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Results of the treatment of pulmonary embolism
DATA FROM REGISTRIES
ZBIGNIEW GĄSIORKATEDRA i KLINIKA KARDIOLOGII SUM Katowice
Session: Pulmonary embolism – new therapeutic optionsPeripheral Interventions in Krakow
8-9.05.2014
No conflict of interest in relation to this presentation
Massive PE SBP <90mmHg n=58
Nonmassive PE SBP >90mmHg n=1817
Anticoagulation 57 (98%) 1790 (98%)
Fibrinolysis 7 (12%) 43 (2%)
Embolectomy 2 (3,4%) -surgical 13 (0,75) – surg.5, cath 8
IVC filter 9 (15%) 273 (15%)
Outcome measures of pts with and without Massive PE
Massive PE SBP <90mmHg n=58
Nonmassive PE SBP >90mmHg n=1817
P
In-patient outcomeMortalityDeath from PEBleeding complications
8 (14%)3 (5%)6 (10%)
54 (3%)16 (0,9%)63 (3,5%)
<0.001<0.02<0.01
30-d outcomeMortalityBleeding complications
n=507 (14%)1 (2%)
n=176332 (2%)23 (1,3%)
<0.01NS
Brian W
1716 pts from 47 hospitals age 70+15 years17% hemodynamically unstable
Treatment:Thrombolytic agents in 185 (10,8%)Percutaneous thrombectomy in 14 (0,8%)Surgery in 2 (0,1%)116 (6,7%) in-hospital deathsDeath or clinical deterioration in 138 (8,0%)
Overall mortality of pulmonary embolectomy 18,8%
ZATPOL
Polish National Registry on
Pulmonary Embolism
Aim:
To assess whether adherence to validated diagnostic criteria affects survival of patients with suspected pulmonary
embolism
Material
0
400
800
1200
1600
2000
I 200
7
II 20
07
III 2
007
IV 2
007
V 2
007
VI 2
007
VII
2007
VIII
200
7
IX 2
007
X 2
007
XI 2
007
XII
2007
I 200
8
II 20
08
III20
08
IV 2
008
V 2
008
VI 2
008
VII
2008
VIII
200
8
IX 2
008
Accepted questionnaires
-2015 patients (40% males, mean age 65 ± 15yrs)
- 80 departments of cardiology in Poland with clinical suspicion of PE
- JAN 2007 – SEP 2008
- 90 days follow-up mortality data available for 1537 (76%) patients
nn = 2015
All-cause mortality
0%
10%
20%
30%
in-hospital mortality(n=2015) 90 days follow-up mortality (n=1537)
PE confirmed ureliable diagnosis PE excluded
p<0.001
p<0.001
7.0% 14.3% 5.0% 15.6% 1 1.5%27.3%
Factors related to all-cause in-hospital mortality
OR 95% CI p
Unreliable diagnosis of PE 2.26 1.52 – 3.36 <0.0001
Symptoms of high-risk PE 9.29 6.49 – 13.3 <0.001
Local positive diagnosis of PE 1.14 0.76 – 1.72 0.51
Age > 75 years 1.74 1.21 – 2.51 0.003
Low clinical probability 0.18 0.06 – 0.51 0.001
Lung disease with respiratory failure 0.98 0.53-1.43 0.95
CHF – NYHA III-IV 1.56 1.04 – 2.32 0.03
ZATPOL – high-risk PE treatment
Locally confirmed high-risk PEn=229
deaths n=68mortality = 30%
Thrombolytic therapyn=89
deaths n= 35mortality = 39%
No Thrombolytic therapyn=140
deaths n=33mortality =24%
ZATPOL – high-risk PE treatment
Thrombolytic therapy introduction
clinical picture - 26 (29%)
clinical picture + ECHO - 34 (38%)
clinical picture + angioCT/arteriography – 29 (33%)
rtPA 100mg/2h
rtPA 50mg/15min
STK 1.5mln j/1-2h
STK 250tys j/h 100tys j/h
76%
ZATPOL - high-risk PE treatment
No Thrombolytictreatment
n = 140
Thrombolytictreatment
n = 89p
Intracranialhaemorrage
0 3 (3.4%) 0.03
Allhaemorrhages
10 (7.1%) 22 (24.7%) <0.001
Haemorrhagic complications
Intracranial haemorrhages leading to death 1.8%
ZATPOL – high-risk PE other treatment methods
• Surgical PULMONARY EMBOLECTOMY - 11 pts
- PE (+) in imaging methods (n=10)
- thrombus in right heart in ECHO (n=1)
- 1 periprocedural death
• Interventional EMBOLECTOMY
- thrombus fragmentation using pig-tail catheter– 3 pts
- 1 death after procedure
• IVC Filter – 3 pts
SEATTLE-II Trial ACC Washington 2014A New Era for Massive and Submassive PE
150 pts (31 massive PE, 119 submassive PE)Ultrasound-facilitated catheter-directed low-dose thrombolysis
24 mg tPA 1mg/h for 24 hoursRESULTS:
1 death attributed to PENo deaths in massive PE within 30 days follow-up
No intracranial hemorrhages
THANK YOU
Results
2015 patients with suspected PE
Locally confirmed
PE
Locally excluded
PE
p
Prevalence 1316 (65%) 699 (35%)
Reliable diagnosis 84% 71% <0.001
Diagnostic process
adhered to ESC
Guidelines
76% 66% 0.003
Reliable diagnosis :
79,9% (95%CI: 78.2 – 81.6 %)