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(Stroke. 2009;40:909.)
© 2009 American Heart Association, Inc.
Original Contributions |
From the Departments of Pharmacology (E.-L.G.) and Public Health and Clinical Medicine (B.S.), Umeå University Hospital, Umeå, Sweden; the Department of Neurology (B.N.), Lund University Hospital, Lund, Sweden; and the Department of Medical Sciences (A.T.), Uppsala University Hospital, Uppsala.
Correspondence to Marie Eriksson, PhD, Department of Public Health and Clinical Medicine, Umeå University, SE-901 85 Umeå, Sweden. E-mail marie.eriksson{at}medicin.umu.se
| Abstract |
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Methods— This study included 24633 stroke events registered in Riks-Stroke, the Swedish national quality register for stroke care, during 2006. Information on background variables and treatment was collected during the hospital stay. After 3 months, the patients living situation and outcome were assessed.
Results— Women were older than men when they had their stroke (mean age, 78.4 versus 73.6 years; P<0.001). On admission to the hospital, women were more often unconscious. Among conscious patients, there was no sex-related difference in the use of stroke unit care. Men and women had equal probability to receive thrombolysis and oral anticoagulants. Women were more likely to develop deep venous thromboses and fractures, whereas men were more likely to develop pneumonia during their hospital stay. Women had a lower 3-month survival, a difference that was associated with higher age and impaired level of consciousness on admission. Women were less often living at home at the 3-month follow-up. However, the difference in residency was not present in patients <85 years who were living at home without community support before the stroke.
Conclusions— Reported sex differences in stroke care and outcome were mainly explained by the womens higher age and lower level of consciousness on admission.
Key Words: outcome registry sex stroke stroke management
| Introduction |
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Overall, results concerning sex differences related to stroke treatment and outcome are inconsistent and not easily interpreted. Additional studies are needed to evaluate possible sex differences and their underlying causes. The study performed by Glader et al on sex differences in Swedish stroke care used data from 2001.2 Since then, stroke care has been improved, eg, more patients have access to care in stroke units, thrombolytic therapy has been approved for acute stroke, and new guidelines on stroke care have been published by the Swedish National Board of Health and Welfare.10 To ensure good care for all patients with stroke, regardless of sex, it is important to further explore possible differences between men and women using recent data.
Our aim was to update results from a previous study that was carried out 5 years ago2 concerning sex-related differences in baseline characteristics, stroke management, and stroke outcome in Sweden. We also aimed to explore possible differences in thrombolytic therapy, secondary complications, secondary prevention, and patient satisfaction between men and women.
| Methods |
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Of the 17459 patients who were alive and followed up 3 months after stroke, 5843 (33.5%) answered the follow-up questionnaire by themselves in writing, 3987 (22.8%) answered in writing with help from a family member or caregiver, 3880 (22.2%) answered by telephone, 507 (2.9%) answered at a visit to the hospital, 1533 (8.8%) had a family member or caregiver who answered, and 1709 (9.8%) answered in some other way. All patients were included in the study independently of how the information was retrieved.
Variable Assessments and Definitions
Level of consciousness on admission to the hospital was recorded using 3 categories based on the Reaction Level Scale.14 Patients with Reaction Level Scale 1 were defined as alert, Reaction Level Scale 2 to 3 as drowsy but responding to stimulus, and Reaction Level Scale 4 to 8 as unconscious. Patients were defined as independent in activities of daily living if they managed dressing, toileting, and walking indoors without assistance from another person. According to a previously published algorithm,15 this corresponds to a score of
3 on the modified Rankin Scale. Depression was self-reported. Patients were asked the following question: "Do you feel depressed?" with 5 fixed response alternatives: "never, nearly never," "sometimes," "often," "always," and "do not know." Patients who answered "often" or "always" were considered to have self-reported depression, and patients who answered "do not know" were considered as missing. General state of health was assessed in a similar way. The patients were asked the following question: "How do you regard your general state of health?" with the alternatives: "very good," "fairly good," "moderately bad," "very bad," and "do not know." Patients who answered "moderately bad" or "very bad" were defined as perceiving their health status as bad. The patients were asked the following question: "Are you satisfied with the care you received in the hospital?," and they were asked 6 additional questions concerning treatment by the staff, rehabilitation, dialogue with the physician and other staff, stroke information about affliction, and where to turn for support after hospitalization. Each question had 5 response alternatives: "very satisfied," "satisfied," "dissatisfied," "very dissatisfied," and "do not know." Patients responding with any of the first 2 alternatives were considered to be satisfied.
Statistical Methods
Age was summarized by mean values and categorical variables by proportions. Differences between men and women were tested using Student t test for age and length of hospital stay and Pearson
2 test for proportions. Because women were older at stroke presentation, age-adjusted analysis was conducted using multiple logistic regression, including sex and age as independent covariates. The results from the multiple regressions are presented as age-adjusted ORs with corresponding 95% CIs. Possible sex differences were further analyzed in more consistent subgroups of patients and by adjustments for additional confounding factors. CIs and probability values were not corrected for multiple testing. All statistical analyses were performed using SAS version 9.1.3.
| Results |
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Hospital Care
Women were less often treated in a stroke unit (P<0.001), a difference that was not explained by womens higher age alone (OR, 0.904; 95% CI, 0.846 to 0.966). More women than men had impaired consciousness on admission (P<0.001). The difference was consistent in all age groups (<65, 65 to 74, 75 to 84, and
85 years) and was not affected by adjustments for the baseline factors presented in Table 1 or type of stroke (OR, 1.449; 95% CI, 1.332 to 1.575). Unconscious patients were less often treated in a stroke unit (59.6% versus 83.1%, P<0.001). After adjustment for level of consciousness on admission, the estimated sex difference in stroke unit care was small and nonsignificant (OR, 0.942; 95% CI, 0.880 to 1.007). In patients
80 years with ischemic stroke, 3.4% received thrombolytic therapy. No difference between men and women was seen (Table 2).
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The mean length of stay in the hospital, including in-hospital rehabilitation, was 17.5 days (median, 11 days) for women and 17.2 days (median, 10 days) for men (P=0.199). Men were more likely than women to be discharged to home (Table 2). The difference in discharge destination was smaller in patients <85 years who were living at home without community support, with a spouse, before their stroke (OR, 0.894; 95% CI, 0.793 to 1.007). Compared with men, women were more likely to experience deep venous thromboses or pulmonary embolism and fractures (Table 2) during their hospital stay. The differences were significant both after age adjustments and in the subgroup of patients who were independent in activities of daily living before stroke (OR, 1.592; 95% CI, 1.182 to 2.143 for deep venous thromboses/pulmonary embolism and OR, 1.490; 95% CI, 1.048 to 2.119 for fractures). Women were less likely to experience pneumonia during the hospital care (P=0.001), and this difference was not affected by age (Table 2) or smoking (OR, 0.740; 95% CI, 0.633 to 0.865 for nonsmokers).
Secondary Prevention
At discharge from the hospital, women were less likely to receive lipid-lowering drugs (P<0.001). After adjustments for age, there were no differences between men and women with respect to antihypertensive treatment or antithrombotic therapy (Table 2). In the group of patients
80 years of age with ischemic stroke and atrial fibrillation, the proportions of patients receiving oral anticoagulants were similar for men and women (P=0.235).
Outcome 3 Months After Stroke
Three months after stroke, 20.2% of the women and 15.2% of the men had died (P<0.001). The womens higher fatality rate, to a large extent, was explained by their higher age and impaired consciousness (Table 3). In contrast, a comparison of men and women with the same level of consciousness on admission showed that the women had a better 3-month survival than the men (OR, 0.899; 95% CI, 0.831 to 0.974). Among patients who were independent before stroke, women were more likely to be dependent after 3 months (P<0.001), but the estimated sex difference decreased and was no longer significant after adjustment for age (OR, 1.079; 95% CI, 0.995 to 1.170).
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At the 3-month follow-up, a total of 13267 (79.4%) of the 16714 stroke survivors with information on residency were living at home. Of the 15734 stroke survivors who were living at home before their stroke, 13097 (83.2%) were still living at home 3 months after their stroke. In patients living at home without community support before stroke, more women than men were living in an institution at follow-up (P<0.001). The difference was not significant in patients <85 years of age or in older patients who were living alone. In older patients,
85 years, who were living with a spouse before stroke, women were more likely than men to be institutionalized (P=0.034; Figure).
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Three months poststroke, more women than men reported depression and bad health status (P<0.001). Those differences were independent of age and level of consciousness. There was no sex-related difference in perceived speech difficulties (Table 3).
Patients Satisfaction
On all measured aspects, independent of age, women were less satisfied with the care they received in the hospital than were men (Table 3). Excluding patients who reported that they often or always felt depressed at the follow-up did not affect the difference (data not shown). Patients who were independent in activities of daily living and were living at home together with a spouse before their stroke, in general, were more satisfied with the care they received in the hospital than other patients (94.5% versus 88.9%, P<0.001). The sex difference in that subgroup was also smaller but remained statistically significant for treatment by the staff (OR, 0.738; 95% CI, 0.592 to 0.919), dialogue with the physician (OR, 0.771; 95% CI, 0.687 to 0.866), dialogue with other staff (OR, 0.869; 95% CI, 0.772 to 0.979), and stroke information (OR, 0.849; 95% CI, 0.759 to 0.950).
Lost to Follow-Up
A total of 1403 (11.4%) men and 1416 (11.5%) women were lost to follow-up. Of the 21545 men and women who were discharged from the hospital alive, patients lost to follow-up were more likely to live in an institution or alone before their stroke. They were also more likely to have had previous strokes.
| Discussion |
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Thromboembolism related to atrial fibrillation has been shown to be more common in women than in men.17 Cardioembolic strokes are more likely to be severe than other stroke subtypes and thus more likely to affect level of consciousness.18 This may explain womens lower level of consciousness at hospital admission.
Womens higher risk of being institutionalized 3 months after stroke in patients
85 years who were living with a spouse before stroke may have sociodemographic causes; womens spouses are generally older, whereas mens spouses are younger.
Men and women were managed alike in most aspects. They were treated similarly in the hospital with respect to stroke thrombolysis and stroke unit care. The sex-related difference in antithrombotic medication that was seen 5 years ago2 has now disappeared. Our observation on the use of antithrombotics is in line with other recent register studies from other populations.3,9 Although those studies reported sex differences in thrombolytic therapy, other previous studies8,19 match our results on this therapy. Womens lower odds of receiving lipid-lowering drugs is in accordance with a study from Scotland.20 Several studies have shown that more men with stroke have a history of myocardial infarction,5,8,16 which may explain our finding of a sex difference.
Other studies have demonstrated that secondary complications are more common in women,21,22 but few studies have had the power to explore sex-related differences in specific secondary complications. Our observation, that men have a higher risk to experience pneumonia, supports the findings by Kapral et al.8 Gargano et al9 studied deep venous thromboses/pulmonary embolism and pneumonia but did not observe the same differences we did. Most poststroke fractures are caused by accidental falls.23 Womens higher risk of fractures after stroke is compatible with womens higher risk of fractures in the general Swedish population >60 years of age24 and their higher risk of osteoporotic fractures.25
Self-reported depression has been previously studied in Riks-Stroke,2,26 and women continue to be more depressed and also perceive their general health as worse than men do 3 months after stroke. Female patients were less satisfied with the care, rehabilitation, dialogue, and information they received during the hospital stay than were male patients. Our finding is in accordance with a survey of 5857 hospital-admitted patients by Woods et al.27 A study on stroke care decision-making has suggested that women worry more about risks and want more information before they make decisions about their stroke care than do men.28 It may be that female patients with stroke need a different type of information or that the information should be presented in a different way than for men.
This study used data from a nationwide quality register that includes all Swedish hospitals that admitted patients with acute stroke. Riks-Stroke has high coverage and the effect of patient selection bias is likely to be small. Our work also has limitations that could potentially affect the interpretation of our results. There was no information on stroke severity, besides level of consciousness on admission, and the information about comorbid conditions was limited. Neither was there any information on lesion size or location from neuroimaging. Many outcome measures were also self-reported rather than assessed clinically. Patient satisfaction with hospital care was assessed 3 months after stroke and there is a risk of recall bias. Eleven percent was lost to follow-up. The proportions lost to follow-up were similar for men and women and it is hence unlikely to have had any substantial effect on differences related to sex.
We chose to present probability values and CIs without adjustments for multiple testing. This reduced the risk of a Type II error (failing to detect a true difference), but enhanced the risk of a Type I error (spurious significant difference). This study had high power, and the main results would still be valid using a significance level of 0.001, which would preserve the risk of an overall Type I error at a low level.
In conclusion, men and women are managed similarly in the hospital on most aspects. Differences related to sex in case fatality and activities of daily living dependency remain but are associated with womens higher age and lower level of consciousness on admission. Studies with more detailed information on, eg, stroke severity and comorbidities, are needed to further explore womens lower level of consciousness at hospital admission and differences in secondary complications.
| Acknowledgments |
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Riks-Stroke is funded by the Swedish National Board of Health and Welfare, Norrländska Strokefonden, Vårdalsstiftelsen, King Gustaf Vs and Queen Victorias Foundation, and the Swedish Medical Research Council.
Disclosures
None.
| Footnotes |
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Received February 18, 2008; revision received May 30, 2008; accepted June 3, 2008.
| References |
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2. Glader EL, Stegmayr B, Norrving B, Terént A, Hulter Åsberg K, Wester PO, Asplund K. Sex differences in management and outcome after stroke: a Swedish national perspective. Stroke. 2003; 34: 1970–1975.
3. Foerch C, Misselwitz B, Humpich M, Steinmetz H, Neumann-Haefelin T, Sitzer M. Sex disparity in the access of elderly patients to acute stroke care. Stroke. 2007; 38: 2123–2126.
4. Niewada M, Kobayashi A, Sandercock PA, Kaminski B, Czlonkowska A. Influence of gender on baseline features and clinical outcomes among 17370 patients with confirmed ischaemic stroke in the international stroke trial. Neuroepidemiology. 2005; 24: 123–128.[CrossRef][Medline] [Order article via Infotrieve]
5. Gargano JW, Reeves MJ. Sex differences in stroke recovery and stroke-specific quality of life: results from a statewide stroke registry. Stroke. 2007; 38: 2541–2548.
6. Paolucci S, Bragoni M, Coiro P, De Angelis D, Fusco FR, Morelli D, Venturiero V, Pratesi L. Is sex a prognostic factor in stroke rehabilitation? A matched comparison. Stroke. 2006; 37: 2989–2994.
7. Holroyd-Leduc JM, Kapral MK, Austin PC, Tu JV. Sex differences and similarities in the management and outcome of stroke patients. Stroke. 2000; 31: 1833–1837.
8. Kapral MK, Fang J, Hill MD, Silver F, Richards J, Jaigobin C, Cheung AM. Sex differences in stroke care and outcomes: results from the Registry of the Canadian Stroke Network. Stroke. 2005; 36: 809–814.
9. Gargano JW, Wehner S, Reeves M. Sex differences in acute stroke care in a statewide stroke registry. Stroke. 2008; 39: 24–29.
10. Norrving B, Wester P, Sunnerhagen KS, Terént A, Sohlberg A, Berggren F, Wester PO, Asplund K. Beyond conventional stroke guidelines: setting priorities. Stroke. 2007; 38: 2185–2190.
11. Asplund K, Hulter Åsberg K, Norrving B, Stegmayr B, Terént A, Wester PO. Riks-Stroke—a Swedish national quality register for stroke care. Cerebrovasc Dis. 2003; 15 (suppl 1): 5–7.[CrossRef][Medline] [Order article via Infotrieve]
12. Hallström B, Jonsson AC, Nerbrand C, Petersen B, Norrving B, Lindgren A. Lund Stroke Register: hospitalization pattern and yield of different screening methods for first-ever stroke. Acta Neurol Scand. 2007; 115: 49–54.[CrossRef][Medline] [Order article via Infotrieve]
13. Appelros P, Hogeras N, Terént A. Case ascertainment in stroke studies: the risk of selection bias. Acta Neurol Scand. 2003; 107: 145–149.[CrossRef][Medline] [Order article via Infotrieve]
14. Starmark JE, Stalhammar D, Holmgren E. The Reaction Level Scale (RLS85). Manual and guidelines. Acta Neurochir (Wien). 1988; 91: 12–20.[CrossRef][Medline] [Order article via Infotrieve]
15. Eriksson M, Appelros P, Norrving B, Terént A, Stegmayr B. Assessment of functional outcome in a national quality register for acute stroke: can simple self-reported items be transformed into the modified Rankin Scale? Stroke. 2007; 38: 1384–1386.
16. Lai SM, Duncan PW, Dew P, Keighley J. Sex differences in stroke recovery. Prev Chronic Dis. 2005; 2: A13.[Medline] [Order article via Infotrieve]
17. Fang MC, Singer DE, Chang Y, Hylek EM, Henault LE, Jensvold NG, Go AS. Gender differences in the risk of ischemic stroke and peripheral embolism in atrial fibrillation: the AnTicoagulation and Risk factors In Atrial fibrillation (ATRIA) study. Circulation. 2005; 112: 1687–1691.
18. Miller PS, Andersson FL, Kalra L. Are cost benefits of anticoagulation for stroke prevention in atrial fibrillation underestimated? Stroke. 2005; 36: 360–366.
19. Katzan IL, Hammer MD, Hixson ED, Furlan AJ, Abou-Chebl A, Nadzam DM. Utilization of intravenous tissue plasminogen activator for acute ischemic stroke. Arch Neurol. 2004; 61: 346–350.
20. Simpson CR, Wilson C, Hannaford PC, Williams D. Evidence for age and sex differences in the secondary prevention of stroke in Scottish primary care. Stroke. 2005; 36: 1771–1775.
21. Davenport RJ, Dennis MS, Wellwood I, Warlow CP. Complications after acute stroke. Stroke. 1996; 27: 415–420.
22. Indredavik B, Rohweder G, Naalsund E, Lydersen S. Medical complications in a comprehensive stroke unit and an early supported discharge service. Stroke. 2008; 39: 414–420.
23. Ramnemark A, Nyberg L, Borssen B, Olsson T, Gustafson Y. Fractures after stroke. Osteoporos Int. 1998; 8: 92–95.[CrossRef][Medline] [Order article via Infotrieve]
24. Johnell O, Kanis JA, Jonsson B, Oden A, Johansson H, De Laet C. The burden of hospitalised fractures in Sweden. Osteoporos Int. 2005; 16: 222–228.[CrossRef][Medline] [Order article via Infotrieve]
25. Johnell O, Kanis J. Epidemiology of osteoporotic fractures. Osteoporos Int. 2005; 16 (suppl 2): S3–7.[CrossRef][Medline] [Order article via Infotrieve]
26. Eriksson M, Asplund K, Glader EL, Norrving B, Stegmayr B, Terént A, Hulter Åsberg K, Wester PO. Self-reported depression and use of antidepressants after stroke: a national survey. Stroke. 2004; 35: 936–941.
27. Woods SE, Heidari Z. The influence of gender on patient satisfaction. J Gend Specif Med. 2003; 6: 30–35.[Medline] [Order article via Infotrieve]
28. Kapral MK, Devon J, Winter AL, Wang J, Peters A, Bondy SJ. Gender differences in stroke care decision-making. Med Care. 2006; 44: 70–80.[CrossRef][Medline] [Order article via Infotrieve]
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