamadeh, Department of Family and Community Medicine, College of Medicine and Medical Sciences, Arabian Gulf University, Manama, Bahrain.

Reza Malekzadeh, Digestive Disease Research Institute, Tehran University of Medical Sciences, Shariati Hospital, Tehran, Iran.

Richard Gillium, Department of Internal Medicine and Department of Community and Family Medicine, Howard University College of Medicine, Washington, DC, USA.

Ronny Westerman, Competence Center Mortality-Follow-Up of the German National Cohort, Federal Institute for Population Research, Wiesbaden, Germany.

Rufus Olusola Akinyemi, Institute for Advanced Medical Research and Training College of Medicine, University of Ibadan, Ibadan, Nigeria.

Rustam Al-Shahi Salman, Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, Scotland.

Samath D. Dharmaratne, Department of Community Medicine, Faculty of Medicine, University of Peradeniya, Peradeniya, Sri Lanka.

Sanjay Basu, Stanford Prevention Research Center, Stanford University School of Medicine, Stanford, CA, USA.

Semaw Ferede Abera, Department of Epidemiology and Biostatistics, School of Public Health, College of Health Sciences, Mekelle University, Mek’ele, Ethiopia.

Soewarta Kosen, Health Economics and Policy Analysis Unit, National Institute of Health Research & Development (NIHRD), Indonesia.

Uchechukwu K. A. Sampson, Center for Translation Research and Implementation Science (CTRIS), National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.

Valeria Caso, Stroke Unit, University of Perugia, Perugia, Italy.

Vasiliy Vlassov, National Research University Higher School of Economics, Moscow, Russia.

Yohannes Adama Melaku, School of Public Health, Mekelle University, Mekele, Ethiopia.

Yoshiohiro Kokubo, Department of Preventive Cardiology, National Cerebral and Cardiovascular Center, Osaka, Japan.

Yukito Shinohara, Tachikawa Hospital, Tokyo.

Yuri Varakin, Research Center of Neurology, Moscow, Russia.

Wenzhi Wang, Beijing Neurosurgical Institute, Beijing, China.

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