Table 4

PE-related death, adverse outcome (death, clinical deterioration or haemodynamic collapse), VTE, major bleeding and their combinations in ‘stable’ PE patient risk groups

Risk cut-off (author, year)Development phaseN studiesType of studyHaemodynamic statusOutcomeTime pointProportion (95% CI)
High-risk group
Low-risk group
Event rate (95% CI)
High-risk group
Low-risk group
Bova et al risk score
(Bova et al 2014)135Derivation and internal validation6 (IPD)BothStable
Stage IIIPE-related death, collapse, VTEIn-hospital5.828
Stage II18.69.7
Stage I75.53.6
Stage IIIPE-related death, collapse, VTE30 days5.829.2
Stage II18.610.8
Stage I75.54.2
Stage IIIPE-related death30 days5.815.5
Stage II18.65.0
Stage I75.51.7
ESC intermediate
(Vanni et al 2011)119External validation1RetrospectiveStablePE-related deathIn-hospital57.6 (53.1 to 62.1)
42.4 (37.9 to 46.9)
6.4 (4.0 to 10.1)
1.0 (0.3 to 4.0)
(Becattini et al 2013)72External validation1ProspectiveStablePE-related deathIn-hospital78.3 (75.4 to 80.9)
21.7 (19.1 to 24.6)
1.8 (1.0 to 3.1)
0.3 (0.00 to 4.1)
Overall1BothStablePE-related deathIn-hospital68.9 (46.1 to 85.2)
31.1 (14.8 to 53.9)
3.4 (0.9 to 11.7)
0.8 (0.2 to 2.7)
(Dellas et al 2014)80External validation1ProspectiveStableAdverse outcome30 days78.1 (72.2 to 83.1)
21.9 (16.9 to 27.8)
10.9 (7 to 16.4)
1 (0.1 to 14.1)
ESC intermediate–high
(Vanni et al 2011)119External validation1RetrospectiveStablePE-related deathIn-hospital14.8 (11.9 to 18.4)
85.2 (81.6 to 88.1)
11.8 (6.0 to 21.8)
2.8 (1.6 to 5.0)
(Becattini et al 2013)72External validation1ProspectiveStablePE-related deathIn-hospital41.8 (38.5 to 45.1)
58.2 (54.9 to 61.5)
1.9 (0.9 to 4.0)
1.0 (0.4 to 2.4)
Overall1StablePE-related deathIn-hospital26.2 (8.2 to 58.7)
73.8 (41.3 to 91.8)
4.9 (0.8 to 25.1)
1.8 (0.6 to 4.8)
(Becattini et al 2013)72External validation1ProspectiveStableDeath adverse outcomeIn-hospital41.8 (38.5 to 45.1)
58.2 (54.9 to 61.5)
8.8 (6.3 to 12.2)
3.2 (1.9 to 5.1)
(Becattini et al 2013)72External validation1ProspectiveStablePE-related death adverse outcomeIn-hospital41.8 (38.5 to 45.1)
58.2 (54.9 to 61.5)
5 (3.1 to 7.7)
2.4 (1.4 to 4.1)
eStiMaTe high
(Jiménez et al 2014)87Derivation1ProspectiveStableDeath adverse outcome VTE30 days3.7 (2.6 to 5.2)
96.3 (94.8 to 97.4)
25.8 (13.5 to 43.7)
3.4 (2.1 to 5.4)
(Jiménez et al 2014)87External validation1ProspectiveStableDeath adverse outcome30 days6.2 (4.5 to 8.6)
93.8 (91.4 to 95.5)
21.2 (10.5 to 38.3)
6.7 (5.2 to 8.7)
(Jiménezet al 2014)87Overall2ProspectiveStableDeath adverse outcome VTE30 days4.8 (2.8 to 8)
95.2 (92 to 97.2)
23.5 (14.7 to 35.4)
5 (2.5 to 9.4)
eStiMaTe high–intermediate
(Jiménez et al 2014)87Derivation1ProspectiveStableDeath adverse outcome VTE30 days74.5 (71.5 to 77.3)
25.5 (22.7 to 28.5)
9.7 (7.6 to 12.2)
0.9 (0.2 to 3.6)
(Jiménez et al 2014)87External validation1ProspectiveStableDeath adverse outcome30 days63.5 (59.3 to 37.5)
36.5 (32.5 to 40.7)
7.1 (4.8 to 10.4)
0.3 (0 to 4)
(Jiménez et al 2014)87Overall2ProspectiveStableDeath adverse outcome VTE30 days69.3 (57.6 to 79)
30.7 (21 to 42.4)
8.6 (6.5 to 11.4)
0.7 (0.2 to 2.4)
FAST=3
(Dellas et al 2014)80External validation1ProspectiveStableAdverse outcome30 days28.4 (23.4 to 34.1)
71.6 (65.9 to 76.6)
22.1 (14.2 to 32.7)
1.5 (0.5 to 4.7)
GPS≥3
(Bova et al 2009)74External validation1ProspectiveStablePE-related deathIn-hospital18.9 (14.1 to 24.9)
81.1 (75.1 to 85.9)
2.6 (0.4 to 16.5)
0.3 (0.0 to 4.7)
Kostrubiec et al (NT-proBNP—cTnT)
(Kostrubiec et al 2005)90Derivation1ProspectiveStable
IntermediateDeath30 days72.0 (62.4 to 79.9)
28.0 (20.1 to 37.6)
20.8 (13.0 to 31.7)
1.7 (0.1 to 22.3)
IntermediatePE-related death30 days69.9 (59.8 to 78.3)
30.1 (21.7 to 40.2)
12.3 (6.3 to 22.7)
1.7 (0.1 to 22.3)
Intermediate–highDeath30 days18.0 (11.6 to 26.8)
82.0 (73.2 to 88.4)
50.0 (28.4 to 71.6)
7.3 (3.3 to 15.3)
Intermediate–highPE-related death30 days16.1 (1.0 to 25.0)
83.9 (75.0 to 90.0)
40.0 (19.2 to 65.2)
2.6 (0.6 to 9.7)
PESI≥II
(Sanchez et al 2013)111External validation1Retrospective (for PESI)StableAdverse outcome30 days75.2 (71.4 to 78.7)
24.8 (21.3 to 28.6)
6 (4.1 to 8.8)
0.8 (0 to 5.2)
PESI≥III
(Palmieri et al 2008)104External validation1ProspectiveStableDeath adverse outcomeIn-hospital69.7 (59.4 to 78.3)
30.3 (21.7 to 40.6)
53.2 (40.9 to 65.2)
11.1 (3.6 to 29.3)
(Sanchez et al 2013)111External validation1Retrospective (for PESI)StableAdverse outcome30 days37.8 (33.8 to 42)
62.2 (58 to 66.2)
9 (5.7 to 13.8)
2.1 (1 to 4.4)
(Vanni et al 2011)119External validation1RetrospectiveStablePE-related deathIn-hospital67 (62.3 to 71.3)
33 (28.7 to 37.7)
6.1 (3.8 to 9.5)
0.7 (0.1 to 5)
PESI≥IV
(Sanchez et al 2013)111External validation1Retrospective (for PESI)StableAdverse outcome30 days17.2 (14.2 to 20.7)
82.8 (79.3 to 85.8)
8.8 (4.5 to 16.6)
3.9 (2.4 to 6.2)
PESI=V
(Sanchez et al 2013)111External validation1Retrospective (for PESI)StableAdverse outcome30 days4 (2.6 to 6)
96 (94 to 97.4)
14.3 (4.7 to 36.1)
4.3 (2.9 to 6.5)
PESI+biomarkers
(Sanchez et al 2013)111External validation1Retrospective (for PESI)StableAdverse outcome30 days
PESI I–II—BNP32.7 (27.8 to 38.0)
67.3 (62.0 to 72.2)
4.7 (2.0 to 10.8)
0.9 (0.2 to 3.6)
PESI I–II—cTnI13.7 (10.3 to 17.9)
86.3 (82.1 to 89.7)
9.1 (3.5 to 21.8)
1.1 (0.3 to 3.3)
PESI I–II—TTE-RVD12.3 (9.0 to 16.5)
87.7 (83.5 to 91.0)
10.8 (4.1 to 25.5)
1.1 (0.4 to 3.5)
PESI III–IV—BNP56.3 (48.8 to 63.4)
43.8 (36.6 to 51.2)
10.1 (5.5 to 17.8)
6.5 (2.7 to 14.7)
PESI III–IV—cTnI24.0 (18.2 to 30.9)
76.0 (69.1 to 81.8)
16.7 (8.2 to 31.0)
5.3 (2.5 to 10.6)
PESI III–IV—TTE-RVD22.8 (17.0 to 29.9)
77.2 (70.1 to 83.0)
10.8 (4.1 to 25.5)
8.8 (4.9 to 15.2)
PESI V—BNP76.2 (54.0 to 89.7)
23.8 (10.3 to 46.0)
18.8 (6.2 to 44.7)
8.3 (0.5 to 62.2)
PESI V—cTnI30.0 (14.1 to 52.7)
70.0 (47.3 to 85.9)
16.7 (2.3 to 63.1)
14.3 (3.6 to 42.7)
PESI V—TTE-RVD23.8 (10.3 to 46.0)
76.2 (54.0 to 89.7)
20.0 (2.7 to 69.1)
12.5 (3.1 to 38.6)
PESI+biomarkers
(Jimenez et al 2011)86Update1Unclear
Prospective
StablePE-related death30 days
cTnI32.1 (28.5 to 36.0)
67.9 (64.0 to 71.5)
10.5 (6.9 to 15.8)
4.2 (2.7 to 6.7)
TTE-RVD20.3 (17.3 to 23.7)
79.7 (76.3 to 82.7)
11.7 (7.0 to 18.7)
4.9 (3.3 to 7.2)
US-DVT38.6 (34.7 to 42.6)
61.4 (57.4 to 65.3)
9.6 (6.4 to 14.2)
4.1 (2.5 to 6.7)
TTE-RVD—cTnI10.0 (7.8 to 12.7)
90.0 (87.3 to 92.2)
15.3 (8.1 to 26.8)
5.3 (3.7 to 7.5)
PESI≥IV—TTE-RVD—cTnI12.7 (9.0 to 17.7)
87.3 (82.3 to 91.0)
20.7 (9.6 to 39.0)
8.0 (5.0 to 12.7)
cTnI—US-DVT13.9 (11.3 to 16.9)
86.1 (83.1 to 88.7)
17.1 (10.4 to 26.8)
4.5 (3.0 to 6.7)
PESI≥IV—cTnI—US-DVT18.0 (13.5 to 23.5)
82.0 (76.5 to 86.5)
24.4 (13.7 to 39.7)
6.4 (3.7 to 11.0)
TTE-RVD—US-DVT8.6 (6.6 to 11.2)
91.4 (88.8 to 93.4)
19.6 (10.9 to 32.7)
5.0 (3.5 to 7.2)
TTE-RVD—cTnI—US-DVT4.1 (2.7 to 6.0)
95.9 (94.0 to 97.3)
20.8 (8.9 to 41.3)
5.6 (4.0 to 7.9)
PESI≥IV—TTE-RVD—US-DVT10.5 (7.2 to 15.2)
89.5 (84.8 to 92.8)
25.0 (11.7 to 45.6)
7.8 (4.9 to 12.4)
PREP—Clin≥II
(Sanchez et al 2010)110Derivation1ProspectiveStableDeath VTE30 days32.3 (28.2 to 36.6)
67.7 (63.4 to 71.8)
12.3 (8 to 18.5)
2.5 (1.2 to 4.9)
PREP—Clin≥III
(Sanchez et al 2010)110Derivation1ProspectiveStableDeath VTE30 days1.9 (1 to 3.6)
98.1 (96.4 to 99)
22.2 (5.6 to 57.9)
4.9 (3.3 to 7.3)
sPESI≥1
(Dellas et al 2014)80External validation1ProspectiveStableAdverse outcome30 days66.1 (60.2 to 71.4)
33.9 (28.6 to 39.8)
11.2 (7.3 to 16.7)
0.5 (0 to 8)
(Lankeit et al 2011)94External validation1ProspectiveStableDeath adverse outcome30 days62.4 (58.1 to 66.4)
37.6 (33.6 to 41.9)
8.8 (6.2 to 12.4)
1 (0.3 to 3.9)
sPESI≥1-hscTnT
(Lankeit et al 2011)94External validation1ProspectiveStableDeath adverse outcome30 days
hscTnT59.3 (55.1 to 63.4)
40.7 (36.6 to 44.9)
8.7 (6.0 to 12.3)
1.9 (0.7 to 4.9)
sPESI≥1-hscTnT75.9 (72.0 to 79.3)
24.1 (20.7 to 28.0)
7.8 (5.5 to 10.8)
0.4 (0.0 to 5.9)
  • In the first column, the cut-off is indicated by the corresponding higher risk group for the cut-off except for the Bova et al135 and Sanchez et al111 (PESI+biomarkers) studies which are displayed in risk categories. Bova's study combined IPD from six studies.

  • BNP, brain natriuretic peptide; cTnI, cardiac troponin I; cTnT, cardiac troponin T; DVT, deep vein thrombosis; GPS, Geneva prognostic score; hscTnT, high-sensitive cardiac troponin T; IPD, individual patient data; NT-proBNP, N-terminal proBNP; PE, pulmonary embolism; PESI, Pulmonary Embolism Severity Index; PREP, Facteurs PRonostiques dans l'Embolie Pulmonaire; sPESI, simplified PESI; TTE-RVD, transthoracic echocardiography-right ventricular dysfunction; US-DVT, ultrasound-detected DVT; VTE, venous thromboembolism.