Contrast Agents in Dentistry

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    INTRODUCTION:

    Image formed on radiograph is as result of differentialattenuation of the x-ray beam by structures through

    which X-ray pass,

    Structures that lack sufficient density to attenuates thebeam do not appear on the radiograph.

    If the densityof a structure of interest is too low to bevisualized on an X-ray image or if the subject contrast

    is too low to meet the specific diagnostic needs ,the

    contrast & the density can be improved artificially

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    The use of artificially induced contrast has beenhelpful in allowing the evaluation of the structures

    that would otherwise be radiographically invisible.

    Use of radiopaque agent is termed as positive contrast

    agent

    whereas use of gas like air, o2, co2 is termed as

    negative contrast agent.When both are used concomitantly, it is known as

    double contrast.

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    WHY CONTRAST MEDIA ARE NECESSARY ?

    1. Different tissues within the body attenuate the X-ray beam todifferent degrees-the degree of attenuation is depends upon

    electrons in the path of the beam with which it interacts.

    2. the no. of electrons in the path of the beam dependds upon

    three factors:a) Thickness of the object

    b) Density : difference between two organs ,such as between ms

    of heart & the air in the lungs,

    c) Atomic no: difference between atomic no. between two tissuessoft tissues composed of elements with low atomic no. and

    bone which is composed of high atomic no.

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    WHY CONTRAST MEDIA ARE NECESSARY ?

    The density of hollow organs is reduced by filling it with gas orair providing negative contrast

    The average atomic no. of the hollow structure such as blood

    vessel can be increased by filling the lumen with liquid such as

    high atomic no.than the blood such as IODINE

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    DEFINATION of contrast :

    It is defined as radiopaque substances that havebeen developed to alter artificially, the density of

    different parts of the patient so altering the subject

    contrast.

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    1. SIALOGRAPHY: It Is The Study Involving Salivary Glands

    2. ATHROGRAPHY: It Is The Study Involving Joints Of The Body

    3. ANGIOGRAPHY: To Study The Blood Vessels

    4. LYMPHOGRAPHY: This Study Involves Lymph Nodes

    5. UROGRAPHY: This Is The Study Carried Out For Kidney

    6. BARIUM SWOLLOW MEAL: This Is The Study Of GIT

    7. COMPUTED TOMOGRAPHY: It Is Used For General Enhancement

    STUDIES INVOLVING CONTRAST AGENTS:

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    REQUIREMENT:

    RADIOPAQUE : it should be adequatelyradiopque to show good contrast.

    MINIMUM SIDE EFFECTS : it should have

    no harmful effects at all i.e should be

    biologically stable.

    LESS VISCOCITY: it should not be so

    viscous that it requires considerable pressure

    to be introduced.LOW SURFACE TENSION: it should have

    low surface tension.

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    Classification

    According to CHARR DH in 19881) Depending upon the nature of material

    a) Iodine based

    b) Noniodine based

    2) Depending upon the solvent

    a) Conventional ionic water soluble

    b) Oil soluble

    3)Depending on the ionic naturea) Monoacidic monomer

    b) Nonacidic monomer

    c) Monoacidic dimer

    d) Non ionic dimer

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    Classification :

    According to WHAIRES E IN 1996Barium sulphate suspensions for investigating the gastrointestinal tract

    Iodine-based aqueous solutions used for all other investigations and divided into:

    Ionic monomers, including:

    * iothalmate (e.g. Conray)

    * metrizoate (e.g. Isopaque)

    * diatrizoate (e.g. Urografin)

    Ionic dimers, including:

    * ioxaglate (e.g. Hexabrix)

    Non-ionic monomers, including:

    * iopamidol (e.g. Niopam)

    * iohexol (e.g. Omnipaque)

    * iopromide (e.g. Ultravist)

    Iodine-based oil solutions such as Lipiodol (iodized poppy seed oil) used for lymphography and sialography

    MR contrast agents (e.g. gadolinium)

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    Chemistry of barium sulphate and iodine

    BARIUM SULPHATE:1) it is a crystalline salt insoluble in water

    2) the mineral barite is composed largely of barium sulphate and

    is common are of barium

    3) although barium is a heavy metal and it is water soluble

    compound are often highly toxic

    4) extreamly low solubility of barium sulphate protects the

    patients from absorbing harmful amounts of metal

    Specific gravity4.5

    Melting point

    1580 degree centigradeDensity4.5 gm/cm3

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    IODINE:-Atomic wt127

    It is the only element which is proved satisfactory for general use

    as an intrvascular contrast media

    Iodine provides the radiopacity

    The other elements of radio contrast media molecule provide no

    radiopoacity but acts as carrier of the iodine and which markdly

    reducing toxicity of molecule

    Over 90% being eliminated by glomerular filtrate by kidneys

    withinn12 hrs

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    General properties of contrast media

    1) VISCOSITYViscocity of contrast medium is important because it helps to

    determine the force required to inject it through a needle or

    catheter into a patient which turn limits the rate at which it can be

    injected

    2) OSMOLALITY:the sensation of heat and discomfort or even pain experienced by

    the patient are directly related to the osmolarity of the contrast

    media

    3)CHEMOTOXICITY:

    Refers to mechanism responsible for causing the toxic effects ofthe contrast media which can not be explained by other means

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    Ideal properties of CONTRAST AGENTS

    1) Safe2) Non Toxic

    3) Should not cross blood brain barrier or placental barrier

    4) Should have similar properties when compared to blood ,body

    fluids,saliva

    5) Should be pharmacologically inert

    6) Opacificaton

    7) Low surfacetention

    8) Easy to inject

    9) Elimination should be easy but the eliminaton time should besufficient

    10) Residual contrast media

    11) Should Be Cost Effective

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    CONTRAST agents in sialography:

    Salivary gland are soft tissue structures , so they can not be visualisedradiographically

    they are visualised by the technique of sialography which involves the technique

    of retrograde filling of luminal system of gland with radiopaque contrast media

    August fredrick 1972merqury as contrast agent

    Carpy 1909 performed 1 st sialography

    Contrast sialography can be performed using either lipid soluble or water

    soluble agents

    A major disadvantage of the lipid soluble agent is that they are not diluted in

    saliva or absorbed by glandular mucosa resulting in optimum opacification ofboth ductal and acinar elements

    used commonly when to see small peripheral masses

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    Water soluble angiographic dyes containing about 28-38% iodineused in contrast sialography

    A major disadvantage with this dyes is that they are easily diluted

    in saliva and get rapidly absorbed across glandular elements

    CLASSIFICATION OF CONTRAST AGENTSUSED IN SIALOGRAPHY:

    1) Lipid soluble or fat soluble contrast media

    2) Water soluble contrast media

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    Lipid soluble contrast media:

    1) Iodised oils:

    a) Ethiodolb) Lipidol

    c) Lipidol uf

    d) Todochioral

    Advantage :1) Opacification : satisfactory

    2) visualization : sharper ,with good resolution of the most

    peripheral ducts

    Disadvantage:1) Produces greater degree of Discomfort

    2) Inflammatory reactions --grannuloma formation,subsequent fibrosis

    3) Gland clouding due to greater amount of contrast medium within the

    lining of fine duct and capillaries

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    2) Water insoluble organic iodine compundse.g-pantoapaque

    myodil

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    Water soluble contrast media:

    e.g_ hypaque 50, urograffin,hypaque 75, renograffin 60

    &73,amipaque ,isopaque ,conray 80&420Properties

    1) Miscibiltythey are miscible with body fluids and saliva

    2) Iodine content-28-30 w/w

    3) Viscosity 2-10 centipores

    4) Hyper tonic compare to saliva and body fluids

    Advantage :

    1) Filling of finer duct system

    2) Discomfortless pain &less discomfort to patient

    3) Excretion- they are rapidly removed from the tissues

    Disadvantages:

    1) Less contrast

    2) Less time retention in body

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    Contrast Media In Arthrography:

    Inability of plain radiography to demostrate either the articularcartilage or bounderies of synovial space needs contrast media

    introduced in to joint space followed by x-ray examination

    When employed in temperomandibularbjoint it is known as

    temperomandibular joint arhtrography

    Pass in 1939 acomplished the 1st

    use of arthrography inevaluating TMJ

    Single contrast arthrography:

    Usually performed by introducing the contrast medium into the

    lower joint space

    The single contrast technique yield mre information about jointdynamics

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    Double contrast arthrography:Performed when the iodinated contrast medium and air

    are introduced in both upper and lower joint space

    Double contrast tech gives more informatics regarding

    joint morphologyWater soluble contrast agents are preffered.

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    Contrast media in lymphangiography

    The demostration of internal architecture of normal sized or

    enlarged lymph nodes requires the ingestion of radiopaque

    contrast media into efferent lymphatics,

    Lipoidol and patient blue violet also called as

    sulphan blue or /acidblue are /commonly usedin lymphangiography

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    Contrast media in computed tomography:

    Need for using contrast media is to obtain the differential change

    in the attenuation values of normal and pathological tissues

    Contrast agents can be administrated prior to C SCAN to allow

    organs and structures to be seen more easily

    Most widely used material is 30 mg of iodine for an avg built

    which can be scaned. 5-15 min later.Agents can be administrated through a vein (iv),by injection or

    taken orally.

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    Contrast Agents Available In Indian Market

    An angiograffin: it contains 0.65 gm meglumindiatrizoate in aq. Sol ( iodine conc.306mg /ml)

    inj.20ml amp and 50 ml vial

    barium sulphate x-ray_ba2so4 400gm

    Magnevist- 469mg gadpenetate acid dimoglumine saltin aq sol 10 ml & 20ml vial

    Radiopaque (iohexol): 10-20-50 ml

    Sunray 280

    Sunray 420Ultravxist 300

    urograffin

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    Anaphylactoid (idiosyncratic)

    unpredictabledose independent

    prevalence 1-2% (0.04 - 0.22% severe)

    fatal 1 in 75,000

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    Risk Factors

    Previous contrast reaction either moderate

    or severeasthma

    allergy history requiring medical treatment

    pretesting poor predictor of reaction

    Repeat Reactions, ionicbronchospasm 40% to facial edema 70%

    decrease to 6 - 9% with pretreatment

    decrease to 0.6% with pretreatment and switchto nonionic

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    Late Reactions

    1 hr to 1 week following contrastinjection

    Headache, myalgias, fever, skin

    reactions

    Risk Factors

    Previous contrast reaction

    Interleukin-2 treatment

    usually self-limited, treat severereactions with steroids

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    Severity of Reactions - Minor

    Nausea & vomitingUrticaria

    Pruritis

    Diaphoresis

    S f

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    Severity of Reactions - Moderate

    FaintnessFacial edema

    Laryngeal edema

    Bronchospasm

    S it f R ti S

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    Severity of Reactions - Severe

    Pulmonary edemaRespiratory arrest

    Cardiac arrest

    Seizures

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    Renal Toxicity(increased serum creatinine by more than 25% or > 0.5mg%)

    2-7%

    Risk Factors5 - 10 fold increase with pre-existing renalinsufficiency (increased creatinine)

    Dehydration

    CHF

    Age > 70

    Taking nephrotoxic drugs (nonsteroidalinflammatory agents, gentomycin etc.)

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    Renal Toxicity(increased serum creatinine by more than 25% or > 0.5

    mg%)direct relationship between serumcreatinine and likelihood

    nephrotoxicity

    Hydrate 100 ml/hr Normal saline 4 hrsprior to procedure, continue for 24

    hours

    Those on hemodialysis do not needextra sessions or dialysis

    immediately following contrast

    administration

    M tf i (Gl h )

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    Metformin (Glucophage)

    oral diabetic agentpatients with renal insufficiency may

    develop lactic acidosis

    withhold drug for 48 hrs after

    contrast administration in all patients

    taking this drug

    T t t C t t R ti

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    Treatment Contrast Reactions

    Nausea & Vomitingusually self-limited

    protracted: Prochlorperazine (Compazine) 5-10

    mg IM

    UrticariaDiphenhydramine (Benadryl) 25 - 50 mg IM,

    caution: drowsiness

    add Cimetidine (Tagamet) 300 mg in 20 ml, IV

    slowly

    T t t C t t R ti

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    Treatment Contrast Reactions

    HypotensionBradycardia (Vasovagal)elevate legs (infuses 700 ml)

    IV fluid (normal saline)

    O2 3 L/min

    atropine 0.6 mg IV push, repeat up to 3 mg total

    Tachycardiaelevate legs

    IV fluid (normal saline) may require > 1 Liter

    O2 3 L/min

    T t t C t t R ti

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    Treatment Contrast Reactions

    Bronchospasm or laryngeal edemaO2 3 L/min

    Epinephrine 1:1000 (0.1 - 0.2 ml subq) or

    1:10,000 1 ml IV over 3 min

    Beta 2 agonist 2 -3 puffs

    albuterol (Proventyl)

    metaproterenol (Alupent)

    terbutaline (Brethaine)

    T t t C t t R ti

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    Treatment Contrast Reactions

    Anaphylactoid

    O2 3 L/min

    IV normal saline

    Epinephrine

    Benadryl 25 - 50 mg IVTagamet 300 mg in 20 ml IV slowly

    Solu-medrol 1 gm IVNote: if patient taking beta blocker

    glucagon 1 - 5 mg IV bolus followed by infusion5-15 ug/min or

    isoproternol 1:5000 (0.2 mg/ml)IV 0.5 - 1.0 ml diluted in 10 ml

    1 mg increments

    T t t C t t R ti

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    Treatment Contrast Reactions

    Seizuresprotect airway

    Diazepam (valium) 5 mg IV slowly

    Suspected pheochromocytoma

    phentolamine (Regitine) 5.0 ml (5 mg) IV bolus

    Pregnancy

    Discard breast milk for 24 hours following

    contrast administration

    E t ti

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    Extravasation

    Elevate extremityIce pack 3x day

    Observe for 2-4 hours if volume > 5ml

    E tra asation

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    Extravasation

    Plastic Surgery Consultation

    ionic > 30 ml

    nonionic > 100 ml

    skin blistering/significant tissue damage

    altered tissue perfusion

    increasing pain after 2-4 hours

    change in sensation distal to site of

    extravasation

    Pretreatment Protocols

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    Pretreatment Protocols

    Reduces minor reactions

    Benadryl 50 mg IM or PO 1 hr before

    procedure

    Prednisone 50 mg PO 13, 7, 1 hr beforeprocedure

    Observe patient at least 30 minutes following

    injection

    Pretreatment Protocols

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    Pretreatment Protocols

    Reduction of Nephrotoxicity

    Creatinine level > 2 mg/dl

    Hydrate patient - Oral fluids if unable to drink use

    IV salineMild Renal Insufficiency Patients add N-acetyl-

    cysteine (Mucomyst) : 600 or 1,200 mg PO BID the

    day before and day of the procedure or 150 mg/kg

    IV over .5 hr or 50 mg/kg IV over 4 hr

    Reference:

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    Reference:

    1) White and pharoh 5th&6thedition

    2) Ultrasound Contrast Media in the Study of Salivary Gland Tumors

    ADOLFO GALLIPOLI1 , IOVANNI MANGANELLA 2 , ELISABETTA DE

    LUTIO DI CASTELGUIDONE ANGELO MASTRO

    3) Alternative and specialized imaging modalities

    4) CONTRAST AGENTS FOR RADIOLOGY PROCEDURES

    5) Contrast Agents for Radiology Procedures: Reimbursement Policy

    (Effective 11/01/2012)1996-2012, Oxford Health Plans, LLC

    6)CONTRAST MEDIA TUTORIALJessica B. Robbins, MD Myron A.

    Pozniak, MD

    7) ACR Manual on Contrast Media Version 8 2012 ACR Committee on Drugs

    and Contrast Media