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. 2013 Aug 16;8:10.3402/ljm.v8i0.22391. doi: 10.3402/ljm.v8i0.22391

Iloprost in pulmonary hypertension due to sub-massive pulmonary embolism: report of two cases

Abdullah Hassan Alsaghir 1,*, Soror Abdullah Alaithan 1, Basima Alsihati 1, Dhia Naji Alhajjaj 1
PMCID: PMC3746081  PMID: 23958458

Patients with acute pulmonary embolism (PE) who has normal systemic arterial pressure and right ventricular (RV) dysfunction are considered to have sub-massive pulmonary embolism (SPE), with 3-month mortality risk of 21% (1). The benefit of the current therapy other than anticoagulation including thrombolytic therapy (TT), embolectomy, and IVC filter insertion, in the absence of cardiogenic shock, is still debated (2). Vasoconstrictive mediators (including thromboxane-A and serotonin) have an important role to play in the increase of peripheral vascular resistance (PVR) and ultimately in developing pulmonary hypertension (PH) in acute phase (3, 4). A study by Idrees et al. described a beneficial effect of inhaled iloprost in five patients with SPE, in whom there is an improvement in WHO-functional class (WHO-FC), 6-min walk distance (6MWD) test, and echocardiographic parameters (5). Iloprost, an inhaled prostacyclin approved for the treatment of patients with pulmonary arterial hypertension, exerts long-term benefits through antiproliferative and antithrombotic effects, but is also a potent acute pulmonary vasodilator with the duration of action of approximately 60 min (6).

Two patients were evaluated at the Dammam Medical Complex, Dammam, Saudi Arabia between June and December 2012. The diagnosis of PE was established by helical computed tomography (CT) angiogram that showed a thrombus at both pulmonary arteries at presentation. They had normal systemic blood pressure, PH documented by echocardiography demonstrated an estimated systolic pulmonary artery pressure >45 mm Hg and findings of RV dysfunction suggestive of acute changes. Both patients received therapeutic anticoagulation with low-molecular-weight heparin and targeted warfarin dose to international normalized ratio of 2–3. They were still symptomatic and required more oxygen, for which they were offered TT. They declined TT, but agreed to receive inhaled iloprost through a nebulized device of 2.5–5.0 µg per inhalation for 15 min, 8× daily for 3 months.

The main efficacy index was defined as the changes in WHO-FC, 6MWD, oxygen saturation, and echocardiography parameters during 3-month inhalation therapy. These parameters were assessed at baseline, 3-month post-inhalation, and 3-month post-cessation of iloprost. Both patients tolerated the treatment well. They showed significant improvement in their clinical symptoms and echocardiographic parameters (Table 1, Figure 1).

Table 1.

Clinical and physiological parameters of both patients before and after iloprost (3 months before and 3 months post-cessation of iloprost)

Measurement Pre-iloprost 3 months post-iloprost 3 months post-cessation of iloprost
Case 1
WHO functional class III I I
6MWD 176 m 408 m 422 m
Oxygen saturation 90% on RA 97% on RA 97% on RA
98% on 2 L/min
sPAP (by echo) >70 mm Hg 30 mm Hg 25 mm Hg
RV dysfunction Severe Normal Normal
Qualitative score
Case 2
WHO functional class IV I I
6MWD 138 m 418 m 434 m
Oxygen saturation 89% on RA 98% on RA 98% on RA
97% on 2 L/min
sPAP (by echo) 80 mm Hg 25 mm Hg 25 mm Hg
RV dysfunction Moderate Normal Normal
Qualitative score

Fig. 1.

Fig. 1

The mean of WHO functional class, 6MWD, and sPAP (by echo) pre- and 3 months post and 3 months post-cessation of iloprost.

In conclusion, iloprost might have favorable acute effects on symptoms, exercise tolerance, and pulmonary hypertension in sub-massive pulmonary embolism.







Abdullah Hassan Alsaghir
Department of Medicine
Dammam Medical Complex
Dammam, Saudi Arabia
Email: asaghir4000@yahoo.com

Soror Abdullah Alaithan
Department of Medicine
Dammam Medical Complex
Dammam, Saudi Arabia

Basima Alsihati
Department of Medicine
Dammam Medical Complex
Dammam, Saudi Arabia

Dhia Naji Alhajjaj
Department of Medicine
Dammam Medical Complex
Dammam, Saudi Arabia

References

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