Mædica - a Journal of Clinical Medicine O RIGINAL
MAEDICA – a Journal of Clinical Medicine 2016; 11(3):186-190
PAPER
Comparison Between Alprostadil and Iloprost in Intravenous Treatment of Patients With Chronic Peripheral Arterial Disease Dan Nicolae TESLOIANUa, Corneliu MOROSANUb, Ene-Cristian ROATAb, Laurentiu SORODOCc a
Department of Cardiology, “Sf. Spiridon” Emergency Clinical Hospital, Iasi, Romania Department of General Surgery, Regional Institute Of Oncology, Iasi, Romania c Department of Internal Medicine, “Sf. Spiridon” Emergency Clinical Hospital, Iasi, Romania b
ABSTRACT Introduction: chronic peripheral arterial disease (PAD) seems to be a “rediscovered” pathology nowadays, brought into spotlight by its strong correlation with other significant cardiovascular disorders. Objectives: to sustain a real benefit from treatment with i.v. prostaglandins (PG) in PAD patients and to directly compare the currently used PG: alprostadil and iloprost. Method: open, non-randomized cohort study, with placebo group (”classical therapy”) reviewing 615 PAD patients with therapeutic approach during 2003-2012 period, divided in 3 subgroups: “classical” therapy; ”classical” therapy + iloprost; ”classical” therapy + alprostadil; patients with Burger’s disease were excluded; multiple factor analysis with statistical results inserted. Results: clear domination of male gender patients, with older female gender patients (p≤0.001); smoking like major risk factor in male and in all patients (p< 0.0001); 124 patients underwent angiography . Conclusion: a real improvement in the clinical status of patients receiving i.v. prostaglandin therapy with no differences between genders, diabetic and non-diabetic patients; alprostadil seems be$er than iloprost. Keywords: Peripheral arterial disease, prostaglandins, iloprost, alprostadil.
BACKGROUND
C
hronic peripheral arterial disease (PAD) seems to be a “rediscovered” pathology, being strongly correlated with other significant cardiovascular disorders (1-3). Despite this, newly guidelines come with no major news: the “classical” therapy takes into account the well-known, but not spectacular in results, naftidrofuryl, pentoxifylline, L-carni-
tine, while buflomedil drops out in many countries (4,5); a salutary note is the absence of contraindication for beta blockers as associated therapy; statins can increase walking perimeter, but in indirect relationship with PAD stage; antiplateles seems to be more effective in reduction of associated cardiovascular risk than in increase of walking perimeter (6); i.v. prostaglandins had only a simple notice (near inositol and proteoglycans) like other therapies, with-
Address for correspondence: Dan Tesloianu, “Sf. Spiridon” Emergency Clinical Hospital, 1t Independentei Boulevard, Iasi, Romania E-mail: [email protected] Article received on the 15rd of June 2015. Article accepted on the 26rd of September 2016.
186
Maedica
A Journal of Clinical Medicine, Volume 11 No.3 2016
COMPARISON BETWEEN ALPROSTADIL AND ILOPROST
IN INTRAVENOUS TREATMENT OF
out conclusive results. An important note is the citation of cilostazol (100 mg twice daily) to improve pain-free walking perimeter in a 2015 update (7). OBJECTIVES
S
ustaining a significant role of i.v. PG in the treatment of PAD patients, in a study on a total number of 615 patients diagnosed and treated for PAD (stages II A-IV) in the Department of Internal Medicine – “Sf. Spiridon” Emergency Clinical Hospital Iasi, during 20032012 period. It was a cohort prospective nonrandomized open study, with placebo group (”classical therapy”). q MATHERIAL AND METHOD
S
tandard protocol for diagnosis and treatment of PAD patients in our clinic included: clinical evaluation with subsequent angiography in patients with stage III – IV (exception for patients with severe associated comorbidities or those which refused the invasive approach); in stage II B angiography was facultative (we preferred to initiate medical therapy; invasive approach only if after one-month-therapy the evolution was unfavorable). Post-angiography remained two options: by-pass surgery or conservative therapy (+/- sympathectomy ) in patients with no surgical solutions or which refuse this solution. ”Classical” therapeutic protocol included a combination between: calcium channel blockers (amlodipine 5-10 mg/day or diltiazem 120360 mg/day), antiplatelet theraphy (ASA 75150 mg/day and/ or clopidogrel 75 mg/day), LMWH (low molecular weight heparin) – fraxiparine/ enoxaparine- in therapeutic doses (in III and IV stages PAD patients), pentoxifylline extended-release 1200 mg/day, statins (simvastatin 40-80 mg/day or atorvastatin 40-80 mg/ day or rosuvastatin 20-40 mg/day) +/- ACE inhibitors (correlated with the level of systemic blood pressure – ramipril 5-10 mg/day or perindopril 5-10 mg/day or quinapril 5-20 mg/day or zofenopril 15-30 mg/day) (8-11). Non-surgical solution is dedicated for patients in II A stages, for patients in II B stages with favorable evolution under conservative therapy and for patients in stage III and IV in presence of absolute/ relative contraindication for by-pass (see above). Due to significant costs, iloprost/ alprostadil therapy was reserved for the following cases:
PATIENTS WITH CHRONIC PERIPHERAL ARTERIAL DISEASE
a. for iloprost – patients in stage II B and III with unfavorable evolution under ”classical” therapy; per primam (+/- sympathectomy) in stage IV PAD patients; b. for alprostadil – patients in stage II B with unfavorable evolution under ”classical” therapy; per primam (+/- sympathectomy) in stage III and IV PAD patients. ”Classical” therapy can be initiated and continued in hospital as well as at home. I. v. prostaglandins therapy should be best initiated in hospital, and continued at home after 5-7 days. Iloprost and alprostadil are synthetic prostaglandins analogues (PGI2/PGE1) with i.v administration and significant action in improvement of endothelial dysfunction at the micro- and macrovascular level. In women, pregnancy must be excluded before start therapy; recomandation for administration must be strictly forward. q RESULTS Tabel1. Demographic data
A.
Total number Median age (years)
Males
Females
P
569
46
≤ 0.0001
63.3+/-11.4
66.6+/-11.3
0.0007
B. Tabel 2. Presence of major cardiovascular risk factors: Risk factor
Males
Females
P
538 (94.6%)
29 (62.3%)
≤0.0001
273 (48%)
36 (78%)
0.02
Dyslipidemia
272 (47.8%)
20 (43.3%)
NS
Elevated blood pressure
304 (53.5%)
43 (48.7%)
NS
Age ≥ 55/65 years
351 (61.5%)
27 (57.6%)
NS
Familial/personal history of cardiovascular disease
380 (66.8%)
42 (91%)
0.03
Smoking Diabetes mellitus
Maedica
A Journal of Clinical Medicine, Volume 11 No.3 2016
187
COMPARISON BETWEEN ALPROSTADIL AND ILOPROST C. Tabel 3. tion of PAD
IN INTRAVENOUS TREATMENT OF
Leriche-Fontaine classifica-
Stage
Males
Females
P
IIA
174 (21.1%)
10 (11.3%)
0.065
IIB
103 (18.1%)
11 (23.9%)
NS
III
204 (34.2%)
19 (41,3%)
NS
IV
88 (14.8%)
6 (13.4%)
NS
D. Angiography: 116 males (19.5%) and 8 females (17.4%) underwent angiography. E. Evolution of conservative treatment possibilities induced the following results: • 292 patients received ”classical” initial therapy: – 184 patients (174M/10F) in stage IIA with good evolution (only 6 with deterioration over time); – 60 patients (56M/4F) in stage IIB: 39 with improvement in clinical status and regression to IIA stage, 15 with stationary evolution, remaining in IIB stage, 16 with deterioration over time; – 34 patients (28M/6F) in stage III: 16 with improvement in clinical status, 18 with deterioration over time; – 14 patients (11M/3F) in stage IV: all with severe evolution and need for amputation. • 60 patients received iloprost therapy: – 34 patients (31M/3F) in stage IIB, with spectacular evolution and increase in walking perimeter: 162 meters +/- 56 meters, after 15-20 days of treatment (p=0.008 vs. ”classical” therapy); – 19 patients (15M/4F) in stage III: all with good evolution and increase in walking distance: 138 meters +/- 42 meters after 15-20 days of treatment (some of them with associated sympathectomy) (p=0.04 vs. ”classical” therapy); – 7 patients (6M/1F) in stage IV: all with associated sympathectomy; 1 with no amputation need; 6 with low level of amputation compared to ”classical” therapy after 15-20 days of treatment (p=0.065 vs. ”classical” therapy); 188
Maedica
A Journal of Clinical Medicine, Volume 11 No.3 2016
PATIENTS WITH CHRONIC PERIPHERAL ARTERIAL DISEASE
Long term follow-up (28-38 months) shows favorable evolution, with only 2 patients needing amputation. Concerning side effects, the most unpleasant one was headache, induced especially by the maximal doses – 18 patients; most frequent adverse effect (50 from 60 patients) was skin flushing of the cephalic extremity; a rarely adverse effect was significant abdominal discomfort, in one case generating treatment stop; another unpleasant phenomenon – superficial phlebitis at the level of catheterisated veins which required frequent changing of peripheral venous catheter position was present in 23 patients; 2 patients presented shivering; dyspnea together with bibasilar pulmonary rales (non-cardiogenic incipient pulmonary edema) was present in 4 patients(11). Even if theoretically, through platelets inhibition, concomitant administration with heparin and/or antiaggregants increases the bleeding risk, we did not observed this fact in our patients. • 263 patients received alprostadil therapy: – 20 patients (15M/5F) in stage II B: immediately spectacular results, with medium increase in walking perimeter with 250 meters +/- 40 meters after 20-30 days therapy (p≤0.005 vs. iloprost); – 170 patients (161M/9F) in stage III: 142 patients with good clinical evolution and improvement in walking perimeter with 191 meters +/- 33 meters; 7 patients needed amputation (p = ns vs. iloprost); the remaining patients underwent sympatectomy followed by good evolution; – 73 patients (70M/3F) in stage IV: 32 with lesions resolution (13 with associated sympathectomy) (p=0.046 vs. iloprost); 31 needed amputation (p=0.055 vs. iloprost); 10 were revascularisated with good evolution. On long term follow-up (14-28 months) only 5 patients had a bad evolution with amputation; the other ones maintained (94 cases) or improved (164 cases) the clinical status achieved after the first approach. A remarkable phenomenon, more pregnant for alprostadil than for iloprost, is the appearance of what we have named ”clear delimitation of viable tissue” observed at PAD patients in stage III and IV. Indeed, after the first days of
COMPARISON BETWEEN ALPROSTADIL AND ILOPROST
IN INTRAVENOUS TREATMENT OF
treatment it appears a clear delimitation between the viable and non-viable tissue. So, it can be noted that the patient’s response after a few days of therapy (sometimes even after first day), could predict an accurate prognosis. Concerning the adverse effects, alprostadil is associated with significantly less side effects in comparison to iloprost treated patients: significant headache - only 2 patients (p=0.0002 vs. iloprost); abdominal discomfort with treatment cessation – 1 patient (p=0.001 vs. iloprost); superficial phlebitis at the level of catheterisated veins which required frequent changing of peripheral venous catheter position was present in 4 patients (p=0.003 vs. iloprost); 11 patients presented shivering (p=0.03 vs. iloprost); dyspnea together with bibasilar pulmonary rales (non-cardiogenic incipient pulmonary edema) was present in 10 patients (p=0.01 vs. iloprost); skin flushing of cephalic extremity was rarely observed (22 patients p=0.0001 vs. iloprost); one patient encountered severe hypotension (ns vs. iloprost). Even if theoretically, through platelets inhibition, concomitant administration with heparin and/ or antiaggregants increases the bleeding risk, we did not observed this fact in our patients, similar to those treated with iloprost. q DISCUSSSION
T
he presented results are a proof for a real hope in PAD patients with unfavorable evolution under ”classical” therapy, the outcomes being directly correlated with the initial stage of PAD. For stage IV PAD patients without surgical possibilities, the association between i.v. prostaglandins and sympathectomy seems to offer the maximum benefit (12). Our results are in general in concordance with the results of other published studies, the number of included cases allowing us pertinent
PATIENTS WITH CHRONIC PERIPHERAL ARTERIAL DISEASE
statistical analysis as well as comparison to other articles (13-19). Our study points for a better outcome for alprostadil treatment versus iloprost treatment in PAD patients, concomitantly proving a significantly better outcome of i.v. prostanglandins vs. ”classical” therapy. The results are additionally validated by the concordance between our general data and that of other studies already published: • clear domination of male gender and older female among patients; • smoking as the most important risk factor in male patients and, concomitantly, in all PAD patients (p≤0.0001); in female patients the most important risk factor is personal or family history of cardiovascular or diabetes, smoking being in the second position. q CONCLUSSION
T
he present study proves additionally benefits by combining ”classical” therapy with i.v. prostaglandins, with no significant differences in prostaglandins effects between genders or regarding presence/absence of diabetes mellitus (19). Regarding the comparison between the two currently used prostaglandins, the superiority of alprostadil versus iloprost is sustained by superior improvement in walking perimeter, quickly installed results, rarely side effects and the so-called ”clear delimitation of viable tissue” phenomenon under perfusion with alprostadil in stage III and IV PAD patients. For patients in stage IV PAD, without surgical solutions, the association between i.v. prostaglandins and sympathectomy seems to offer a maximum benefit. q Conflict of interests: none declared. Financial support: none declared.
R"#"$"%&"' 1.
2.
Creager MA, Libby P. Braunwald’s Heart Disease a Textbook of Cardiovascular Disease. 10th ed. Philadelphia: Elsevier Saunders; 2015;1312-1316. Criqui MH, Gallal W. Peripheral arterial disease – epidemiological aspects. Vascular Medicine 2001;6 (suppl 1):3-7.
3.
4.
Tesloianu D, Spiridon M, Şorodoc L, et al. Arteriopatia obliteranta a membrelor inferioare – O “Cenusareasa” a Cardiologiei. Un review a 910 cazuri. Revista Medicala Romana 2013;11-17; Tendera M, Aboyans V,Bartelink ML, et al. ESC Guidelines on the diagnosis
Maedica
5.
and treatment of peripheral artery diseases. European Heart Journal 2011;32:2851–2906. Heidrich H, Schmidt T, Fahrig C. Are there predictors for the outcome of a PGE1 treatment in peripheral arterial disease with critical limb ischaemia? Abstr. in. Vasa 2015;34:101-107.
A Journal of Clinical Medicine, Volume 11 No.3 2016
189
COMPARISON BETWEEN ALPROSTADIL AND ILOPROST 6.
Hia( WR. Preventing atherothrombotic events in peripheral arterial disease: the use of antiplatelet therapy. Journal of Internal Medicine 2002;251:193–206. 7. Yang HA. Peripheral Artery Disease (PAD) Guidelines: Screening, Lower Extremity PAD, Renal Arterial Stenosis (Updating the 2011 Guideline), 2015, h#p://emedicine.medscape.com/ article/2500033-overview. 8. Gherasim L, Dimulescu D. Gherasim L (ed): Medicina interna, vol. II, Ed. Medicala, Bucuresti 1996;1013-1023. 9. Olin JW. Buerger’s disease: in Rutherford RB (ed): Vascular Surgery 4th ed. Philadelphia: WB Saunders; 2000;350364. 10. Fiessinger JN, Schafer M. Trial of iloprost versus aspirin treatment for critical limb ischemia of trombangiitis obliterans. The TAO study, Lancet 1990;335:555-558. 11. Reisin L, Marmor A, Rabinowitz B, et
190
Maedica
12.
13.
14.
15.
IN INTRAVENOUS TREATMENT OF
PATIENTS WITH CHRONIC PERIPHERAL ARTERIAL DISEASE
al. Safety of prostaglandin E1 for the treatment of peripheral arterial occlusive disease in patients with congestive heart failure. The Alprostadil Investigators, Am J Ther 1997;4:365374; Davidovic LB, Vranes MR, Lotina SI, et al. Intraarterial perfusion of prostaglandin E1 a$er lumbar sympathectomy or reconstruction on femoropopliteal segment, Int Angiol 1991;10:178-181. Gruss JD. Effects of adjuvant PGE1 therapy following profundoplasty in patients with severe limb ischemia. Early and long-term results. Vasa 1997;26:117-121. Occhionorelli S, Mascoli F, Vasquez G. Use of PGE1 in severe ischemia of the lower extremities. Clinical study, Minerva Cardioangiol 1995;43:247-256. Amendt K. PGE1 and other prostaglandins in the treatment of intermi#ent
A Journal of Clinical Medicine, Volume 11 No.3 2016
16.
17.
18.
19.
claudication: a meta-analysis, Angiology 2005;56:409-415. Cesarone MR, Belcaro G, Nicolaides AN, et al.Treatment of severe intermittent claudication: ORACLE-PGE1 short term study. A randomized 40-week study. Evaluation of efficacy and costs, Minerva Cardioangiol 2002;50:683-690. Cachovan M, Roga(i W. Improvement of peripheral and cardiopulmonary performance a$er a short-term exercise program with additive prostaglandin E1; Angiology 2001;52:381-391. Gardner AW, Afaq A. Management of lower extremity peripheral arterial. J Cardiopulm Rehabil Prev. 2008;28:349– 357; Stiegler H, Diehm C, Grom E, et al. Placebo controlled, double-blind study of the effectiveness of i.v.prostaglandin E1 in diabetic patients with stage IV arterial occlusive disease, Vasa Suppl 1992;35:164-166
MAEDICA – a Journal of Clinical Medicine 2016; 11(3):186-190
PAPER
Comparison Between Alprostadil and Iloprost in Intravenous Treatment of Patients With Chronic Peripheral Arterial Disease Dan Nicolae TESLOIANUa, Corneliu MOROSANUb, Ene-Cristian ROATAb, Laurentiu SORODOCc a
Department of Cardiology, “Sf. Spiridon” Emergency Clinical Hospital, Iasi, Romania Department of General Surgery, Regional Institute Of Oncology, Iasi, Romania c Department of Internal Medicine, “Sf. Spiridon” Emergency Clinical Hospital, Iasi, Romania b
ABSTRACT Introduction: chronic peripheral arterial disease (PAD) seems to be a “rediscovered” pathology nowadays, brought into spotlight by its strong correlation with other significant cardiovascular disorders. Objectives: to sustain a real benefit from treatment with i.v. prostaglandins (PG) in PAD patients and to directly compare the currently used PG: alprostadil and iloprost. Method: open, non-randomized cohort study, with placebo group (”classical therapy”) reviewing 615 PAD patients with therapeutic approach during 2003-2012 period, divided in 3 subgroups: “classical” therapy; ”classical” therapy + iloprost; ”classical” therapy + alprostadil; patients with Burger’s disease were excluded; multiple factor analysis with statistical results inserted. Results: clear domination of male gender patients, with older female gender patients (p≤0.001); smoking like major risk factor in male and in all patients (p< 0.0001); 124 patients underwent angiography . Conclusion: a real improvement in the clinical status of patients receiving i.v. prostaglandin therapy with no differences between genders, diabetic and non-diabetic patients; alprostadil seems be$er than iloprost. Keywords: Peripheral arterial disease, prostaglandins, iloprost, alprostadil.
BACKGROUND
C
hronic peripheral arterial disease (PAD) seems to be a “rediscovered” pathology, being strongly correlated with other significant cardiovascular disorders (1-3). Despite this, newly guidelines come with no major news: the “classical” therapy takes into account the well-known, but not spectacular in results, naftidrofuryl, pentoxifylline, L-carni-
tine, while buflomedil drops out in many countries (4,5); a salutary note is the absence of contraindication for beta blockers as associated therapy; statins can increase walking perimeter, but in indirect relationship with PAD stage; antiplateles seems to be more effective in reduction of associated cardiovascular risk than in increase of walking perimeter (6); i.v. prostaglandins had only a simple notice (near inositol and proteoglycans) like other therapies, with-
Address for correspondence: Dan Tesloianu, “Sf. Spiridon” Emergency Clinical Hospital, 1t Independentei Boulevard, Iasi, Romania E-mail: [email protected] Article received on the 15rd of June 2015. Article accepted on the 26rd of September 2016.
186
Maedica
A Journal of Clinical Medicine, Volume 11 No.3 2016
COMPARISON BETWEEN ALPROSTADIL AND ILOPROST
IN INTRAVENOUS TREATMENT OF
out conclusive results. An important note is the citation of cilostazol (100 mg twice daily) to improve pain-free walking perimeter in a 2015 update (7). OBJECTIVES
S
ustaining a significant role of i.v. PG in the treatment of PAD patients, in a study on a total number of 615 patients diagnosed and treated for PAD (stages II A-IV) in the Department of Internal Medicine – “Sf. Spiridon” Emergency Clinical Hospital Iasi, during 20032012 period. It was a cohort prospective nonrandomized open study, with placebo group (”classical therapy”). q MATHERIAL AND METHOD
S
tandard protocol for diagnosis and treatment of PAD patients in our clinic included: clinical evaluation with subsequent angiography in patients with stage III – IV (exception for patients with severe associated comorbidities or those which refused the invasive approach); in stage II B angiography was facultative (we preferred to initiate medical therapy; invasive approach only if after one-month-therapy the evolution was unfavorable). Post-angiography remained two options: by-pass surgery or conservative therapy (+/- sympathectomy ) in patients with no surgical solutions or which refuse this solution. ”Classical” therapeutic protocol included a combination between: calcium channel blockers (amlodipine 5-10 mg/day or diltiazem 120360 mg/day), antiplatelet theraphy (ASA 75150 mg/day and/ or clopidogrel 75 mg/day), LMWH (low molecular weight heparin) – fraxiparine/ enoxaparine- in therapeutic doses (in III and IV stages PAD patients), pentoxifylline extended-release 1200 mg/day, statins (simvastatin 40-80 mg/day or atorvastatin 40-80 mg/ day or rosuvastatin 20-40 mg/day) +/- ACE inhibitors (correlated with the level of systemic blood pressure – ramipril 5-10 mg/day or perindopril 5-10 mg/day or quinapril 5-20 mg/day or zofenopril 15-30 mg/day) (8-11). Non-surgical solution is dedicated for patients in II A stages, for patients in II B stages with favorable evolution under conservative therapy and for patients in stage III and IV in presence of absolute/ relative contraindication for by-pass (see above). Due to significant costs, iloprost/ alprostadil therapy was reserved for the following cases:
PATIENTS WITH CHRONIC PERIPHERAL ARTERIAL DISEASE
a. for iloprost – patients in stage II B and III with unfavorable evolution under ”classical” therapy; per primam (+/- sympathectomy) in stage IV PAD patients; b. for alprostadil – patients in stage II B with unfavorable evolution under ”classical” therapy; per primam (+/- sympathectomy) in stage III and IV PAD patients. ”Classical” therapy can be initiated and continued in hospital as well as at home. I. v. prostaglandins therapy should be best initiated in hospital, and continued at home after 5-7 days. Iloprost and alprostadil are synthetic prostaglandins analogues (PGI2/PGE1) with i.v administration and significant action in improvement of endothelial dysfunction at the micro- and macrovascular level. In women, pregnancy must be excluded before start therapy; recomandation for administration must be strictly forward. q RESULTS Tabel1. Demographic data
A.
Total number Median age (years)
Males
Females
P
569
46
≤ 0.0001
63.3+/-11.4
66.6+/-11.3
0.0007
B. Tabel 2. Presence of major cardiovascular risk factors: Risk factor
Males
Females
P
538 (94.6%)
29 (62.3%)
≤0.0001
273 (48%)
36 (78%)
0.02
Dyslipidemia
272 (47.8%)
20 (43.3%)
NS
Elevated blood pressure
304 (53.5%)
43 (48.7%)
NS
Age ≥ 55/65 years
351 (61.5%)
27 (57.6%)
NS
Familial/personal history of cardiovascular disease
380 (66.8%)
42 (91%)
0.03
Smoking Diabetes mellitus
Maedica
A Journal of Clinical Medicine, Volume 11 No.3 2016
187
COMPARISON BETWEEN ALPROSTADIL AND ILOPROST C. Tabel 3. tion of PAD
IN INTRAVENOUS TREATMENT OF
Leriche-Fontaine classifica-
Stage
Males
Females
P
IIA
174 (21.1%)
10 (11.3%)
0.065
IIB
103 (18.1%)
11 (23.9%)
NS
III
204 (34.2%)
19 (41,3%)
NS
IV
88 (14.8%)
6 (13.4%)
NS
D. Angiography: 116 males (19.5%) and 8 females (17.4%) underwent angiography. E. Evolution of conservative treatment possibilities induced the following results: • 292 patients received ”classical” initial therapy: – 184 patients (174M/10F) in stage IIA with good evolution (only 6 with deterioration over time); – 60 patients (56M/4F) in stage IIB: 39 with improvement in clinical status and regression to IIA stage, 15 with stationary evolution, remaining in IIB stage, 16 with deterioration over time; – 34 patients (28M/6F) in stage III: 16 with improvement in clinical status, 18 with deterioration over time; – 14 patients (11M/3F) in stage IV: all with severe evolution and need for amputation. • 60 patients received iloprost therapy: – 34 patients (31M/3F) in stage IIB, with spectacular evolution and increase in walking perimeter: 162 meters +/- 56 meters, after 15-20 days of treatment (p=0.008 vs. ”classical” therapy); – 19 patients (15M/4F) in stage III: all with good evolution and increase in walking distance: 138 meters +/- 42 meters after 15-20 days of treatment (some of them with associated sympathectomy) (p=0.04 vs. ”classical” therapy); – 7 patients (6M/1F) in stage IV: all with associated sympathectomy; 1 with no amputation need; 6 with low level of amputation compared to ”classical” therapy after 15-20 days of treatment (p=0.065 vs. ”classical” therapy); 188
Maedica
A Journal of Clinical Medicine, Volume 11 No.3 2016
PATIENTS WITH CHRONIC PERIPHERAL ARTERIAL DISEASE
Long term follow-up (28-38 months) shows favorable evolution, with only 2 patients needing amputation. Concerning side effects, the most unpleasant one was headache, induced especially by the maximal doses – 18 patients; most frequent adverse effect (50 from 60 patients) was skin flushing of the cephalic extremity; a rarely adverse effect was significant abdominal discomfort, in one case generating treatment stop; another unpleasant phenomenon – superficial phlebitis at the level of catheterisated veins which required frequent changing of peripheral venous catheter position was present in 23 patients; 2 patients presented shivering; dyspnea together with bibasilar pulmonary rales (non-cardiogenic incipient pulmonary edema) was present in 4 patients(11). Even if theoretically, through platelets inhibition, concomitant administration with heparin and/or antiaggregants increases the bleeding risk, we did not observed this fact in our patients. • 263 patients received alprostadil therapy: – 20 patients (15M/5F) in stage II B: immediately spectacular results, with medium increase in walking perimeter with 250 meters +/- 40 meters after 20-30 days therapy (p≤0.005 vs. iloprost); – 170 patients (161M/9F) in stage III: 142 patients with good clinical evolution and improvement in walking perimeter with 191 meters +/- 33 meters; 7 patients needed amputation (p = ns vs. iloprost); the remaining patients underwent sympatectomy followed by good evolution; – 73 patients (70M/3F) in stage IV: 32 with lesions resolution (13 with associated sympathectomy) (p=0.046 vs. iloprost); 31 needed amputation (p=0.055 vs. iloprost); 10 were revascularisated with good evolution. On long term follow-up (14-28 months) only 5 patients had a bad evolution with amputation; the other ones maintained (94 cases) or improved (164 cases) the clinical status achieved after the first approach. A remarkable phenomenon, more pregnant for alprostadil than for iloprost, is the appearance of what we have named ”clear delimitation of viable tissue” observed at PAD patients in stage III and IV. Indeed, after the first days of
COMPARISON BETWEEN ALPROSTADIL AND ILOPROST
IN INTRAVENOUS TREATMENT OF
treatment it appears a clear delimitation between the viable and non-viable tissue. So, it can be noted that the patient’s response after a few days of therapy (sometimes even after first day), could predict an accurate prognosis. Concerning the adverse effects, alprostadil is associated with significantly less side effects in comparison to iloprost treated patients: significant headache - only 2 patients (p=0.0002 vs. iloprost); abdominal discomfort with treatment cessation – 1 patient (p=0.001 vs. iloprost); superficial phlebitis at the level of catheterisated veins which required frequent changing of peripheral venous catheter position was present in 4 patients (p=0.003 vs. iloprost); 11 patients presented shivering (p=0.03 vs. iloprost); dyspnea together with bibasilar pulmonary rales (non-cardiogenic incipient pulmonary edema) was present in 10 patients (p=0.01 vs. iloprost); skin flushing of cephalic extremity was rarely observed (22 patients p=0.0001 vs. iloprost); one patient encountered severe hypotension (ns vs. iloprost). Even if theoretically, through platelets inhibition, concomitant administration with heparin and/ or antiaggregants increases the bleeding risk, we did not observed this fact in our patients, similar to those treated with iloprost. q DISCUSSSION
T
he presented results are a proof for a real hope in PAD patients with unfavorable evolution under ”classical” therapy, the outcomes being directly correlated with the initial stage of PAD. For stage IV PAD patients without surgical possibilities, the association between i.v. prostaglandins and sympathectomy seems to offer the maximum benefit (12). Our results are in general in concordance with the results of other published studies, the number of included cases allowing us pertinent
PATIENTS WITH CHRONIC PERIPHERAL ARTERIAL DISEASE
statistical analysis as well as comparison to other articles (13-19). Our study points for a better outcome for alprostadil treatment versus iloprost treatment in PAD patients, concomitantly proving a significantly better outcome of i.v. prostanglandins vs. ”classical” therapy. The results are additionally validated by the concordance between our general data and that of other studies already published: • clear domination of male gender and older female among patients; • smoking as the most important risk factor in male patients and, concomitantly, in all PAD patients (p≤0.0001); in female patients the most important risk factor is personal or family history of cardiovascular or diabetes, smoking being in the second position. q CONCLUSSION
T
he present study proves additionally benefits by combining ”classical” therapy with i.v. prostaglandins, with no significant differences in prostaglandins effects between genders or regarding presence/absence of diabetes mellitus (19). Regarding the comparison between the two currently used prostaglandins, the superiority of alprostadil versus iloprost is sustained by superior improvement in walking perimeter, quickly installed results, rarely side effects and the so-called ”clear delimitation of viable tissue” phenomenon under perfusion with alprostadil in stage III and IV PAD patients. For patients in stage IV PAD, without surgical solutions, the association between i.v. prostaglandins and sympathectomy seems to offer a maximum benefit. q Conflict of interests: none declared. Financial support: none declared.
R"#"$"%&"' 1.
2.
Creager MA, Libby P. Braunwald’s Heart Disease a Textbook of Cardiovascular Disease. 10th ed. Philadelphia: Elsevier Saunders; 2015;1312-1316. Criqui MH, Gallal W. Peripheral arterial disease – epidemiological aspects. Vascular Medicine 2001;6 (suppl 1):3-7.
3.
4.
Tesloianu D, Spiridon M, Şorodoc L, et al. Arteriopatia obliteranta a membrelor inferioare – O “Cenusareasa” a Cardiologiei. Un review a 910 cazuri. Revista Medicala Romana 2013;11-17; Tendera M, Aboyans V,Bartelink ML, et al. ESC Guidelines on the diagnosis
Maedica
5.
and treatment of peripheral artery diseases. European Heart Journal 2011;32:2851–2906. Heidrich H, Schmidt T, Fahrig C. Are there predictors for the outcome of a PGE1 treatment in peripheral arterial disease with critical limb ischaemia? Abstr. in. Vasa 2015;34:101-107.
A Journal of Clinical Medicine, Volume 11 No.3 2016
189
COMPARISON BETWEEN ALPROSTADIL AND ILOPROST 6.
Hia( WR. Preventing atherothrombotic events in peripheral arterial disease: the use of antiplatelet therapy. Journal of Internal Medicine 2002;251:193–206. 7. Yang HA. Peripheral Artery Disease (PAD) Guidelines: Screening, Lower Extremity PAD, Renal Arterial Stenosis (Updating the 2011 Guideline), 2015, h#p://emedicine.medscape.com/ article/2500033-overview. 8. Gherasim L, Dimulescu D. Gherasim L (ed): Medicina interna, vol. II, Ed. Medicala, Bucuresti 1996;1013-1023. 9. Olin JW. Buerger’s disease: in Rutherford RB (ed): Vascular Surgery 4th ed. Philadelphia: WB Saunders; 2000;350364. 10. Fiessinger JN, Schafer M. Trial of iloprost versus aspirin treatment for critical limb ischemia of trombangiitis obliterans. The TAO study, Lancet 1990;335:555-558. 11. Reisin L, Marmor A, Rabinowitz B, et
190
Maedica
12.
13.
14.
15.
IN INTRAVENOUS TREATMENT OF
PATIENTS WITH CHRONIC PERIPHERAL ARTERIAL DISEASE
al. Safety of prostaglandin E1 for the treatment of peripheral arterial occlusive disease in patients with congestive heart failure. The Alprostadil Investigators, Am J Ther 1997;4:365374; Davidovic LB, Vranes MR, Lotina SI, et al. Intraarterial perfusion of prostaglandin E1 a$er lumbar sympathectomy or reconstruction on femoropopliteal segment, Int Angiol 1991;10:178-181. Gruss JD. Effects of adjuvant PGE1 therapy following profundoplasty in patients with severe limb ischemia. Early and long-term results. Vasa 1997;26:117-121. Occhionorelli S, Mascoli F, Vasquez G. Use of PGE1 in severe ischemia of the lower extremities. Clinical study, Minerva Cardioangiol 1995;43:247-256. Amendt K. PGE1 and other prostaglandins in the treatment of intermi#ent
A Journal of Clinical Medicine, Volume 11 No.3 2016
16.
17.
18.
19.
claudication: a meta-analysis, Angiology 2005;56:409-415. Cesarone MR, Belcaro G, Nicolaides AN, et al.Treatment of severe intermittent claudication: ORACLE-PGE1 short term study. A randomized 40-week study. Evaluation of efficacy and costs, Minerva Cardioangiol 2002;50:683-690. Cachovan M, Roga(i W. Improvement of peripheral and cardiopulmonary performance a$er a short-term exercise program with additive prostaglandin E1; Angiology 2001;52:381-391. Gardner AW, Afaq A. Management of lower extremity peripheral arterial. J Cardiopulm Rehabil Prev. 2008;28:349– 357; Stiegler H, Diehm C, Grom E, et al. Placebo controlled, double-blind study of the effectiveness of i.v.prostaglandin E1 in diabetic patients with stage IV arterial occlusive disease, Vasa Suppl 1992;35:164-166
