Lowering iodinated contrast concentration in infrainguinal endovascular interventions: a three-armed randomized controlled non-inferiority trial.

OBJECTIVES: To determine the influence of lowering iodinated contrast concentration on confidence of interventional radiologists in diagnosing and treating lesions during endovascular interventions in patients with symptomatic peripheral arterial disease (PAD).
METHODS: A randomized controlled non-inferiority trial was performed in 60 patients. Intervention was performed with contrast concentrations (in mg of iodine per mL, mgI/mL) of 300 (standard), 240, or 140 mgI/mL. Primary outcome was confidence (score 0-100 %) of radiologists in diagnosing and treating arterial lesions. Secondary outcomes were procedural iodine load and image quality (i.e. non-diagnostic, limited, diagnostic, exemplary).
RESULTS: Median confidence scores in diagnosing lesions were 100 % (range 81-100 %) for the 300 group (n = 21), 100 % (range 82-100 %) for the 240 group (n = 19), and 100 % (range 91-100 %) for the 140 group (n = 20) (both p = 1.00 compared to the 300 group). Median scores for treating lesions in the 240 and 140 groups, 100 % (range 79-100 %, p = 0.40), and 100 % (range 63-100 %, p = 0.25), respectively, were not lower compared to the 300 group (median 100 %, range 78-100 %). Procedural iodine load was lower in the 240 (24.3 ± 7.6 g, p = 0.022) and 140 groups (17.8 ± 5.6 g, p < 0.001) compared to the 300 group (29.7 ± 6.3 g). Image quality was diagnostic for all groups.
CONCLUSION: Using iodine contrast of 140 mgI/mL for diagnosis and interventions in PAD patients significantly reduces administered iodine load without compromising image quality. Future use of lower iodine dose is recommended. KEY POINTS: • Lower iodinated contrast concentration during endovascular intervention does not decrease radiologist's confidence. • Image quality of standardized angiographies remains diagnostic using 140 mgI/mL iodinated contrast concentration. • Iodine load during intervention can be decreased by >40 % when using 140 mgI/mL. • Implementing the use of a lower iodinated contrast concentration will reduce the costs of the procedure.

RCT Entities:   Population Interventions Outcomes

Introduction

The use of intravascular iodinated contrast media carries a risk of contrast-induced nephropathy (CIN), which is associated with an increase in morbidity and mortality [1]. CIN can be defined as an impairment in renal function, i.e. an increase in serum creatinine by more than 25 % or 44 μmol/L, occurring within 3 days following intravascular contrast administration without an alternative aetiology [2]. The incidence of CIN is low in patients with a normal renal function, but can be as high as 25 % in patients with impaired renal function, especially secondary to diabetes mellitus [3].

Patients with intermittent claudication (IC) or critical limb ischemia (CLI) due to peripheral arterial disease (PAD), often have several risk factors for developing CIN after an endovascular intervention. To prevent CIN in high risk patients, hydration using saline or bicarbonate is recommended, but based on the consensus of experts and small or retrospective studies [1]. Other strategies, such as N-acetylcysteine [4] or statin pretreatment [5], are also accepted approaches to prevention of CIN, though not evidence-based.

In the 1980s and 1990s, many studies were performed on finding the right contrast medium and concentration [6, 7]. In 1992, Ugolotti et al showed that with concentrations of 150 mg iodine per mL (mgI/mL) adequate images of the lower limb could be acquired [8]. With improved technical specifications for angiographic equipment achieved during the last few decades, such as a higher image resolution, lowering the iodinated contrast concentration might be an appropriate way to prevent CIN, especially since a higher volume use of iodinated contrast is associated with the risk of CIN [9]. Currently, many interventional radiologists use a contrast concentration of about 300 mg iodine per mL (mgI/mL) for lower limb angiography and interventions. Lowering this concentration might compromise the image quality, especially in patients with CLI and multi-level disease.

The aim of this study was to compare the confidence of interventional radiologists in performing an endovascular intervention in patients with PAD between three different concentrations of iodinated contrast.

Materials and methods

This trial was reported according to the extended Consolidated Standards of Reporting Trials (CONSORT) 2010 statement [10]. This trial was registered in advance at www.trialregister.nl (trial identification NTR3406). Ethical approval was obtained from the local ethics committee.

Trial design

The trial was designed as a prospective, multicentre, three-armed, double-blind randomized controlled non-inferiority trial and was carried out in two hospitals.

For the three arms, iohexol 300 mgI/mL, considered the control group, iohexol 240 mgI/mL, and iohexol 140 mgI/mL contrast concentrations were used.

Participants

All patients (≥18 years) presenting at the vascular surgery outpatient clinic referred for digital subtraction angiography (DSA) were eligible for this study. In all patients, vascular status was evaluated by duplex ultrasound before they were referred for intervention.

Inclusion criteria were:

IC (Fontaine stage II) or CLI (Fontaine stage III or IV) due to PAD

Ankle-brachial pressure index (ABPI) <0.90, or drop in ABPI >0.15 after exercise, or toe-brachial pressure index (TBPI) <0.70

Duration of complaints > 2 weeks

Scheduled for DSA with anterograde femoral artery puncture

Written informed consent

Exclusion criteria were:

renal failure; serum creatinine > 130 μmol/L

inability to give informed consent

participation in another study

Baseline characteristics of the included patients were recorded using a standardized case record form and comprised patient demographics, risk factors for atherosclerosis, history of coronary artery disease, transient ischemic attack (TIA) or stroke, family history of cardiovascular disease, and renal failure.

Patient characteristics

Sixty consecutive patients were included between April 2012 and July 2014, of which 21, 19, and 20 were randomly allocated to respectively the control, 240, and 140 groups. The mean age of all patients was 70.8 ± 9.5 years, 38 (63 %) were male, 26 (43 %) had diabetes, and 35 (58 %) had CLI (Table 1).

Table 1

Baseline characteristics

	Total	300 group(control)	240 group	140 group
No. of patients	60	21	19	20
Age, years (SD)	70.8 (9.5)	73.1 (7.6)	70.2 (12.4)	68.8 (8.0)
Male sex (%)	38 (63)	10 (48)	15 (79)	13 (65)
BMI, kg/m2 (SD)	25.9 (6.5)	26.4 (7.2)	25.1 (3.7)	26.2 (8.0)
Diabetes (%)	26 (43)	9 (43)	9 (47)	8 (40)
Hypertension (%)	51 (85)	16 (76)	17 (89)	18 (90)
Hyperlipidemia (%)
No	18 (30)	4 (19)	6 (32)	8 (40)
Yes	19 (32)	6 (29)	9 (47)	4 (20)
Unknown, statin use	16 (27)	7 (33)	3 (16)	6 (30)
Unknown	7 (12)	4 (19)	1 (5)	2 (10)
Smoking (%)
Current	29 (48)	10 (48)	7 (37)	12 (60)
Former	5 (8)	2 (9)	2 (11)	1 (5)
Never	26 (43)	9 (43)	10 (53)	7 (35)
CAD (%)	12 (20)	4 (19)	3 (16)	5 (25)
TIA or stroke (%)	12 (20)	3 (14)	3 (16)	6 (30)
Family history of CVD (%)	30 (50)	10 (48)	9 (47)	11 (55)
Previous treatment (%)
Ipsilateral revasc.	16 (27)	4 (19)	8 (42)	4 (20)
Fontaine stage (%)
Fontaine II	25 (42)	9 (43)	8 (42)	8 (40)
Fontaine III	11 (18)	2 (9)	2 (11)	7 (35)
Fontaine IV	24 (40)	10 (48)	9 (47)	5 (25)
ABI, median (IQR)	0.63 (0.50-0.82)	0.57 (0.42-0.77)	0.71 (0.59-0.85)	0.63 (0.50-0.83)
Absolute toe pressure, mmHg (IQR)	42 (16-66)	40 (0-75)	45 (13-64)	52 (18-68)

ABI, ankle brachial pressure index; BMI, body mass index; CAD, coronary artery disease; CVD, cardiovascular disease; IQR, interquartile range; SD, standard deviation; TIA, transient ischemic attack

Interventions

Endovascular interventions were performed by interventional radiologists who had experience in interventional radiology varying between 1 and 25 years. In total, seven interventional radiologists performed procedures for this trial.

Diagnostic DSA and intervention were done with three different doses of contrast media. In the control group, iohexol 300 was used, and in the experimental groups, iohexol 240 and iohexol 140 contrast (respectively, Omnipaque 300, 240, and 140 mgI/mL, Amersham Health, Buckinghamshire, UK).

After antegrade puncture of the common femoral artery, angiography was performed according to a standardized procedure. Angiography of the superficial femoral artery and popliteal artery was done through a 5 French endhole catheter. Using a contrast power injector, 10 mL of contrast was injected at a rate of 5 mL/s, and an anteroposterior angiography was made. The catheter tip was then placed in the popliteal artery at the level of the knee joint. Standard projection images of the crural arteries, i.e. anteroposterior and oblique projections, and one lateral projection of the foot, were made with 10 mL of contrast at a rate of 3 mL/s. When femoropopliteal or crural arterial segments were not in the field of view during the first acquisition, a second, more distal, acquisition was made.

Arterial recanalisation was performed according to standard procedures, i.e. initial balloon angioplasty, and only in residual significant stenosis or dissection a stent was placed. At any time during the procedure, the interventional radiologist had the ability to change to the standard concentration (300 mgI/mL), if image quality was judged too poor for adequate diagnostic evaluation or intervention.

Primary outcomes

Primary outcomes were the confidence score in diagnosing arterial stenosis or occlusion and the confidence in treating arterial stenosis or occlusion. The confidence scores were assessed using a visual analogue scale (VAS) ranging between 0 % confidence and 100 % confidence. These outcomes were scored by the interventional radiologist performing the procedure.

Secondary outcomes

Secondary outcomes were volume of contrast used during intervention, image quality of the standardized angiographies, interobserver agreement in assessing arterial lesions, contrast-to-noise ratio (CNR), and the pain score of the patient during contrast injection.

Image quality was assessed separately for the femoropopliteal, crural, and foot angiographies by three interventional radiologists (radiologist performing the procedure, SS, and DDB) according to the Radlex® image quality scoring criteria [11]: [0] non-diagnostic (unacceptable for diagnostic purposes); (1) limited (acceptable, with some technical defects but still adequate for diagnostic purposes); (2) diagnostic (acceptable, with no technical defects likely to impair diagnosis); (3) exemplary (good, most adequate for diagnostic purposes).

For each artery, i.e. superficial femoral artery, popliteal artery, tibioperoneal trunk, anterior tibial artery, posterior tibial artery, peroneal artery, plantar artery, and dorsal pedal artery, two radiologists (SS, DDB; respectively, 1 year and 3 years experience in interventional radiology) scored whether the artery was (1) fully patent or stenosis <50 %, (2) stenosis >50 %, or (3) occluded. Foot arteries were judged as “not assessable” if distal foot arteries were not visualized at all due to crural occlusions.

CNR was assessed by the following formula:

Here, the mean intensity value in the artery () subtracted by the mean intensity value in the adjacent tissue () is considered the contrast between the artery and the tissue. The noise is defined as the standard deviation of the intensity of the adjacent tissue (SD). These values were assessed by one observer (SJ), by drawing a region of interest (ROI) in patent arteries of femoropopliteal, crural, and foot angiographies, and a ROI in adjacent tissue. The ROI in the artery was drawn distally from the contrast injection site. All CNRs were calculated using the DSA images.

The pain score of the patient during contrast injection on a 4-point scale (no, mild, moderate, or severe pain), and volume of contrast used was recorded by the interventional radiologist performing the procedure.

Sample size

In a previous study assessing physicians confidence scores, the mean confidence score for therapeutic decision making based on DSA in patients with PAD was 8.1 ± 1.4 (standard deviation, SD) on a scale of 10, with 0 being absolutely uncertain and 10 being absolutely certain [12]. In our design, the radiologists were asked to rate confidence on a scale of 0 to 100 %. Therefore, the SD of the confidence score was 14. Since using a lower iodine concentration would be beneficial for the patient, we set the boundary for acceptable loss of confidence in the 240 or 140 group compared to the control group at 10 %.

To evaluate whether the mean difference (delta) of maximal 10 % of the 240 or 140 group is not inferior to the 300 group, with a power of 80 % (Zb = 0.842) and significance level of 0.10 (Za = 1.28), and under the assumption that the SD of the groups would be 14, 18 patients were needed per group. Therefore, 60 patients were included in total.

Randomization

Randomization was computer-based in a 1:1:1 ratio using minimization (biased coin randomization). Stratification was applied for the Fontaine classification (stage II versus stage III and IV) and presence of diabetes with the coin bias factor set at 80 %. Randomization was performed by the coordinating investigator after informed consent was obtained.

Blinding

To ensure that the interventional radiologist was blinded for the contrast concentration, the coordinating investigator supplied the contrast directly for the power injector and for contrast injection by hand. Patients were also blinded to the allocated contrast concentration.

Statistical analysis

The confidence of the interventional radiologist in diagnosing or in treating arterial stenosis or occlusion of the 240 and 140 groups was compared separately to the control group by a one-sided Mann-Whitney U test.

The volume of contrast material used in the 240 and 140 groups per patient was compared separately to the control group by two-sided independent samples t-test.

The interobserver variation in confidence in diagnosing arterial stenosis or occlusion and in grading imaging quality was evaluated by means of weighted kappa statistics including 95 % confidence interval (95 % CI).

The CNR scores were compared between groups using the Mann-Whitney U test.

The pain scores during contrast injection were compared between groups using the Χ test.

All analyses were done using SPSS (SPSS 20 Inc., Chicago, IL, USA). A p-value < 0.05 was used as an indicator for statistical significance.

Results

Intervention

Single above the knee interventions were performed in 42 (70 %) patients, single below the knee interventions in eight (13 %) patients, and both above and below the knee interventions in five (8 %) patients. In five (8 %) patients no intervention was performed. One patient was evaluated for dissection, which could not be treated endovascularly, in two patients an occlusion could not be passed with the catheter, and in two patients no significant stenosis was found (false positive duplex ultrasound). Out of 60 angiographies, 59 femoropopliteal, 53 crural, and 52 lateral foot angiographies were available for evaluation by the three observers. One femoropopliteal angiography was not made since the superficial femoral artery was proximally occluded. Seven crural and eight lateral foot angiographies were not made according to the standard operating procedure, since the tip of the catheter could not be placed at the level knee joint in the popliteal artery due to proximal occlusions in five patients, or due to the risk of dissection during advancement of the catheter in the artery in one patient, or since the radiologist refrained from imaging due to pain complaints during contrast injection in two patients.

In total 68 lesions were treated, of which 66 (97 %) were technically successful. Revascularization was not successful in one patient in the control group and one in the 140 group. Intervention characteristics are listed in Table 2.

Table 2

Intervention characteristics

	300 group(control)n (%)	240 groupn (%)	140 groupn (%)
Number of patients	21	19	20
ATK intervention	14 (67)	13 (68)	15 (75)
BTK intervention	2 (10)	4 (21)	2 (10)
ATK/BTK intervention	3 (14)	0 (0)	2 (10)
No intervention	2 (10)	2 (11)	1 (5)
Total interventions	26	20	22
PTA	15 (58)	11 (55)	15 (68)
PTA + stent	6 (23)	4 (20)	1 (5)
Subintimal angioplasty	3 (11)	4 (20)	3 (13.5)
Subintimal + stent	2 (8)	1 (5)	3 (13.5)

ATK, above the knee (i.e. femoropopliteal arterial segments); BTK, below the knee; PTA, percutaneous transluminal angioplasty

Confidence scores

The median confidence score of the radiologist in diagnosing arterial lesions was 100 % (range 81-100 %) for the control group. The median confidence scores in the 240 and 140 groups were respectively 100 % (range 82-100 %) and 100 % (range 91-100 %). The confidence scores of the 240 (p = 1.00) and 140 group (p = 1.00) were not inferior compared to the control group.

The median confidence score of the radiologist for treating arterial lesions was 100 % (range 78-100 %) for the control group. The median scores in the 240 and 140 groups were respectively 100 % (range 79-100 %) and 100 % (range 63-100 %). Confidence scores for the 240 and 140 groups were not inferior compared to the control group, with p-values of respectively 0.40 and 0.25 (Table 3).

Table 3

Confidence scores of radiologists

	300 group(control)n (%)	240 groupn (%)	140 groupn (%)
Confidence in diagnosing arterial lesion in % (range)	100 (81-100)	100 (82-100)	100 (91-100)
p-value*	NA	1.0	1.0
Confidence in treating arterial lesions in % (range)	100 (78-100)	100 (79-100)	100 (63-100)
p-value*	NA	0.40	0.25

*p-values given are compared to the control group.

Volume of contrast used

In the control group the interventional radiologist used a mean of 99 ± 21 mL of contrast per patient. For the 240 and 140 groups this was respectively 101 ± 32 mL and 127 ± 40 mL, with p-values compared with control-group of respectively 0.77 and 0.008. For the control group this resulted in an iodine load per patient of 29.7 ± 6.3 g, and for the 240 and 140 groups respectively in a load of 24.3 ± 7.6 g and 17.8 ± 5.6 g. The iodine loads in the 240 and 140 groups were both significantly lower than the control group, with respective p-values of 0.022 and <0.001. See Table 4 for the contrast volume and iodine load per group.

Table 4

Secondary outcomes

	300 group(control)n (%)	240 groupn (%)	p-value 240 vs. control	140 groupn (%)	p-value 140 vs. control
Volume contrast used in ml (SD)T	99 (21)	101 (32)	0.77	127 (40)	0.008
Iodine load in grams (SD)T	29.7 (6.3)	24.3 (7.6)	0.022	17.8 (5.6)	<0.001
CNR in median (IQR)M
Total	34.9 (23.0-44.0)	27.2 (17.9-46.6)	0.13	28.0 (17.5-38.7)	0.083
Femoropopliteal	35.0 (28.3-44.2)	44.4 (27.2-50.7)	0.43	34.8 (20.9-62.5)	0.68
Crural	33.9 (22.9-53.8)	28.9 (20.5-61.2)	0.74	25.1 (12.7-37.9)	0.082
Foot	30.8 (13.2-38.9)	13.9 (11.6-19.6)	0.018	25.5 (14.2-35.9)	0.74
Pain during contrast injection*	300 group	240 group	140 group
No	6	11	17
Mild	3	2	2
Moderate	3	5	0
Severe	8	1	0
p-value compared to control X	NA	0.055	0.001

CNR, contrast-to-noise ratio; IQR, interquartile range; SD, standard deviation

* In two patients, severity of pain was not assessed, since one patient was sedated. For the other patient pain was not recorded

NA, not assessed

T Compared using two-sided independent samples t test

M Compared using Mann-Whitney U test

X Compared using Χ test

Image quality

In all patients, the allocated contrast concentration was used and was adequate for diagnostic evaluation and intervention in all patients according to the interventional radiologist performing the procedure. The radiologist performing the intervention scored one crural acquisition as limited quality in the control group, and one pedal acquisition as non-diagnostic and limited quality. One pedal acquisition in the 240 group was scored as limited quality. In the 140 group, no acquisition was scored as non-diagnostic or limited quality. For all other acquisitions, the radiologist performing the procedure scored the images as diagnostic or exemplary quality (Fig. 1).

Fig. 1

Standardized angiographic acquisitions using (A) 300, (B) 240, and (C) 140 mgI/mL

For the two radiologists assessing all standardized image acquisitions, one radiologist scored a pedal acquisition as non-diagnostic, and two pedal acquisitions as limited quality in the control-group. In the 240 group, one radiologist scored one crural angiography and one pedal angiography as limited quality. Both radiologists scored in the 140 group one pedal angiography as limited quality. All other angiographies were either scored as diagnostic or exemplary by both observers.

Arterial stenosis or occlusion

A total of 408 out of 480 possible arterial segments were assessed for patency. As mentioned, due to occlusions, risk of dissection or pain complaints, 38 arteries could not be imaged according to protocol. Furthermore, either the plantar artery or dorsal pedal artery was not visualized due to proximal occlusion in 33 patients and were, therefore, scored as “not assessable”. In one patient, the tibioperoneal trunk was absent due to anatomical variation. Interobserver agreement was highest for the control-group with a weighted kappa value of 0.85 (95 %CI, 0.77-0.93). Interobserver agreement was also excellent for the 240 and 140 groups with weighted kappa values of respectively 0.82 (95 %CI, 0.72-0.91) and 0.81 (95 %CI, 0.72-0.91). See Table 5 for the interobserver agreement of arterial lesions between both radiologists.

Table 5

Interobserver agreement of arterial lesions per group

CONTROL GROUP
	Radiologist 2
Radiologist 1	Patent	Stenosis >50 %	Occlusion	Total
Patent	85	1	2	88
Stenosis >50 %	3	20	0	23
Occlusion	2	3	24	29
Total	90	24	26	140
20 arteries were not assessable.
Kappa = 0.85 (95 %CI 0.77-0.93)
240 GROUP
	Radiologist 2
Radiologist 1	Patent	Stenosis >50 %	Occlusion	Total
Patent	75	2	2	79
Stenosis >50 %	6	14	2	22
Occlusion	0	1	28	29
Total	81	17	32	130
30 arteries were not assessable
Kappa = 0.82(95 %CI 0.72-0.91)
140 GROUP
	Radiologist 2
Radiologist 1	Patent	Stenosis >50 %	Occlusion	Total
Patent	80	1	3	84
Stenosis >50 %	6	20	1	27
Occlusion	1	2	24	27
Total	87	23	28	138
22 arteries were not assessable
Kappa = 0.81(95 %CI 0.72-0.91)

Interobserver agreement in scoring standardized angiographies for the presence of arterial stenosis more than 50 % and occlusion. Radiologist 1, DDB (3 years experience in interventional radiology); Radiologist 2, SS n1 year experience in interventional radiology)

Contrast-to-noise ratio

The CNR was highest for the control-group with a median ratio of 34.9 (IQR 23.0-44.0) .The CNR for the 240 and 140 groups was 27.2 (IQR 17.9-46.6) and 28.0 (IQR 17.5-38.7), with respective p-values of 0.13 and 0.083 compared to the control group. In general, the CNR was highest in the femoropopliteal arteries and lowest in the pedal arteries. See Table 4 for the CNR scores.

Pain during contrast injection

During contrast injection 14 (70 %) patients in the control group had some pain, which was severe in eight (40 %). Seven (42 %) patients in the 240 group had some pain during contrast injection. In the 140 group, 17 (89 %) patients had no pain and two (11 %) patients had mild pain during contrast injection. The Χ test showed no significant difference in pain scores between the control group and the 240 group (p = 0.055) and a significant difference between the control group and the 140 group (p = 0.001). See Table 4 for the pain scores.

Discussion

This trial showed that the confidence of the interventional radiologist in diagnosing and treating lower limb arterial stenoses or occlusions in patients with PAD in the 240 and 140 groups were not inferior to the control group. The volume of contrast used in the 140 group was larger than in the control group and the 240 group. However, the iodine load in the 140 group was significantly lower, with a reduction of 40 % compared to the standard contrast concentration. The image quality for the femoropopliteal, crural, and foot angiographies was generally diagnostic or exemplary. Moreover, the CNR remained relatively high enough for adequate diagnosis and treatment. Furthermore, patients in the 140 group had significantly less discomfort during contrast injection.

Implications for clinical practice

As recommended by the updated European Society of Urogenital Radiology (ESUR) Contrast Media Safety Committee guidelines, unnecessarily large contrast doses should be avoided to prevent CIN, and low or iso-osmolar contrast media should be used [1]. Furthermore, it has been shown that patients receiving an iodine load (in grams) higher than their estimated glomerular filtration rate eGFR value (in mL/min) are significantly more likely to develop CIN [13], and that in patients with occlusive vascular disease, a higher cumulative contrast agent exposure was an independent predictor of renal failure and death [14]. Since the iodine load is significantly reduced with lower concentrations, and confidence during intervention and image quality remained high, future lower limb arterial interventions, i.e. distal from the common femoral artery, in patients with PAD should be performed with the 140 mgI/mL contrast. As this study did not evaluate the incidence of CIN between groups, future studies should evaluate the effect of using lower contrast concentrations on the incidence of CIN.

Substitution of iodinated contrast media by carbon dioxide or gadolinium-based contrast media has been studied extensively. However, for carbon dioxide, studies reported poor visualization of the infrapopliteal arteries and discomfort in patients [15-21]. Likewise, gadolinium chelates are expensive and can only be used in low concentrations, resulting in low attenuation and image quality, especially in distal vessels, compared to iodinated contrast material [22, 23]. Moreover, gadolinium does more harm to renal function than equal concentrations of iodinated contrast medium [24, 25].

Limitations

Patients with renal insufficiency, i.e. serum creatinine equal to or higher than 130 μmol/L, were excluded in this trial, since we anticipated that participating in this trial could result in a higher contrast load compared to current clinical practice. However, in hindsight, the iodine load for the patients participating in this trial on average was as low as 24.0 mgI, and especially in the 240 and 140 groups. Since patients with renal insufficiency have a higher risk for CIN [3] and we excluded these patients, a relevant patient population was missed. Yet in our opinion, the results of this trial are also applicable for this patient population, since we do not expect a correlation between the outcomes of this trial and renal function.

The initial design of this study included the assessment of serum creatinine within 3 days following intervention to assess whether CIN had occurred to have direct evidence of the effect of using lower iodine concentrations on renal function. However, early in the trial this was removed from protocol, since patients were reluctant to reappear at the medical centre for blood withdrawal. We judged that we could refrain from creatinine assessment without compromising the study question, since the sample size calculations of this trial were based on confidence scores and not on the incidence of CIN. To evaluate whether there would be a difference between groups in the incidence of CIN, would have required a considerably larger study population.

Finally, our study showed that using a lower concentration leads to a higher injected volume of contrast. One could argue, therefore, that this could lead to an increased risk of CIN, since studies already have shown that a larger volume of contrast increases the risk of CIN [9, 26, 27]. However, as the number of milligrams iodine injected is a derivative of the volume injected, our opinion is that it is not the volume injected which increases the risk of CIN, but merely the milligrams of iodine injected.

Conclusion

Using an iodine contrast concentration of 140 mgI/mL will lead to a significant reduction of administered iodine load, thereby minimizing the risk for CIN, without compromising image quality. Use of low iodine dose contrast during DSA in PAD patients is recommended.