key: cord-0026415-fn0kaotc authors: Ogawa, Hiroaki; Kitsios, Georgios D.; Iwata, Mitsunaga; Terasawa, Teruhiko title: Sputum Gram stain for diagnosing causative bacterial pathogens and guiding antimicrobial therapies in community-acquired pneumonia: a systematic review and meta-analysis protocol date: 2019-04-17 journal: Fujita Med J DOI: 10.20407/fmj.2018-019 sha: 4e0721e80d01990f579ad6518bb807561f1ee42e doc_id: 26415 cord_uid: fn0kaotc OBJECTIVES: The clinical role of sputum Gram stain for rapid etiologic pathogen diagnosis in patients with community-acquired pneumonia (CAP) remains an unresolved controversy. Variability in protocols and reporting of diagnostic performance in different studies has hampered assessments of clinical utility and interpretation. Since the last meta-analysis published in 1996, several reports and resources to accurately evaluate the diagnostic accuracy of sputum Gram stain have become available. Therefore, we will conduct a systematic review and meta-analysis of the clinical validity and utility of sputum Gram stain. METHODS: We will search PubMed, Ovid MEDLINE, Embase, and The Cochrane Controlled Register of Trials (CENTRAL) databases from inception through July 30, 2018, with no language restriction and perform a full-text evaluation of potentially relevant articles. We will include prospective and retrospective studies that assess sputum Gram stain in adults (aged ≥18 years) with CAP. Two reviewers will independently extract data and rate each study’s validity with standard quality assessment tools. We will subsequently perform standard and latent-class random-effects model meta-analyses to quantitatively synthesize the diagnostic accuracy and yield. Finally, we will assess the totality of evidence by the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) approach for diagnostic tests and strategies. RESULTS: Results of the analysis will be submitted for publication in a peer-reviewed journal. CONCLUSIONS: This systematic review and meta-analysis will provide a 30-year synopsis of clinical evidence on sputum Gram stain in patients with CAP. Community-acquired pneumonia (CAP) is an acute infection of the lung that develops in community-dwelling persons who have not been hospitalized in recent months or have not received regular medical or nonmedical healthcare. 1 Despite advances in effective antimicrobial therapies, lower respiratory tract infections were the fourth most common cause of death and the leading infectious cause of death worldwide in 2016. 2 Although mortality from pneumonia has been decreasing in the United States, with 50,000 annual deaths in 2015, approximately 1 million adults were hospitalized with pneumonia in the same year, making it the second most common cause of admissions in the United States. 3 In Japan, pneumonia remains the third most common cause of death, and approximately 120,000 people died of pneumonia in 2015. 4 Gram staining of expectorated sputum is a simple, easily performed, widely available, and inexpensive test for patients with pneumonia. Multiple pathogens can be assessed simultaneously with sputum Gram stain, and the test has a short turnaround time. 5 When performed by experienced observers with specimens of acceptable quality, the sputum Gram stain can assist in establishing the correct pathogen diagnosis in CAP and in directing appropriate antibiotic therapies. However, the wide variability in reported sensitivity and specificity of heterogeneously conducted studies has led to inconsistent adoption of the test in clinical practice. 6 In addition, inadequate sputum samples are not uncommon, and processing of the specimens and microscopic diagnosis of causative bacteria by visual assessment are highly operator-dependent. 7 Other factors, such as collection and transport of the specimens, can affect timely initiation of antimicrobial therapies, which is an important measure related to pneumonia-associated mortality. 8 Furthermore, to our knowledge, no robust evidence exists to support a pathogendirected treatment strategy over the guideline-recommended empirical broad-spectrum antibiotic treatment. 9 Therefore, current clinical guidelines for patients with CAP inconsistently recommend sputum Gram stain only in selected indications. [10] [11] [12] Nevertheless, a theoretical rationale for pathogen-directed therapies was that rapid detection of pneumonia etiologies could spare the use (and misuse) of broad-spectrum antibiotics to control the emergence of antibiotic resistance. In the past two decades since the publication of the metaanalysis of sputum Gram stain in patients with CAP in 1996, 6 13 For this reason, several approaches to account for the imperfectness of reference standards have been implemented to calculate corrected accuracy in primary studies. 14 Thus, the naïvely synthesized uncorrected accuracy estimates in the 1996 meta-analysis could be inaccurate. Furthermore, the 1996 metaanalysis focused on diagnostic accuracy for detecting Strep. pneumoniae only and failed to include diagnostic accuracy for detecting other potentially important pathogens or the overall diagnostic yield to assess the full range of performance in this modality to simultaneously assess multiple pathogens. Given the emergence of the aforementioned contemporary reference standard and alternative or add-on tests and the approaches available that adjust for theoretically biased results, we plan a comprehensive overview and quantitative synthesis of the clinical data on sputum Gram stain for identifying causative pathogens of CAP. This systematic review and meta-analysis protocol follows the preferred reporting items for systematic review and metaanalysis protocols 2015 statement (PRISMA-P). 15 We have followed the framework for assessing levels of clinical effectiveness of diagnostic tests proposed by Fryback and Thornbury 16 We chose, a priori, these six common, clinically significant, and morphologically discernible bacterial pathogens of CAP as the target pathogens; 5 previous studies 9, 17 and guidelines 18 have proposed specific antibiotics for these six bacteria. We will also assess a combined pathogen category, named "mixed (aerobic and anaerobic) oral flora," as a target pathogen of interest. Research Question 2 (diagnostic impact; Fryback Level 3): What is the proportion of patients for whom sputum Gram stain (alone or in combination; separately analyzed) is useful in diagnosing specific pathogens for patients with CAP? Research Question 3 (management decision impact; Fryback Level 4): How often does sputum Gram stain (alone or in combination; separately analyzed) change diagnostic or therapeutic strategies planned before testing for patients with CAP? Research Question 4 (patient-relevant outcomes; Fryback Level 5): What is the comparative effectiveness between diagnostic and management strategies guided by sputum Gram stain and those not guided by sputum Gram stain for patients with CAP? In this question, we will, assess as specific patient-relevant outcomes, (1) failure rates of primary therapies, (2) overall failure rates of primary and subsequent-line therapies, (3) length of hospital stay, (4) in-hospital mortality, and (5) all harms observed. Here, we will define failure as a patient whose signs and symptoms of pneumonia do not improve within a study-specified time-frame after initiation of the initial antibiotic treatment and is therefore judged a "treatment failure" by the study. Research Question 5 (effect modifiers): What factors modify the aforementioned effectiveness measures? We will search PubMed and MEDLINE, Embase, and the Cochrane Register of Controlled Trials (CENTRAL) via Ovid databases from inception through July 30, 2018, using the freetext terms "sputum," "Gram stain," and "pneumonia," and their synonyms. As additional searches, we will peruse the reference lists of previously reported systematic reviews and metaanalyses. A pulmonologist investigator who specializes in pneumonia microbiome (GDK) will check whether there are any missing publications that are relevant. No language restrictions will be set. We will include any prospective or retrospective cohort or cross-sectional studies that included at least ten patients with CAP and that assessed the outcomes of interest listed under the PICO framework (Table 1 ). We will also include randomized controlled trials and non-randomized studies of intervention of any size that assessed the effectiveness of sputum Gram stain in patients with CAP (e.g., test-directed versus no test strategies). We will exclude conference abstracts, primary studies with the outcome data unextractable from the publication, and studies based on modeling without using primary data. Two reviewers will independently screen abstracts, and all potentially eligible articles considered by at least one reviewer will be retrieved. Then, the two reviewers will independently peruse the retrieved full-text articles and determine the final inclusion. Any discrepant results will be resolved by consensus. Adjudication by a third reviewer will be made in case of unresolved discrepancies. Data will be extracted by two reviewers. One primary reviewer will extract the following descriptive data, and (at least) one reviewer will verify all extracted data. Two independent reviewers will extract any numerical data on the outcomes of interest. Disagreements will be resolved by consensus including a third reviewer. In the case of missing or unresolved numerical data, we will contact the study authors for clarification by email. We will send two additional email correspondences if no response is received within 2 weeks of a previous correspondence attempt. We will extract study, patient, and test characteristics as descriptive data. Study characteristics will include study identification, study location (country, city), study period (enrollment year), study design, enrollment methods (consecutive or not), number of centers, clinical setting, definition of CAP, exclusion criteria, comparator tests if any, and types of reference standard adopted. Patient characteristics will include number of patients, average age (range), male sex (%), presence of chronic obstructive pulmonary disease (%), immunocompromised host (%), suspected aspiration pneumonia (%), prognostic index (e.g., pneumonia severity index), prior antibiotics use, identified pathogens [Strep. pneumoniae (%), H. influenzae (%), M. catarrhalis (%), K. pneumoniae (%), P. aeruginosa (%), Staph. aureus (%), mixed oral flora (%)], nonpneumonia causes (%), and unidentified pathogens or causes (%). Test characteristics will include timing of sampling, sampling methods, time between sampling and Gram stain, staining methods, validity criteria of adequate samples, adequate samples [n/N (%)], performers of Gram stain and experience, and interpreter of test results and experience. We will assess sensitivity and specificity as the outcome measure of diagnostic accuracy (the primary outcome of interest). We will define sensitivity as TP/(TP+FN) and specificity as TN/(FP+TN), where TP indicates true-positive (positive index and reference standard tests), FP indicates falsepositive (index test positive and reference standard test negative), FN indicates false-negative (index test negative and reference standard test positive), and TN indicates true-negative (index and reference standard tests negative) results from the 2×2 contingency table including cross-classified count data according to whether the index and reference standard tests are positive or negative. Here, we will consider the morphological visual assessment of each specific bacterium observed after Gram staining as the index test. We will assess diagnostic yield as the measure of diagnostic impact (as the secondary outcome). We will define diagnostic yield as the number of cases with a correct diagnosis by testing (any correctly diagnosed bacteria by sputum Gram stain; this number should correspond to the total number of TP cases for all Gram stain-assessable bacteria) divided by the number of all tested cases. We will perform a subgroup analysis of diagnostic yield for patients with sputum samples of adequate quality. As the measure of management decision impact, we will calculate the post-test percentage change in the diagnostic or therapeutic interventions planned before performing sputum Gram stain in a study cohort. The respective percentage changes will be defined as the number of patients for whom the diagnostic or therapeutic interventions planned before testing are altered based on the test results (regardless of whether the interventions are either increased or decreased) divided by the total number of patients who undergo sputum Gram stain. Regarding the patient-relevant outcomes listed in Research Question 4, we will assess the association of use versus non-use of sputum Gram stain with the numbers of failure of antibiotic therapies, in-hospital deaths from any cause, and all harms observed as the binary outcomes; or length of hospital stay as the continuous outcome. For each study, we will calculate the risk ratio for each of the binary outcomes and the difference in length of hospital stay as the respective outcome measure. We will accept any reference standard test adopted in eligible studies. However, before analysis, we will specify commonly available clinical tests for each target pathogen as the reference standards and will define their results to uniformly construct the 2×2 table. Table 2 describes the operational definitions of the final diagnosis for the target pathogens by the reference standard tests. To assess the risk of bias and concerns regarding the applicability of studies of diagnostic accuracy and yield, two reviewers will independently assess patient selection, index test, reference standard, and their flow and timing based on the revised Quality Assessment of Diagnostic Accuracy Studies instrument tool (QUADAS-2). 21 Discrepant ratings will be resolved by consensus. For non-randomized studies of intervention, we will use the ROBINS-I tool [Risk Of Bias In Non-randomized Studies -of Interventions, formerly known as A Cochrane Risk Of Bias Assessment Tool for Non-Randomized Studies of Interventions (ACROBAT-NRSI)], a recently proposed risk of bias assessment tool by the Cochrane Risk of Bias Group. 22 For randomized controlled trials, we will use the revised tool to assess risk of bias in randomized trials (RoB 2 tool). 23 We will rate each methodological quality item as "yes," "no," or "unclear" (due to no or less clear reporting) for each eligible study. Then, we will rate the overall validity for each study as being of low, intermediate, or high risk of bias. For each specific pathogen, we will calculate sensitivity and specificity for each study with their corresponding 95% confidence intervals (CI) and then obtain summary estimates of sensitivity and specificity with their corresponding 95% CI by using bivariate random-effects meta-analysis with the exact binomial likelihood when ≥4 studies are available. 24, 25 We will assess between-study heterogeneity visually by plotting sensitivity and specificity separately in forest plots and in the receiver operating characteristic (ROC) space. We will construct hierarchical summary ROC curves (HSROC) 26 and confidence regions for summary sensitivity and specificity when appropriate. 24, 25 We will calculate "adjusted" summary estimates of sensitivity and specificity, and summary ROC curves by a Bayesian latentclass model (LCM) meta-analysis to adjust for imperfect reference standard(s), as proposed by Dendukuri. 27 In the main analysis, we will use a vague prior distribution (0%-100%) for the sensitivity and specificity of all adopted imperfect reference standard(s). In sensitivity analysis, we will use informative prior distributions for specific reference standard(s) adopted. For example, we will use a sensitivity of 74.0% (range, 66.6%-82.3%) and specificity of 97.2% (range, 92.7%-99.8%) for urine-based pneumococcal antigen tests based on the ranges reported in a meta-analysis accounting for the imperfect reference standard. 28 However, a pulmonologist investigator who specializes in pneumonia microbiome (GDK) will propose clinically relevant ranges of accuracy estimates for any imperfect reference standard tests adopted in the primary studies. Regarding the change in diagnosis, diagnostic or therapeutic managements, and patient-relevant outcomes, we will first perform qualitative syntheses through graphs and tables. If feasible, we will then calculate summary estimates of diagnostic yield and percentage change in diagnostic and therapeutic management by the random-effects meta-analysis of proportions, and summary risk ratios and differences by the standard Bayesian hierarchical random-effects meta-analysis. 29, 30 Additional analyses We will perform subgroup or univariable meta-regression analysis on study year (before versus after 2000), study location (United States and Europe versus other regions), use of a urinebased Pneumococcus test as reference standard (yes versus no), and performers/interpreter of test (physicians versus lab technicians; experienced personnel versus less experienced personnel). We will also assess the relationship between diagnostic yield and the prevalence of Strep. pneumoniae and H. influenzae, two of the most frequently identified pathogens for which sputum Gram stain is expected to be particularly useful. We will assess the totality of evidence by the Grading of Recommendations Assessment, Development, and Evaluation Sputum Gram stain in community-acquired pneumonia: a systematic review protocol (GRADE) approach and strength of recommendations for diagnostic tests and strategies. 31 We will not perform statistical tests for funnel plot asymmetry because the required tests do not allow for valid assessment of the extent and impact of missing data in studies of diagnostic accuracy. 32 All aforementioned statistical analyses will be performed using Stata SE, version 13.1 (College Station, TX, USA) and WinBUGS 1.4.3 (MRC Biostatistics, Cambridge, UK) or OpenBUGS 3.2.3 (OpenBUGS Project Management Group; www.openbugs.net) from within Stata. All P-values will be twosided, and statistical significance will be defined as P<0.05. Sputum Gram stain is an inexpensive, readily available, and rapid test; together with other available rapid antigen detection tests, it is a pragmatic tool for rapid pathogen-directed antimicrobial therapy across different care settings. Although advanced sequencing-based molecular diagnostics are currently under development, such techniques remain investigational and have not been clinically validated. 33 Thus, the diagnostic performance of sputum Gram staining and its impact on patient outcomes represent important and clinically relevant questions. Use of the LCM meta-analysis has the potential to perform statistical corrections for the biased accuracy estimates reported in culture-based primary studies of sputum Gram stain in the absence of perfect reference standards, which is a strength of our analysis. Our comprehensive assessment of diagnostic accuracy and yield for all relevant bacterial pathogens also elucidates additional roles of sputum Gram stain, not limited to its role in diagnosing Strep. pneumoniae, in the management of CAP. In conclusion, by conducting a 30-year field synopsis of this topic, including standard and LCM meta-analysis of diagnostic accuracy and yield, we hope to clarify the true diagnostic accuracy of sputum Gram stain for various bacterial pathogens on which further studies can be performed to address clinical impacts of pathogen-directed treatment strategies for patients with CAP. Community-acquired pneumonia World Health Organization. The top 10 causes of death Top 20 Pneumonia Facts-2015 Deaths by causes (the condensed list of causes of death for Japan), sex and age: Japan Clinical Methods: The History, Physical, and Laboratory Examinations Sputum gram's stain in community-acquired pneumococcal pneumonia. A meta-analysis Diagnostic tests for agents of community-acquired pneumonia Antibiotic therapy for adults hospitalized with community-acquired pneumonia: a systematic review Comparison between pathogen directed antibiotic treatment and empirical broad spectrum antibiotic treatment in patients with community acquired pneumonia: a prospective randomised study Infectious Diseases Society of America/ American Thoracic Society consensus guidelines on the management of community-acquired pneumonia in adults Diagnosis and management of community and hospital acquired pneumonia in adults: summary of NICE guidance Guidelines for the management of adult lower respiratory tract infections-full version Chapter 9: options for summarizing medical test performance in the absence of a "gold standard Latent class models in diagnostic studies when there is no reference standard-a systematic review Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015 statement The efficacy of diagnostic imaging Validation of sputum Gram stain for treatment of community-acquired pneumonia and healthcare-associated pneumonia: a prospective observational study Guideline Update from the Dutch Working Party on Antibiotic Policy (SWAB) and Dutch Association of Chest Physicians (NVALT) Systematic survey of randomized trials evaluating the impact of alternative diagnostic strategies on patient-important outcomes Diagnostic tests often fail to lead to changes in patient outcomes QUADAS-2: a revised tool for the quality assessment of diagnostic accuracy studies ROBINS-I: a tool for assessing risk of bias in non-randomised studies of interventions A revised tool for assessing risk of bias in randomized trials Bivariate analysis of sensitivity and specificity produces informative summary measures in diagnostic reviews A unification of models for meta-analysis of diagnostic accuracy studies A hierarchical regression approach to metaanalysis of diagnostic test accuracy evaluations Bayesian meta-analysis of the accuracy of a test for tuberculous pleuritis in the absence of a gold standard reference Systematic review and meta-analysis of a urine-based pneumococcal antigen test for diagnosis of community-acquired pneumonia caused by Streptococcus pneumoniae Simulation-Based Comparison of Methods for Meta-Analysis of Proportions and Rates Metaanalysis using Bayesian methods Grading quality of evidence and strength of recommendations for diagnostic tests and strategies Cochrane Handbook for Systematic Reviews of Diagnostic Test Accuracy Version 1.0. The Cochrane Collaboration Translating lung microbiome profiles into the nextgeneration diagnostic gold standard for pneumonia: a clinical investigator's perspective This is an Open access article distributed under the Terms of Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author(s) and source are credited Sputum Gram stain in community-acquired pneumonia: a systematic review protocol The authors report no conflicts of interest in this work. TT was supported in part by The Ministry of Education, Culture, Sports, Science and Technology, Japan (Numbers 26461518 and 26460755). GDK was supported in part by the National Heart, Lung, and Blood Institute of the National Institutes of Health, United States Department of Health and Human Services, USA (K23HL139987). The funding sources had no role in the design or conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; or decision to submit the manuscript for publication.