Next Article in Journal
Revealing the Mysteries of Acute Myeloid Leukemia: From Quantitative PCR through Next-Generation Sequencing and Systemic Metabolomic Profiling
Next Article in Special Issue
Mechanical Thrombectomy for Acute Ischemic Stroke in Patients with Malignancy: A Systematic Review
Previous Article in Journal
Anatabine, Nornicotine, and Anabasine Reduce Weight Gain and Body Fat through Decreases in Food Intake and Increases in Physical Activity
Previous Article in Special Issue
Selective Serotonin Reuptake Inhibitors for the Prevention of Post-Stroke Depression: A Systematic Review and Meta-Analysis
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Pneumonia in Acute Ischemic Stroke Patients with Proximal Occlusions within the Anterior Circulation after Endovascular Therapy or Systemic Thrombolysis

1
Department of Neurology, Klinikum Bremen-Mitte, St.-Jürgen-Street 1, 28177 Bremen, Germany
2
Department of Neuroradiology, Klinikum Bremen-Mitte, St.-Jürgen-Street 1, 28177 Bremen, Germany
3
Department of Neurology, University of Göttingen, Robert-Koch-Street 40, 37075 Göttingen, Germany
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2022, 11(3), 482; https://doi.org/10.3390/jcm11030482
Submission received: 17 December 2021 / Revised: 15 January 2022 / Accepted: 17 January 2022 / Published: 18 January 2022
(This article belongs to the Special Issue New Frontiers in Cerebrovascular Disorders)

Abstract

:
While endovascular treatment (ET) improves clinical outcomes in patients with proximal vessel occlusions compared to thrombolysis (IVT), the impact of ET on the frequency of stroke-associated pneumonia (SAP) is uncertain. We compared the rates of SAP in patients with large vessel occlusions in the anterior circulation after IVT or ET. We also determined risk factors for SAP, as well as the impact of SAP on early clinical outcomes. A total of 544 patients were treated with IVT, and 1061 patients received ET (with or without IVT). The rates of SAP did not differ significantly between ET (217/1061; 20%) and IVT (100/544; 18%) (p = 0.3). Overall, the occurrence of SAP was significantly associated with mortality and a poor clinical outcome. In the multivariable regression analysis, age, sex, the presence of dysphagia, early signs of ischemia on imaging and a history of stroke and mechanical ventilation were all significantly associated with the occurrence of SAP. In patients with large vessel occlusions, the introduction of ET did not result in lower rates of SAP compared with IVT. There is an ongoing need to reduce the rates of SAP in this patient population, for which the risk factors found here could become useful.

1. Introduction

After the publication of several landmark trials, endovascular treatment (ET) in addition to intravenous thrombolysis (IVT) has become the standard treatment for patients with proximal intracranial occlusions of the anterior circulation [1,2,3,4,5]. In these trials, ET was beneficial in all patient groups studied. A positive clinical effect of ET has also been observed in everyday clinical practice and, thus, outside of randomized trials [6]. In contrast to overwhelming clinical efficacy, the potential impact of ET on other stroke-associated complications has received little attention to date. In this context, the development of stroke-associated pneumonia (SAP) plays an important role. In fact, SAP is associated with multiple poor functional outcomes, including death (up to sixfold), neurological deterioration and a prolonged stay in hospital [7,8,9,10,11,12,13,14]. In contrast to the positive effect of ET on clinical outcome, the overall rates of SAP were high and comparable between IVT and ET in the MR CLEAN trial (11% after ET vs. 15% after IVT) [1]. Likewise, the rates of SAP did not differ significantly between ET or IVT in the ESCAPE trial (4.2% vs. 6%) [4] or the REVASCAT trial (14.6% vs. 8.7%) [3]. Therefore, the question arises as to whether ET reduces the frequency of SAP in addition to improving clinical outcomes compared with IVT. In addition, the relatively high rates of SAP in the aforementioned trials support the notion that there is an ongoing need to identify risk factors for this potentially devastating complication, especially in severely affected patients with large vessel occlusions.
The purpose of this study was to use our prospectively obtained large-volume stroke center database to compare the rates of SAP in patients with anterior circulation large vessel occlusions in two periods. During the first time period, all patients received systemic thrombolysis and, during the second time period, endovascular treatment with stent retrievers or aspiration devices was routinely used (with or without systemic thrombolysis). In the second step, we determined risk factors for SAP in this patient population.

2. Materials and Methods

2.1. Study Population

We identified patients with occlusions of the distal intracranial carotid artery and/or middle cerebral artery (M1 and M2 segment) who received treatment from January 2008 to December 2019. Patients with occlusions beyond the M2 segment were excluded. In addition, the current analysis excluded patients with posterior circulation strokes and bilateral strokes. Before November 2012 all patients had received systemic thrombolysis. The inclusion and exclusion criteria of thrombolytic therapy and the drug dose of our institution are mainly based on the NINDS study protocol. It can be treated up to 4.5 h after symptom onset, and there is no upper age limit for eligibility.
After November 2012, endovascular treatment with and without systemic thrombolysis (utilizing no upper age limit or specific imaging selection criteria) was routinely performed in patients who presented within 6 h (within 4.5 h in patients additionally treated with rt-PA) of symptom onset. At our institution ET is usually performed under conscious sedation, whilst general anesthesia is only used in very restless patients or those with limited vigilance.
In all patients, the following demographic data and stroke risk factors were gathered: age, gender, arterial hypertension, diabetes and atrial fibrillation. The time to thrombolysis (or to thrombectomy in patients without prior systemic thrombolysis) from stroke onset was likewise noted.
At our institution, all patients with acute cerebrovascular disorders are routinely screened for dysphagia within the first few hours after admission by a dysphagia-trained member of nursing staff. Patients who fail this initial screening remain “Nil by Mouth” until subsequently observed by a speech therapist within the first 24 h after admission. A standardized clinical evaluation based on the Munich Swallowing Score (MUCSS) for the assessment of the functional level of swallowing of saliva, fluids and food is used to quantify the severity of dysphagia [15]. In this study, the presence or absence of dysphagia was based on the results of speech therapists.
Our local stroke register has been approved by our local ethics committee (Ärztekammer Bremen) and is part of a nationwide mandatory quality assurance program for acute stroke treatment (Stroke Register of Northwestern Germany). The identity of individual patients is anonymous. Within this quality assurance program, no specific informed consent from patients or their relatives is required.

2.2. Imaging Techniques

Nonenhanced CT (NCT) and CT angiographic acquisitions before treatment were performed on a 4-row Multisection CT scanner (Siemens Volume Zoom, Siemens Medical Solutions, Forchheim, Germany).
NCT was performed with a patient in a head holder in the transverse plane. Incremental CT acquisitions of the brain were obtained by using the following parameters: 120 kVp, 250 mA, 2 s scan time and 5 mm section thickness.
CT angiography covered the region from the fifth vertebral body up to the vertex by using the following parameters: 120 kVp, 200 mAs, 4 × 1 mm collimation, 5.5 mm/rotation table feed and 0.5 s rotation time. CTA images were obtained after a single bolus contrast material (100 mL) injected intravenously at a flow rate of 4 mL/s using a power injector. In order to determine hemorrhagic, intracerebral complications as well as the final infarct sizes, CT or MR scans were obtained 1–3 days after treatment or immediately in the case of clinical worsening.

2.3. Image Analysis

All CT and MR images were analyzed jointly on a widescreen high-resolution monitor by 2 readers (a board-certified neuroradiologist with 21 years of neuroimaging review experience and a stroke neurologist with 19 years of neuroimaging review experience). With the exception of involvement, both readers were blinded to clinical and outcome data.
In order to detect early irreversible ischemia with a higher sensitivity than on plain CT images, the Alberta Stroke Programme Early CT Score was assessed on CTA source images (CTA-SI-ASPECTS) [16]. Follow-up CT or MR scans were used to determine the final ASPECTS as a marker of infarct extent, as well as the occurrence of symptomatic intracranial hemorrhages (SICH) by using the ECASS III definition.

2.4. End Points and Analyses

At our stroke center, the diagnosis of SAP is based on a combination of the following CDC criteria within 7 days of stroke onset [17]:
  • Fever (<38 °C) with no other known cause;
  • New onset of purulent sputum, change in character of sputum, increased respiratory secretions or increased suctioning requirements;
  • New onset or worsening of cough, dsypnea or tachypnea with increased respiratory rates;
  • Rales, crackles or bronchial breath sounds;
  • Worsening gas exchange;
  • Leukocytosis or leukopenia;
  • Positive chest radiograph.
In a first step, we compared the rates of SAP after either IVT or ET. In a second step, we then determined clinical and radiological risk factors for SAP, regardless of treatment modality. In addition, we analyzed the impact of SAP on mRS at the time of hospital discharge.

2.5. Statistical Analysis

Continuous values were expressed as mean ± standard deviation (SD) or as median ± interquartile range (IQR). Nominal variables were expressed as counts and percentages. For comparisons of categorical data, two-tailed chi-square statistics with Yates correction and univariate Fisher’s exact test were used. The Fisher’s exact test was used when the predicted contingency table cell values were less than five. Analyses of continuous variables were performed with an unpaired Student’s t-test or, in cases of abnormally distributed data, with a Mann–Whitney U test.
A stepwise forward multiple-regression analysis was applied to determine the independent predictors for SAP. The following variables were considered: age; sex; initial NIHSS; treatment modality (i.v. thrombolysis alone, thrombectomy with thrombolysis and thrombectomy without thrombolysis); location of occlusion; presence of dysphagia; mechanical ventilation; history of a prior stroke; prestroke dependency (mRS ≥ 3); presence of hypertension; diabetes; hyperlipidemia; atrial fibrillation; baseline source image ASPECTS; and location in right or left hemisphere. Results are presented as odds ratios (ORs) with a 95% confidence interval (CI).
A value of p < 0.05 was considered to indicate a statistically significant difference. All statistical analyses were performed with SPSS (Version 22, SPSS Inc., Chicago, IL, USA).

3. Results

From January 2008 to December 2019, a total of 1605 patients with anterior circulation large vessel occlusions were treated (544 with systemic thrombolysis (IVT group) and 1061 patients with endovascular therapy (ET group)). Table 1 summarizes the baseline characteristics of both treatment groups. For the majority of risk factors, both treatment groups were well balanced. However, patients in the ET group were more severely affected and more often had early signs of ischemia than patients in the IVT group. These differences likely reflect higher rates of ICA/Carotid T occlusions and treatment times beyond 4.5 h or with unknown times of symptom onset in the ET group.
Significantly more patients in the ET group than in the IVT group had a favorable early clinical outcome (mRS 0–2)(32% vs. 26%; p < 0.05), as well as an excellent clinical outcome (mRS 0–1) (18% vs. 13%; p < 0.05). In addition, the final infarct sizes were significantly smaller after ET than after IVT (Table 2).
Overall, 317/1605 patients (19.7%) developed pneumonia. The rates of SAP did not differ significantly between ET (217/1061; 20%) and IVT (100/544; 18%) (p = 0.3). This result was also not affected when adjusting for potentially confounding variables between both treatment groups (ORadjusted, 1.1; 95% CI 0.8–1.5, p = 0.4).
Table 3 summarizes the baseline characteristics of patients with and without SAP.
Notably, patients with SAP were significantly older (78 years vs. 72 years, p < 0.001), more severely affected (initial NIHSS: 16 vs. 14, p < 0.001), more often had a dysphagia (89% vs. 58%, p < 0.001) and were significantly more often functionally impaired (mRS ≥ 3) before the current stroke event (22% vs. 12%, p < 0.001) than those without SAP, respectively. Atrial fibrillation and a prior stroke event were significantly more common in patients with SAP. Mechanical ventilation was also significantly associated with the rates of SAP.
Clinical and imaging outcome data for both groups are provided in Table 4. Patients with SAP were more likely to die within the hospital than patients without SAP (19% vs. 12%, p < 0.001). The rates of a poor outcome (mRS 5–6 at the time of discharge) were significantly higher in patients with SAP than without SAP (59% vs. 29%, p < 0.001). Vice versa, the rates of a good outcome (mRS 0–2 at the time of discharge) were significantly lower in patients with SAP compared to those without SAP (5% vs. 36%, p < 0.001). SAP was also associated with larger infarcts and a longer stay in hospitals.
In multivariate regression analysis, age, sex, the presence of dysphagia, early signs of ischemia on imaging (i.e., the SI-ASPECTS) and a history of stroke and mechanical ventilation were all significantly associated with the occurrence of SAP (Table 5).

4. Discussion

Based on a large dataset, the frequency of SAP in patients with large-vessel intracranial occlusions within the anterior circulation was similar between systemic thrombolysis alone and endovascular therapy with or without thrombolysis. Regardless of the treatment modality, we identified several risk factors for SAP in this patient population, including age, sex (male), the presence of dysphagia, early signs of ischemia on imaging and a history of stroke and mechanical ventilation.
In our patient population approximately 20% of all patients developed SAP after either IVT or ET. This high rate of SAP is within the range reported in previous randomized trials dealing with comparable patient populations [1,2]. In the MR CLEAN trial, the overall rate of SAP in patients with large vessel occlusions in the anterior cerebral circulation was 13% [1]. In the SWIFT PRIME trial, nearly 20% of the patients developed SAP after ET [2]. In contrast, the rates of SAP after either IVT or ET were lower in the ESCAPE trial (approximately 5%), likely reflecting a highly selected patient population with less comorbid conditions [4].
In all aforementioned trials, the rates of SAP in patients with proximal vessel occlusions were comparable after ET or IVT, despite the fact that ET improved clinical outcomes. In good agreement with this finding, the rates of SAP were nearly identical after either ET or IVT in this patient population in our case series. As in the randomized trials, ET also improved clinical and radiological outcomes in our series, compared with IVT. Taken together, these results clearly show that improved clinical outcome after ET does not automatically translate into reduced rates of SAP.
In broader stroke-patient populations, SAP has repeatedly been associated with poor clinical outcomes, including death [8,9,14]. Likewise, we observed a close relation between SAP and poor outcomes in patients with large vessel occlusions after either IVT or ET, supporting the notion that pneumonia is an important modifiable risk factor in this patient population. Future studies should, thus, address the question as to whether the use of prophylactic antibiotics could further improve clinical outcomes after ET in patients at high risk of SAP. Irrespective of treatment modality, several factors, including advanced age, sex, dysphagia, mechanical ventilation and early signs of ischemia were significantly associated with SAP in our study. Comparable factors have been identified in previous studies dealing with broader stroke-patient populations and have also been incorporated into risk scores for SAP [18,19]. The increased risk of SAP in older patients after either ET or IVT likely reflects higher instances of comorbid conditions, as well as impairments of swallowing and cough reflexes [20]. As in previous studies, we found an inverse association between female sex and SAP [21]. Although the reasons for the lower rates of SAP in females remain unclear, it could be speculated that women have a healthier lifestyle than men with lower rates of smoking and less alcohol consumption. In addition, female hormones could also contribute to this finding. In fact, female hormones have been shown to inhibit inflammatory reactions to bacterial antigens und could, thus, reduce the severity of respiratory infections [22]. Female hormones have also been associated with a more vigorous immune response, at least in animal models [22]. On the other hand, the vast majority of our female patients were in their menopause, suggesting that further, currently unknown sex-specific mechanisms must also contribute to the lower risk of SAP in females.
As expected, and in good agreement with several previous reports, mechanical ventilation was also significantly associated with the risk of pneumonia in our cohort in both treatment groups [23,24]. Against the background of this increased risk, there is an ongoing discussion as to whether ET should be performed under conscious sedation or general anesthesia [24]. However, our data should be interpreted with caution, since mechanical ventilation was only applied in severely affected patients, thus likely reflecting a selection bias.
In the past few years, several clinical risk scores for predicting SAP in broader stroke populations have been developed [25]. The majority of these predictive risk models were based on routinely available variables and commonly included age, atrial fibrillation, dysphagia, stroke severity as determined by the NIHSS and sex. It is noteworthy that NIHSS and atrial fibrillation were not significantly associated with SAP in the multivariate analyses in our study. This finding is likely attributable to the fact that our stroke patients with large vessel occlusions were more severely affected and more often had a cardio-embolic stroke due to atrial fibrillation than the patients entered in the aforementioned risk models.
The major strengths of our study include the large dataset and the use of uniform treatment algorithms. However, the present report also has limitations. The data were obtained retrospectively in a single academic center, and the impact of ET or IVT on SAP was determined in a nonrandomized fashion. Hence, the study method holds all drawbacks of observational design and limits the generalizability of our results. Several important risk factors for SAP were not considered in our analyses including details on nasogastric tube interventions, laboratory markers and the use of certain medications, which have been linked to the presence or absence of SAP [26,27,28]. Furthermore, dysphagia was only dichotomized as either absent or present, thus using a rather broad classification scheme of this important risk factor for SAP. In addition, we did not consider the time of onset and timecourse of pneumonia, which play a crucial role in the interpretation of stroke and pneumonia with respect to causality, especially in mechanically ventilated patients and those with signs of pneumonia already at the time of admission. Although we studied a rather large patient population and found comparable SAP rates after ET or IVT, we might have missed a significant difference between both groups. Using our data, however, more than 9000 patients in each treatment group would be needed to detect a potential significant difference, making a Type II error unlikely. Finally, we used mRS at the time of discharge to assess clinical outcome instead of the widely accepted 3 months.

5. Conclusions

In patients with acute large vessel occlusions, the overall frequency of SAP is high in everyday clinical practice and comparable between ET and IVT. Regardless of treatment modality, SAP is significantly associated with mortality and an overall poor clinical outcome. Thus, there is an ongoing need to reduce the rates of SAP in this patient population, for which the risk factors found in this study could become useful.

Author Contributions

Conceptualization: H.M., C.R., P.P. and A.K.; methodology: H.M., C.R., P.P. and A.K.; software: not applicable; validation: H.M. and A.K.; formal analysis: H.M., P.P. and A.K.; investigation: not applicable; resources: A.K.; data curation: H.M., C.R., A.S., M.P., M.A., J.D., S.G., P.P. and A.K.; writing—original draft preparation: H.M., C.R., P.P. and A.K.; writing—review and editing: A.S., M.P., M.A., J.D. and S.G.; visualization: not applicable; supervision: A.K., C.R. and P.P. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted according to the Declaration of Helsinki and approved by the local ethics committee (Ärztekammer Bremen).

Informed Consent Statement

According to institutional review board approval, informed consent was not necessary since clinical data had been collected retrospectively as part of a legally enforced national quality control program.

Data Availability Statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Berkhemer, O.A.; Fransen, P.S.S.; Beumer, D.; Van Den Berg, L.A.; Lingsma, H.F.; Yoo, A.J.; Schonewille, M.D.W.J.; Jan Abert Vos, M.D.; Paul, M.D.J.; Nedercorn, M.D.; et al. A Randomized Trial of Intraarterial Treatment for Acute Ischemic Stroke. N. Engl. J. Med. 2015, 372, 11–20. [Google Scholar] [CrossRef] [Green Version]
  2. Saver, J.L.; Goyal, M.; Bonafe, A.; Diener, H.C.; Levy, E.I.; Pereira, V.M.; Albers, G.W.; Cognard, C.; Cohen, D.J.; Hacke, W.; et al. Stent-Retriever Thrombectomy after Intravenous t-PA vs. t-PA Alone in Stroke. N. Engl. J. Med. 2015, 372, 2285–2295. [Google Scholar] [PubMed] [Green Version]
  3. Jovin, T.G.; Chamorro, A.; Cobo, E.; de Miquel, M.A.; Molina, C.A.; Rovira, A.; Roman, L.S.; Serena, J.; Abilleira, S.; Ribo, M.; et al. Thrombectomy within 8 Hours after Symptom Onset in Ischemic Stroke. N. Engl. J. Med. 2015, 372, 2296–2306. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Goyal, M.; Demchuk, A.M.; Menon, B.K.; Eesa, M.; Rempel, J.L.; Thornton, J.; Roy, D.; Jovin, T.G.; Willinsky, R.A.; Sapkota, B.L.; et al. Randomized Assessment of Rapid Endovascular Treatment of Ischemic Stroke. N. Engl. J. Med. 2015, 372, 1019–1030. [Google Scholar] [CrossRef]
  5. Campbell, B.C.V.; Mitchell, P.J.; Kleinig, T.J.; Dewey, H.M.; Churilov, L.; Yassi, N.; Yan, B.; Dowling, R.J.; Parsons, M.W.; Oxley, T.J.; et al. Endovascular Therapy for Ischemic Stroke with Perfusion-Imaging Selection. N. Engl. J. Med. 2015, 372, 1009–1018. [Google Scholar] [CrossRef] [Green Version]
  6. Kastrup, A.; Brunner, F.; Wasser, K.; Hildebrandt, H.; Roth, C.; Winterhalter, M.; Papanagiotou, P. Endovascular therapy versus thrombolysis in patients with anterior circulation stroke in everyday clinical practice. Int. J. Stroke 2016, 11, 544–548. [Google Scholar] [CrossRef]
  7. Westendorp, W.F.; Nederkoorn, P.J.; Vermeij, J.D.; Dijkgraaf, M.G.; van de Beek, D. Post-stroke infection: A systematic review and meta-analysis. BMC Neurol. 2011, 11, 110. [Google Scholar] [CrossRef] [Green Version]
  8. Rohweder, G.; Ellekjær, H.; Salvesen, Ø.; Naalsund, E.; Indredavik, B. Functional outcome after common poststroke complications occurring in the first 90 days. Stroke 2015, 46, 65–70. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  9. Ingeman, A.; Andersen, G.; Hundborg, H.H.; Svendsen, M.L.; Johnsen, S.P. In-hospital medical complications, length of stay, and mortality among stroke unit patients. Stroke 2011, 42, 3214–3218. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  10. Kwan, J.; Hand, P. Infection after acute stroke is associated with poor short-term outcome. Acta Neurol. Scand. 2007, 115, 331–338. [Google Scholar] [CrossRef]
  11. Boehme, A.K.; Kulick, E.R.; Canning, M.; Alvord, T.; Khaksari, B.; Omran, S.; Willey, J.Z.; Elkind, M.S. Infections increase the risk of 30-day readmissions among stroke survivors: Analysis of the National Readmission Database. Stroke 2018, 49, 2999–3005. [Google Scholar] [CrossRef] [PubMed]
  12. Popović, N.; Stefanović-Budimkić, M.; Mitrović, N.; Urošević, A.; Milošević, B.; Pelemiš, M.; Jevtović, M.; Beslać-Bumbaširević, L.; Jovanović, D. The frequency of poststroke infections and their impact on early stroke outcome. J. Stroke Cerebrovasc. Dis. 2013, 22, 424–429. [Google Scholar] [CrossRef]
  13. Ji, R.; Wang, D.; Shen, H.; Pan, Y.; Liu, G.; Wang, P.; Wang, Y.; Li, H.; Wang, Y. Interrelationship among common medical complications after acute stroke: Pneumonia plays an important role. Stroke 2013, 44, 3436–3444. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Finlayson, O.; Kapral, M.; Hall, R.; Asllani, E.; Selchen, D.; Saposnik, G. Risk factors, inpatient care, and outcomes of pneumonia after ischemic stroke. Neurology 2011, 77, 1338–1345. [Google Scholar] [CrossRef]
  15. Bartolome, G.; Starrost, U.; Schröter-Morrasch, H.; Schilling, B.; Fischbacher, L.; Kues, L.; Graf, S.; Ziegler, W. Validation of the Munich Swallowing Score (MUCSS) in patients with neurogenic dysphagia: A preliminary study. NeuroRehabilitation 2021, 49, 445–457. [Google Scholar] [CrossRef]
  16. Wasser, K.; Papanagiotou, P.; Brunner, F.; Hildebrandt, H.; Winterhalter, M.; Roth, C.; Kastrup, A. Impact of ASPECTS on computed tomography angiography source images on outcome after thrombolysis or endovascular therapy in large vessel occlusions. Eur. J. Neurol. 2016, 23, 1599–1605. [Google Scholar] [CrossRef]
  17. Horan, T.C.; Andrus, M.; Dudeck, M.A. CDC/NHSN surveillance definition of health care-associated infection and criteria for specific types of infections in the acute care setting. Am. J. Infect. Control 2008, 36, 309–332. [Google Scholar] [CrossRef]
  18. Hoffmann, S.; Malzahn, U.; Harms, H.; Koennecke, H.C.; Berger, K.; Kalic, M.; Walter, G.; Meisel, A.; Heuschmann, P.U. Development of a clinical score (A2DS2) to predict pneumonia in acute ischemic stroke. Stroke 2012, 43, 2617–2623. [Google Scholar] [CrossRef] [Green Version]
  19. Kishore, A.K.; Vail, A.; Bray, B.D.; Chamorro, A.; Napoli, M.D.; Kalra, L.; Langhorn, P.; Montaner, J.; Roffe, C.; Rudd, A.G.; et al. Clinical risk scores for predicting stroke-associated pneumonia: A systematic review. Eur. Stroke J. 2016, 1, 76–84. [Google Scholar] [CrossRef] [PubMed]
  20. Petroianni, A.; Ceccarelli, D.; Conti, V.; Terzano, C. Aspiration pneumonia Pathophysiological aspects, prevention and management: A review. Panminerva Med. 2006, 48, 231–239. [Google Scholar]
  21. Colbert, J.F.; Traystman, R.J.; Poisson, S.N.; Herson, P.S.; Ginde, A.A. Sex-Related Differences in the Risk of Hospital-Acquired Sepsis and Pneumonia Post Acute Ischemic Stroke. J. Stroke Cerebrovasc. Dis. 2016, 25, 2399–2404. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Falagas, M.E.; Mourtzoukou, E.G.; Vardakas, K.Z. Sex differences in the incidence and severity of respiratory tract infections. Respir. Med. 2007, 101, 1845–1863. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Eker, O.F.; Saver, J.L.; Goyal, M.; Jahan, R.; Levy, E.I.; Nogueira, R.G.; Yavagal, D.R.; Bonafe, A. Impact of anesthetic management on safety and outcomes following mechanical thrombectomy for ischemic stroke in SWIFT PRIME cohort. Front. Neurol. 2018, 9, 702. [Google Scholar] [CrossRef]
  24. Zhang, Y.; Jia, L.; Fang, F.; Ma, L.; Cai, B.; Faramand, A. General Anesthesia Versus Conscious Sedation for Intracranial Mechanical Thrombectomy: A Systematic Review and Meta-analysis of Randomized Clinical Trials. J. Am. Heart Assoc. 2019, 8, e011754. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Westendorp, W.F.; Vermeij, J.D.; Hilkens, N.A.; Brouwer, M.C.; Algra, A.; van der Worp, H.B.; Dippel, D.W.J.; van de Beek, D.; Nederkoorn, P.J. Development and internal validation of a prediction rule for poststroke infection and poststroke pneumonia in acute stroke patients. Eur. Stroke J. 2018, 3, 136–144. [Google Scholar] [CrossRef] [PubMed]
  26. Caldeira, D.; Alarcão, J.; Vaz-Carneiro, A.; Costa, J. Risk of pneumonia associated with use of angiotensin converting enzyme inhibitors and angiotensin receptor blockers: Systematic review and meta-analysis. BMJ 2012, 345, e4260. [Google Scholar] [CrossRef] [Green Version]
  27. Sykora, M.; Siarnik, P.; Diedler, J. β-Blockers, Pneumonia, and Outcome after Ischemic Stroke. Stroke 2015, 46, 1269–1274. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  28. Warusevitane, A.; Karunatilake, D.; Sim, J.; Lally, F.; Roffe, C. Safety and effect of metoclopramide to prevent pneumonia in patients with stroke fed via nasogastric tubes trial. Stroke 2015, 46, 454–460. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Table 1. Baseline characteristics of acute ischemic stroke patients with large vessel occlusions in the anterior circulation after either thrombolysis or endovascular therapy.
Table 1. Baseline characteristics of acute ischemic stroke patients with large vessel occlusions in the anterior circulation after either thrombolysis or endovascular therapy.
IVTETp-Value
(n = 544)(n = 1061)
Age74 ± 1274 ± 130.2
  Mean (yrs)
Female294 (54)569 (54)0.9
Hypertension451 (83)858 (81)0.3
Atrial fibrillation270 (50)488 (46)0.2
Diabetes112 (21)223 (21)0.8
Prior stroke83 (15)191 (18)0.2
Prestroke dependency89 (16)142 (13)0.1
NIHSS *13 (10–17)15 (11–18)<0.01
  (median, IQR)
Dysphagia353 (65)673 (63)0.5
Imaging
Side of Occlusion
Right hemisphere255 (47)514 (48)0.6
Location of Occlusion **
  ICA78 (14)172 (16)0.3
  Carotid-T17 (3)153 (14)<0.01
  M1 MCA301 (55)555 (53)0.2
  M2 MCA148 (27)181 (17)<0.01
Baseline SI-ASPECTS ***
  (median, IQR)9 (7–10)8 (7–10)<0.05
Mechanical ventilation38 (7)99 (9)0.1
* NIHSS = National Institutes of Health Stroke Scale; ** most proximal occlusion location; *** SI-ASPECTS = Source image Alberta Stroke Program Early CT Score (only for anterior circulation strokes); ICA: indicates internal carotid artery; MCA: indicates middle cerebral artery.
Table 2. Clinical and radiological outcomes according to treatment.
Table 2. Clinical and radiological outcomes according to treatment.
Endovascular
Therapy
Thrombolysis Alonep Value
n = 1061n = 544
Clinical outcomes
mRS * 0–2336 (32)142 (26)<0.05
mRS 0–1190 (18)73 (13)p < 0.05
mRS 5–6346 (33)222 (41)p < 0.05
Death139 (13)73 (13)p = 0.9
Radiological outcome
Infarct size **7 (5–8)6 (3–8)p < 0.01
(Median, IQR)
* mRS = modified Rankin Scale; ** using the follow-up ASPECTS = Alberta Stroke Program Early CT Score.
Table 3. Baseline characteristics of patients with and without stroke-associated pneumonia.
Table 3. Baseline characteristics of patients with and without stroke-associated pneumonia.
Non-SAPSAPp-Value
Age
Mean (yrs)
72 ± 1378 ± 10<0.01
Female705 (55)158 (50)0.1
Hypertension1023 (79)266 (84)0.07
Atrial fibrillation591 (46)167 (53)<0.05
Diabetes257 (20)78 (25)0.07
Prior stroke200 (15)74 (23)<0.001
Prestroke dependency161 (12)70 (22)<0.001
NIHSS *
(median, IQR)
14 (10–17)16 (13–19)<0.001
Dysphagia744 (58)282 (89)<0.001
Imaging
Side of Occlusion
Right hemisphere620 (48)150 (48)1
Location of Occlusion **
ICA192 (15)59 (19)0.1
Carotid–T134 (10)35 (11)0.7
M1 MCA698 (54)158 (50)0.5
M2 MCA264 (20)65 (20)1
Baseline SI–ASPECTS ***
(median, IQR)
9 (7–10)8 (6–10)<0.001
SICH46 (4)13 (4)0.6
Treatment
i.v. Alteplase alone444 (34)100 (31)0.7
Endovascular therapy
with thrombolysis476 (40)126 (40)1
Endovascular therapy
without thrombolysis368 (28)91 (29)1
Mechanical ventilation89 (7)48 (15)<0.001
* NIHSS = National Institutes of Health Stroke Scale; ** most proximal occlusion location; *** SI-ASPECTS = Source image Alberta Stroke Program Early CT Score (only for anterior circulation strokes); ICA indicates internal carotid artery; MCA indicates middle cerebral artery.
Table 4. Clinical and imaging outcomes in patients with and without SAP at the time of discharge.
Table 4. Clinical and imaging outcomes in patients with and without SAP at the time of discharge.
Non-SAP
(n = 1288)
SAP
(n = 317)
p-Value
mRS at discharge
(mean ± SD)
3.3 ± 1.84.6 ± 1.1<0.001
mRS 0–2 (n; %)461 (36)17 (5)<0.001
mRS 5–6 (n; %)380 (29)188 (59)<0.001
Death (n; %)151 (12)61 (19)<0.001
Infarct size *
(median, IQR)
7 (5–8)5 (3–7)<0.001
Length of hospital stay (days)
(median; IQR)
6 (4–9)8 (6–12)<0.001
mRS modified Rankin scale; * using the follow-up Alberta Stroke Program Early CT Score.
Table 5. Multivariable odds ratios and 95% confidence intervals of SAP in patients with large vessel occlusions in the anterior circulation.
Table 5. Multivariable odds ratios and 95% confidence intervals of SAP in patients with large vessel occlusions in the anterior circulation.
Odds RatioCI LowerCI Higherp Value
Age *1.031.011.04<0.001
Female0.60.50.9<0.01
Initial NIHSS **1.020.991.10.09
Dsyphagia4.53.16.8<0.001
Prior stroke1.71.22.5<0.01
Baseline SI-ASPECTS ***0.90.80.9<0.05
Mechanical ventilation21.33.2<0.01
CI, confidence interval; NIHSS, National Institutes of Health Stroke Scale; * per 1 year increase; ** per 1 point increase; *** per 1 point increase.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Muhl, H.; Roth, C.; Schröter, A.; Politi, M.; Alexandrou, M.; Dahl, J.; Gindorf, S.; Papanagiotou, P.; Kastrup, A. Pneumonia in Acute Ischemic Stroke Patients with Proximal Occlusions within the Anterior Circulation after Endovascular Therapy or Systemic Thrombolysis. J. Clin. Med. 2022, 11, 482. https://doi.org/10.3390/jcm11030482

AMA Style

Muhl H, Roth C, Schröter A, Politi M, Alexandrou M, Dahl J, Gindorf S, Papanagiotou P, Kastrup A. Pneumonia in Acute Ischemic Stroke Patients with Proximal Occlusions within the Anterior Circulation after Endovascular Therapy or Systemic Thrombolysis. Journal of Clinical Medicine. 2022; 11(3):482. https://doi.org/10.3390/jcm11030482

Chicago/Turabian Style

Muhl, Henning, Christian Roth, Andreas Schröter, Maria Politi, Maria Alexandrou, Janina Dahl, Susanne Gindorf, Panagiotis Papanagiotou, and Andreas Kastrup. 2022. "Pneumonia in Acute Ischemic Stroke Patients with Proximal Occlusions within the Anterior Circulation after Endovascular Therapy or Systemic Thrombolysis" Journal of Clinical Medicine 11, no. 3: 482. https://doi.org/10.3390/jcm11030482

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop