Treatment of thromboangiitis obliterans (Buerger's disease) with bosentan
© De Haro et al; licensee BioMed Central Ltd. 2012
Received: 1 August 2011
Accepted: 14 February 2012
Published: 14 February 2012
This study assessed the effectiveness and safety of bosentan when administered to thromboangiitis obliterans (Buerger's disease) patients.
A clinical pilot study was designed in which patients with ulcer and/or pain at rest were treated with bosentan p.o. at a dose of 62.5 mg twice daily during the first month, which was thereafter up-titrated to 125 mg twice daily. The study endpoints were clinical improvement rate, major or minor amputation rate, haemodynamic changes, changes in endothelial function and angiographic changes.
Seven out of 12 patients were male (58%). Median age was 39 years (range 29-49). The median follow-up was 20 months (range 11-40). All patients were smokers. With bosentan treatment, new ischaemic lesions were observed in only one patient. Overall, clinical improvement was observed in 12 of the 13 extremities (92%). Only two out of 13 extremities underwent amputation (one major and one minor) after bosentan treatment. After being assessed by digital arteriography with subtraction or angio-magnetic resonance imaging, an increase of distal flow was observed in 10 out of the 12 patients. All patients experienced a statistically significant improvement in their BAFMD values (mean: 1.8 at baseline; 6.6 at the end of the treatment; 12.7 three months after the end of the treatment; p < 0.01).
Bosentan treatment may result in an improvement of clinical, angiographic and endothelial function outcomes. Bosentan should be investigated further in the management of TAO patients. Larger studies are required to confirm these results.
Buerger's disease, also known as thromboangiitis obliterans (TAO), is a thrombotic, occlusive, non-atherosclerotic, segmental vasculitis of small and medium-sized arteries and veins, which may involve both upper and lower extremities. The onset usually occurs in people of around the age of 45, and is more frequent in male smokers. As a consequence of the increase in tobacco use, an increase in the incidence of TAO in women has been observed in the last 20 years [1, 2].
Intermittent claudication and, in more advanced cases, pain at rest are the predominant clinical symptoms. Distal ischaemic lesions (trophic and ulcerations) are frequently observed by means of physical examination. Clinical course is characterised by alternating periods of exacerbation with periods of remission. Angiographic studies reveal a distal and segmental involvement of the vasculature of the extremities. Recanalisation is frequently demonstrated, showing a typical image (corkscrew collateral vessels) . Skin disorders such as migrating phlebitis or Raynaud-like colour changes may be associated with TAO.
Giving up smoking is the most important therapeutic measure in TAO patients . In fact, it leads to dramatic improvement of the symptoms and lesions. Amongst the drugs used to manage TAO, prostacyclin (PGI2) or its analogues (iloprost, beraprost, trepostinil sodium), aspirin or streptokinase (as a thrombolytic) are the most important. Revascularisation by means of a by-pass surgery or endovascular procedure is usually not possible as a consequence of the predominantly diffuse and distal location of the lesions in the veins and arteries involved. Endothelin-1 (ET-1) is a potent vasoconstrictor peptide, which exerts its action by targeting two transmembrane receptors (ETA and ETB). Pharmacologic ET-1 receptor blockade, may be single (ETA or ETB) or dual (both, ETA and ETB) . Bosentan is a dual ET-1 receptor antagonist, administered orally, which is approved in the European Union to treat pulmonary arterial hypertension in systemic sclerosis patients and to prevent the occurrence of new digital ulcers in systemic sclerosis patients with ongoing digital ulcers. The results of a small retrospective study [6–8] and a prospective study  suggested that bosentan could have a role in healing ongoing digital ulcers in systemic sclerosis.
Based on these previously reported studies on digital ulcers in Systemic Sclerosis patients, we designed a pilot study in order to assess both the safety and effectiveness of bosentan in the pharmacologic management of ischaemic symptoms and ulcers in TAO patients, the results of which are reported herein.
In order to be included in the study, the patients had to have a previous diagnosis of TAO, fulfilling the Shionoya criteria : 1) onset of distal ischaemic symptoms in one extremity before the age of 50 years, 2) smoker or history of smoking, 3) distal ischaemia of the extremity confirmed by a non-invasive test (ankle-brachial index [ABI], toe-brachial index or partial pressures), 4) absence of thrombophilia, autoimmune disease, diabetes, hyperlipidaemia, trauma or a proximal source of underlying embolism, 5) arterial tree proximal to the distal segment of the healthy superficial femoral artery, and 6) occlusive distal disease with specific elements or actual pathological findings demonstrated angiographically or by means of angio-magnetic resonance imaging. The consecutive patients included in this study were required to meet the following inclusion criteria: critical ischaemia in any extremity, pain at rest or non-healing ischaemic ulcers, present for at least four weeks with no evidence of improvement in response to conventional treatment; not being candidates for surgical or endovascular revascularisation of the extremity studied; objective confirmation of the ischaemia in the affected extremity by means of an ABI at rest of less than 0.6, if it was the lower extremity, or a partial pressure of less than 50 mmHg in the upper extremity, in two consecutive assessments at least one week apart. In each patient included with pathological conditions in the upper extremities was performed a study to assess blood flow in the upper limb affection performing an Allen test, the determination of the Digital/Brachial Index (DBI), Radial/Brachial Index (RBI) or Ulnar/Brachial Index (UBI) and the determination of the partial pressure in the radial artery. DBI, RBI and UBI indexes were defined as the ratio of the segmental arterial pressures of the digital arteries, radial and ulnar, respectively, and the partial pressure in the brachial artery.
We considered a ratio < 0.7 in DBI, RBI and UBI as an indicator of an inadequate blood perfusion in the upper limb [11–13]. Conventional treatment includes: advice for patients on giving up smoking; surgical or endovascular revascularisation of the extremity when possible, peripheral sympathectomy; prostanoid vasodilator iloprost (in a 21-day cycle). The exclusion criteria were as follows: any known contraindication for treatment with bosentan such as patients with liver failure or liver diseases, with anaemia or pregnant women; presence of arteriosclerotic risk factors, apart from smoking (hypertension, hyperlipidaemia and/or diabetes mellitus), any other medical or psychological condition which may represent, in the investigator's opinion, a contraindication to either bosentan treatment or to adequately performing the treatment and procedures of the study. Patients with other causes or forms of peripheral vasculopathy such as popliteal entrapment syndrome, cystic adventitial disease, collagenopathy and hypercoagulability (e.g. the presence of Factor V Leiden or antiphospholipid syndrome) were also excluded from the study.
The study was designed as a pilot, open-label, non-controlled, non-randomised, single centre clinical study, where patients previously diagnosed with TAO received treatment with bosentan in a compassionate use programme. No concomitant medication was administered during the study period except analgesics and antibiotics.
The study protocol was approved by the Institutional Review Board of the participating centre and regulatory authorities. Patients were required to give written informed consent before enrolment.
The study endpoints were clinical improvement rate (absence of new trophic lesions, ulcer healing process, pain relief, complete absence of pain), major or minor amputation rate, haemodynamic changes as measured by means of ABI, changes in endothelial function as measured by means of the brachial artery flow-mediated dilation test (BAFMD), and angiographic changes as measured by an arteriography with digital subtraction or angio-magnetic resonance imaging (MRI).
Clinical therapeutic success was defined as the complete healing of the distal ischaemic trophic lesion or complete ischaemic pain relief at rest if the patient presented no lesion.
All included patients received a treatment regimen with bosentan for compassionate use, after strict compliance with the inclusion criteria and the absence of exclusion criteria were ascertained. Bosentan therapy consisted of a month's treatment with 62.5 mg twice daily (bid) administered orally. The initial dose was doubled to 125 mg bid after the first month if significant adverse events attributable to bosentan were ruled out. This full-dose regimen (125 mg/12 h) was maintained for the following three months or until total healing of the ulcers, provided that the liver function tests and blood cell count remained within the normal range. Patients were given analgesic treatment, as necessary, to control pain at rest. The ischaemic lesions and necrotic ulcers were treated with standard daily care and antibiotherapy as necessary. Special methods of treatment were not used and nor was absolute bed rest prescribed during the study period.
All patients were monitored fortnightly on an outpatient basis, at baseline, weekly for the first eight weeks after the start of bosentan treatment, and monthly thereafter. Baseline assessments included medical history, concomitant medication requirements, (mainly analgesics or antibiotics), and a complete physical examination. Laboratory assessments, such as liver function tests and blood cell counts were performed, as well as frequent immunological tests.
In addition, a pregnancy test was performed in women of childbearing age. The ischaemic ulcers were documented with colour photographs for all patients before the BAFMD was assessed. The target extremity for assessment purposes was defined as the one presenting the trophic lesion or causing pain at rest.
Baseline haemodynamic studies included the ABI at rest, and the partial brachial pressures (absolute value).
Bioactivity of bosentan was assessed by means of BAFMD, as an indirect measurement of the endothelial function that is based on the capacity of nitric oxide (NO) production released by the endothelium, which may lead to arterial dilation. This measurement is achieved by means of an ultrasonography, a non-invasive technique based on parietal stress, caused by increased flow after a period of ischaemia. This causes the opening of ionic channels, thereby increasing the concentration of intracellular calcium and stimulating the enzymatic activity of endothelial NO synthase. As a result, there is a relaxation of smooth muscle, together with dilation of the brachial artery .
Measurement of BAFMD: Before the test, all patients fasted for a minimum of 12 hours and were advised not to partake in physical exercise or smoke. They were placed in dorsal decubitus, in a calm environment and under controlled room temperature. A Doppler ultrasound machine (HD11 XE, PHILIPS, Eindhoven, The Netherlands) was used with a L12-3-MHz linear probe. After obtaining an image at rest, ischaemia was applied at a pressure of 250 mmHg over a period of five minutes. Another image was obtained 60 seconds after releasing ischaemia. The BAFMD was calculated as the as the post-ischaemic diameter after 60 seconds, minus the diameter at rest, divided by the diameter at rest and expressed as a percentage.
BAFMD was assessed according to a previously described technique , in each patient before and after treatment with bosentan and three months after the end of treatment. An arteriography with digital subtraction (or an angio-MRI) was performed at baseline and three months after the last dose of bosentan.
During follow-up, all the information on the clinical symptoms, evolution of trophic lesions, presence/absence of major or minor amputation, smoking and patient's physical activity was collected. This information was obtained directly from the guided anamnesis, physical examination and photographs that were taken at the successive follow-up visits.
Outcome assessments and techniques
The criteria we used to document the changes in the status of the target extremity were taken from the Inter-Society Consensus for the Management of Peripheral Arterial Disease (TASC II) consensus-based standard recommendations . The haemodynamic effect of bosentan on macrocirculation was determined by means of the ABI, which was obtained by taking the systolic pressure figure in the posterior tibial artery at maleolar level or the dorsalis pedis artery and dividing this measurement by the brachial artery systolic pressure. These measurements were always taken with the patient in the supine position and following a rest period of 15 minutes, using a continuous bidirectional Doppler ultrasound device. The drug's bioactivity was shown through the monitoring of the improvement in patient endothelial function, produced by the treatment and indirectly measured by means of BAFMD, as was previously described.
Qualitative variables were described by frequencies and percentages and quantitative variables by mean ± standard error or median and range. Differences between time points were compared, using the Wilcoxon test for dependent samples and the Friedman test for repeated measurements. The threshold of statistical significance was established as p < 0.05. Statistical analyses were performed using SSPS version 16.0.
Patient characteristics and results of brachial artery flow-mediated dilation test
Give up smoking
Pre-treatment clinical results
Post-treatment clinical results
BAFMD 3 months after
PG + LS
Ulcer in toe
Ulcer in toes
Ulcer in fingers
Ulcer in fingers
Pain at rest
Pain relief Claudicates 300 m
Ulcer in toes
Ulcer in toes
Ulcer in toe
Ulcer in toe
PG + LS
Ulcer in forefoot
PG + LS
Ulcer in toes
Healing. Amp. 3rd toe
2 BP (permeable) + PG
Ulcer in toe
Ulcer in fingers
Seven patients were male (58%). The median age of the patients was 39 years (range 29-49). Seven patients (58%) had previously been diagnosed with at least one episode of phlebitis migrans. All patients were current smokers and had been heavy smokers for years. Eight patients (67%) were unable to completely abstain from smoking during the follow-up.
We discarded the presence of associated autoimmune diseases in patients due to all the immunological testing included, as tests for C-reactive protein, rheumatoid factor, antinuclear antibodies, anti-DNA antibodies, antiribonucleoprotein antibodies, anti-Ro antibodies, anti-Sm antibodies, anti-Jo-1 antibodies and antineutrophil cytoplasmic antibodies were negative. Levels of complement C3 and C4, and thyroid stimulating hormone, were normal in all patients. Tests for anticardiolipin antibodies were negative, as were tests for syphilis, HIV, and hepatitis B and C. Diagnoses of cardiogenic or aortic embolism, early-onset occlusive atherosclerotic disease, collagen disease and hypercoagulable state were excluded.
As shown by angiography, the infrapopliteal arteries were involved in the 10 patients with lesions on the lower extremities, whereas the upper extremities were involved in three patients (25%). Either a digital arteriography with subtraction or an angio-MRI documented the typical findings of Buerger's disease in all 12 patients at baseline. These findings included segmental occlusive disease, mainly affecting the tibial, forearm and digit vessels, as well as the plantar and palmar arches, although this involvement extended proximally to the popliteal artery in two cases. In all cases the typical corkscrew collateral vessels were observed and the proximal vessels to the superficial femoral artery were free of any sign of disease.
During the follow-up, no new ischaemic lesions were observed in the target extremities in all but one patient whose ulcer had begun to heal and who, three months after the end of bosentan treatment, had a relapse of an ulcer on their toe. This relapse was treated with a new four-month course of bosentan which managed to heal the lesion. Only one patient required prolonging the administration of bosentan beyond four months in order to achieve total healing of the ulcers.
Overall, clinical improvement was observed in 12 of the 13 extremities (92%) treated, while only one extremity which presented lesions at the level of the forefoot ultimately required major amputation below the knee. Of the 12 extremities that improved, ten (77%) achieved complete clinical therapeutic success (healing or complete pain relief) [Table 1]. Moreover, a minor amputation of one toe was performed with conservation of the extremity and healing of the ulcers of the other toes in one patient. Two out of 13 extremities (15%) underwent amputation (one major and one minor) after bosentan treatment. Thus, an extremity conservation rate of 92% was achieved.
All 10 of the lower extremities treated presented an ABI lower than 0.6 before treatment. After the end of bosentan treatment, the ABI increased by more than 0.1 in two patients. These differences were statistically non-significant when compared with baseline values. None of the three target upper extremities, which presented a partial pressure below 50 mmHg at baseline, experienced an increase in partial pressure above 10 mmHg after bosentan treatment.
The BAFMD test was well tolerated in all patients. Baseline endothelial function was reduced in all patients (mean BAFMD = 1.8 ± 1.3%). After the end of bosentan treatment, all patients experienced a significant improvement in their values at this endpoint (mean BAFMD = 6.5 ± 1.3%), making this difference statistically significant (p = 0.002). Three months after the end of treatment with bosentan, the BAFMD values were also higher than they were at the end of the treatment, reaching a mean value of 12.7 ± 2.9% (p < 0.001).
No patient suffered serious adverse effects due to treatment with bosentan leading to withdrawal of the treatment. The repeated liver enzyme measurements remained within the range of normality. Moreover, blood cell counts were normal in all but one patient who presented haemoglobin values in the lower limit and was treated with enteral iron. We did not find statistical differences in the levels of blood pressure in our patients after the administration of Bosentan. The only documented bosentan-associated adverse event was the occurrence of transient oedema in the lower extremities in 3 patients (25%), consistent with the vasodilatory effect of the distal bed associated with bosentan use. No new safety signals were observed.
As TAO is associated with both distal ulcers in the extremities and the possibility of amputation, it frequently involves social problems and a worsening in the quality of life of the affected patients . Only a few pharmacological and surgical options (of controversial efficacy) are available to date . New therapeutic options with a higher efficacy than the current ones are clearly needed in order to properly manage patients affected by TAO.
Our study is a small pilot study and, as a result, it is not possible to draw firm conclusions from it. On the contrary, its objective should be to generate hypotheses which firstly require further confirmation in larger prospective studies, and secondly, a definitive assessment in comparative randomised trials. In any case, the characteristics of this disease, the low incidence and the lack of effective treatments that improve the course of the disease or correct the cause, contributes to serious ethical difficulties in carrying out this type of studies in this particular disease. We consider special and important the value of the results obtained in our study and the immediate applicability in the clinical practice. This study should be considered in this setting. However, our results show that bosentan therapy was associated with several clinical and endothelial function-related outcomes in patients with TAO, which may be promising. This report adds data to previous single reports [18, 19] on the efficacy of bosentan and the management of patients with TAO.
Both clinical improvement and complete healing of the ulcers were achieved in the majority of the target extremities despite the documented failure to give up smoking in the majority of the patients. Moreover, the only major amputation was performed in a patient who gave up smoking definitively. This result compares favourably with a 19% major amputation rate in 69 patients who continued smoking, previously reported in a series involving 110 patients with TAO . The prostacyclin analogue iloprost has shown modest efficacy in randomised clinical trials. In a trial of intravenous iloprost versus aspirin , healing of ulcers was higher in the iloprost arm and was observed in 18 out of 52 patients receiving iloprost (35%). In another trial, an oral formulation of iloprost was not better than placebo with regard to this outcome . In the aggregate, the efficacy results shown by prostacyclin analogues when used for the management of TAO are far from satisfactory. On the contrary, in our study, 10 out of 12 ulcers have improved (83%), of which eight have healed. Although these results are from a small study and are not comparable with those from randomised trials, they seem to be promising.
Giving up smoking, the only therapeutic procedure that has proven to be successful in TAO, was achieved in only four out of 12 patients (33%). This unsatisfactory rate is in accordance with previous reports which highlight the fact that it was extremely difficult for patients who are heavy smokers to give up smoking despite having strongly been advised to do so, as well as having received full information about the benefits of giving up smoking, especially in terms of avoiding amputations . Patients reported their tobacco consumption and no medical diagnostic test was used to confirm the absolute cessation of smoking, which represents a limitation of this clinical study.
The majority of our patients had been treated with prostanoids, bosentan being the frontline pharmacological regimen in only two patients. Moreover, four out of the 13 target extremities had been surgically treated (lumbar sympathectomy or by-pass procedures). Thus, almost all patients included in this study should be considered refractory to previous therapeutic strategies. Taken together, the data on previous treatments as well as the high rate of smoking continuation reveal that the patients in our study were difficult to manage, given that they presented previous negative prognostic factors.
A possible explanation for the bosentan pharmacodynamic effect on endothelial function is based on the endothelial function impairment observed in patients with peripheral arterial disease in general  and in TAO patients in particular . In addition, bosentan has shown that it can improve endothelial function, at least in patients with systemic sclerosis . Thus, there is a mechanistic background to explain our results on endothelial function, which was indirectly measured in our study by means of BAFMD. In fact, BAFMD results clearly improved in every patient treated and also in the overall mean value.
Moreover, an elevated serum ET-1 level has been observed in patients with TAO, supporting a possible mechanistic explanation of the clinical benefit of bosentan in these patients . Adverse events of bosentan treatment were as expected. Notably, liver tolerance was excellent and anaemia required iron supplementation in only one patient. Compliance with the treatment was also excellent (monitored by pill counts in every follow-up visit) with no patients needing to withdraw from the treatment as a consequence of adverse events.
The hypothesis that bosentan treatment in TAO patients results in an improvement of clinical, angiographic and endothelial function outcomes is supported by the results of this small pilot study. Bosentan should be investigated further with regard to TAO patient management. New clinical trials with a control group should be performed to confirm our results. In the meantime, bosentan should be considered as a promising investigational agent for treating these patients.
List of abbreviations
brachial artery flow-mediated dilation test
angio-magnetic resonance imaging
The authors would like to thank Lola Montilla from Trial Form Support, Spain for her contribution in the preparation of this manuscript.
Written consent for publication was obtained from the patient(s) or their relative(s).
- Olin J, Young J, Graor R, Ruschhaupt W, Bartholomew J: The changing clinical spectrum of thromboangiitis obliterans (Buerger's disease). Circulation. 1990, 82 (5 Suppl 4): 3-8.Google Scholar
- Yorukoglu Y, Ilgit E, Zengin M, Nazliel K, Salman E, Yucel E: Thromboangiitis obliterans (Buerger's disease in women-a reevaluation). Angiology. 1993, 44: 527-532. 10.1177/000331979304400704.View ArticlePubMedGoogle Scholar
- Yoshimuta T, Akutsu K, Okajima T, Tamori Y, Kubota Y, Takeshita S: Corkscrew collaterals in Buerger's disease. Can J Cardiol. 2009, 25: 365-10.1016/S0828-282X(09)70099-6.View ArticlePubMedPubMed CentralGoogle Scholar
- Cooper LT, Henderson SS, Ballman KV, Offord KP, Tse TS, Holmes DR, Hurt RD: A prospective, case-control study of tobacco dependence in thromboangiitis obliterans (Buerger's Disease). Angiology. 2006, 57: 73-78. 10.1177/000331970605700110.View ArticlePubMedGoogle Scholar
- Watts SW: Endothelin receptors: what's new and what do we need to know?. Am J Physiol Regul Integr Comp Physiol. 2010, 298: R254-260. 10.1152/ajpregu.00584.2009.View ArticlePubMedGoogle Scholar
- Launay D, Diot E, Pasquier E, Mouthon L, Boullanger N, Fain O, Jego P, Carpentier P, Hatron PY, Hachulla E: Bosentan for treatment of active digital ulcers in patients with systemic sclerosis. Presse Med. 2006, 35: 587-592. 10.1016/S0755-4982(06)74645-0.View ArticlePubMedGoogle Scholar
- Funauchi M, Kishimoto K, Shimazu H, Nagare Y, Hino S, Yano T, Kinoshita K: Effects of bosentan on the skin lesions: an observational study from a single center in Japan. Rheumatol Int. 2009, 29: 769-775. 10.1007/s00296-008-0789-z.View ArticlePubMedGoogle Scholar
- Riccardi MT, Chialà A, lannone F, Grattagliano V, Covelli M, Lapadula G: Treatment of digital ulcers in systemic sclerosis with endothelin-1 receptor antagonist (bosentan). Reumatismo. 2007, 59: 135-139.PubMedGoogle Scholar
- Tsifetaki N, Botzoris V, Alamanos Y, Argyriou E, Zioga A, Drosos AA: Bosentan for Digital Ulcers in Patients with Systemic Sclerosis: A Prospective 3-year Follow up Study. J Rheumatol. 2009, 36: 1550-1551. 10.3899/jrheum.080992.View ArticlePubMedGoogle Scholar
- Shionoya S: Diagnostic criteria of Buerger's disease. Int J Cardiol. 1998, 66 (Suppl 1): S243-5.View ArticlePubMedGoogle Scholar
- Zimmerman NB: Occlusive vascular disorders of the upper extremity. Hand Clin. 1993, 9 (1): 139-50.PubMedGoogle Scholar
- Ouriel K: Noninvasive diagnosis of upper extremity vascular disease. Semin Vasc Surg. 1998, 11 (2): 54-9.PubMedGoogle Scholar
- Ruch D, Koman LA, Smith TL: Chronic vascular disorders of the upper extremity. J Am Society Surg Hand. 2001, 1 (1): 73-80. 10.1053/jssh.2001.21780.View ArticleGoogle Scholar
- Maldonado FJ, Miralles J de H, Aguilar EM, Gonzalez AF, García JR, García FA: Relationship between noninvasively measured endothelial function and peripheral arterial disease. Angiology. 2009, 60 (6): 725-731. 10.1177/0003319708327787.View ArticlePubMedGoogle Scholar
- Norgren L, Hiatt WR, Dormandy JA, Nehler MR, Harris KA, Fowkes FG: TASC II Working Group. Inter-Society Consensus for the Management of Peripheral Arterial Disease (TASC II). J Vasc Surg. 2007, 45 (Suppl S): S5-67.View ArticlePubMedGoogle Scholar
- Ohta T, Ishioashi H, Hosaka M, Sugimoto I: Clinical and social consequences of Buerger Disease. J Vasc Surg. 2004, 39: 176-180. 10.1016/j.jvs.2003.08.006.View ArticlePubMedGoogle Scholar
- Puéchal X, Fiessinger JN: Thromboangiitis obliterans or Buerger's disease:challenges for the rheumatologist. Rheumatology. 2007, 46: 192-199.View ArticlePubMedGoogle Scholar
- Todoli JA, Hernández MM, Arrébola MA: Efficacy of bosentan in digital ischemic ulcers. Ann Vasc Surg. 2010, 24 (5): 690.e1-4. 10.1016/j.avsg.2010.03.011.View ArticleGoogle Scholar
- De Haro J, Florez A, Fernandez JL, Acin F: Treatment of Buerger disease (thromboangiitis obliterans) with bosentan: a case report. BMJ Case Reports. 2009, doi:10.1136/bcr.08.2008.0691. Published online: May 12th 2009. [http://casereports.bmj.com/content/2009/bcr.08.2008.0691]Google Scholar
- Fiessinger JN, Schäfer M: Trial of iloprost versus aspirin treatment for critical limb ischaemia of thromboangiitis obliterans. The TAO Study. Lancet. 1990, 335: 555-557. 10.1016/0140-6736(90)90346-7.View ArticlePubMedGoogle Scholar
- The European TAO Study Group: Oral iloprost in the treatment of thromboangiitis obliterans (Buerger's disease): A double-blind, randomized, placebo-controlled trial. Eur J Vasc Endovasc Surg. 1998, 15: 300-307.View ArticleGoogle Scholar
- Szuba A, Cooke JR: Thromboangiitis Obliterans. An Update on Buerger's Disease. West J Med. 1998, 168: 255-260.PubMedPubMed CentralGoogle Scholar
- Makita S, Nakamura M, Murakami H, Komoda K, Kawazoe K, Hiramori K: Impaired endothelium-dependent vasorelaxation in peripheral vasculature of patients with thromboangiitis obliterans (Buerger's disease). Circulation. 1996, 94 (9 Suppl 2): 211-215.Google Scholar
- Sfikakis PP, Papamichael C, Stamatelopoulos KS, Tousoulis D, Fragiadaki KG, Katsichti P, Stefanadis C, Mavrikakis M: Improvement of vascular endothelial function using the oral endothelin receptor antagonist bosentan in patients with systemic sclerosis. Arthritis Rheum. 2007, 56: 1985-1993. 10.1002/art.22634.View ArticlePubMedGoogle Scholar
- Czarnacki M, Gacka M, Adamiec R: A role of endothelin 1 in the pathogenesis of thromboangiitis obliterans (initital news). Przegl Lek. 2004, 61 (12): 1346-50.PubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2261/12/5/prepub
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