| Literature DB >> 28228310 |
A Vamsidhar1, D Rajasekhar2, V Vanajakshamma1, A Y Lakshmi1, K Latheef1, C Siva Sankara1, G Obul Reddy1.
Abstract
OBJECTIVE: The aim of this study is to prospectively assess the diagnostic accuracy of pulmonary embolism severity index, echocardiogram, computed tomography pulmonary angiogram (CTPA), and N-terminal pro b-type natriuretic peptide (NT-proBNP) for predicting adverse events in acute pulmonary embolism patients.Entities:
Keywords: Echocardiogram; NT-proBNP; Pulmonary embolism; Qanadli index; Right ventricle
Mesh:
Substances:
Year: 2016 PMID: 28228310 PMCID: PMC5319130 DOI: 10.1016/j.ihj.2016.07.010
Source DB: PubMed Journal: Indian Heart J ISSN: 0019-4832
Baseline characteristics of study population.
| Characteristic | Total cohort ( | With AEs ( | Without AEs ( | |
|---|---|---|---|---|
| Age (years) | 41.20 ± 12.98 | 34.56 ± 6.56 | 44.05 ± 14.09 | 0.06 |
| Male | 24 (80%) | 8 (88.9%) | 16 (76.2%) | |
| Female | 6 (20%) | 1 (11.1%) | 5 (23.8%) | 0.64 |
| Chest pain | 10 (33.3%) | 1 (11.1%) | 9 (42.9%) | 0.20 |
| Dyspnea | ||||
| NYHA Class-1 | 1 (3.3%) | 0 | 1 (4.8%) | |
| NYHA Class-2 | 7 (23.3%) | 0 | 7 (33.3%) | |
| NYHA Class-3 | 13 (43.3%) | 3 (33.3%) | 10 (47.6%) | |
| NYHA Class-4 | 9 (30.0%) | 6 (66.7%) | 3 (14.3%) | 0.004 |
| Hemoptysis | 05 (16.7%) | 1 (11.1%) | 4 (19%) | 0.99 |
| Syncope | 6 (20%) | 0 | 6 (28.6%) | NA |
| Altered Sensorium | 1 (3.3%) | 1 (11.1%) | 0 | NA |
| Recent Surgery/trauma | 8 (26.7%) | 1 (11.1%) | 7 (33.3%) | 0.42 |
| Cancer | 2 (6.7%) | 0 | 2 (9.5%) | NA |
| Stroke | 1 (3.3%) | 0 | 1 (4.8%) | NA |
| CAD | 2 (6.7%) | 0 | 2 (9.5%) | NA |
| Dyslipidemia | 13 (43.3%) | 3 (33.3%) | 10 (47.6%) | 0.75 |
| Smoking | 9 (30%) | 5 (55.6%) | 4 (19%) | 0.12 |
| Hypertension | 4 (13.3%) | 0 | 4 (19%) | NA |
| Diabetes | 3 (10%) | 0 | 3 (14.28%) | NA |
| HR, bpm | 118.50 ± 15.65 | 121.0 ± 13.49 | 117.19 ± 16.62 | 0.55 |
| SBP, mm of Hg | 114.33 ± 16.63 | 115.56 ± 10.14 | 113.81 ± 18.95 | 0.79 |
| DBP, mm of Hg | 73.20 ± 9.30 | 73.33 ± 5.0 | 73.14 ± 10.74 | 0.96 |
| Respiratory rate | 29.33 ± 5.91 | 31.22 ± 4.24 | 28.52 ± 6.42 | 0.26 |
| Sr. Creatinine, mg/dl | 1.08 ± 0.24 | 1.16 ± 0.21 | 1.05 ± 0.24 | 0.24 |
| Sr. Sodium, mg/dl | 136.33 ± 4.52 | 137.44 ± 4.67 | 135.86 ± 4.49 | 0.39 |
| Sr. Potassium, mg/dl | 4.07 ± 0.71 | 3.82 ± 0.76 | 4.17 ± 0.67 | 0.22 |
| ICU Stay, days | 2.89 ± 2.22 | 4.44 ± 2.19 | 2.16 ± 1.86 | 0.006 |
AE, adverse events; HR, heart rate; SBP, systolic blood pressure; DBP, diastolic blood pressure; SPO2, pulse oxymetry oxygen saturation; Sr., serum; TLT, thrombolytic therapy; IQR, intra quartile range.
Significant p-value (p < 0.05).
Combined adverse events in study population.
| Combined adverse events | Total cohort ( |
|---|---|
| Secondary thrombolysis | 8 (26.7%) |
| Mechanical ventilator | 2 (6.7%) |
| Inotropes | 2 (6.7%) |
| In-hospital deaths | 2 (6.7%) |
Prognostic variables in patients with and without adverse events.
| Characteristic | Total cohort ( | With AEs ( | Without AEs ( | |
|---|---|---|---|---|
| PESI score | 90.03 ± 25.44 | 87.89 ± 18.20 | 90.95 ± 28.34 | 0.77 |
| Echocardiographic parameters | ||||
| Echo RV/LV ratio | 1.05 ± 0.16 | 1.07 ± 0.09 | 1.02 ± 0.16 | 0.38 |
| RVEDD, mm | 42.53 ± 7.96 | 45.0 ± 5.54 | 41.48 ± 8.7 | 0.27 |
| TR JV, m/s | 2.77 ± 1.07 | 3.08 ± 0.87 | 2.73 ± 0.98 | 0.36 |
| Echo RV dysfunction | ||||
| Yes | 22 (73.3%) | 09 (100%) | 13 (61.9%) | – |
| No | 08 (26.7%) | 00 (0%) | 08 (38.1%) | |
| Qanadli index | 19.37 ± 7.55 | 25.0 ± 4.33 | 16.95 ± 7.39 | 0.005 |
| CT RV/LV ratio | 1.44 ± 0.44 | 1.57 ± 0.35 | 1.38 ± 0.45 | 0.27 |
| IVS bowing | ||||
| Yes | 17 (56.7%) | 8 (88.9%) | 9 (42.9%) | |
| No | 13 (43.3%) | 1 (11.1%) | 12 (57.1%) | 0.04 |
| Median NTproBNP, pg/ml | 2032.50 | 3451.0 | 1392.5 | 0.0094 |
| (IQR) | (550.0–4082.0) | (2425.0–6784.0) | (315.0–2506.0) | |
AE, adverse events; echo, echocardiography; RVD, right ventricular dysfunction; TRJV, tricuspid regurgitation jet velocity; PAOI, pulmonary vascular obstruction index; RV, right ventricle; LV, left ventricle.
Significant p-value (p < 0.05).
ROC analysis of various prognostic tools in predicting adverse events.
| Variable | Cut-off | AUC | 95% CI | Sensitivity (%) | Specificity (%) | PPV | NPV | |
|---|---|---|---|---|---|---|---|---|
| Qanadli index | >19 | .807 | 0.651–0.963 | 0.009 | 100 | 52.38 | 47.4 | 100 |
| NT-proBNP | >729 | .772 | 0.593–0.952 | 0.020 | 100 | 38.10 | 40.91 | 100 |
| RV/LV ratio on echocardiogram | >0.95 | .709 | 0.525–0.893 | 0.074 | 100 | 42.86 | 42.9 | 100 |
| CT RV/LV ratio | >1.15 | .646 | 0.446–0.845 | 0.213 | 100 | 42.9 | 42.9 | 100 |
| RVEDD | >47 | .675 | 0.463–0.886 | 0.135 | 55.56 | 85.7 | 62.5 | 81.8 |
AUC, area under curve; PPV, positive predictive value; NPV, negative predictive value; NT-proBNP, N-terminal pro-brain natriuretic peptide; RV, right ventricle; LV, left ventricle; CT, computed tomography; RVEDD, right ventricular end diastolic diameter.
Fig. 1Receiver operating characteristics of prognostic parameters in predicting adverse events.
Relationship between right ventricular dysfunction and other prognostic parameters.
| Echocardiographic RVD vs. | Correlation coefficient | |
|---|---|---|
| SBP | −0.412 | 0.024 |
| PESI score | 0.449 | 0.013 |
| Qanadli index | 0.694 | <0.0001 |
| NT-proBNP | 0.767 | <0.0001 |
| CT RV/LV ratio | 0.675 | <0.0001 |
SBP, systolic blood pressure; PESI, pulmonary embolism severity index; NT-proBNP, N-terminal pro-brain natriuretic peptide; CT, computed tomography; RV, right ventricle; LV, left ventricle.
Significant p-value (p < 0.05).