Meta-Analysis: Outcomes in Patients with Suspected Pulmonary Embolism Managed with Computed Tomographic Pulmonary Angiography

7 December 2004 | Volume 141 Issue 11 | Pages 866-874

Background: Spiral computed tomographic pulmonary angiography (CTPA) is increasingly being used in the evaluation of patients with clinically suspected pulmonary embolism (PE). However, CTPA as a definitive diagnostic test may be limited by inadequate sensitivity, especially in instances of isolated subsegmental emboli.

Purpose: To assess the safety of withholding anticoagulation in patients with suspected PE and negative results on CTPA.

Data Sources: All relevant studies identified in MEDLINE (1966 to March 2004) and EMBASE (1974 to 2004) and in bibliographies of key articles. The search was not limited to the English language.

Study Selection: The authors selected all published studies that used CTPA to evaluate suspected PE and reported at least 3 months of follow-up in patients not receiving anticoagulation on the basis of a negative CTPA result.

Data Extraction: Two reviewers independently rated study quality on the basis of predetermined criteria. Data were extracted on participants, CTPA technique, diagnostic studies performed, prevalence of PE, number of patients with negative or indeterminate CTPA results who were followed, and subsequent rates of venous thromboembolism and fatal PE.

Data Synthesis: Twenty-three studies reported on 4657 patients with negative CTPA results who did not receive anticoagulation. The 3-month rate of subsequent venous thromboembolic events was 1.4% (95% CI, 1.1% to 1.8%), and the 3-month rate of fatal PE was 0.51% (CI, 0.33% to 0.76%).

Limitations: The CTPA technology used varied across studies and was not applied uniformly in the same step of diagnostic algorithms. Only 1 study used CTPA as the sole diagnostic test.

Conclusion: The rate of subsequent venous thromboembolism after negative results on CTPA is similar to that seen after negative results on conventional pulmonary angiography. It appears to be safe to withhold anticoagulation after negative CTPA results.

Editors' Notes Top Editors' Notes Methods Results Discussion Author & Article Info References Context Is it safe to withhold anticoagulation in adults with suspected pulmonary embolism (PE) and negative results on spiral computed tomographic pulmonary angiography (CTPA)? Contribution This meta-analysis summarized data from 23 studies that reported rates of thromboembolism among patients with suspected PE who did not receive anticoagulation after negative results on CTPA. Among 4657 patients, the 3-month risks for a thromboembolic event and fatal PE were 1.4% and 0.51%, respectively. Cautions Studies used early-generation CT technology and different diagnostic algorithms for thromboembolism. Implications Withholding anticoagulation from patients with low to moderate probability of PE and negative results on CTPA appears reasonable. –The Editors

 

Pulmonary embolism (PE) remains a major cause of morbidity and mortality (1). The limitations of clinical examination in establishing a diagnosis of PE, as well as the perils of unnecessary anticoagulation and untreated clots, mandate use of judicious objective diagnostic testing in the evaluation of this disorder. Spiral computed tomographic pulmonary angiography (CTPA) has become an integral part of the diagnostic evaluation for suspected PE, given its widespread availability, ease of acquisition, favorable performance characteristics (2), and utility in revealing alternative diagnoses (3, 4). Researchers have been cautiously optimistic that CTPA may be useful as a definitive study to exclude PE (5).

However, CTPA is often applied as part of an algorithmic screening approach that includes other diagnostic tests, including pretest prediction models, D-dimer testing, lower-extremity compression ultrasonography, and lung scintigraphy (3, 6-13). Many of these algorithms recommend conventional pulmonary angiography (CPA) as the gold standard (14). Although screening algorithms are reported to have good efficacy, they remain cumbersome to apply (15) and may be considerably underused in clinical practice (16). Some recent investigations suggest that CTPA merits consideration as a definitive diagnostic study (17-19). However, many authors remain unconvinced that negative CTPA results alone can reliably exclude clinically significant pulmonary emboli (20, 21).

Bates and Ginsberg (20) have proposed that acceptance of CTPA as a definitive study would require establishment of its interobserver and intraobserver variability and study characteristics, determination of its accuracy, and an assessment of outcomes after anticoagulation is withheld because of a negative test result. The first 2 criteria have been evaluated (21, 22). In the current study, we performed a systematic review of the literature and conducted a meta-analysis of eligible studies to determine the safety and efficacy of withholding systemic anticoagulation after negative results on CTPA for PE.

Methods

Top Editors' Notes Methods Results Discussion Author & Article Info References

We searched MEDLINE (1966 to March 2004) and EMBASE (1974 to 2004) using the terms pulmonary embolism, computed x-ray tomography, CTPA, angiography, sensitivity and specificity, prognosis, and recurrence. We augmented our search by reviewing the reference lists of retrieved articles and review articles, our personal files, and reference lists of related articles in our files. Our medical librarian performed an independent search to ensure completeness. The search was not limited to the English language, but only published reports were included (Figure 1).

View larger version (29K): [in this window] [in a new window]   Figure 1. Flow diagram of study selection. CTPA = computed tomographic pulmonary angiography; PE = pulmonary embolism.

 

Study Identification and Eligibility

We attempted to identify all published studies that examined the rate of subsequent symptomatic venous thromboembolism (VTE) in patients who did not receive anticoagulation after negative or indeterminate CTPA results. To be included in the analysis, studies had to 1) have a consecutive sample or a well-defined reason for a selected sample (for example, inclusion of only patients with underlying cardiopulmonary disease or those referred to specialty centers); 2) define the diagnostic strategy used to confirm or exclude VTE; 3) withhold anticoagulation or clearly state the reason for administering anticoagulation when VTE was excluded (patients who received anticoagulation were excluded from the final analysis); 4) have a minimum of 3 months of follow-up; and 5) report subsequent symptomatic VTE events and the means of confirmation.

Study Quality

Two reviewers independently rated each study's quality. Because there are no validated tools for quality assessment of outcome studies, we adapted the McMaster criteria for evaluating the validity of studies about prognosis (23). Studies were assessed for presence of 9 features: description of patient sample characteristics, description of inclusion and exclusion criteria, potential selection bias, length of follow-up, completeness of follow-up, description of patients lost to follow-up, description of reasons for incomplete follow-up, definition of outcomes at the start of the study, and objectivity of outcomes. The intraclass correlation coefficient for agreement between the 2 raters on overall quality rating for all included studies was 0.85 (P < 0.001). Disagreements were resolved by consensus. In addition to abstracted data on patients, CTPA performance, and outcomes, we recorded the number of patients who had initial nondiagnostic CTPA results and follow-up of these patients if reported. Patients who received anticoagulation despite initial negative results on CTPA were excluded from the final analysis. Although some studies included a longer follow-up period, we limited our analysis to the first 3 months after negative results on CTPA because events after 3 months are likely to be new rather than recurrences.

Statistical Analysis

The rates of subsequent VTE events and fatal PE were calculated from the abstracted numbers for each study. Extracted outcomes were the proportion of individuals with negative results on CTPA who subsequently experienced pulmonary emboli, fatal or otherwise. These data were combined by using an approximation to the inverse variance approach, effectively weighting each study according to its sample size (24). The 95% CI for each study and for the overall effect was calculated by using exact binomial methods. Heterogeneity was assessed visually with Galbraith plots (25). Publication bias was assessed visually by using funnel plots and by statistically using the method of Egger and colleagues (26). The sensitivity of our results to potential publication bias was assessed by using the methods of Duval and Tweedie (27). We performed sensitivity analyses, assessing the effects of type of study (prospective vs. retrospective), year of study, whether patients were consecutive or selected, generation of computed tomography (CT) scanner, the thickness of CT cuts, caudocranial image acquisition, view box interpretation, and the prevalence of PE.

Role of the Funding Source

No funding was received in support of this review.

Results

Top Editors' Notes Methods Results Discussion Author & Article Info References

We identified 640 abstracts in our search. Most were excluded because they did not include outcome data on patients not treated with anticoagulants (Figure 1). Among the 27 remaining articles, 4 were excluded: 3 had insufficient follow-up data (4, 28, 29) and 1 reported duplicate data (30) that were presented as part of the final report of a prospective study (31). Therefore, 23 articles were included in our analysis (3, 6, 11-13, 15, 17-19, 31-44). One of these (33) included 35 patients from another study (32).

Qualitative Review

The 23 studies included 15 prospective and 8 retrospective trials (Table). Study samples ranged from 54 to 1512, averaging 403 patients. Seventeen of the included studies examined consecutive patients, and 6 included selected patient samples. Overall, the mean prevalence of PE was 19.8% (range, 13% to 42%). Three studies (34, 37, 38) enrolled only patients in whom PE had been excluded and therefore did not report on prevalence in the sample. Nine of the studies included images obtained in the caudocranial direction, and 15 interpreted images on view box stations. The average CT scanner thickness was 2.1 mm (range, 2 to 5 mm). Ten prospective studies used CTPA with other diagnostic methods as part of a predetermined algorithm (3, 6, 11-13, 31-33, 35, 40). Pretest probability was used in 6 studies (6, 12, 13, 31, 32, 35), lung scintigraphy in 5 (11, 12, 31, 32, 35), lower-extremity compression ultrasonography in 6 (3, 13, 31-33, 40), and D-dimer testing in 4 (6, 11, 33, 40). Fourteen studies (3, 12, 13, 15, 17-19, 31, 33, 36, 37, 39, 41, 43) used objective imaging to confirm subsequent VTE events, while only 6 (3, 13, 15, 18, 34, 39) used autopsy confirmation or central adjudication to confirm fatal events.

View this table: [in this window] [in a new window]   Table. Data Extracted from Individual Studies

 

Twenty-one of the studies included a small proportion of patients (n = 492) who received anticoagulation despite negative results on CTPA. The reasons for anticoagulation included presence of deep venous thrombosis on concomitant ultrasonography (n = 70), chronic VTE (n = 68), and cardiac arrhythmias or other cardiac abnormalities (n = 204). Four patients had positive results on another test (ventilation–perfusion scanning or CPA) that suggested PE, while 65 patients (13%) were listed as having nonthromboembolic disorders. The reason for anticoagulation was not stated in 63 patients. Only 18 patients received anticoagulation because of persistent high clinical suspicion of PE despite negative results on CTPA. These patients were not included in our analysis of outcomes.

Overall quality ratings ranged from 3 to 9 (Appendix Table). Common quality problems included inadequately clear inclusion and exclusion criteria in 6 studies, potential selection bias in 16 studies, incomplete follow-up in 13 studies, inadequate description of the patients lost to follow-up in 14 studies, inadequate description of the reason for incomplete follow-up in 7 studies, and problems with the objectivity of outcome assessment in 9 studies.

View this table: [in this window] [in a new window]   Appendix Table. Quality Ratings of Included Studies

 

Three studies (3, 6, 12) met all 9 criteria assessing methodologic quality. In an observational study, Perrier and colleagues (6) performed CTPA in 299 consecutive outpatients who had suspected PE and plasma D-dimer levels greater than 500 µg/L; PE was diagnosed by using a previously validated strategy (10) that did not include CTPA results. Thirty-four patients with negative CTPA results initially received a diagnosis of PE by ventilation–perfusion scanning, lower-extremity compression ultrasonography, or CPA; these patients received anticoagulation. At 3-month follow-up, none of the 157 patients who did not have PE on CTPA and did not receive anticoagulation had experienced recurrent or fatal PE. Of note, despite its strengths, this study was not included in our pooled event rate because CTPA results did not influence patient management and subsequent VTE events could not be assigned to CTPA results.

Ost and colleagues (12) performed CTPA in 103 patients with high pretest clinical suspicion for PE and nondiagnostic results on ventilation–perfusion scanning. Three of 71 patients with negative CTPA results subsequently developed nonfatal VTE at 6-month follow-up, with a negative predictive value of 96% when clinical outcome was used as the reference standard. Van Strijen and associates (3) studied 510 consecutive patients with suspected PE by using sequential single-detector CTPA and lower-extremity compression ultrasonography. Two of 248 patients with negative results on CTPA and no alternative diagnosis had positive results on lower-extremity compression ultrasonography. Of the 376 patients who had negative results on diagnostic studies and did not receive anticoagulation, 3 subsequently developed VTE during 3-month follow-up (VTE rate, 0.8% [CI, 0.2% to 2.3%]).

Quantitative Review

When all extracted data were pooled, 4657 patients were eligible for analysis. The rate of subsequent VTE (both nonfatal and fatal) among these studies ranged from 0% to 4.9%, with no evidence of heterogeneity. Over all studies, the pooled rate of VTE during 3-month follow-up among patients with negative CTPA results was 1.4% (CI, 1.1% to 1.8%) (Figure 2, top). Fatal PE occurred in 24 patients (pooled risk, 0.51% [CI, 0.33% to 0.76%]) (Figure 2, bottom).

View larger version (24K): [in this window] [in a new window]   Figure 2. Forest plots of total venous thromboembolism (VTE) events (top) and fatal pulmonary embolism (PE) events (bottom). The number of patients for each study is the number of patients eligible for outcome assessment, and the event rates are a combination of recurrent VTE and fatal PE (see Table). Values in parentheses on the right-hand side of the figure are the upper bound of the CI unless otherwise indicated.

 

Among the 15 prospective studies, 2361 patients were eligible for analysis. Subsequent VTE events occurred in 39 patients (pooled risk, 1.2% [CI, 0.6% to 1.8]), and fatal PE occurred in 15, yielding a pooled rate of 0.26% (CI, –0.5% to 52.5%). Of the 9 studies that followed patients for longer than 3 months, 8 studies, 5 of them prospective, recorded at least a mean of 6 months of follow-up. Only 1 subsequent PE was documented beyond the 3-month follow-up period (44).

Sensitivity Analysis

Our reported study outcomes for both total VTE and fatal PE rates were not affected by year of study, study type (prospective vs. retrospective), patient sample (consecutive vs. selected), the generation of the scanner, the thickness of scanner cuts, caudocranial image acquisition, image reading (view box vs. no view box), performance of other studies as part of the study protocol, or the prevalence of PE (P > 0.2 for all comparisons).

Publication Bias

We found no evidence of publication bias by examining funnel plots (data not shown) or by performing the Egger test (26) (overall VTE rate, P = 0.07; fatal PE, P > 0.2). Because tests for publication bias are relatively insensitive, we corrected for potential unpublished data by using the Duval and Tweedie (27) meta-trim method, which produced an adjusted overall PE rate of 1.1% (CI, 0.8% to 1.5%) and no change in the fatal PE rate.

Outcomes after Inconclusive, Nondiagnostic, or Suboptimal CTPA Results

Sixteen studies (3, 6, 11-13, 15, 17, 19, 32, 34, 38-42, 44) explicitly reported that 327 patients had CTPA results described as inconclusive, indeterminate, uninterpretable, nondiagnostic, or suboptimal. Seventy-four of these 327 patients, from 8 studies (3, 6, 12, 15, 32, 38, 40, 41), were classified separately. They were not excluded from the final analysis, did not receive anticoagulation empirically, and either underwent additional diagnostic evaluation or were followed clinically. Twelve patients (16.2%) subsequently received a diagnosis of VTE.

Discussion

Top Editors' Notes Methods Results Discussion Author & Article Info References

Our data suggest that it is safe to withhold anticoagulation in patients with negative results on CTPA. Our literature review and meta-analysis of 23 studies revealed that the 3-month rate of subsequent VTE after negative results on CTPA is very low (VTE, 1.4% [CI, 1.1% to 1.8%]; fatal PE, 0.51% [CI, 0.33% to 0.76%]). This low rate of recurrent VTE is similar to that seen after negative results on CPA (45, 46). In the Prospective Investigation of Pulmonary Embolism Diagnosis (PIOPED) study (45), the largest pre-CTPA study with outcome data, rates of subsequent VTE and fatal PE were 1.6% (CI, 0.3% to 2.9%) and 0.53% (CI, 0.16% to 1.9%), respectively. Van Beek and coworkers (46) performed a systematic review of all prospective trials (including PIOPED) that included outcome data on patients who did not receive anticoagulation after negative results on CPA. They reported summary rates of 1.7% (CI, 1.7% to 2.7%) for VTE and 0.30% (CI, 0.02% to 0.70%) for fatal PE.

Although CTPA for diagnosis of PE was first assessed in 1992 (47), recent literature reviews have concluded that sufficient evaluation of this method is still lacking (21, 22). The important missing piece of information is whether it is safe to withhold anticoagulation after negative CTPA results. Our findings suggest that rates of subsequent events in patients with negative CTPA results are similar to rates observed after negative results on CPA. Although CTPA has not been proven to be accurate as CPA, much of the literature on CTPA has used early-generation CT scanners with a limited number of detectors. More recent literature has shown that the use of multidetector CT scanners and more sophisticated reconstruction algorithms allows better identification of higher-generation pulmonary arteries and improved diagnostic yield (48-52). In addition, multidetector scanners can perform image acquisition approximately twice as quickly as single-detector scanners and may reduce the number of technically inadequate studies (48). Nonetheless, our results suggest that even early-generation CTPA is safe for management of patients with suspected acute PE.

Two of the most methodologically robust prospective studies we reviewed combined CTPA with lower-extremity compression ultrasonography (3, 6). One of these studies reported, however, that the 3-month VTE recurrence rate would have been 1.3% if anticoagulation had been withheld only because of normal CTPA results (that is, if no lower-extremity compression ultrasonography had been performed) (3). Our sensitivity analysis did not show that the way CTPA was performed—alone or in combination—had any significant effect on the pooled rates of VTE and fatal PE. However, we did find that among patients who received anticoagulation despite negative CTPA results, 14% were treated because venous ultrasonography had revealed acute DVT. Had these patients been left untreated because of negative CTPA results, the subsequent VTE rate may have been slightly higher. Therefore, the role of CTPA without concomitant lower-extremity imaging is still undefined. Computed tomographic venography has shown promise as an adjunctive study when added to CTPA and may increase the diagnostic yield (53-55); recent studies (53, 54) suggest that this test may be more sensitive at detecting DVT than concomitant lower-extremity ultrasonography.

Only 6 studies combined an assessment of clinical probability with imaging. Although the PIOPED study (45) demonstrated that a pretest clinical estimate of PE was very valuable in dictating management after lung scintigraphy, and although clinical prediction scoring systems for PE have been devised and validated (9, 56, 57), the influence of clinical pretest probability on dictating diagnostic strategy after negative results on "screening" CTPA is unknown. Furthermore, if CTPA were applied as a definitive study (a step our meta-analysis would support), any influence of pretest probability would not be important. Pretest probability assessments should be used to select patients for CTPA, since recent publications support the exclusion of PE based on a low pretest probability and negative results on D-dimer testing (7-11, 13).

Some of the included studies documented a high rate of subsequent VTE after inconclusive results on CTPA, although not all allowed extraction of these data. Criteria for nondiagnostic CTPA results, which varied among studies, were arguably subjective but were generally defined by a combination of insufficient contrast enhancement (for example, inadequate vessel clarity past the central pulmonary arteries), inter-reader variability, and technical considerations (for example, significant motion or imaging artifact). Nondiagnostic results after CTPA are not uncommon (13, 41, 44) and occur with frequency similar to that of nondiagnostic results on CPA (58, 59). However, CTPA results that are inconclusive for PE do not modify the prior probability of disease (6). It would be important to know whether the subsequent rate of VTE in this population correlated with the number of inconclusive studies, but we could not extract these data from the information provided by the primary authors. In our review, the cumulative rate of subsequent VTE among patients who had inconclusive CTPA results but did not receive anticoagulation was high (16.2%). This finding supports the recommendation that when a viable alternative diagnosis is not revealed incidentally, additional testing is indicated (6, 12). Improvements in technical quality (37, 60) and interpretation (61) of CTPA results may decrease the frequency of nondiagnostic results, but until such improvements are realized, CPA, repeated CTPA, or serial lower-extremity ultrasonography should be performed to confirm or exclude PE. Local resources and expertise should dictate study selection.

Studies included in our review had several important limitations. Our search was not limited to the English language but included only published studies. However, we could find no evidence of publication bias. Prospective studies used a variety of diagnostic algorithms, as detailed earlier. No two management strategies were identical, although we found no evidence of heterogeneity in outcomes between studies. Although a majority of studies (16) enrolled consecutive patients, there were some differences in patient selection. Autopsy or objective diagnostic testing was usually used to confirm recurrent VTE; however, clinical suspicion or adjudication committee opinion was used on occasion. Rarely, means of confirmation were not described. Follow-up was not complete in most studies.

In addition, CTPA techniques varied both across and within studies. Moreover, all studies used early-generation CT technology, and none of the studies used reconstruction algorithms for interpretation. Thus, our findings may not be directly applicable to patients imaged with variable-thickness scanning, although advances in data acquisition would probably improve outcomes after negative results on CTPA.

In sum, the rate of subsequent VTE after negative results on CTPA appears to be very low. We found that CTPA compares favorably with CPA as a definitive study to confirm or exclude PE. Ideally, a trial that randomly assigns patients to evaluation with CTPA versus CPA as the definitive diagnostic study, withholds anticoagulation in all patients with negative imaging results, and rigorously documents subsequent VTE events would provide clear guidance on the management of patients with suspected PE. However, given the very low rates of subsequent VTE previously documented in patients managed according to CPA results, as well as in patients managed with CTPA as we have shown here, such a trial would require the enrollment of more than 10 000 patients to detect a clinically significant difference in subsequent VTE rates. Therefore, it is unlikely to be performed. In the absence of such a trial or prospective trials examining clinical outcomes when CTPA is used as the sole diagnostic examination, imaging of the lower extremities (either lower-extremity ultrasonography or CT venography) should be performed concurrently. Withholding anticoagulation seems to be safe in patients managed in this way.

Author and Article Information

Top Editors' Notes Methods Results Discussion Author & Article Info References

From Walter Reed Army Medical Center, Washington, DC, and the Uniformed Services University of the Health Sciences, Bethesda, Maryland.

Disclaimer: The opinions or assertions contained herein are the private views of the authors and are not to be construed as official or as reflecting the views of the U.S. Department of the Army or the U.S. Department of Defense.

Acknowledgments: The authors thank Christopher Bennett, MD, for his expertise with CTPA and Mr. Robert J. Mohrman for his assistance with the literature search.

Potential Financial Conflicts of Interest: None disclosed.

Requests for Single Reprints: Lisa K. Moores, MD, Uniformed Services University of the Health Sciences, Walter Reed Army Medical Center, 6900 Georgia Avenue NW, Washington, DC 20307; e-mail, Lisa.Moores{at}na.amedd.army.mil.

Current Author Addresses: Drs. Moores, W.L. Jackson, and Schorr: Uniformed Services University of the Health Sciences, Walter Reed Army Medical Center, 6900 Georgia Avenue NW, Washington, DC 20307.

Dr. J.L. Jackson: Uniformed Services University, 4301 Jones Bridge Road, Bethesda, MD 20814.

References

Top Editors' Notes Methods Results Discussion Author & Article Info References

1. Goldhaber SZ. Pulmonary embolism. N Engl J Med. 1998;339:93-104. [PMID: 9654541].[Free Full Text]

2. Safriel Y, Zinn H. CT pulmonary angiography in the detection of pulmonary emboli: a meta-analysis of sensitivities and specificities. Clin Imaging. 2002;26:101-5. [PMID: 11852216].[Medline]

3. van Strijen MJ, de Monyé W, Schiereck J, Kieft GJ, Prins MH, Huisman MV, et al. Single-detector helical computed tomography as the primary diagnostic test in suspected pulmonary embolism: a multicenter clinical management study of 510 patients. Ann Intern Med. 2003;138:307-14. [PMID: 12585828].[Abstract/Free Full Text]

4. Kim KI, Müller NL, Mayo JR. Clinically suspected pulmonary embolism: utility of spiral CT. Radiology. 1999;210:693-7. [PMID: 10207469].[Abstract/Free Full Text]

5. Gurney JW. No fooling around: direct visualization of pulmonary embolism [Editorial]. Radiology. 1993;188:618-9. [PMID: 8351321].[Free Full Text]

6. Perrier A, Howarth N, Didier D, Loubeyre P, Unger PF, de Moerloose P, et al. Performance of helical computed tomography in unselected outpatients with suspected pulmonary embolism. Ann Intern Med. 2001;135:88-97. [PMID: 11453707].[Abstract/Free Full Text]

7. Kruip MJ, Leclercq MG, van der Heul C, Prins MH, Büller HR. Diagnostic strategies for excluding pulmonary embolism in clinical outcome studies. A systematic review. Ann Intern Med. 2003;138:941-51. [PMID: 12809450].[Abstract/Free Full Text]

8. Wells PS, Anderson DR, Rodger M, Stiell I, Dreyer JF, Barnes D, et al. Excluding pulmonary embolism at the bedside without diagnostic imaging: management of patients with suspected pulmonary embolism presenting to the emergency department by using a simple clinical model and D-dimer. Ann Intern Med. 2001;135:98-107. [PMID: 11453709].[Abstract/Free Full Text]

9. Wells PS, Ginsberg JS, Anderson DR, Kearon C, Gent M, Turpie AG, et al. Use of a clinical model for safe management of patients with suspected pulmonary embolism. Ann Intern Med. 1998;129:997-1005. [PMID: 9867786].[Abstract/Free Full Text]

10. Perrier A, Desmarais S, Miron MJ, de Moerloose P, Lepage R, Slosman D, et al. Non-invasive diagnosis of venous thromboembolism in outpatients. Lancet. 1999;353:190-5. [PMID: 9923874].[Medline]

11. Lorut C, Ghossains M, Horellou MH, Achkar A, Fretault J, Laaban JP. A noninvasive diagnostic strategy including spiral computed tomography in patients with suspected pulmonary embolism. Am J Respir Crit Care Med. 2000;162:1413-8. [PMID: 11029354].[Abstract/Free Full Text]

12. Ost D, Rozenshtein A, Saffran L, Snider A. The negative predictive value of spiral computed tomography for the diagnosis of pulmonary embolism in patients with nondiagnostic ventilation-perfusion scans. Am J Med. 2001;110:16-21. [PMID: 11152860].[Medline]

13. Musset D, Parent F, Meyer G, Maître S, Girard P, Leroyer C, et al. Diagnostic strategy for patients with suspected pulmonary embolism: a prospective multicentre outcome study. Lancet. 2002;360:1914-20. [PMID: 12493257].[Medline]

14. Sautter RD. Pulmonary arteriography: the gold standard [Letter]. Arch Intern Med. 1987;147:202 [PMID: 3813724].

15. Gottsäter A, Berg A, Centergård J, Frennby B, Nirhov N, Nyman U. Clinically suspected pulmonary embolism: is it safe to withhold anticoagulation after a negative spiral CT? Eur Radiol. 2001;11:65-72. [PMID: 11194920].[Medline]

16. Goodman LR, Lipchik RJ. Diagnosis of acute pulmonary embolism: time for a new approach [Editorial]. Radiology. 1996;199:25-7. [PMID: 8633154].[Free Full Text]

17. Donato AA, Scheirer JJ, Atwell MS, Gramp J, Duszak R Jr. Clinical outcomes in patients with suspected acute pulmonary embolism and negative helical computed tomographic results in whom anticoagulation was withheld. Arch Intern Med. 2003;163:2033-8. [PMID: 14504116].[Abstract/Free Full Text]

18. Lombard J, Bhatia R, Sala E. Spiral computed tomographic pulmonary angiography for investigating suspected pulmonary embolism: clinical outcomes. Can Assoc Radiol J. 2003;54:147-51. [PMID: 12866238].[Medline]

19. Krestan CR, Klein N, Fleischmann D, Kaneider A, Novotny C, Kreuzer S, et al. Value of negative spiral CT angiography in patients with suspected acute PE: analysis of PE occurrence and outcome. Eur Radiol. 2004;14:93-8. [PMID: 12942280].[Medline]

20. Bates SM, Ginsberg JS. Helical computed tomography and the diagnosis of pulmonary embolism [Editorial]. Ann Intern Med. 2000;132:240-2. [PMID: 10651607].[Free Full Text]

21. Rathbun SW, Raskob GE, Whitsett TL. Sensitivity and specificity of helical computed tomography in the diagnosis of pulmonary embolism: a systematic review. Ann Intern Med. 2000;132:227-32. [PMID: 10651604].[Abstract/Free Full Text]

22. Mullins MD, Becker DM, Hagspiel KD, Philbrick JT. The role of spiral volumetric computed tomography in the diagnosis of pulmonary embolism. Arch Intern Med. 2000;160:293-8. [PMID: 10668830].[Abstract/Free Full Text]

23. Laupacis A, Wells G, Richardson WS, Tugwell P. Users' guides to the medical literature. V. How to use an article about prognosis. Evidence-Based Medicine Working Group. JAMA. 1994;272:234-7. [PMID: 8022043].[Medline]

24. Egger M, Smith G, Altman D. Systematic Reviews in Health Care. Meta-Analysis in Context. 2nd ed. London: BMJ Publishing Group; 2001.

25. Galbraith RF. A note on graphical presentation of estimated odds ratios from several clinical trials. Stat Med. 1988;7:889-94. [PMID: 3413368].[Medline]

26. Egger M, Davey Smith G, Schneider M, Minder C. Bias in meta-analysis detected by a simple, graphical test. BMJ. 1997;315:629-34. [PMID: 9310563].[Abstract/Free Full Text]

27. Duval S, Tweedie R. Trim and fill: A simple funnel-plot-based method of testing and adjusting for publication bias in meta-analysis. Biometrics. 2000;56:455-63. [PMID: 10877304].[Medline]

28. Mayo JR, Remy-Jardin M, Müller NL, Remy J, Worsley DF, Hossein-Foucher C, et al. Pulmonary embolism: prospective comparison of spiral CT with ventilation-perfusion scintigraphy. Radiology. 1997;205:447-52. [PMID: 9356627].[Abstract/Free Full Text]

29. Cross JJ, Kemp PM, Walsh CG, Flower CD, Dixon AK. A randomized trial of spiral CT and ventilation perfusion scintigraphy for the diagnosis of pulmonary embolism. Clin Radiol. 1998;53:177-82. [PMID: 9528867].[Medline]

30. Ferretti GR, Ayanian D, Ranchoup Y, Thony F, Bosson JL, Coulomb M. [CT x-ray evaluation of abdominal and pelvic veins in patients suspected of acute pulmonary embolism with negative Doppler sonography]. J Radiol. 1998;79:327-30. [PMID: 9757258].[Medline]

31. Ferretti GR, Bosson JL, Buffaz PD, Ayanian D, Pison C, Blanc F, et al. Acute pulmonary embolism: role of helical CT in 164 patients with intermediate probability at ventilation-perfusion scintigraphy and normal results at duplex US of the legs. Radiology. 1997;205:453-8. [PMID: 9356628].[Abstract/Free Full Text]

32. Blachere H, Latrabe V, Montaudon M, Valli N, Couffinhal T, Raherisson C, et al. Pulmonary embolism revealed on helical CT angiography: comparison with ventilation-perfusion radionuclide lung scanning. AJR Am J Roentgenol. 2000;174:1041-7. [PMID: 10749247].[Abstract/Free Full Text]

33. Bourriot K, Couffinhal T, Bernard V, Montaudon M, Bonnet J, Laurent F. Clinical outcome after a negative spiral CT pulmonary angiographic finding in an inpatient population from cardiology and pneumology wards. Chest. 2003;123:359-65. [PMID: 12576352].[Abstract/Free Full Text]

34. Garg K, Sieler H, Welsh CH, Johnston RJ, Russ PD. Clinical validity of helical CT being interpreted as negative for pulmonary embolism: implications for patient treatment. AJR Am J Roentgenol. 1999;172:1627-31. [PMID: 10350303].[Abstract/Free Full Text]

35. Garg K, Welsh CH, Feyerabend AJ, Subber SW, Russ PD, Johnston RJ, et al. Pulmonary embolism: diagnosis with spiral CT and ventilation-perfusion scanning—correlation with pulmonary angiographic results or clinical outcome. Radiology. 1998;208:201-8. [PMID: 9646814].[Abstract/Free Full Text]

36. Goodman LR, Lipchik RJ, Kuzo RS, Liu Y, McAuliffe TL, O'Brien DJ. Subsequent pulmonary embolism: risk after a negative helical CT pulmonary angiogram—prospective comparison with scintigraphy. Radiology. 2000;215:535-42. [PMID: 10796937].[Abstract/Free Full Text]

37. Kavanagh EC, O'Hare A, Hargaden G, Murray JG. Risk of pulmonary embolism after negative MDCT pulmonary angiography findings. AJR Am J Roentgenol. 2004;182:499-504. [PMID: 14736689].[Abstract/Free Full Text]

38. Lomis NN, Yoon HC, Moran AG, Miller FJ. Clinical outcomes of patients after a negative spiral CT pulmonary arteriogram in the evaluation of acute pulmonary embolism. J Vasc Interv Radiol. 1999;10:707-12. [PMID: 10392937].[Medline]

39. Nilsson T, Olausson A, Johnsson H, Nyman U, Aspelin P. Negative spiral CT in acute pulmonary embolism. Acta Radiol. 2002;43:486-91. [PMID: 12423459].[Medline]

40. Perrier A, Roy PM, Aujesky D, Chagnon I, Howarth N, Gourdier AL, et al. Diagnosing pulmonary embolism in outpatients with clinical assessment, D-dimer measurement, venous ultrasound, and helical computed tomography: a multicenter management study. Am J Med. 2004;116:291-9. [PMID: 14984813].[Medline]

41. Remy-Jardin M, Remy J, Baghaie F, Fribourg M, Artaud D, Duhamel A. Clinical value of thin collimation in the diagnostic workup of pulmonary embolism. AJR Am J Roentgenol. 2000;175:407-11. [PMID: 10915683].[Abstract/Free Full Text]

42. Remy-Jardin M, Tillie-Leblond I, Szapiro D, Ghaye B, Cotte L, Mastora I, et al. CT angiography of pulmonary embolism in patients with underlying respiratory disease: impact of multislice CT on image quality and negative predictive value. Eur Radiol. 2002;12:1971-8. [PMID: 12136315].[Medline]

43. Swensen SJ, Sheedy PF 2nd, Ryu JH, Pickett DD, Schleck CD, Ilstrup DM, et al. Outcomes after withholding anticoagulation from patients with suspected acute pulmonary embolism and negative computed tomographic findings: a cohort study. Mayo Clin Proc. 2002;77:130-8. [PMID: 11838646].[Medline]

44. Tillie-Leblond I, Mastora I, Radenne F, Paillard S, Tonnel AB, Remy J, et al. Risk of pulmonary embolism after a negative spiral CT angiogram in patients with pulmonary disease: 1-year clinical follow-up study. Radiology. 2002;223:461-7. [PMID: 11997553].[Abstract/Free Full Text]

45. Value of the ventilation/perfusion scan in acute pulmonary embolism. Results of the prospective investigation of pulmonary embolism diagnosis (PIOPED). The PIOPED Investigators. JAMA. 1990;263:2753-9. [PMID: 2332918].[Abstract]

46. van Beek EJ, Brouwerst EM, Song B, Stein PD, Oudkerk M. Clinical validity of a normal pulmonary angiogram in patients with suspected pulmonary embolism—a critical review. Clin Radiol. 2001;56:838-42. [PMID: 11895301].[Medline]

47. Remy-Jardin M, Remy J, Wattinne L, Giraud F. Central pulmonary thromboembolism: diagnosis with spiral volumetric CT with the single-breath-hold technique—comparison with pulmonary angiography. Radiology. 1992;185:381-7. [PMID: 1410342].[Abstract/Free Full Text]

48. Lawler LP, Fishman EK. Multi-detector row CT of thoracic disease with emphasis on 3D volume rendering and CT angiography. Radiographics. 2001;21:1257-73. [PMID: 11553832].[Abstract/Free Full Text]

49. Qanadli SD, Hajjam ME, Mesurolle B, Barré O, Bruckert F, Joseph T, et al. Pulmonary embolism detection: prospective evaluation of dual-section helical CT versus selective pulmonary arteriography in 157 patients. Radiology. 2000;217:447-55. [PMID: 11058644].[Abstract/Free Full Text]

50. Patel S, Kazerooni EA, Cascade PN. Pulmonary embolism: optimization of small pulmonary artery visualization at multi-detector row CT. Radiology. 2003;227:455-60. [PMID: 12732699].[Abstract/Free Full Text]

51. Ghaye B, Szapiro D, Mastora I, Delannoy V, Duhamel A, Remy J, et al. Peripheral pulmonary arteries: how far in the lung does multi-detector row spiral CT allow analysis? Radiology. 2001;219:629-36. [PMID: 11376246].[Abstract/Free Full Text]

52. Simon M, Boiselle PM, Choi JR, Rosen MP, Reynolds K, Raptopoulos V. Paddle-wheel CT display of pulmonary arteries and other lung structures: a new imaging approach. AJR Am J Roentgenol. 2001;177:195-8. [PMID: 11418425].[Free Full Text]

53. Loud PA, Katz DS, Bruce DA, Klippenstein DL, Grossman ZD. Deep venous thrombosis with suspected pulmonary embolism: detection with combined CT venography and pulmonary angiography. Radiology. 2001;219:498-502. [PMID: 11323478].[Abstract/Free Full Text]

54. Cham MD, Yankelevitz DF, Shaham D, Shah AA, Sherman L, Lewis A, et al. Deep venous thrombosis: detection by using indirect CT venography. The Pulmonary Angiography-Indirect CT Venography Cooperative Group. Radiology. 2000;216:744-51. [PMID: 10966705].[Abstract/Free Full Text]

55. Ghaye B, Dondelinger RF. Non-traumatic thoracic emergencies: CT venography in an integrated diagnostic strategy of acute pulmonary embolism and venous thrombosis. Eur Radiol. 2002;12:1906-21. [PMID: 12136309].[Medline]

56. Wicki J, Perneger TV, Junod AF, Bounameaux H, Perrier A. Assessing clinical probability of pulmonary embolism in the emergency ward: a simple score. Arch Intern Med. 2001;161:92-7. [PMID: 11146703].[Abstract/Free Full Text]

57. Chunilal SD, Eikelboom JW, Attia J, Miniati M, Panju AA, Simel DL, et al. Does this patient have pulmonary embolism? JAMA. 2003;290:2849-58. [PMID: 14657070].[Abstract/Free Full Text]

58. Remy-Jardin M, Remy J. Spiral CT angiography of the pulmonary circulation. Radiology. 1999;212:615-36. [PMID: 10478224].[Abstract/Free Full Text]

59. Stein PD, Athanasoulis C, Alavi A, Greenspan RH, Hales CA, Saltzman HA, et al. Complications and validity of pulmonary angiography in acute pulmonary embolism. Circulation. 1992;85:462-8. [PMID: 1735144].[Abstract/Free Full Text]

60. Remy-Jardin M, Remy J, Artaud D, Deschildre F, Duhamel A. Peripheral pulmonary arteries: optimization of the spiral CT acquisition protocol. Radiology. 1997;204:157-63. [PMID: 9205239].[Abstract/Free Full Text]

Read all Rapid Responses

Using CTPA to Diagnose Pulmonary Embolism

Shaun D Frost

Annals Online, 8 Dec 2004 [Full text]

CT pulmonary angiography and suspected pulmonary embolism: a word of caution

Philippe Girard

Annals Online, 13 Dec 2004 [Full text]

CT Pulmonary Angiography should be part of a diagnostic strategy for pulmonary embolism.

Pieter W. Kamphuisen, et al.

Annals Online, 24 Dec 2004 [Full text]

The Applicability of a Negative Computed Tomographic Pulmonary Angiogram in Clinical Practice

Jeremy P Smith

Annals Online, 20 Jan 2005 [Full text]

Defining the Role of CTPA in Suspected Pulmonary Embolism

Lisa K Moores, et al.

Annals Online, 9 Feb 2005 [Full text]