Infections Up to 76 Days After Stroke Increase Disability and Death
verfasst von:
Annastazia E. Learoyd, Lisa Woodhouse, Laurence Shaw, Nikola Sprigg, Daniel Bereczki, Eivind Berge, Valeria Caso, Hanne Christensen, Ronan Collins, Anna Czlonkowska, Anwar El Etribi, Tracy D. Farr, John Gommans, Ann-Charlotte Laska, George Ntaios, Serefnur Ozturk, Stuart J. Pocock, Kameshwar Prasad, Joanna M. Wardlaw, Kevin C. Fone, Philip M. Bath, Rebecca C. Trueman, on behalf of the ENOS Trial investigators
Early infection after stroke is associated with a poor outcome. We aimed to determine whether delayed infections (up to 76 days post-stroke) are associated with poor outcome at 90 days. Data came from the international Efficacy of Nitric Oxide Stroke (ENOS, ISRCTN99414122) trial. Post hoc data on infections were obtained from serious adverse events reports between 1 and 76 days following stroke in this large cohort of patients. Regression models accounting for baseline covariates were used to analyse fatalities and functional outcomes (modified Rankin Scale (mRS), Barthel Index, Euro-Qol-5D) at 90 days, in patients with infection compared to those without infection. Of 4011 patients, 242 (6.0%) developed one or more serious infections. Infections were associated with an increased risk of death (p < 0.001) and an increased likelihood of dependency (measured by mRS) compared to those of all other patients (p < 0.001). This remained when only surviving patients were analysed, indicating that the worsening of functional outcome is not due to mortality (p < 0.001). In addition, the timing of the infection after stroke did not alter its detrimental association with fatality (p = 0.14) or functional outcome (p = 0.47). In conclusion, severe post-stroke infections, whether occurring early or late after stroke, are associated with an increased risk of death and poorer functional outcome, independent of differences in baseline characteristics or treatment. Not only are strategies needed for reducing the risk of infection immediately after stroke, but also during the first 3 months following a stroke. This study is registered: ISRCTN registry, number ISRCTN99414122, ClinicalTrials.gov Identifier, NCT00989716.
The online version of this article (doi:10.1007/s12975-017-0553-3) contains supplementary material, which is available to authorized users.
Members of the ENOS Trial investigators are listed in ENOS trial investigators. Lancet. 2015;385(9968):617–28
Introduction
Approximately 15 million people in the world have a stroke each year [1]. Of these, 30.0% will develop infections in the first week post-stroke [2], which is associated with an increase in the likelihood of death [3, 4] and the extent of disability [5, 6]. These data, combined with the growing body of evidence from other neurological disorders, indicate that infection has a detrimental effect on the damaged brain [7, 8].
The risk of infection is increased after a stroke due to immunosuppression [9, 10], dysphagia and aspiration [11], cannulation/catherisation [12] and reduced mobility [13]. However, only a few studies have examined the effect of infections beyond the first 14 days after a stroke, and these showed that infections in the period from 14 up to 30 days post-stroke were associated with increased dependence on hospital discharge and increased mortality [14, 15].
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The international multicentre Efficacy of Nitric Oxide in Stroke (ENOS) trial [16] collected data on all serious adverse events until 90 days post-randomisation, including common infections such as pneumonia and urinary tract infections [17]. Using the data collected in this trial, we aimed to perform a post hoc examination of the effect of infection up to 76 days post-stroke on survival and functional outcome and quality of life at 90 days post-randomisation.
Methods
ENOS Trial
The ENOS was an international multicentre trial of transdermal glyceryl trinitrate (GTN) or no GTN [16] in patients with acute ischaemic stroke and high blood pressure. Those taking antihypertensive medication were also randomised to continue or temporarily stop their medication in a partial factorial design. Patients were randomised within 48 h of stroke onset and treated for 7 days. This study is registered: ISRCTN registry, number ISRCTN99414122, ClinicalTrials.gov Identifier, NCT00989716.
Data collection for the ENOS was performed using a secure web interface and included the collection of baseline demographic (age, sex) and clinical variables (comorbidities, stroke type, subtype and severity [Scandinavian Stroke Scale, SSS]). Baseline data and main results have been reported previously [16, 18].
Target Population for the Present Analysis
In addition to the ENOS exclusion criteria [16, 19], the following patients were excluded (Fig. 1): those with a previous stroke (to reduce chance of patients having previous disability/dependency), those with a non-stroke diagnosis and patients with serious adverse events (SAEs) reported after 76 days (in an attempt to prevent SAEs directly affecting outcome at 90 days). SAEs were defined as those events that were fatal, caused disability, were life-threatening, led to hospital admission, prolonged discharge in a hospitalised patient or were associated with birth defects in a child born to a trial participant (http://www.nottingham.ac.uk/~nszwww/enos/enosprotocolv15.pdf). SAEs that arose at any time point from the randomisation to final follow-up at day 90 were adjudicated blinded to treatment assignment by Daniel Bereczki and Nikola Sprigg.
Fig. 1
Criteria used for selection of patients for analysis of the effects of infection. Patients were excluded due to lack of defined stroke type, previous stroke or serious adverse events (SAEs) after 76 days. Remaining patients were grouped based on the absence of SAEs or the presence of infections, secondary stroke-related cerebral events (SSRCEs) or other SAEs. Patients with infections were compared to all three of the other patient groups (individually or combined (termed: all other patients)) to assess the effect of infection on case fatality and functional outcome
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Patients included in the analysis were grouped based on the presence of different types of SAEs. SAEs were categorised as infection, secondary stroke-related cerebral event (SSRCE) or other SAE. SSRCE was defined as cerebral oedema, complication or extension of initial stroke, haemorrhagic transformation, intracerebral/extracerebral/intracranial bleeds, transient ischaemic attack or recurrent stroke. These are known to worsen the outcomes being measured. Other SAEs included any other event ranging from falls to cardiac events (Supplementary Table I). Patients with no reported SAEs but who had died by 90 days (as determined by the outcome measures) were also placed in the other SAE category. Patients with multiple SAEs were categorised as SSRCEs (if they had at least one SSRCE) or infection (if they had no SSRCEs, but had infection). Patients with infection were also categorised by their time of presentation after randomisation: within 7 days (early), 8–28 days (intermediate) and 29–76 days (late). This was to allow the effect of infections acquired at different time points to be delineated.
Outcome Measures
The outcome measures were case fatalities (by 90 days), functional/vital status as measured by the modified Rankin Scale (mRS, primary outcome) and activities of daily living (Barthel Index and Euro-QoL-5D Health Utility State [HUS]). The telephone-Mini Mental State Examination (t-MMSE), modified Zung Depression Scale (ZDS), modified Telephone Interview for Cognitive Status (TICS-M), EuroQol-Visual Analogue Scale (EQ-VAS) and verbal fluency (animals named in 1 min) were also assessed in the ENOS trial but not used in the analysis due to insufficient numbers of responses in the subgroups (<20). All functional measures were determined by telephone at 90 days by an assessor blinded to treatment and other clinical details.
Statistics
All analyses were performed using SPSS, version 22. Data are number (%), mean (standard deviation, SD) or median (interquartile range, IQR). Significance is taken at p < 0.05. Adjustments for multiplicity of testing were not performed.
Case fatalities in patients with infections were compared to fatalities in all other patients, or to patients with either SSRCEs or other SAEs using Cox regression with infection, SSRCEs and other SAEs as time-updated covariates. This second analysis allowed patients with infection to be compared to other patient groups of a similar size whom also experienced serious adverse events. To control for factors which are known to alter outcome, other covariates were also included in these analyses: age, sex, hypertension, diabetes, use of alteplase, stroke type and severity at baseline, and the ENOS treatment groups. An additional model (analysing just patients with infection) was used to assess the effect of time of infection on fatality across the patient group.
Functional outcome (mRS, Barthel Index and HUS) in patients with infection and all other patients (without SAEs, with SSRCEs or with other SAEs) was analysed using ordered probit regression. The covariates described above were included in the analysis. Ordered probit regression was repeated using only patients who survived to 90 days in order to separate the effect of infection on functional outcome from that on mortality, as the functional outcome measures included death in the scoring system. To assess if the time that infection developed influenced outcome within the surviving population, regressions compared functional outcome in patients acquiring infections at each time points (1–7, 8–28 and 29–76 days post-stroke) to functional outcome in all other patients. An additional model (analysing just patients with infection) was used to assess the effect of time of infection on dependency across the patient group. To control further for baseline differences and confirm the findings of regression analysis, patients with infections were paired with those that had no SAEs. These paired groups were compared using ordered probit regression without covariates (see Supplemental Table II and Figure II for full details).
Results
Participants and SAE Occurrence
Of the 4011 patients enrolled into the ENOS trial, 703 were excluded from this analysis. Of the remaining patients, 760 developed SAEs with 1091 SAEs reported in total. Two hundred ninety-three (26.9%) of these SAEs were infections, which occurred in 242 patients. Thirty of these patients were removed from the infection group due to the additional presence of a SSRCE. Out of the 293 reported infections, 192 (65.5%) were pneumonia and 57 (19.5%) were urinary tract infections. Of the remaining SAEs reported, 260 (23.8%) were SSRCEs and 538 (49.3%) were other SAEs occurring in 242 and 306 patients, respectively. The characteristics of patients with infections, SSRCEs, other SAEs or no SAEs are shown in Table 1.
Table 1
Baseline characteristics of all patients in the ENOS trial and groups of patients used in this study
Variable
All patients
Patients with:
Infections
SSRCEs
Other SAEs
No SAEs
No. of patients
4011
212
242
306
2524
Age (years)
70.3 (12.2)
77.8 (9.9)
72.5 (12.7)
72.7 (11.1)
68.7 (12.1)
Sex, male
2297 (57.3%)
118 (55.7%)
119 (49.2%)
157 (51.3%)
1486 (58.9%)
Risk factors
Hypertension
2607 (65.0%)
134 (63.2%)
165 (68.2%)
195 (63.7%)
1549 (61.4%)
Diabetes
699 (17.4%)
35 (16.5%)
48 (19.8%)
45 (14.7%)
396 (15.7%)
Thrombolysis
425 (10.6%)
27 (12.7%)
32 (13.2%)
45 (14.7%)
252 (10.0%)
Stroke type
Ischaemic
3342 (83.3%)
181 (85.4%)
197 (81.4%)
275 (89.9%)
2097 (83.1%)
Haemorrhagic
629 (15.7%)
31 (14.6%)
45 (18.6%)
31 (10.1%)
427 (16.9%)
Pre-morbid mRS
0 (0–1)
0 (0–1)
0 (0–0)
0 (0–0)
0 (0–0)
SSS score (/58)
36 (24–44)
22 (12–30)
26 (14–39)
32 (21–41)
38 (28–46)
GTN treatment
2000 (49.9%)
108 (50.9%)
135 (55.8%)
167 (54.6%)
1230 (48.7%)
Time to treatment
26.0 (12.9)
27.7 (12.6)
23.7 (12.8)
25.6 (14.2)
26.2 (12.7)
Developed SAEs
1057 (26.4%)
Death by 90 days
494 (12.3%)
113 (53.3%)
125 (51.9%)
91 (29.7%)
0 (0%)
Data is described as number (% of patients in group) for categorical data, mean (SD) for continuous data or median (IQR) for ordinal data
The incidence rate of infections, SSRCEs and other SAEs followed a non-linear pattern with more SAEs reported shortly after stroke onset. The median number of days between stroke onset and SAE occurrence was 4 (2–12) days for SSRCEs, 11 (3–32) days for infections and 14 (4–33) days for other SAEs.
Case Fatality Rate in Patients with Infections, SSRCEs or Other SAEs
Infections significantly increased the likelihood of fatality (Fig. 2a; hazard ratio [HR] = 6.47, 95% confidence interval [CI] = 5.01–8.35, p < 0.001) compared to all patients, irrespective of other covariates. When compared to SSRCEs or other SAEs (Fig. 2b), both infections (HR = 1.94, 95% CI = 1.50–2.51, p < 0.001) and SSRCEs (HR = 2.02, 95% CI = 1.53–2.68, p < 0.001) increased the likelihood of fatality. The occurrence of other SAEs did not affect fatality rate (HR = 0.83, 95% CI = 0.62–1.10, p = 0.19). Analysis of the infection group alone showed that the timing of infection did not affect fatality (HR = 0.99, 95% CI = 0.99–1.00, p = 0.14), indicating that late infections were as likely to cause death as those presenting in the days after stroke. In addition, 58.4% of patients destined to die after their infection did so in the first 2 days (Supplementary Figure I).
Fig. 2
Descriptive Kaplan-Meier graphs for patients developing infections between 1 and 76 days post-stroke and other groups of patients. a Patients with infections (n = 212) in comparison to all other patients (after exclusions, n = 3072). b Patients with infections in comparison to those with secondary stroke-related cerebral events (SSRCEs, n = 242) or with other serious adverse events (SAEs, n = 306)
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Functional Outcome in Patients with Infection
Infections significantly increased the likelihood of dependency as measured by the mRS (Fig. 3a; odds ratio [OR] = 2.90, 95% CI = 2.46–3.42, p < 0.001) compared to that of all other patients irrespective of other covariates. This finding was also present for the Barthel Index (Table 2, OR = 0.34, 95% CI = 0.28–0.40, p < 0.001) and the HUS (OR = 0.62, 95% CI = 0.53–0.72, p < 0.001).
Fig. 3
Distributions in modified Rankin Scale scores at day 90 for stroke patients with infections and all other patients. a All patients with serious adverse events (SAEs) between 1 and 76 days post-stroke and patients without SAEs. b Patients who survived to 90 days only. c Surviving patients were split into patients who acquired infections or other SAEs between 1–7, 8–28 and 29–76 days post-stroke. The infection group had higher Rankin Scores even when non-surviving patients were removed, indicating more dependency. This was maintained when patients were split into groups based on time of infection occurrence. OR odds ratio, CI confidence interval
Table 2
Median scores (IQR) for Barthel Index and Health Utility State (HUS) in the comparison of stroke patients with infection and all other patients at defined time points
Group
n
Barthel
HUS
All patients
Infection
209–212
−5 (−5 to 30)*
0.00 (0.00–0.03)*
Other patients
2995–3009
85 (50 to 100)
0.64 (0.19–0.81)
Surviving patients
Infection
94–97
35 (8 to 75)*
0.03 (−0.10 to 0.59)*
Other patients
2798–2812
90 (60 to 100)
0.66 (0.26 to 0.81)
Between 1 and 7 days
Infection
48–50
30 (5 to 71)*
0.03 (−0.09 to 0.59)*
Other patients
2631–2645
90 (65 to 100)
0.69 (0.26 to 0.85)
Between 8 and 28 days
Infection
23–24
43 (6 to 83)*
0.03 (−0.10 to 0.59)*
Other patients
2570–2582
90 (65 to 100)
0.69 (0.26 to 0.85)
Between 29 and 76 days
Infection
23
40 (20 to 80)*
0.15 (−0.09 to 0.64)
Other patients
2567–2579
90 (65 to 100)
0.69 (0.27 to 0.85)
*p < 0.05 compared to other patients
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To establish that the reduction in functional outcome was not simply due to the increased mortality in the infection group, as the functional outcome measures include death as a score, the analysis was repeated using only patients who survived until 90 days. Patients who had infections continued to exhibit a significantly worse functional outcome overall, as measured by the mRS (Fig. 3, OR = 1.71, 95% CI = 1.37–2.14, p < 0.001), than patients with no SAE. This difference was evident for infections between 1 and 7 days post-stroke (OR = 1.89, 95% CI = 1.38–2.58, p < 0.001), 8–28 days post-stroke (OR = 1.79, 95% CI = 1.15–2.80, p = 0.010) and 29–76 days post-stroke (OR = 1.56, 95% CI = 1.00–2.43, p = 0.049). Analysis of surviving infection patients alone showed that the timing of infection did not affect functional outcome (OR = 1.00, 95% CI = 0.99–1.01, p = 0.47). An additional analysis where patients with infection and patients without SAE were paired to control for variables such as age and stroke severity found similar results, whereby patients with infections consistently had reduced functional outcomes (Supplementary Figure II).
Infections at all three points were also associated with reduced functional outcome as measured by the Barthel Index (1–7 days: OR = 0.54, 95% CI = 0.40–0.72, p < 0.001; 8–28 days: OR = 0.57, 95% CI = 0.38–0.86, p = 0.007; 29–76 days: OR = 0.53, 95% CI = 0.35–0.81, p = 0.003). When measured using the HUS, patients with infections between 1 and 7 days post-stroke (OR = 0.62, 95% CI = 0.46–0.83, p = 0.001) or 8–28 days post-stroke (OR = 0.66, 95% CI = 0.43–1.00, p = 0.049) had significantly worse functional outcome with a trend toward worse functional outcome in patients with infection between 29 and 76 days post-stroke (OR = 0.67, 95% CI = 0.45–1.02, p = 0.063).
Discussion
The aim of this analysis was to determine whether severe infection at different time points post-stroke increases case fatality and dependency at 90 days post-stroke. Our study indicates that infections, at all time points assessed between 1 and 76 days, are associated with a higher incidence of death or dependency at 90 days. The time of infection onset did not alter the effect on death or functional outcome, demonstrating that infections that develop weeks after a stroke are as detrimental as those occurring within the first 7 days.
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This work supports the current literature showing the detrimental effects of infection [3‐6] and of systemic inflammation [20]. The likelihood of fatality after infection in these stroke patients is much higher than that seen in other patient populations with pneumonia [21, 22], comparable to that after SSRCEs. In addition, these infections are associated with poor post-stroke recovery (independent to causing fatality) at much later time points than those which are established in the literature [14, 15, 23]. This highlights the need for long-term consideration of infections in patient care with measures to allow early identification and treatment. Unfortunately, prophylactic antibiotics do not, in themselves, appear to reduce rates of pneumonia infection, or improve functional outcome [24, 25]. Instead, measures to reduce aspiration such as awareness, diagnosis and management of dysphagia [26] or antiemetic treatment to reduce vomiting/regurgitation [27] are likely be more effective with ongoing trials hoping to address this [28]. However, no analyses of the use of preventive measures or the incidence of dysphagia were completed here due to lack of data.
Within this analysis, it is unclear how infections are contributing to functional deficits. Previous studies have shown that general medical complications after a stroke do influence rates of death and disability [23, 29] and any adverse event is likely to have some effect on functional outcome. Time is critical when undergoing therapy, with rehabilitation being most effective in the first 30 days post-stroke [30]. However, the detrimental effect of later infections (from 29 to 76 days post-stroke) means that it is likely that infections are having a larger impact than just interfering with therapy. Mechanisms have been suggested for the effect of infection including an increased risk of further SAEs [31] and the development of an autoimmune response against the brain [32]. Inflammatory processes seem to be a likely contributor to the effect of infection. Pro-inflammatory T lymphocytes [32] and inflammatory markers such as IL-6 [20] have both been linked to poor outcome in stroke patients. Meanwhile, work in animal models has shown that activation of the peripheral immune system by lipopolysaccharide shortly after a stroke leads to increased microglia activation and neutrophil infiltration within the stroke infarct [33, 34] and worsens functional outcome [33, 35]. Finally, it has been shown in animal models of neurodegenerative diseases that peripheral inflammation leads to the reactivation of microglia within the brain [36]. It is possible that this is also occurring in stroke patients who get infections, particularly those with infections at later time points when the initial inflammatory responses to stroke onset are resolving.
Limitations
The strength of this study is that the data are based on a large multinational cohort of patients with high-fidelity data collection. However, there are several limitations to this study. First, this is a post hoc analysis of previously collected data from the ENOS database. During its conception, the ENOS investigators did not plan to investigate the effects of post-stroke infection and only collected most of their outcome measures for use as secondary outcomes [16]. This resulted in some gaps in data potentially reducing the numbers of patients in this analysis. Therefore, only those outcome measures with sufficient numbers of patients were used in this study.
Second, information on infection was not collected prospectively but rather using SAE reports which are known to show variability within and between sites and regions [37]. Therefore, it is possible that some SAEs were missed, particularly at later time points after hospital discharge. This is reflected in the incidence of SAEs and infections in this patient population. Only 23.4% of patients included in the analysis developed SAEs and only 27.9% of these patients had infections. In total, this means approximately 6.5% of patients developed infections, a lower frequency than that generally reported in the literature (30% on average [17]).
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Third, the reliance on SAE reports to identify infections means that only serious infections were included in this analysis. Severity has been shown to have a role in determining how detrimental an infection is to post-stroke recovery [2, 23] and the fact that the effect of infection on fatality is higher than that of some previous reports supports this [3, 4]. Because of this, this dataset cannot be used to say that any infection is harmful to recovery regardless of time of infection. We can only be certain that severe infections are detrimental to functional outcome irrespective of time post-stroke.
Finally, as the patients with infection are on average older and have worse stroke severity, it is likely that their rate of death [38] and disability [39] would be higher without the additional complications of infection. It could be argued that these patients developed infections because they had worse functional outcome [40] rather than infection causing their decline, or that these patients may be given palliative care for their infections rather than aggressive treatment. Both of these factors would contribute to the high levels of death and disability. The influence of older age and stroke severity was accounted for by their inclusion as covariates within the analyses and by the use of patient pairing in an additional analysis of functional outcomes (Supplementary Table II and Figure II). Additionally, there is evidence at earlier time points post-stroke [14, 15], and from other diseases [7, 8], that infection accelerates the decline of neurological function, so the potential of infection to inhibit or limit recovery still needs to be taken seriously.
Summary
Infection at both early (1–7 days) and later (≤76 days) time points post-stroke is detrimental to a person’s functional recovery and survival from a stroke. Further work should establish whether it is possible to initiate prompt treatment of all infections to reduce their effects on mortality and functional outcome. In addition, work should be undertaken to investigate the mechanisms by which infections lead to increased deficits. Investigation into this area may be able to establish time periods of particular importance in post-stroke recovery, determine the types of infections which have the greatest influence or define the effect of post-stroke infection on a range of functional outcomes.
Acknowledgements
We would like to thank the patients and investigators who took part in ENOS (as listed in the main publication [16]) and the National Institute for Health Research Stroke Research Network nurses/coordinators who contributed to recruitment into ENOS. The ENOS trial was primarily funded by the UK Medical Research Council (grant G0501797). Other funders who supported the trial were the Agency for Science, Technology, and Research (Singapore), BUPA Foundation (UK), Hypertension Trust (UK), Queen Elizabeth II Health Sciences Centre Research Fund (Canada), Reichstadt family (UK), and The Stroke Association (UK, through its funding of the Division of Stroke, University of Nottingham, Nottingham, UK). AEL was funded by the Biotechnology and Biological Sciences Research Council. PB is the Chief Investigator of the ENOS and is the Stroke Association Professor of Stroke Medicine. The ENOS was sponsored by the University of Nottingham. Neither funder nor sponsor had any input into the study.
Compliance with Ethical Standards
Conflict of Interest
The authors declare that they have no conflict of in terest.
Sources of Funding
This work was supported by the Medical Research Council [grant number G0501797] and the Biotechnology and Biological Sciences Research Council [grant number BB/F016956/1]. Other funders who supported the ENOS trial were the Agency for Science, Technology, and Research (Singapore), BUPA Foundation (UK), Hypertension Trust (UK), Queen Elizabeth II Health Sciences Centre Research Fund (Canada), Reichstadt family (UK), and The Stroke Association (UK, through its funding of the Division of Stroke, University of Nottingham, Nottingham, UK). PB is the Chief Investigator of the ENOS and is the Stroke Association Professor of Stroke Medicine. ENOS was sponsored by the University of Nottingham. Neither funder nor sponsor had any input into the study.
Ethical Approval
All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
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Infections Up to 76 Days After Stroke Increase Disability and Death
verfasst von
Annastazia E. Learoyd Lisa Woodhouse Laurence Shaw Nikola Sprigg Daniel Bereczki Eivind Berge Valeria Caso Hanne Christensen Ronan Collins Anna Czlonkowska Anwar El Etribi Tracy D. Farr John Gommans Ann-Charlotte Laska George Ntaios Serefnur Ozturk Stuart J. Pocock Kameshwar Prasad Joanna M. Wardlaw Kevin C. Fone Philip M. Bath Rebecca C. Trueman on behalf of the ENOS Trial investigators
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