Introduction

Contrast-induced nephropathy (CIN) refers to acute kidney injury (AKI) after intravenous or intra-arterial administration of contrast media (CM). Several definitions and classifications on AKI exist and are proposed in the nephrological literature [1, 2] The most widely used CIN definition is from the Contrast Media Safety Committee (CMSC) of the European Society of Urogenital Radiology (ESUR): an increase in serum creatinine (SC) of at least 25 % or 44 μmol/l within 3 days after CM administration in absence of an alternative aetiology [3]. The incidence is highly dependent on renal function prior to CM administration and additional risk factors, of which diabetes mellitus is the most important one. Incidence varies from less than 2 % in the general population up to 50 % in patients with advanced kidney disease [4]. CIN is the third most common cause of hospital acquired renal failure, with an incidence of 11 % [5]. Furthermore, CIN is associated with increased morbidity and mortality within 2 years following occurrence [3, 4].

In recent years, a controversy emerged as to whether CIN incidence is dependent on the administration route. Recently updated guidelines state that the CIN incidence is higher after intra-arterial administration than after intra-venous administration [3]. This is supported by literature, for example, intra-arterial peripheral digital subtraction angiography has shown a CIN incidence of up to 14.3 % [6]. A recent meta-analysis regarding CIN incidence after contrast-enhanced computed tomography (CT) has shown a pooled CIN incidence of 6.4 % [7]. In a group of 747 patients, who underwent 944 procedures with intra-venous CM administration, CIN incidence was 2.4 %. All high-risk patients received pre- and post-hydration in accordance with current guidelines [8]. On the other hand, a recently published study, describing 170 patients who received both intra-arterial and intra-venous CM within 1 year, showed a similar CIN incidence of 14 % in the intra-arterial group and 11.7 % in the intra-venous group. It was concluded that CIN incidence is similar after intra-arterial and intravenous CM administration, after adjustment for patient-related risk factors [9].

Second, several authors question the existence of CIN. In a 2006 published literature analysis, the authors found only two articles on intra-venous CM administration with a control group that received no CM. In both articles, the incidence of significant changes in SC was not significantly different between the group receiving intra-venous CM and the group receiving no CM [10]. A change in SC of at least 25 % during a 5-day period occurred in more than 50 % of patients who had not received CM [11]. The authors conclude that the role of CM in nephropathy may have been overestimated. A recently published meta-analysis describes a similar incidence of acute kidney injury between the group receiving CM and the control group [12]. In a recently published retrospective study of over 157,000 CT scans in over 53,000 patients, no significant difference in acute kidney injury was found between contrast-enhanced and non-contrast scans [13]. As a counterbalance, another recently published retrospective study showed that CIN does exist after intra-venous CM administration, but only in subtypes of patients [14]. All patients who underwent CT over a 10-year period with sufficient SC data and stable renal function were included, 8,826 underwent non-enhanced CT and 8,826 underwent contrast-enhanced CT. Intra-venous low-osmolar CM proved to be a nephrotoxic risk factor in patients with a stable estimated glomerular filtration rate (eGFR) less than 30 ml/kg/1.73 m2, with a trend towards significance at eGFR 30–44 ml/kg/1.73 m2. Intra-venous low-osmolar CM were not risk factors in patients with eGFR ≥45 ml/kg/1.73 m2 [14]. CIN incidence in the group with eGFR ≤30 ml/kg/1.73 m2 was 36.4 %, compared with 19.4 % in the non-enhanced CT group [14].

Although randomised controlled trials with a control group receiving no CM are widely lacking, results of these recently published retrospective studies provide a trend that CIN incidence has probably been overestimated in the past, but that CIN can occur in patients with decreased kidney function.

The following article reviews the pharmacology of CM, the pathophysiology of CIN and discusses some preventive strategies, all for iodinated CM.

Pharmacology of CM

History

The modern era of CM started back in 1953 when Vernon Wallingford, a chemist working for the Mallinckrodt Company in St. Louis, MO, USA, synthesised a new class of chemical compounds. This molecule contained three iodine atoms covalently bound to an aromatic ring structure, a so-called benzoic acid derivate [15].

The compound Wallingford synthesised was called sodium acetrizoate (Fig. 1) and was marketed as Urokon®. This was the first ionic, high-osmolar CM and it set a new standard in CM. Soon ‘me too’ CM were developed, such as sodium diatrizoate (Urografin®; Schering, Berlin, Germany) in 1954 and sodium iothalamate (Conray; Mallinckrodt, St. Louis, MO, USA) in 1963. These CM were the dominant CM throughout the 1960s-1980s and sodium diatrizoate still remains in use today for non-vascular radiology exams [16–18].

Fig. 1
figure 1

The structural formula of sodium acetrizoate (Urokon); the first high-osmolar and ionic contrast agent

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During the period in which ionic CM were introduced and administered extensively, it became clear that the CM could cause serious adverse effects related to the high osmolality and ionicity of the injected fluids. Torsten Almèn, a Swedish radiologist, realised the role of osmolality when he observed pain during administration of CM in angiography and compared it to swimming in the almost isotonic Baltic Sea with the eyes open which does not hurt. He hypothesised that high osmolality caused the pain and developed a chemical process to covert high-osmolar ionic CM into low-osmolar non-ionic CM. This resulted in the synthesis of metrizamide in 1968 (Fig. 2) [19]. Only after several pharmaceutical companies declined Almèn’s ideas on low-osmolar CM was he able to persuade a Norwegian pharmaceutical company, Nyegaard, to further develop and market metrizamide (Amipaque®). In the 1970s and 1980s the second generation non-ionic CM (Fig. 3) with increased solubility, such as iohexol (Omnipaque®; GE, Amersham, UK), iopromide (Ultravist®; Bayer Healthcare, Berlin, Germany), iomeprol (Iomeron®; Bracco, Milano, Italy), ioversol (Optiray®; Mallinckrodt, St. Louis, MO, USA) and Iobitridol (Xenetix®; Guerbet, Aulnay-sous-Bois, France), were developed and introduced in patient care in the next decade [16, 17].

Fig. 2
figure 2

The structural formula of metrizamide (Amipaque); the first non-ionic contrast medium developed by Almen et al.

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Fig. 3
figure 3

The structural formula of iohexol (Omnipaque); an example of a highly soluble polycarboxylated contrast medium

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Simultaneous to the development of the new low-osmolar CM was the introduction of an ionic dimeric compound, meglumine-sodium ioxaglate (Hexabrix®; Guerbet, Aulnay-sous-Bois, France) in 1979. Furthermore, non-ionic dimers were developed which proved to be iso-osmolar to blood. First, the iso-osmolar iotrolan (Isovist®; Bayer Healthcare, Berlin, Germany) was introduced in 1994 and soon after its introduction withdrawn due to a high reported number of delayed reactions. Currently, the only non-ionic dimer (Fig. 4) on the market is iodixanol (Visipaque®; GE, Amersham, UK) [20–23]. Since 1995, not a single iodinated contrast medium has been introduced which is still marketed internationally today.

Fig. 4
figure 4

The structural formula of iodixanol (Visipaque); a non-ionic dimer consisting of two aromatic rings, each containing three iodine atoms

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In summary, currently four types of contrast medium are available. High-osmolar ionic monomers, low-osmolar ionic dimers, low-osmolar non-ionic monomers and iso-osmolar non-ionic dimers (Table 1).

Table 1 Pharmacological and pharmacokinetic parameters of iodinated CM [23]
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Chemical composition

The tri-iodobenzene basis of sodium acetrizoate molecule contains 84 % iodine and thus it displays excellent radio-opaque properties. The other positions on the aromatic ring, numbers 1, 3 and 5, are available for side chains to improve physicochemical and pharmacokinetic properties such as solubility, osmolality, protein binding and tolerance [15–18].

The hydrophilic side chains in sodium acetrizoate are an acid group (−COOH at position 1) and an acetamido group (−NHCOCH3 at position 3) to enhance solubility, salt formation and to reduce protein binding, as can be seen in Fig. 1. The –COOH group at position 1 is responsible for the ionicity, as it forms a cation conjugated with sodium or meglumine in solutions. Adding another acetamido group at position 5 created sodium diatrizoate [16, 17].

In metrizamide, the first non-ionic iodinated contrast medium developed by Almen and colleagues, an acetamide (−NHCOCH3) group was placed at both positions 3 and 5 of the aromatic ring. Novel in the development of metrizamide was adding a derivative of glucose, containing four hydroxyl groups, at position 1 of the aromatic ring. This proved an important step to decrease the osmolality by eliminating the effect of positive and negative ions in the contrast solution and retaining radio-opaque properties [16–19].

Metrizamide proved poorly soluble and thus was of limited use in intravenous contrast administration. Soon, however, highly soluble polycarboxylated agents (Fig. 3) followed, such as iohexol and ioversol. The solubility in these agents is improved by adding more carboxyl groups to the tri-iodinated aromatic structure [16–19].

Reduction of osmolality and further increasing the number of iodine atoms in the molecules led to the development of dimeric non-ionic CM. These structures consist of two aromatic rings containing a total of six iodine atoms covalently bound to the ring (Fig. 4). The introduction of these non-ionic dimers proved to reduce osmolality without significantly influencing radio-opaque quality or systemic reactions upon administration. Generally, dimers display a higher viscosity than monomeric CM [16, 17].

Pharmacokinetic properties

After intravenous administration, CM are distributed rapidly into extracellular body compartments, and rapid decreases in plasma concentrations can be measured. The plasma concentration–time plot of contrast medium pharmacokinetics displays the characteristics of a classical bi-exponential model.

Several factors determine the pharmacokinetic properties of a contrast medium. The side chains of the aromatic rings influence solubility, osmolality, protein binding and toxicity profile. Lipophilic side chains, for example, will lower the solubility in water and tend to have high plasma protein binding, whereas a carboxyl (−COOH) group can form salts and enhance solubility and osmolality. Hydrophilic side chains such as acetamide groups (−NHCOCH3) and polyhydroxylated groups (containing several –OH groups) further improve solubility in water, tolerability and are able to reduce protein binding. The latter property is of importance to ensure rapid glomerular filtration. Non-ionic CM generally are very hydrophilic [16, 17].

The amount of particles in a certain volume determines the osmolality. It takes both cell membrane penetrating particles and non-penetrating particles into account. Penetrating solutes can enhance the cell volume by attracting water after passing the cell membrane, whereas non-penetrating solutes outside the cell will attract water from the cell. High osmolality is one of the co-factors responsible for tolerability of CM. Ionic CM are molecules with an electrical charge and solutions in water contain cations such as sodium or meglumine. In general, these solutions contain more particles per millilitre and thus have a higher osmolality than non-ionic CM. High osmolar CM are less tolerable than low-osmolar or iso-osmolar CM. Non-ionic CM do not have an electrical charge and generally have a lower osmotic contribution than ionic CM [16, 17]. Generally, if a larger number of iodine atoms are covalently bound in a molecule, this molecule will be more difficult to dissolve in water. The addition of large numbers of hydrophilic carboxyl groups, cation forming groups or hydroxyl groups is needed to achieve adequate solubility in aqueous solutions for use of the molecule as a contrast agent.

Another important physicochemical property is viscosity. Viscosity, best described as thickness or internal friction, of a fluid determines the infusion rate that can be achieved. Fluids with a high viscosity will be infused over a longer period of time compared with fluids with a low viscosity when the same infusion system is used. After intravenous injection, fluids with a high viscosity can influence local circulation on a larger scale than fluids with a low viscosity, since the latter will mix more easily with blood.

Recent data from animal studies suggest that iso-osmolar non-ionic dimers compared with low-osmolar non-ionic monomers significantly increase urine viscosity, lead to increased kidney iodine retention and increase the formation of vacuoles in the renal tubular epithelium of the cortex predominantly in the proximal and distal tubulus [24].

After intravascular administration, CM are distributed rapidly over intravascular and extracellular fluids, i.e. the CM have a short distribution half-life (t½d). Usually, the time for the CM to distribute evenly over the fluids is several minutes, ranging from 2 to 30 min. Plasma protein binding is approximately 1-3 % [16].

CM are not metabolised in the human body, but eliminated quickly through glomerular filtration by the kidney. The time to clear half of the amount of contrast medium in the blood, or elimination half-life (t½el), is approximately 1–2 h.

In patients with normal renal function approximately 100 % of the contrast medium is excreted in the first 24 h after administration. In patients with decreased renal function the elimination half-life can increase to 40 h or more [25]. Alternative routes of elimination, such as biliary elimination, are slow. Haemodialysis and peritoneal dialysis are efficient methods to remove CM from the blood [25, 26].

An overview of physicochemical and pharmacokinetic properties can be found in Table 1.

Pathophysiology of CIN

The pathophysiology of CIN is complex and partially understood. What exactly happens inside a human kidney in vivo can only be speculated from the results of mainly animal and laboratory studies.

Under physiological resting conditions, 25 % of the cardiac output is directed towards the kidneys. The majority is directed towards the cortex, to optimise glomerular filtration and reabsorption of water and salts. The medullary blood flow is low. Its function is to preserve osmotic gradients and enhance urinary concentration [27]. Blood flow to the renal medulla is derived from efferent arterioles of juxtamedullary glomeruli. At the corticomedullary junction, these efferent arterioles give rise to the so-called distal vasa recta (DVR). These DVR gradually form a capillary bed that penetrates deep into the inner medulla. These capillaries eventually coalesce to form ascending vasa recta (AVR). The transformation from DVR to capillary to AVR occurs gradually with accompanying histological changes in the composition of the vessel wall [28].

Hypoxic medullary injury plays a critical role in CIN [29]. This is caused by three different but potentially interacting pathways: haemodynamic effects of CM, the effect of reactive oxygen species (ROS) and free radicals and direct CM molecule tubular cell toxicity [30].

Haemodynamic effects

Under physiological circumstances, regional PO2 levels of the renal medulla can be as low as 20 mmHg [31]. The most vulnerable part of hypoxic damage is the deeper portion of the outer medulla that contains the metabolically active thick ascending limbs of the loop of Henle. In this part of the tubular system, an osmotic gradient is generated by active reabsorption of sodium, a process that requires a large amount of oxygen [27]. The haemodynamic response to intra-arterial injection of contrast medium is biphasic: a brief initial increase in renal blood flow, followed by a prolonged decline of 10-25 % below baseline [29, 30, 33]. This predomintantly reflects a decline in cortical blood flow, as 10 % of renal blood flow represents medullary flow [29] Declines of outer medullary PO2 by 50-67 % after contrast medium administration to 9-15 mmHg have been reported [29, 32]. The mechanism for medullary hypoxia is a combination of a decline in regional microcirculatory blood flow and increased oxygen demand of tubular cells [29, 32].

Injection of contrast medium leads to a transient increase in renal plasma flow, glomerular filtration and urinary output [29]. The higher the osmolality of the injected contrast medium, the higher these effects are. Both by osmotic load, as by the effect of endothelin release, more sodium has to be reabsorbed by distal tubular cells [29, 31, 32]. This leads to increased oxygen consumption [31, 33].

The decline in regional blood flow has been attributed to the response of vaso-active mediators to contrast medium administration. Basically, an imbalance occurs between vasoconstrictive and vasodilatative mediators. Many mediators have been related to contrast medium administration. Prominent medullary vasodilatators are adenosine, dopamine, nitric oxide (NO), atrial natriuretic peptide (ANP) and prostaglandin E2 [27, 31, 33]. Vasconstrictors act more on the cortical vessels, to decrease glomerular filtration [29]. Potent vasoconstrictors are vasopressin, angiotensin II and endothelin [27, 31]. Potential additional participants, both dilatative and constrictive in the pathophysiology, are: serotonin, bradykinin, leukotriens, histamine and catecholamines [33]. To what extent each mediator plays a role is unknown. Furthermore, the distribution of receptor mediator subtypes in the cortex and medulla may be responsible for different regional haemodynamic responses [29, 33].

More insight on the medullar microvasculature response to CM has been given by Sendeski et al. [34]. The average DVR diameter is 12-18 μm, close to that of a red blood cell. On isolated rat DVRs, it was shown that micro-perfusion with Iodixanol leads to a diameter reduction of 48 %. This was due to a decreased NO production and an increase reactivity of DVR to angiotensin II. Addition of a free radical scavenger, prevented Iodixanol and angiotensin-II-induced vasoconstriction [34]. Additional research from the same group showed that Iodixanol has a more pronounced vasconstrictive effect on afferent arterioles than on efferent arterioles. Decreased NO availability and increased superoxide concentration explained the increased tone and reactivity of afferent arterioles [35].

Reactive oxygen species (ROS)

Free radicals are atoms or molecules that contain one or more unpaired electrons [30]. Examples are superoxide (O2-) and hydroxyl radical (OH-) [32]. These molecules are changed into water after successive reduction reactions [30]. Less aggressive reacting molecules, such as H2O2, are called ROS [30, 32]. Under physiological conditions, medullary tubular ROS formation plays an important role in cellular signalling processes, regulation of regional microcirculation and tubular transport by its effects on NO concentration and tubular transport activity [36]. Medullary hypoxia develops after contrast medium administration, both by decreased medullary blood flow and increased oxygen demand of tubular cells due to increased sodium reabsorption. This leads to increased ROS formation and oxidative stress, an imbalance between oxidants and antioxidants in favour of oxidants. The mechanisms of increased ROS formation are complex and only partially understood [36]. Once exceeding the cellular scavenging capacities, ROS lead to the so-called ischaemia-reperfusion injury [36]. This refers to cellular injury caused by combined effects of hypoxia and ROS-mediated oxidative damage. The latter affects mitochondrial and nuclear DNA, membrane lipids and cellular proteins [36]. ROS play an important role in altered renal microcirculation. They trigger and increase angiotensin-II- and endothelin-I-induced vasoconstriction. Furthermore, bioavailability of the vasodilatative NO is reduced by ROS [36].

Tubular cell toxicity

Direct toxic effects of CM can only be studied in vitro, for the effect of other cell injury mechanisms such as hypoxia, can be ruled out [37]. In general, the toxic effects of high osmolar CM are more pronounced than the effects of low- or iso-osmolar CM [37]. Cytoxic effects of CM on glomerular mesangial cells include apoptotic effects, associated with elevated intracellular ROS levels [37]. The latter shows how pathophysiological CIN mechanisms interact and enhance each other. More effects of CM on tubular cells have been described, including redistribution of membrane proteins, reduction of extracellular Ca2+, DNA fragmentation, disruption of intercellular junctions, reduced cell proliferation, apoptosis and altered mitochondrial function [37].

In conclusion, CIN is a consequence of medullary ischaemia by both increased oxygen consumption of tubular cells and decreased perfusion. This leads to the formation of ROS, which enhance the effect of vasoconstrictive mediators and reduce the bioavailability of vasodilatative mediators. Furthermore, ROS formation leads to oxidative damage to tubular cells. CM also have a direct toxic effect on tubular cells, with increased ROS formation as a consequence. These three interacting pathways can finally lead to tubular necrosis.

Prevention

Regarding prevention, international guidelines exist, such as the ACR manual on contrast media [38]. Probably the most widely used guideline on CIN prevention is the one by the CMSC of the ESUR, which can be easily checked on-line and has recently been updated [3, 26]. A summary on the practical aspects of both guidelines is displayed in Table 2.

Table 2 Summary of practical aspects of guidelines
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Updated CIN Guideline by the CMSC of the ESUR

After more than 10 years, the CMSC guideline on CIN was in need of revision and the updated guideline was published very recently [3]. The list of patient-related risk factors has been updated and now also includes factors related to cardiovascular instability like a low haematocrit level, periprocedural hypotension, a recent myocardial infarction (<24 h), and use of an intra-aortic balloon pump, which can be present in many clinical high-care patients. The procedure-related risk factors have not changed to a great deal, but in high risk patients it is important to use the minimal dose of low- or iso-osmolar contrast medium necessary for a diagnostic examination. An essential, but often forgotten, point is that alternative imaging methods should be considered first and in high-risk patients scheduled for CT, there is still an underuse of MRI in daily practice.

One of the major new things in the guideline is the fact that the route of contrast medium administration is discriminative in assessing the risk. Based on the data and reviews of intravenous CM administration studies, it was concluded that the risk of CIN in intravenous CM administration is lower than the risk of intra-arterial CM administration. In intravenous CM administration, several studies have shown that the risk of CIN increases if eGFR is ≤45 ml/min/1.73 m2. For intra-arterial contrast medium administration a cut-off eGFR of <60 ml/min/1.73 m2 has been maintained.

Volume expansion is still considered the backbone of CIN prevention, with no indication for pharmacological prophylaxis, such as N-acetylcysteine (NAC). The results of the published studies on NAC vary considerably, with most studies finding no significant benefit [39]. In the preventive schemes of fluid administration, intravenous is still considered superior to oral fluid administration due to a better control of the volume expansion. Intravenous infusion of 1.0-1.5 ml/kg/h saline 0.9 % starting 6 h before and continuing 6 h after contrast medium administration has proven to be an effective prevention scheme. Another major new item in the guideline is the fact that intravenous administration of 3 ml/kg/h sodium bicarbonate 1.4 %, starting 1 h before and continuing at a dose of 1 ml/kg/h for 3 h after the contrast medium administration is an adequate alternative in elective examinations, and the preferred schedule in emergency situations.

Volume expansion: bicarbonate versus saline

Central volume expansion leads to an increased intravascular volume. As a consequence, renal blood flow and diuresis increases, leading to decreased contact time of contrast medium with renal tubular cells. Supression of the renin-angiotensin system occurs, leading to a general renal vasodilatation [3, 4, 40]. Volume expansion is a safe procedure, with six adverse events reported in 511 procedures (1.2 %) [8].

An ongoing controversy in intravenous hydration is whether to use NaCl 0.9 % or NaHCO3 1.4 % intravenously. NaHCO3 1.4 % is commercially available and therefore widely used for volume expansion. It equals NaHCO3 167 mEq/l, the closest commercially available product to the researched NaHCO3 154 mEq/l. The hypothesis behind the possible increased protective effect of NaHCO3 is as follows: the use of NaHCO3 leads to alkalisation of renal tubular fluid; in a more alkali environment, ROS formation is impaired [3, 40].

The first published randomised controlled trial (RCT) on this subject by Merten et al. [41] described 119 patients undergoing either coronary angiography (CAG), CT, diagnostic or therapeutic angiography or TIPS procedure. They were randomly assigned to receive either NaCl 154 mEq/l in 5 % dextrose and H2O or NaHCO3 154 mEq/l in 5 % dextrose and H2O. Both solutions were intravenously administered at 3 ml/kg/h for 1 h before CM administration and 1 ml/kg/h for 6 h after CM administration. CIN incidence in the NaHCO3 group was 1.7 % versus 13.6 % in the NaCl group [41]. This RCT shows convincing evidence in favour of NaHCO3 hydration, but the used hydration schedule for NaCl was rather unusual. Most hydration schedules with NaCl, use isotonic saline (0.9 %) and a much longer pre- and post-hydration time of up to 12 h.

The results of this RCT, triggered the performance of new RCTs regarding NaHCO3 versus NaCl. Two trails compared the effect of a single bolus of NaHCO3 before CAG or PCI [42, 43]. Both RCTs showed significantly less CIN in the group treated with the NaHCO3 bolus [42, 43]. One RCT created its own mixture of NaHCO3 with NaCl 0.45 % [44]. The results of this trial are therefore not comparable to any of the other published RCTs. For four other RCTs, the schedule of Merten et al. [41] was used for prior and post NaHCO3 hydration, as described in the section above. This schedule has been compared with several NaCl schedules in mainly cardiology patient groups with different stages of renal impairment [45–48]. Another RCT uses the same NaHCO3 concentration, but administers 1 ml/kg/h from 6 h before till 6 h after contrast medium administration [49]. The final RCT uses a more or less comparable schedule of NaHCO3 150 mEq/l at a rate of 3 ml/kg/h for 1 h before contrast medium administration and 1.5 ml/kg/h for 4 h after CM administration [50] The results of these more or less comparable RCTs are displayed in Table 3.

Table 3 Characteristics of RCT of NaHCO3 versus saline pre- and post-hydration
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Recently an abstract has been published online describing the results of a randomised controlled trial regarding 1 h pre-hydration with 250 ml NaHCO3 1.4 % versus 4–12 h pre- and post-hydration with 1,000 ml NaCl 0.9 %. CIN incidence was 3.3 % in the NaHCO3 group and 3.7 % in the NaCl 0.9 % group [51]. This indicates that a short NaHCO3 pre-hydration schedule can be safely used in CIN prevention, which can lead to a reduction in hospital stay and therefore a reduction in costs [51].

From these seven more or less comparable RCTs on intravenous volume expansion, four show a statistically significant difference in favour of NaHCO3. None of these RCT’s has an outcome in favour of NaCl. Therefore, the CMSC conclusion that pre- and post-hydration with NaHCO3 is at least equal to NaCl, is justifiable.

Conclusions

The pharmacology of iodinated CM is simple. A quick distribution within the extra-vascular space, no metabolisation and excretion solely by glomerular filtration. The pathophysiology of CIN has three branches that interact with each other: haemodynamic effects, formation of ROS and tubular cell toxicity. Prevention is extensively described in guidelines. Recently, ESUR guidelines have been updated.