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      Chest Computed Tomography Findings and Validation of Clinical Criteria of Stroke Associated Pneumonia

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          Abstract

          Dear Sir: Multiple terms have been used to describe chest infection in stroke patients. Pneumonia in Stroke Consensus (PISCES) Group has set stroke associated pneumonia (SAP) diagnostic criteria consensus [1] as a starting point in the identification of this pathology. However, SAP assessment still involves a particular challenge [2], especially if chest radiography is taken into account, due to significant interobserver variability in interpretation and its limited use in the early stages [3]. In fact, the wide SAP incidence range in stroke units (3.9% to 44% [4]) reflects the insufficient evidence about diagnostic accuracy of clinical symptoms or laboratory tests for SAP [2]. Thorax high resolution computed tomography (THRCT) is a useful adjunct to conventional radiography and an accurate study to identify underlying findings in stroke patients, which could serve as a guide in risk score or diagnostic criteria validation. To describe for the first time SAP imaging pattern on THRCT, and to evaluate diagnostic performance of SAP clinical criteria based on THRCT findings, we conducted a monocentric, prospective, observational study (approved by our Institutional Review Committee [ID 0103-M1-14]). The patients eligible for the study were those with ischemic stroke and National Institutes of Health Stroke Scale (NIHSS) ≥10 on admission, stroke symptoms onset to inclusion time was ≤24 hours, and informed consent signed by the patient or a relative at inclusion. Mechanical ventilation pneumonia patients transferred from intensive care unit and stroke patients with antibiotic therapy received within last 24 hours before hospital admission were excluded. Dysphagia was evaluated within the first 24 hours with the Acute Stroke Dysphagia Screen test [5]. Chest radiography and laboratory test were run following neurologist criteria during admission. A non-contrast THRCT was performed between 5th and 7th day of admission in all included patients, independently of the suspicion or not of respiratory infection. Every THRCT was evaluated by two skilled thorax radiologists, and discrepancies reviewed by another expert thorax radiologist, all blinded to the clinical data. In this study, SAP was diagnosed by treating physician according to diagnostic categories established by the PISCES criteria [2]. These categories are probable and definite SAP. Forty-five patients were included. Three patients died and one presented with psychomotor agitation before THRCT performance, so they were excluded for the study. PISCES probable SAP rate was 19.5% (n=8). Baseline characteristics of the sample are shown in Table 1. There was no patient with PISCES definite SAP according to treating physician criteria. Moreover, chest radiography low quality was insufficient to a correct interpretation of some cases to be considered definitive SAP. The pattern of radiological findings in THRCT of the full sample and regarding probable SAP are shown in Figure 1. Sensitivity, specificity, positive predictive value, negative predictive values of clinical criteria for any low respiratory tract infection (LRTI) and bronchopneumonia alone are shown in Table 2. Clinical criteria showed high sensitivity and specificity for both any LRTI and bronchopneumonia (87.5%/96.9% and 100%/91.6%). The C statistic for clinical criteria was 0.92 (95% confidence interval [CI], 0.78 to 1.00) for any LRTI and 0.96 (95% CI, 0.89 to 1.00) for bronchopneumonia. Our study shows for the first time thorax computed tomography (CT) radiological findings of stroke associated respiratory infections, and this allowed us to conduct the first prospective study for external validation of PISCES clinical criteria, using THRCT as an accurate image test to confirm or rule out clinical suspicions. Our SAP rate (12.2%), identified on thorax CT, remains within the limits currently described in a systematic review [6]. Our cohort is representative of standard stroke care in severe strokes with large vessel occlusions with 63.4% receiving intravenous thrombolysis and 31.7% thrombectomy; these reperfusion therapies did not influence SAP rate (Supplementary Table 1). Clinical presentation of pneumonia in patients who had stroke can be non-specific; since cough is impaired [7] and sputum microbiological samples have limited availability and poor clinical yield [6]. The use of chest radiography is recommended by international guidelines [1] when pneumonia is suspected. However, chest radiography has been demonstrated to be an insensitive method, with <40% of new infiltrates on chest radiography in a stroke population [8] and a low accuracy test [3]. Some limitations of the present study are small sample size and the low quality of chest radiography, avoiding correct interpretation and making comparison between radiological tests difficult. However, we believe that even with such small sample size our study brings objective data on the descriptive findings of respiratory infections using chest CT for the first time in stroke patients, showing its usefulness and feasibility. In fact, this is the first time we can separate bronchitis and lobar condensation, under the same clinical presentation. Probably an increase of sample size will identify even a broader spectrum of findings in SAP. Given high accuracy on thorax CT in SAP diagnosis, a negative THRCT in patients with clinical suspicion, could guide further studies that allow us antibiotic saving, avoiding antibiotic resistance development in hospitalized patients. This study shows that PISCES criteria exhibit a high sensitivity for LRTI and bronchopneumonia detection, defining an interesting tool for screening patients in case of suspected SAP. Although further validation is needed, and multicentric studies will be probably required to get adequate sample size for such type of complex studies, PISCES criteria set an interesting starting point that could be associated with other infection biomarkers to guide future prophylactic antibiotic clinical trials.

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          Most cited references6

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          Stroke-Associated Pneumonia: Major Advances and Obstacles

          Background: Stroke-associated pneumonia (SAP) has been implicated in the morbidity, mortality and increased medical cost after acute ischemic stroke. The annual cost of SAP during hospitalization in the United States approaches USD 459 million. The incidence and prognosis of SAP among intensive care unit (ICU) patients have not been thoroughly investigated. We reviewed the pathophysiology, microbiology, incidence, risk factors, outcomes and prophylaxis of SAP with special attention to ICU studies. Methods: To determine the incidence, risk factors and prognosis of acute SAP, PubMed was searched using the terms ‘pneumonia' AND ‘neurology intensive unit' and the MeSH terms ‘stroke' AND ‘pneumonia'. Non-English literature, case reports and chronic SAP studies were excluded. Studies were classified into 5 categories according to the setting they were performed in: neurological intensive care units (NICUs), medical intensive care units (MICUs), stroke units, mixed studies combining more than one setting or when the settings were not specified and rehabilitation studies. Results: The incidences of SAP in the following settings were: NICUs 4.1-56.6%, MICUs 17-50%, stroke units 3.9-44%, mixed studies 3.9-23.8% and rehabilitation 3.2-11%. The majority of NICU and MICU studies were heterogeneous including different neurovascular diseases, which partly explains the wide range of SAP incidence. The higher incidence in the majority of ICU studies compared to stroke units or acute floor studies is likely explained by the presence of mechanical ventilation, higher stroke severity causing higher rates of aspiration and stroke-induced immunodepression among ICU patients. The short-term mortality of SAP was increased among the mixed and stroke unit studies ranging between 10.1 and 37.3%. SAP was associated with worse functional outcome in the majority of stroke unit and floor studies. Mortality was less consistent among NICU and MICU studies. This difference could be due to the heterogeneity of ICU studies and the effect of small sample size or other independent risk factors for mortality such as the larger neurological deficit, mechanical ventilation, and age, which may simultaneously increase the risk of SAP and mortality confounding the outcomes of SAP itself. The pathophysiology of SAP is likely explained by aspiration combined with stroke-induced immunodepression through complex humeral and neural pathways that include the hypothalamic-pituitary-adrenal axis, parasympathetic and sympathetic systems. Conclusions: A unified definition of SAP, strict inclusion criteria, and the presence of a long-term follow-up need to be applied to the future prospective studies to better identify the incidence and prognosis of SAP, especially among ICU patients.
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            Chest radiograph vs. computed tomography scan in the evaluation for pneumonia.

            To determine, in an Emergency Department (ED) population, the incidence of pneumonia diagnosed on thoracic computed tomography (CT) in the setting of negative or non-diagnostic chest radiographs (CXR). This is a retrospective chart review of all ED visits of adult patients ultimately diagnosed with "pneumonia" in whom both CXR and CT were obtained. We note cases in which the CXR was either negative or non-diagnostic for pneumonia and the CT noted a definitive infiltrate consistent with pneumonia. Of the 1,057 patients diagnosed with pneumonia, both CXR and CT were performed in 97 cases. Of this group, there were 26 patients (27%), in whom the CXR was either negative or non-diagnostic, but the CT noted an infiltrate/consolidation consistent with pneumonia. In our retrospective review of ED patients, we find that in 27% of cases in which both a CXR and a CT scan were performed in the work-up of varied chief complaints, pneumonia was demonstrated on CT in the face of a negative or non-diagnostic CXR. This analysis demonstrates the need for further studies regarding the appropriate radiographic evaluation of pneumonia, particularly in high-risk patients.
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              Validation of a dysphagia screening tool in acute stroke patients.

              Although many dysphagia screening tools exist, none has high sensitivity and reliability or can be administered quickly with minimal training. To design and validate a swallowing screening tool to be used by health care professionals who are not speech language pathologists to identify dysphagia and aspiration risk in acute stroke patients. In a prospective study of 300 patients admitted to the stroke service at an urban tertiary care hospital, interrater and test-retest reliabilities of a new tool (the Acute Stroke Dysphagia Screen) were established. The tool was administered by nursing staff when patients were admitted to the stroke unit. A speech language pathologist blinded to the results with the new tool administered the Mann Assessment of Swallowing Ability, a clinical bedside evaluation, with dysphagia operationally defined by a score less than 178. The mean time from admission to screening with the new tool was 8 hours. The mean time between administration of the new tool and the clinical bedside evaluation was 32 hours. For the new tool, interrater reliability was 93.6% and test-retest reliability was 92.5%. The new tool had a sensitivity of 91% and a specificity of 74% for detecting dysphagia and a sensitivity of 95% and a specificity of 68% for detecting aspiration risk. The Acute Stroke Dysphagia Screen is an easily administered and reliable tool that has sufficient sensitivity to detect both dysphagia and aspiration risk in acute stroke patients.
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                Author and article information

                Journal
                J Stroke
                J Stroke
                JOS
                Journal of Stroke
                Korean Stroke Society
                2287-6391
                2287-6405
                May 2019
                17 April 2019
                : 21
                : 2
                : 217-219
                Affiliations
                [a ]Stroke Research Program, Institute of Biomedicine of Seville (IBIS)/ University Hospital Virgen del Rocio/CSIC/University of Seville, Seville, Spain
                [b ]Department of Radiology, University Hospital Virgen del Rocio, Seville, Spain
                [c ]Department of Radiology, Vall d’Hebron University Hospital, Barcelona, Spain
                [d ]Neurovascular Research Laboratory, Vall d’Hebron Research Institute (VHIR), Barcelona, Spain
                [e ]Department of Neurology, University Hospital Virgen Macarena, Seville, Spain
                Author notes
                Correspondence: Joan Montaner Villalonga Neurovascular Research Laboratory, Institute of Biomedicine of Seville (IBIS), Calle Antonio Maura Montaner, 41013 Sevilla, Spain Tel: +34-955923067 Fax: +34-955923101 E-mail: jmontaner-ibis@ 123456us.es
                Article
                jos-2018-03251
                10.5853/jos.2018.03251
                6549062
                30991796
                6ddc9589-7a53-43b8-8188-d014896219df
                Copyright © 2019 Korean Stroke Society

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 19 November 2018
                : 17 January 2019
                : 18 January 2019
                Categories
                Letter to the Editor

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