4.2. Procedure Data and Technical Success
Technical success of performing the procedure was 100%. All 47 patients underwent angiography via common femoral artery (CFA) and access method was antegrade in 41 (87.2%). One technical failure due to diffuse atherosclerosis and unsuccessful placement of guide wire was reported. In 97.2%, initial technical success was obtained.
The most frequent angioplasty location was anterior tibial artery (ATA) performed in 33 patients (70.2%) and then the tibioperoneal trunk performed in 19 patients (40.4%) (
Table 3). Isolated ATA angioplasty was performed in 36 % but concurrent multi vessel intervention was performed in 64%. In six patients, concurrent femoropopliteal involvement was seen in whom angioplasty was done. There was no major complication during and after the procedure. The most frequent minor complication was hematoma seen in five patients (10.6%). They did not need any intervention.
| Angiography Characteristics | No. (%) |
|---|
| Access | |
| Retrograde | 41 (87.2) |
| Antegrade | 6 (12.8) |
| Angioplasty location | |
| Anterior tibial artery | 33 (70.2) |
| Posterior tibial artery | 18 (38.3) |
| Peroneal artery | 15 (31.9) |
| Tibioperoneal trunk | 19 (40.4) |
| Concurrent femoropopliteal | 6 (12.8) |
| Minor complication | |
| Hematoma | 5 (10.6) |
| Pseudoaneurysm | 1 (2.1) |
| Arterial spasm | 2 (4.3) |
4.3. Clinical Outcome and Follow up Data
Mean follow up time was 9.7 ± 6.6 months (1 - 30). Mean ABI 6 months after the procedure was 0.68 ± 0.12 (0.4 - 0.9). Among the patients with data of ABI before and 6 months after the procedure, the mean improvement of ABI was 0.17 ± 0.11 (0 - 0.5) (change from 0.51 ± 0.08 to 0.68 ± 0.12) (P < 0.001). Improved ABI ( > 0.1) was detected in 78% of patients (primary clinical success).
Among 14 patients with rest pain at the beginning of the study, for 12 patients we had data for evaluation of rest pain after 3 and 6 months. Among these patients, eight (66.7%) reported complete improvement of rest pain and the others reported relative rest pain improvement (four patients, 33.3%). Therefore, all patients reported improvement in rest pain 3 and 6 months after the procedure (P < 0.001). Pain improvement was statistically similar in different TASC classes and pain improvement was not different between two groups of TASC [A,B] vs. [C,D] patients (P = 0.58). Clinical results of pain improvement after 6 months was similar to 3 months follow up data. Among 11 patients with pain improvement after 6 months, eight reported complete improvement (72.7%) and three reported improvement in rest pain (27.3%). Thus, all patients reported improvement after 6 months (P < 0.001) and the pattern of improvement was not statistically different between TASC groups of [A,B] vs. [C,D] patients (P = 0.9) (
Table 4).
| Baseline | 3-Month follow-up | 6-Month follow-up | 12-Month follow-up |
|---|
| Rest pain | N = 14 (29.8) | N = 12 | N = 11 | |
| Complete improvement | Relative improvement | Complete improvement | Relative improvement | |
| 8 (66.7) | 4 (33.3) | 8 (72.7) | 3 (27.3) | |
| P < 0.001 | P < 0.001 | |
| Rest pain improvement in different TASC subgroups | Rest pain improvement in different TASC subgroups | |
| TASC [A,B] | TASC [C,D] | TASC [A,B] | TASC [C,D] | |
| 5/5 (100) | 7/7 (100) | 5/5 (100) | 6/6 (100) | |
| P > 0.9 | P > 0.9 | |
| Claudication | N = 35 (74.5) | N = 32 | N = 28 | N = 12 |
| Complete improve | Relative improve | Stable disease | Worsening | Complete improve | Relative improve | Stable disease | Worsening | Complete improve | Relative improve | Stable disease | Worsening |
| 14 (43.8) | 10 (31.3) | 6 (18.8) | 2 (6.3) | 16 (57.1) | 7 (25) | 4 (14.3) | 1 (3.6) | 9 (75) | 2 (16.7) | 1 (8.3) | |
| P < 0.001 | P < 0.001 | P < 0.001 |
| Claudication improvement in different TASC subgroups | Claudication improvement in different TASC subgroups | Claudication improvement in different TASC subgroups |
| TASC [A,B] | TASC [C,D] | TASC [A,B] | TASC [C,D] | TASC [A,B] | TASC [C,D] |
| 13/16 (81.3) | 11/16 (68.8) | 11/15 (73.3) | 12/13 (92.3) | 5/6 (83.3) | 6/6 (100) |
| P = 0.69 | P = 0.33 | P = 0.9 |
| Chronic ulcer | N = 37 (78.7) | N = 29 | N = 25 | N = 12 |
| Complete improvement | Relative improvement | Stable disease | Worsening | Complete improvement | Relative improvement | Stable disease | Worsening | Complete improvement | Relative improvement | Stable disease | Worsening |
| 7 (24.1) | 13 (44.8) | 7 (24.1) | 2 (6.9) | 8 (32) | 15 (60) | 0 (0) | 2 (8) | 4 (33.3) | 6 (50) | 1 (8.3) | 1 (8.3) |
| P < 0.001 | P < 0.001 | P < 0.001 |
| Chronic ulcer improvement in different TASC subgroups | Chronic ulcer improvement in different TASC subgroups | Chronic ulcer improvement in different TASC subgroups |
| TASC [A,B] | TASC [C,D] | TASC [A,B] | TASC [C,D] | TASC [A,B] | TASC [C,D] |
| 10/13 (76.9) | 10/16 (62.5) | 11/12 (91.7) | 12/13 (92.3) | 5/7 (71.4) | 5/5 (100) |
| P = 0.45 | P = 0.9 | P = 0.47 |
Abbreviation: TASC, transatlantic intersociety characteristics
a Values are expressed as No. (%).
Among 35 patients with claudication before angioplasty, the data of 32 were available after 3 months. Among them, 14 reported complete improvement (43.8%) (P < 0.001) and 10 reported relative improvement (31.3%). Thus, totally 24 patients experienced improvement in claudication (P < 0.001). Among the remaining eight patients, six reported no change in their claudication (18.8%) and only two patients (6.2%) experienced worsening of claudication. Totally, 28 of these patients completed 6 month follow up; in which, 16 (57%) reported complete and seven (25%) reported relative improvement (P < 0.001). Among 12 patients with one-year follow up, 11 reported improvement (91.7%, nine complete, and two relative) (P < 0.001). Claudication improvement was not statistically different among TASC [A,B] group vs. TASC [C,D] group after 3, 6 and 12 months follow up (all Ps > 0.3) (
Table 4).
Among 37 patients with chronic ulcer, 29 completed 3 month follow up of whom seven (24.1%) reported complete ulcer healing and 13 (44.8%) experienced relative ulcer healing [P < 0.02]. Seven patients (24.1%) showed no improvement in ulcer and two (6.9%) showed deterioration in their ulcer. These figures were 8 (32%), 15 (60%) and two (8%) for complete improvement, relative improvement and worsening of ulcer, respectively in 6 month follow up [P < 0.001 for improvement in 6 months] Again, frequency of ulcer improvement was not statistically different between TASC group of [A,B] vs. [C,D] in all follow up sessions [Ps > 0.45] (
Table 4).
Restenosis occurred in four patients who underwent angioplasty and stent placement. We had major amputation in nine patients (19.1%) that was above the knee in two patients. Mean amputation time was 2.5 ± 2 months after the procedure (range: 20 days-5 month). In two patients, amputations were performed in the first month after angioplasty and in one patient, acute ischemia and thrombosis of ATA occurred immediately after the procedure, that despite repeated angioplasty, amputation was unavoidable. No amputation occurred in TASC A patients, one amputation in TASC B patients (6.3%), five in TASC C patients (29.4%) and three in TASC D patients (30%) (P = 0.059 for comparing group [A,B] vs. [C,D]). Mean amputation time in patients with TASC [C,D] was 2.7 ± 2 months. Comparing the survival pattern of amputation in two TASC groups of [A,B] vs. [C,D] using log rank test showed a statistical significant difference between these groups (P = 0.04). Primary patency was finally estimated as 76.1.
Mortality rate was 25.5% (12 cases). The leading causes of death were myocardial infarction (MI) and sepsis. Each of them were responsible for death in three patients. Other causes were liver failure, renal failure and miscellaneous causes. Mean death time was 4.8 ± 3.7 months after the procedure (range: 1 - 12 months). Overall survival in one year was 74.5%. Two related mortalities occurred due to ischemia deterioration, tissue loss, limb gangrene and sepsis as a consequence. Six mortalities occurred in patients who underwent amputation. No death occurred in TASC A patients, three in TASC B patients (18.8%), four in TASC C patients (23.5%), and five in TASC D patients (50%) (P = 0.18). Mean mortality time in patients with TASC [A,B] was 6.7 ± 5.5 months and it was 4.1 ± 3 months in TASC [C,D] group (P = 0.7). Comparing survival pattern of death in two TASC groups of [A,B] vs. [C,D] using log rank test showed no statistical significant difference between these groups (P = 0.04). Primary patency was finally estimated as 76.1%.