| Applebaum et al. [17] | United States and India | Pre- and post-procedure comparison (no control group) | Atherosclerotic heart disease, age 55 ± 8 years | 18 (male, 78%) |
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Machine: Cardiomedics, Inc., Irvine, California
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2 flexible cuffs
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Cuff pressure up to a point at which the peak diastolic pressure wave reached the height of the systolic pressure wave on the finger plethysmography (150–180 mmHg for most patients)
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1 session, duration 30 min |
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History of recent lower extremity thrombophlebitis, severe ischemia, or trauma including surgical incision and amputation
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Moderate to severe aortic regurgitation
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Severe congestive heart failure
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Uncontrolled hypertension
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Uncontrolled arrhythmia
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Thrombolytic or anticoagulation agents use | Renal artery blood flow, measured every 5 minutes during and immediately after the counterpulsation with duplex ultrasonography (angle correction of ≤60°) |
| Werner et al. [18] | Germany | Pre- and post-procedure comparison (no control group) | Healthy volunteers, age 28 ± 4 years | 16 |
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Machine: Vasomedical Inc., Westbury, New York, and Cardiomedics Inc., Irvine, California
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2 cuffs (calves and thighs)
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Cuff pressure of 200 mmHg
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1 session, duration 1 h | No available data | Changes in flow volume in carotid, vertebral, hepatic, renal, and internal iliac arteries, measured by duplex ultrasonography |
| Werner et al. [19] | Germany | Pre- and post-procedure comparison in (1) cirrhotic patients and (2) healthy subjects |
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Cirrhotic patients diagnosed by hepatologists, age 54.4 ± 10.5 years
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Healthy subjects, age 23.7 ± 2.5 years | 16 cirrhotic patients and 12 healthy subjects (male, 50%) |
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Machine: Vasomedical Inc., Westbury, New York
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2 cuffs (calves and upper thighs)
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Cuff pressure of 250–300 mmHg
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1 session (performed in the early afternoon), duration 2 h |
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Aortic regurgitation
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Aortic aneurysm
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Atrial fibrillation
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Deep venous thrombosis, leg ulcer, marked peripheral edema
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INR >2 (Screened by electrocardiogram, echocardiogram, and duplex sonography of the lower extremities) |
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GFR by inulin clearance (continuous infusion)
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Renal plasma flow by aminohippurate sodium clearance (continuous infusion)
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Continuous radial artery blood pressure, monitored by vascular unloading technique
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Plasma concentrations of endothelin-1, measured by ELISA kit
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Plasma concentrations of renin, ANP, ADH, epinephrine and N-epinephrine, measured by radioimmunoassay
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Urinary volume determined every 30 min
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Urinary excretion rates of sodium and chloride, measured by flame photometry
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Urinary osmolality, measured by freezing point depression |
| Onuigbo [20] | United States | Case series | Hemodialysis patients with IDH and hypoalbuminemia refractory to conventional treatments | 3 | Using sequential compression device as a mini-EECP
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Machine: Flowtron Excel deep venous thrombosis prophylaxis system (Huntleigh Healthcare, Poland)
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Cuff pressures of 40 mmHg
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The cuff is applied to the calves throughout the hemodialysis session, and inflation of the cuffs is alternated between both calves every other minute. | Not stated |
|
| Ruangkanchanasetr et al. [21] | Thailand | Longitudinal pre- and post-procedure comparison (no control group) | Age ≥18 years with chronic stable angina and/or heart failure | 30 (male, 76.7%, chronic angina 76.7%, heart failure 23.3%) |
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Machine: Vasomedical Inc., Westbury, New York
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35 sessions of 1-h daily EECP treatment over a period of 7–8 weeks
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Cuff pressure and amount: not specify |
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Unstable angina, acute myocardial Infarction, decompensated heart failure in the preceding one month
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Undergoing coronary angiography or coronary artery bypass grafting in the preceding 1 month
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Blood pressure >180/110 mmHg
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Severe symptomatic peripheral vascular disease
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GFR <15 mL/min/1.73 m2 |
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Serum creatinine, measured by enzymatic methods
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Serum cystatin C, measured by particle-enhanced immunonephelometric assay
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Estimated GFR using combination of serum creatinine and cystatin C
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NT-proBNP, measured by a sandwich immunoassay
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Non-invasive blood pressure measurement (The median follow-up time after starting EECP treatment was 16 months) |
| Wu et al. [22] | Taiwan | Longitudinal pre- and post-procedure comparison (no control group) | Hemodialysis patients with coronary artery disease and angina refractory to medical treatment and unable or unwilling for revascularization | 36 (male, 61.3%) |
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Machine: Vasomedical Inc., Westbury, New York
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Duration of 1- or 2-h daily EECP treatment for 5 days per week to reach total of 35 h
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Cuff pressures of 260–300 mmHg to achieve mean peak diastolic augmentation of 1.6 |
|
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Angina symptom, measured by Canadian Cardiovascular Society Angina Grading scale
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Angina medications
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Myocardial perfusion, assessed by Thallium-201 imaging with pharmacological stress
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Cardiovascular events (Assess immediately after complete 35 h of EECP and 1 year after complete the therapy) |
| Zhang et al. [23] | China | Randomized, non-sham-controlled | Age >18 years undergoing a diagnostic contrast-enhanced computed tomography with estimated GFR using CKD-EPI of 60–89 mL/min/1.73 m2 | 121 (male, 62%, hypertension 56%, diabetes 27%) |
|
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Blood pressure >180/100 mmHg
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Hemorrhagic disease or bleeding tendency including INR >2
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Uncontrolled tachyarrhythmia
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Severe aortic insufficiency
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Acute heart failure
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Arterial dissection or aneurysm
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Lower-extremityvenous thrombosis
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Infection, pregnancy, thyroid disease, tumor
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Recent exposure to contrast media or nephrotoxic drugs |
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Increase of serum cystatin C ≥10% at 24th h after contrast exposure
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Iopromide contrast clearance measurement using plasma concentration of iopromide at 2nd, and 3rd h
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Conventional diagnosis of contrast-induced kidney injury using serum creatinine concentration at 48th h
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Adverse clinical events |
| Zeng et al. [24] | China | Prospective cohort, compared with active comparator (standard dose of 0.9% NaCl hydration) | Age ≥18 years with estimated GFR <60 mL/min/1.73 m2 not on dialysis; Receiving coronary angiography and percutaneous intervention | 230 (male, 76%, diabetes 36.1%, hypertension 77%, mean estimated GFR 42 mL/min/1.73 m2) | A once daily 1-h session of EECP therapy at 24 h before and 48–72 h after the intervention | (1) patients who had used iodinated contrast medium 30 d before inclusion, (2) patients with AKI due to other clear causes, (3) patients requesting withdrawal, (4) patients who failed to receive the re-examination of renal function indicators on time after surgery, (5) patients who underwent hemodialysis within 48 h after surgery, and (6) patients with uremia who received long-term hemodialysis. | Serum creatinine increase ≥0.3, ≥0.5 mg/dL or ≥25% relative to baseline value within 48–72 h after iodinated contrast exposure |