Copyright: ©Author(s) 2026.
World J Cardiol. Jun 26, 2026; 18(6): 120186
Published online Jun 26, 2026. doi: 10.4330/wjc.120186
Published online Jun 26, 2026. doi: 10.4330/wjc.120186
Table 1 Characteristics of studies included in the analysis
| Ref. | Chartier et al[23] | Torbicki et al[14] | Pierre-Justin and Pierard[15] | Seghda et al[7] | Bikdeli et al[18] |
| Design | Retrospective analysis of a hospital registry | Subgroup analysis of the ICOPER international prospective registry | Prospective single-center study | Prospective cohort study | Analysis of data from the international prospective RIETE registry |
| Country/center | France (Dijon/Lille) | Multicenter (52 centers, 7 countries) | Martinique (France), Fort-de-France | Burkina Faso, Ouagadougou | Multicenter (international) |
| Inclusion period | January 1986-January 1998 January | 1995-November 1996 November | 1997-June 1999 | March 2012-September 2015 | March 2001-September 2019 |
| Total patients with PE (n) | 341 (for the period 1992–1997) | 2454 | 335 | 250 | 42620 |
| RHT (n) | 38, 28 from 1992 to 1997 | 42 of 1135 in whom echocardiography was performed | 12 | 11 | 443 of 18803 in whom echocardiography was performed. Post hoc analysis n = 124 |
| Prevalence of RHT | 8.2% (28/341) in 1992-1997 | 3.7% (42/1135) | 4.0% (12/335) | 4% (11/250) | 2.4% (443/18803) |
| RHT morphology | Worm-like (36/38), spherical (2/38) | Not described | Mobile: 9 (75%)-coil, 3 (25%)-ball | Mobile thrombi. Specific shape not described | Not described |
| Location of RHT | RA-30, RV-6, both chambers-2 | RA/RV | All-RA (free-floating, could prolapse into RV) | RA in all cases (100%) | Right heart chambers |
| PE severity | Severe: NYHA IV-84% (32/38), cardiogenic shock-53% (20/38), cardiac arrest-47% (18/38) | More severe course than without RHT: More frequent hypotension, tachycardia, RV dysfunction, and heart failure | Massive PE: All in ICU, syncope (100%), hypotension (mean SBP 96 mmHg), acute pulmonary heart disease in all | All-high/intermediate-high risk | In those who received reperfusion therapy-more frequent hypotension (SBP < 100 mmHg), tachycardia (HR ≥ 110/minutes), syncope, hypoxemia, and RV hypokinesis |
| Anticoagulant monotherapy (1st line) (n) | 8 | 17 | 5 (including 3 with absolute contraindications to thrombolysis) | 5 | 62 (post hoc analysis) |
| Mortality with anticoagulant monotherapy (as first-line treatment) | In-hospital: 5/8 (62.5%) | 14-day: 4/17 (23.5%); | In-hospital: 3/5 (60%)-all with contraindications to thrombolysis | 30-day: 4/5 (80%) | 30-day post hoc analysis-7/62 (11.3%) |
| Thrombolysis (1st line) (n) | 9 | 24 | 7 | 6 | 62 (post hoc analysis) |
| Mortality with thrombolysis (as first-line treatment) | 2/9 (22.2%) | 14-day: 5/24 (20.8%); | 1/7 (14.3%) | 30-day: 1/6 (16.7%) | 30-day post hoc analysis-6/62 (9.7%) |
| Confirmed thrombus lysis | Echocardiographic monitoring was used, but data on the frequency of thrombus lysis are not presented | Not described | In 7 of 9 patients (77.8%) who received thrombolysis, complete thrombus lysis and resolution of RV overload were documented on echocardiography at 12 hours | In all 6 patients who received thrombolysis, complete thrombus lysis was documented on follow-up echocardiography | Not described |
| Major bleeding | Not described | Not described | None reported | 2/11 (18.2%) in the RHT group | Absolute values not provided in the article. Post hoc analysis: 6/62 (9.7%). Reperfusion: 4/62 (6.5%) |
| Recurrent PE | Not observed during the follow-up period | Not described | 0% during hospitalization and 1-year follow-up in survivors | Not described | Not described |
| Early mortality (14-day/in-hospital) | 17/38 (44.7%) | 9/42 (21.4%) | 4/12 (33.3%) | ||
| 30-day mortality | 4/12 (33.3%) | 5/11 (45.4%) | 40/443 (9.0%), in post hoc analysis-13/124 (10.5%) | ||
| Follow-up period | Mean 47.2 months (range 1-70 months) | 3 months | 12 months | 30 days | 30 days |
| Mortality during the follow-up period | 20/38 (52.6%). Among the discharged: 3/21 (14.2%) | 12/42 (28.6%) | 4/12 (33.3%), among the discharged: 0% | 5/11 (45.4%) | 40/443 (9.0%) from PE: 24/443 (5.4%) |
| Authors’ key conclusion on treatment | No significant difference in mortality between methods. Thrombolysis is recommended as a rapid and accessible first-line therapy, especially in the absence of contraindications. Surgery remains the classic method, and catheter-based techniques are an alternative when contraindications exist | Patients with RA/RV thrombi have a higher risk of death, especially if treated with heparin alone. The authors suggest that anticoagulation alone may be insufficient even in clinically stable patients, and more aggressive methods (thrombolysis, embolectomy) should be considered, although this requires further research | Thrombolysis is an effective, rapid, and safe first-line therapy for patients with mobile thrombi. Heparin alone (monotherapy) in severe forms is ineffective and leads to 100% mortality. Surgery is a rescue method when thrombolysis fails | Thrombolysis significantly reduced mortality in the group with thrombi. In the absence of thrombolysis, 30-day survival was < 25%. Thrombolysis is the preferred option when surgical or percutaneous embolectomy is not available | Reperfusion therapy (predominantly thrombolysis) in patients with acute PE and concomitant RHT did not demonstrate a statistically significant reduction in 30-day mortality compared with anticoagulant monotherapy; however, the point estimate of effect (OR = 0.65 for PE-related death) does not rule out clinically meaningful benefit, and the wider confidence intervals indicate the need for further research |
- Citation: Pereverzeva KG, Yakushin SS, Peregudova NN. Anticoagulants vs thrombolytic therapy for the management of right heart thrombus in pulmonary embolism: A systematic review. World J Cardiol 2026; 18(6): 120186
- URL: https://www.wjgnet.com/1949-8462/full/v18/i6/120186.htm
- DOI: https://dx.doi.org/10.4330/wjc.120186