Peripheral artery disease

Peripheral artery disease

An arterial insufficiency ulcer in a person with severe peripheral artery disease
Classification and external resources
Specialty Vascular surgery
ICD-10 I73.9
ICD-9-CM 443.9
DiseasesDB 31142
MedlinePlus 000170
eMedicine med/391 emerg/862
MeSH D016491

Peripheral artery disease (PAD), also known as peripheral vascular disease (PVD), peripheral artery occlusive disease, and peripheral obliterative arteriopathy, is a narrowing of the arteries other than those that supply the heart or the brain.[1] When narrowing occurs in the heart it is called coronary artery disease while in the brain it is called cerebrovascular disease. Peripheral artery disease most commonly affects the legs, but other arteries may also be involved.[2] The classic symptom is leg pain when walking which resolves with rest, known as intermittent claudication.[3] Other symptoms including skin ulcers, bluish skin, cold skin, or poor nail and hair growth may occur in the affected leg.[4] Complications may include an infection or tissue death which may require amputation; coronary artery disease, or stroke.[2] Up to 50% of cases of PAD are without symptoms.[3]

The main risk factor is cigarette smoking.[2] Other risk factors include diabetes, high blood pressure, and high blood cholesterol.[5] The underlying mechanism is usually atherosclerosis.[6] Other causes include artery spasm.[1] PAD is typically diagnosed by finding an ankle-brachial index (ABI) less than 0.90, which is the systolic blood pressure at the ankle divided by the systolic blood pressure of the arm.[7] Duplex ultrasonography and angiography may also be used.[8] Angiography is more accurate and allows for treatment at the same time; however, it is associated with greater risks.[7]

It is unclear if screening for disease is useful as it has not been properly studied.[9][10] In those with intermittent claudication from PAD, stopping smoking and supervised exercise therapy improves outcomes.[11][12] Medications, including statins, ACE inhibitors, and cilostazol also may help.[12][13] Aspirin does not appear to help those with mild disease but is usually recommended in those with more significant disease.[14][15] Anticoagulants such as warfarin are not typically of benefit.[16] Procedures used to treat the disease include bypass grafting, angioplasty, and atherectomy.[17]

In 2010 about 202 million people had PAD worldwide.[5] In the developed world it affects about 5.3% of 45 to 50 years olds and 18.6% of 85- to 90-year-olds.[5] In the developing world it affects 4.6% of people between the ages of 45 to 50 and 15% of people between the ages of 85 to 90.[5] In the developed world PAD is equally common among men and women while in the developing world women are more commonly affected.[5] In 2013 PAD resulted in about 41,000 deaths up from 16,000 deaths in 1990.[18]

Signs and symptoms

Up to 50% of people with PAD may have no symptoms.[3] Symptoms of PAD in the legs and feet are generally divided into 2 categories:

  1. Intermittent claudication—pain in muscles when walking or using the affected muscles that is relieved by resting those muscles. This is due to the unmet oxygen demand in muscles with use in the setting of inadequate blood flow.
  2. Critical limb ischemia, consisting of:

Medical signs of PAD in the legs, due to inadequate perfusion, include:

PAD in other parts of the body depends on the organ affected. Renal artery disease can cause renovascular hypertension. Carotid artery disease can cause strokes and transient ischemic attacks.

Causes

The illustration shows how PAD can affect arteries in the legs. Figure A shows a normal artery with normal blood flow. The inset image shows a cross-section of the normal artery. Figure B shows an artery with plaque buildup that's partially blocking blood flow. The inset image shows a cross-section of the narrowed artery.

Risk factors contributing to PAD are the same as those for atherosclerosis:[19][20]

Risk factors

Peripheral arterial disease is more common in the following populations of people:[24][36]

Diagnosis

Measuring the ankle-brachial index

Upon suspicion of PAD, the first-line study is the ankle brachial pressure index (ABPI/ABI). When the blood pressure readings in the ankles is lower than that in the arms, blockages in the arteries which provide blood from the heart to the ankle are suspected. Normal ABI range of 1.00 to 1.40.The patient is diagnosed with PAD when the ABI is ≤ 0.90 . ABI values of 0.91 to 0.99 are considered ‘‘borderline’’ and values >1.40 indicate noncompressible arteries. PAD is graded as mild to moderate if the ABI is between 0.41 and 0.90, and an ABI less than 0.40 is suggestive of severe PAD. These relative categories have prognostic value.[24]

In people with suspected PAD but normal resting ABIs, exercise testing of ABI can be done. A base line ABI is obtained prior to exercise. The patient is then asked to exercise (usually patients are made to walk on a treadmill at a constant speed) until claudication pain occurs (or a maximum of 5 minutes), following which the ankle pressure is again measured. A decrease in ABI of 15%-20% would be diagnostic of PAD.[24][36]

It is possible for conditions which stiffen the vessel walls (such as calcifications that occur in the setting of long term diabetes) to produce false negatives usually, but not always, indicated by abnormally high ABIs (> 1.40). Such results and suspicions merit further investigation and higher level studies.[37]

If ABIs are abnormal the next step is generally a lower limb doppler ultrasound examination to look at site and extent of atherosclerosis. Other imaging can be performed by angiography,[19] where a catheter is inserted into the common femoral artery and selectively guided to the artery in question. While injecting a radiodense contrast agent an X-ray is taken. Any flow limiting stenoses found in the x-ray can be identified and treated by atherectomy, angioplasty or stenting. Contrast angiography is the most readily available and widely used imaging technique.

Modern multislice computerized tomography (CT) scanners provide direct imaging of the arterial system as an alternative to angiography.

Magnetic resonance angiography (MRA) is a noninvasive diagnostic procedure that uses a combination of a large magnet, radio frequencies, and a computer to produce detailed images to provide pictures of blood vessels inside the body. The advantages of MRA include its safety and ability to provide high-resolution three-dimensional (3D) imaging of the entire abdomen, pelvis and lower extremities in one sitting.[38][39]

Classification

Peripheral artery occlusive disease is commonly divided in the Fontaine stages, introduced by René Fontaine in 1954 for chronic limb ischemia:[36][40]

  • Stage IIA: Claudication when walking a distance of greater than 200 meters
  • Stage IIB: Claudication when walking a distance of less than 200 meters

A classification introduced by Robert B. Rutherford in 1986 and revised in 1997 consists of four grades and seven categories:[36][41]

The TASC (and TASC II) classification suggested PAD treatment by severity of disease seen on angiogram.[36] More recently classifications, such as the Society for Vascular Surgery "Wound, Ischemia and Foot Infection" (WIFI) classification, take into account that ischemia and angiographic disease patterns are not the only determinants of amputation risk.[42]

Screening

It is not clear if screening for disease is useful as it has not been properly studied.[9]

Treatment

Depending on the severity of the disease, the following steps can be taken, according to the following guidelines:[43]

Lifestyle changes

Medication

Cilostazol or pentoxifylline can improve symptoms in some.[44][45]

Treatment with other drugs or vitamins are unsupported by clinical evidence, "but trials evaluating the effect of folate and vitamin B-12 on hyperhomocysteinemia, a putative vascular risk factor, are near completion".[43]

Revascularization

After a trial of the best medical treatment outline above, if symptoms persist, patients may be referred to a vascular or endovascular surgeon. The benefit of revascularization is thought to correspond to the severity of ischemia and the presence of other risk factors for limb loss such as wound and infection severity.[42]

Guidelines

An updated consensus guideline from the American College of Cardiology and American Heart Association for the diagnosis and treatment of lower extremity, renal, mesenteric and abdominal aortic PAD was compiled in 2013, combining the 2005 and 2011 guidelines.[24]

Prognosis

Individuals with PAD have an "exceptionally elevated risk for cardiovascular events and the majority will eventually die of a cardiac or cerebrovascular etiology";[51] prognosis is correlated with the severity of the PAD as measured by the Ankle brachial pressure index (ABPI).[51] Large-vessel PAD increases mortality from cardiovascular disease significantly. PAD carries a greater than "20% risk of a coronary event in 10 years".[51]

There is a low risk that an individual with claudication will develop severe ischemia and require amputation, but the risk of death from coronary events is three to four times higher than matched controls without claudication.[43] Of patients with intermittent claudication, only "7% will undergo lower extremity bypass surgery, 4% major amputations, and 16% worsening claudication", but stroke and heart attack events are elevated, and the "5-year mortality rate is estimated to be 30% (versus 10% in controls)".[51]

Epidemiology

The prevalence of peripheral artery disease in the general population is 12–14%, affecting up to 20% of those over 70;[51] 70%–80% of affected individuals are asymptomatic; only a minority ever require revascularisation or amputation. Peripheral artery disease affects 1 in 3 diabetics over the age of 50.

In the USA peripheral arterial disease affects 12–20 percent of Americans age 65 and older. Approximately 10 million Americans have PAD. Despite its prevalence and cardiovascular risk implications, only 25 percent of PAD patients are undergoing treatment.

The incidence of symptomatic PAD increases with age, from about 0.3% per year for men aged 40–55 years to about 1% per year for men aged over 75 years. The prevalence of PAD varies considerably depending on how PAD is defined, and the age of the population being studied. Diagnosis is critical, as people with PAD have a four to five times higher risk of heart attack or stroke.

The Diabetes Control and Complications Trial, and the U.K. Prospective Diabetes Study trials, in people with type 1 and type 2 diabetes, respectively, demonstrated that glycemic control is more strongly associated with microvascular disease than macrovascular disease. It may be that pathologic changes occurring in small vessels are more sensitive to chronically elevated glucose levels than is atherosclerosis occurring in larger arteries.[52]

Research

In those who have developed critically poor blood flow to the legs it is unclear if autotransplantation of autologous mononuclear cells is useful or not.[53]

Only one randomized controlled trial has been conducted comparing vascular bypass to angioplasty for the treatment of severe PAD.[54] The trial found no difference in amputation-free survival between vascular bypass and angioplasty at the planned clinical endpoint, however the trial has been criticized as being underpowered, limiting endovascular options, and comparing inappropriate endpoints.[55] As of 2015, a second trial is being conducted regarding the optimal revascularization for severe PAD.[56]

In 2011 pCMV-vegf165 was registered in Russia as the first-in-class gene therapy drug for treatment of peripheral artery disease, including the advanced stage of critical limb ischemia.[57][58]

See also

References

  1. 1 2 "What Is Peripheral Vascular Disease?" (PDF). https://www.heart.org. 2012. Retrieved 26 February 2015. External link in |website= (help)
  2. 1 2 3 "What Is Peripheral Arterial Disease?". http://www.nhlbi.nih.gov/. August 2, 2011. Retrieved 25 February 2015. External link in |website= (help)
  3. 1 2 3 Violi, F; Basili, S; Berger, JS; Hiatt, WR (2012). "Antiplatelet therapy in peripheral artery disease.". Handbook of experimental pharmacology (210): 547–63. doi:10.1007/978-3-642-29423-5_22. PMID 22918746.
  4. ↑ "What Are the Signs and Symptoms of Peripheral Arterial Disease?". http://www.nhlbi.nih.gov/. August 2, 2011. Retrieved 26 February 2015. External link in |website= (help)
  5. 1 2 3 4 5 Fowkes, FG; Rudan, D; Rudan, I; Aboyans, V; Denenberg, JO; McDermott, MM; Norman, PE; Sampson, UK; Williams, LJ; Mensah, GA; Criqui, MH (19 October 2013). "Comparison of global estimates of prevalence and risk factors for peripheral artery disease in 2000 and 2010: a systematic review and analysis.". Lancet 382 (9901): 1329–40. doi:10.1016/s0140-6736(13)61249-0. PMID 23915883.
  6. ↑ "What Causes Peripheral Arterial Disease?". http://www.nhlbi.nih.gov/. August 2, 2011. Retrieved 26 February 2015. External link in |website= (help)
  7. 1 2 Ruiz-Canela, M; Martínez-González, MA (2014). "Lifestyle and dietary risk factors for peripheral artery disease.". Circulation journal : official journal of the Japanese Circulation Society 78 (3): 553–9. doi:10.1253/circj.cj-14-0062. PMID 24492064.
  8. ↑ "How Is Peripheral Arterial Disease Diagnosed?". August 2, 2011. Retrieved 27 March 2015.
  9. 1 2 Andras, A; Ferket, B (Apr 7, 2014). "Screening for peripheral arterial disease". The Cochrane database of systematic reviews 4: CD010835. doi:10.1002/14651858.CD010835.pub2. PMID 24711093.
  10. ↑ U.S. Preventive Services Task Force (Dec 15, 2014). "Peripheral artery disease screening and cardiovascular disease risk assessment with the ankle-brachial index in adults: recommendation statement.". Am Fam Physician. 90 (12): 858A–858D. PMID 25591190.
  11. ↑ Fokkenrood, HJ; Bendermacher, BL; Lauret, GJ; Willigendael, EM; Prins, MH; Teijink, JA (23 August 2013). "Supervised exercise therapy versus non-supervised exercise therapy for intermittent claudication.". The Cochrane database of systematic reviews 8: CD005263. doi:10.1002/14651858.CD005263.pub3. PMID 23970372.
  12. 1 2 Hankey, GJ; Norman, PE; Eikelboom, JW (1 February 2006). "Medical treatment of peripheral arterial disease.". JAMA 295 (5): 547–53. doi:10.1001/jama.295.5.547. PMID 16449620.
  13. ↑ Bedenis, R; Stewart, M; Cleanthis, M; Robless, P; Mikhailidis, DP; Stansby, G (31 October 2014). "Cilostazol for intermittent claudication.". The Cochrane database of systematic reviews 10: CD003748. doi:10.1002/14651858.CD003748.pub4. PMID 25358850.
  14. ↑ Lin, JS; Olson, CM; Johnson, ES; Whitlock, EP (3 September 2013). "The ankle-brachial index for peripheral artery disease screening and cardiovascular disease prediction among asymptomatic adults: a systematic evidence review for the U.S. Preventive Services Task Force.". Annals of internal medicine 159 (5): 333–41. doi:10.7326/0003-4819-159-5-201309030-00007. PMID 24026319.
  15. ↑ Poredos, P; Jezovnik, MK (March 2013). "Is aspirin still the drug of choice for management of patients with peripheral arterial disease?". VASA. Zeitschrift fur Gefasskrankheiten 42 (2): 88–95. doi:10.1024/0301-1526/a000251. PMID 23485835.
  16. ↑ Hauk, L (15 May 2012). "ACCF/AHA update peripheral artery disease management guideline.". American family physician 85 (10): 1000–1. PMID 22612053.
  17. ↑ "How Is Peripheral Arterial Disease Treated?". http://www.nhlbi.nih.gov. August 2, 2011. Retrieved 26 February 2015. External link in |website= (help)
  18. ↑ GBD 2013 Mortality and Causes of Death, Collaborators (17 December 2014). "Global, regional, and national age-sex specific all-cause and cause-specific mortality for 240 causes of death, 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013.". Lancet 385 (9963): 117–71. doi:10.1016/S0140-6736(14)61682-2. PMC 4340604. PMID 25530442.
  19. 1 2 3 Peripheral Arterial Disease at Merck Manual of Diagnosis and Therapy Professional Edition. Retrieved August 9, 2010.
  20. 1 2 Joosten MM, Pai JK, Bertoia ML, Rimm EB, Spiegelman D, Mittleman MA, Mukamal KJ (Oct 2012). "Associations between conventional cardiovascular risk factors and risk of peripheral artery disease in men". JAMA 308 (16): 1660–7. doi:10.1001/jama.2012.13415. PMID 23093164.
  21. ↑ Price J, Mowbray P, Lee A, Rumley A, Lowe G, Fowkes F (1999). "Relationship between smoking and cardiovascular risk factors in the development of peripheral arterial disease and coronary artery disease; Edinburgh Artery Study Edinburgh Artery Study". European heart journal 20 (5): 344–353. doi:10.1053/euhj.1998.1194.
  22. ↑ Smith GD, Shipley M, Rose G (1990). "Intermittent claudication, heart disease risk factors, and mortality. The Whitehall Study". Circulation 82 (6): 1925–1931. doi:10.1161/01.cir.82.6.1925.
  23. ↑ Cole C, Hill G, Farzad E, Bouchard A, Moher D, Rody K, Shea B (1993). "Cigarette smoking and peripheral arterial occlusive disease". Surgery 114 (4): 753.
  24. 1 2 3 4 5 Rooke, TW; Hirsch, AT; Misra, S; Sidawy, AN; Beckman, JA; Findeiss, L; Golzarian, J; Gornik, HL; Jaff, MR; Moneta, GL; Olin, JW; Stanley, JC; White, CJ; White, JV; Zierler, RE; American College of Cardiology Foundation Task, Force; American Heart Association Task, Force (9 April 2013). "Management of patients with peripheral artery disease (compilation of 2005 and 2011 ACCF/AHA Guideline Recommendations): a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines.". Journal of the American College of Cardiology 61 (14): 1555–70. doi:10.1016/j.jacc.2013.01.004. PMID 23473760.
  25. ↑ Kannel WB, McGee D (1979). "Diabetes and glucose tolerance as risk factors for cardiovascular disease: the Framingham study". Diabetes Care 2 (2): 120–126. doi:10.2337/diacare.2.2.120.
  26. ↑ Creager MA, Lüscher TF, Cosentino F, Beckman JA (2003). "Diabetes and vascular disease pathophysiology, clinical consequences, and medical therapy: part I.". Circulation 108 (12): 1527–1532. doi:10.1161/01.cir.0000091257.27563.32.
  27. ↑ Lüscher TF, Creager MA, Beckman JA, Cosentino F (2003). "Diabetes and vascular disease pathophysiology, clinical consequences, and medical therapy: Part II.". Circulation 108 (13): 1655–1661. doi:10.1161/01.cir.0000089189.70578.e2.
  28. ↑ Beks P, Mackaay A, De Neeling J, De Vries H, Bouter L, Heine R: Peripheral arterial disease in relation to glycaemic level in an elderly Caucasian population: the Hoorn study. Diabetologia 1995, 38(1):86-96.
  29. ↑ Unit ES: Efficacy and safety of cholesterol-lowering treatment: prospective meta-analysis of data from 90 056 participants in 14 randomised trials of statins. Lancet 2005, 366:1267-1278.
  30. ↑ Kannel W, McGee D (1985). "Update on some epidemiologic features of intermittent claudication: the Framingham Study". Journal of the American Geriatrics Society 33 (1): 13.
  31. ↑ Selvin E, Erlinger TP: Prevalence of and risk factors for peripheral arterial disease in the united states results from the national health and nutrition examination survey, 1999–2000. Circulation 2004, 110(6):738-743.
  32. ↑ Hooi JD, Kester AD, Stoffers HE, Overdijk MM, van Ree JW, Knottnerus JA (2001). "Incidence of and risk factors for asymptomatic peripheral arterial occlusive disease: a longitudinal study". American Journal of Epidemiology 153 (7): 666–672. doi:10.1093/aje/153.7.666. PMID 11282794.
  33. ↑ Allison MA, Denenberg JO, Criqui MH (2011). "Family History of Peripheral Artery Disease Is Associated With Prevalence and Severity of Peripheral Artery Disease". Journal of the American College of Cardiology 58 (13): 1386–92. doi:10.1016/j.jacc.2011.06.023. PMID 21920269.
  34. ↑ Valentine RJ, Guerra R, Stephan P, Scoggins E, Clagett GP, Cohen J (2004). "Family history is a major determinant of subclinical peripheral arterial disease in young adults". Journal of vascular surgery 39 (2): 351–356. doi:10.1016/j.jvs.2003.07.011.
  35. ↑ Ridker PM, Stampfer MJ, Rifai N (2001). "Novel risk factors for systemic atherosclerosis". JAMA: the journal of the American Medical Association 285 (19): 2481–2485. doi:10.1001/jama.285.19.2481.
  36. 1 2 3 4 5 TASC II Guidelines
    * Norgren L, Hiatt WR, Dormandy JA; Hiatt; et al. (2007). "Inter-Society Consensus for the Management of Peripheral Arterial Disease (TASC II)". Eur J Vasc Endovasc Surg. 33 (Suppl 1): S1–75. doi:10.1016/j.ejvs.2006.09.024. PMID 17140820.
    * Norgren L, Hiatt WR, Dormandy JA, TASC II Working Group, et al. (2007). "Inter-Society Consensus for the Management of Peripheral Arterial Disease (TASC II)". J Vasc Surg. 45 (Suppl S): S5–67. doi:10.1016/j.jvs.2006.12.037. PMID 17223489.
    * Norgren L, Hiatt WR, Dormandy JA (2007). "Inter-Society Consensus for the Management of Peripheral Arterial Disease". Int Angiol. 26 (2): 81–157. PMID 17489079.
  37. ↑ Vowden P, Vowden K (March 2001). "Doppler assessment and ABPI: Interpretation in the management of leg ulceration". Worldwide Wounds. - describes ABPI procedure, interpretation of results, and notes the somewhat arbitrary selection of "ABPI of 0.8 has become the accepted endpoint for high compression therapy, the trigger for referral for a vascular surgical opinion and the defining upper marker for an ulcer of mixed aetiology"
  38. ↑ Leiner T, Kessels AG, Nelemans PJ, Vasbinder GB, de Haan MW, Kitslaar PE, Ho KY, Tordoir JH, van Engelshoven JM699-708; Kessels; Nelemans; Vasbinder; De Haan; Kitslaar; Ho; Tordoir; Van Engelshoven (May 2005). "Peripheral arterial disease: comparison of color duplex US and contrast-enhanced MR angiography for diagnosis". Radiology 235 (2): 699–708. doi:10.1148/radiol.2352040089. PMID 15858107.
  39. ↑ Leiner, T (February 2005). "Magnetic resonance angiography of abdominal and lower extremity vasculature". Top Magn Reson Imaging 16 (1): 21–66. doi:10.1097/01.rmr.0000185431.50535.d7. PMID 16314696.
  40. ↑ Fontaine R, Kim M, Kieny R; Kim; Kieny (1954). "Die chirugische Behandlung der peripheren Durchblutungsstörungen. (Surgical treatment of peripheral circulation disorders)". Helvetica Chirurgica Acta (in German) 21 (5/6): 499–533. PMID 14366554.
  41. ↑ Rutherford, Robert B.; Baker, J. Dennis; Ernst, Calvin; Johnston, K. Wayne; Porter, John M.; Ahn, Sam; Jones, Darrell N. (September 1997). "Recommended standards for reports dealing with lower extremity ischemia: Revised version". Journal of Vascular Surgery 26 (3): 517–538. doi:10.1016/S0741-5214(97)70045-4. PMID 9308598.
  42. 1 2 Mills JL, Sr; Conte, MS; Armstrong, DG; Pomposelli, FB; Schanzer, A; Sidawy, AN; Andros, G; Society for Vascular Surgery Lower Extremity Guidelines, Committee (January 2014). "The Society for Vascular Surgery Lower Extremity Threatened Limb Classification System: risk stratification based on wound, ischemia, and foot infection (WIfI).". Journal of vascular surgery 59 (1): 220–34.e1–2. doi:10.1016/j.jvs.2013.08.003. PMID 24126108.
  43. 1 2 3 Burns P, Gough S, Bradbury AW; Gough; Bradbury (March 2003). "Management of peripheral arterial disease in primary care". BMJ 326 (7389): 584–8. doi:10.1136/bmj.326.7389.584. PMC 1125476. PMID 12637405.
  44. ↑ Robless P, Mikhailidis DP, Stansby GP; Mikhailidis; Stansby (2008). Robless, Peter, ed. "Cilostazol for peripheral arterial disease". Cochrane Database Syst Rev (1): CD003748. doi:10.1002/14651858.CD003748.pub3. PMID 18254032.
  45. ↑ Salhiyyah, Kareem; Senanayake, Eshan; Abdel-Hadi, Mohammed; Booth, Andrew; Michaels, Jonathan A (2012). Salhiyyah, Kareem, ed. "Pentoxifylline for intermittent claudication". Cochrane Database of Systematic Reviews (Systematic Review) 1: CD005262. doi:10.1002/14651858.CD005262.pub2. PMID 22258961.
  46. ↑ Fowkes FG, Gillespie IN; Gillespie (2000). Fowkes, Gerry, ed. "Angioplasty (versus non surgical management) for intermittent claudication". Cochrane Database Syst Rev (2): CD000017. doi:10.1002/14651858.CD000017. PMID 10796469.
  47. ↑ Twine CP, Coulston J, Shandall A, McLain AD; Coulston; Shandall; McLain (2009). Twine, Christopher P, ed. "Angioplasty versus stenting for superficial femoral artery lesions". Cochrane Database Syst Rev (2): CD006767. doi:10.1002/14651858.CD006767.pub2. PMID 19370653.
  48. ↑ Johnston KW, Rae M, Hogg-Johnston SA, Colapinto RF, Walker PM, Baird RJ, Sniderman KW, Kalman P (1987). "5-year results of a prospective study of percutaneous transluminal angioplasty". Annals of surgery 206 (4): 403–413. doi:10.1097/00000658-198710000-00002.
  49. ↑ Emmerich J (2005). "Current state and perspective on medical treatment of critical leg ischemia: gene and cell therapy". The international journal of lower extremity wounds 4 (4): 234–241. doi:10.1177/1534734605283538.
  50. ↑ Ambler, GK; Radwan, R; Hayes, PD; Twine, CP (17 March 2014). "Atherectomy for peripheral arterial disease.". The Cochrane database of systematic reviews 3: CD006680. doi:10.1002/14651858.CD006680.pub2. PMID 24638972.
  51. 1 2 3 4 5 Shammas NW (2007). "Epidemiology, classification, and modifiable risk factors of peripheral arterial disease". Vasc Health Risk Manag 3 (2): 229–34. doi:10.2147/vhrm.2007.3.2.229. PMC 1994028. PMID 17580733.
  52. ↑ Selvin E, Wattanakit K, Steffes MW, Coresh J, Sharrett AR; Wattanakit; Steffes; Coresh; Sharrett (April 2006). "HbA1c and peripheral arterial disease in diabetes: the Atherosclerosis Risk in Communities study". Diabetes Care 29 (4): 877–82. doi:10.2337/diacare.29.04.06.dc05-2018. PMID 16567831.
  53. ↑ Moazzami, K; Moazzami, B; Roohi, A; Nedjat, S; Dolmatova, E (19 December 2014). "Local intramuscular transplantation of autologous mononuclear cells for critical lower limb ischaemia.". The Cochrane database of systematic reviews 12: CD008347. doi:10.1002/14651858.CD008347.pub3. PMID 25525690.
  54. ↑ "Bypass versus angioplasty in severe ischaemia of the leg (BASIL): multicentre, randomised controlled trial.". Lancet 366: 1925–34. Dec 2005. doi:10.1016/S0140-6736(05)67704-5. PMID 16325694.
  55. ↑ Conte, MS (May 2010). "Bypass versus Angioplasty in Severe Ischaemia of the Leg (BASIL) and the (hoped for) dawn of evidence-based treatment for advanced limb ischemia.". Journal of vascular surgery 51 (5 Suppl): 69S–75S. doi:10.1016/j.jvs.2010.02.001. PMID 20435263.
  56. ↑ Menard, MT; Farber, A (March 2014). "The BEST-CLI trial: a multidisciplinary effort to assess whether surgical or endovascular therapy is better for patients with critical limb ischemia.". Seminars in vascular surgery 27 (1): 82–84. doi:10.1053/j.semvascsurg.2015.01.003. PMID 25812762.
  57. ↑ "Gene Therapy for PAD Approved". 6 December 2011. Retrieved 5 August 2015.
  58. ↑ Deev, R.; Bozo, I.; Mzhavanadze, N.; Voronov, D.; Gavrilenko, A.; Chervyakov, Yu.; Staroverov, I.; Kalinin, R.; Shvalb, P.; Isaev, A. (13 March 2015). "pCMV-vegf165 Intramuscular Gene Transfer is an Effective Method of Treatment for Patients With Chronic Lower Limb Ischemia". Journal of cardiovascular pharmacology and therapeutics 20: 473–82. doi:10.1177/1074248415574336. PMID 25770117. Retrieved 5 August 2015.

External links

This article is issued from Wikipedia - version of the Thursday, February 04, 2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.