Friday 2 November 2012

Pediatric Sedation






TABLE – I

Chloral Hydrate in Pediatric sedation

  1. Method of Administration.
20 to 75 mg / kg orally or rectally (maximum single dose, 1.0g; if a second dose in given, the maximum total dose in either 100 mg / kg or 2.0 g, whichever is lower).

  1. Contraindications
    1. Compromised hepatic function.
    2. History of obstructive sleep apnea*
    3. Previous unfavorable experience with chloral hydrate.
  2. Advantages
No specific advantages for sedation and treatment of children with fractures.
 
  1. Disadvantages
    1. Prolonged time to peak effect (as long as 60 min).
    2. Difficult to titrate.
    3. Prolonged observation period required.

* Caution is required when using any sedative medication in patients with obstructive sleep apnea.


TABLE – II

Benzidiazepines in Pediatric Sedation

  1. Method of Administration.
    1. Diazepam: 0.1 to 0.3 mg / kg IV or PO. IM administration should be avoided because it is painful.
    2. Midazolam
1.      PO: 0.5 – 0.75 mg / kg.
2.      Nasal: 0.3 – 0.4 mg / kg*
3.      IM: 0.03 – 0.1 mg / kg.
4.      IV: 0.05 – 0.1 mg / kg.
  1. Contraindications
    1. Previous unfavorable experience with benzodiazepines.
    2. (?) Early pregnancy (possible teratogenicity).
    3. Altered state of consciousness.
  2. Advantages
    1. Generally provide excellent sedation and amnesia.
                  B. Reversible if necessary (flumazenil, 10 mg / kg, upto a total dose of 1.0 mg.
  1. Disadvantages
    1. No analgesic effect.
    2. Respiratory depression, especially with parenteral administration.
    3. Combination with narcotics may lead to oversadation or respiratory arrest.

* Many children find the intranasal administration of midazolam to be very unpleasant. This    
    method of administering midazolam is not recommended.





TABLE – III

Opioids in Pediatric Sedation

  1. Method of Administration.
    1. Morphine: 0.05 – 0.1 mg / kg IM or IV.
    2. Meperidine: 0.5 – 1.0 mg / kg IM or IV.
    3. Fentanyl: In increments of 0.001 mg / kg IV (maximum total dose, 0.004 – 0.005 mg / kg).
    4. Nalbuphine: 0.1 mg / kg IM or IV.
    
      Patients younger than 3 months old should be given no more than half of these doses initially. IV titration to desired effect is the ideal way to administer all Sedative medications.
  1. Contraindications
    1. Altered state of consciousness.
    2. Previous unfavorable experience (excludes that medication only).
    3. Sedation for non painful procedure.
  2. Advantages
    1. Provide excellent analgesia.
    2. Reversible if necessary (naloxone 0.001 – 0.005 mg / kg IV titrated to effect).
  3. Disadvantages
    1. Risk of respiratory depression and apnea.
    2. Increased risk of respiratory depression and apnea when combined with other sedatives.
    3. No amnestic effects.
  4. Additional side effects (more likely when used in recurrent doses for treatment of pain).

Nausea, vomiting, pruritus, constipation, decreased gastric motility.

TABLE – IV

Fentanyl and Midazolam in Pediatric Sedation*

  1. Method of Administration IV titration to effect.
    1. Midazolam: In increments of 0.05 mg / kg to a maximum of 0.1 mg / kg. Wait 5 min between doses.
    2. Fentanyl: Begin 5 min after last midazolam dose. Give in increments of 0.001 mg / kg to a maximum of 0.003 mg / kg, wait 2 to 3 min between doses.
  2. Contrandications
    1. Altered state of consciousness.
    2. Previous unfavorable experience with either medication.
    3. Specific contraindications to benzodiazepines or opioids (seen Tables 2 and 3).
  3. Advantages
    1. Provides sedation, amnesia (midazolam), and analgesia (fentanyl).
    2. Reversible if necessary (see Tables 2 and 3).
  4. Disadvantages
    1. Additive respiratory depressant effects.
    2. Additive depressant effects on protective airway reflexes with increased risk for regurgitation and aspiration of gastric contents.

* An excellent review of the advantages and problems associated with this drug regimen is provided in Yaster M, Nichols DG, Deshpande JK, Wetzel RC.
Miazolam – fentanyl intravenous sedation in children: case report of respiratory arrest. Pediatrics 1990;86:463-467.







TABLE – V

Ketamine in Pediatric Sedation

1.       Method of Administration and Dosage.
A.     IM: 4 mg / kg.
B.     IV: 1 – 2 mg / kg.
C.     PO: 6 – 10 mg / kg.
D.     Rectal: 5 – 10 mg / kg.

2.       Contraindications
A.     Altered state of consciousness.
B.     Increased intracranial pressure.
C.     Active upper respiratory infections (increased quantity of secretions and possible increased risk of laryngospasm).
D.     Full stomach.
E.      Prior unfavorable experience with ketamine.
F.      Patients older than 16 yrs old (increased incidence of emergence phenomena).

3.       Advantages
A.     Provides Sedation, amnesia, intense analgesia.
B.     Sympathetic-mediated activity may be beneficial for children with asthma.

4.       Disadvantages
A.     Increases production of saliva and tracheobronchial secretions; coadministration of glycopyrrolate 0.01 mg / kg recommended.
B.     Potential for loss of the airway from:
1.      Laryngospasm secondary to increased secretions.
2.      Aspiration from laryngeal incompetence.
3.      Apnea.
C.     Emergence phenomena: Rare in young children. No advantage to quiet  
      environment. Midazolam may help, but may contribute to oversedation.  



















TABLE – VI

Dosing Schedules and Formulations for Nonsteroidal Anti-inflammatory Drugs in children.


Agent
Dose
Formulations*
Ibuprofen (oral)
5 -10 mg / kg q6h (pubilished dose is for treatment of fever, not specifically for analgesia).
100 mg / 5 mL suspension
Tablets: 200, 300, 400, 600, 800 mg.
Naproxen (oral)
5 – 7.5 mg / kg q12h
125 mg / 5 mL suspension
Tablets: 250, 375, 500 mg.
Ketorolac (IM, IV)
0.5 mg / kg q6h
Injectable 30 mg / mL.
Choline Magnesium
50 mg / kg / day
500 mg salicylate / 5 mL solution
Trisalicylate (Trilisate) (oral) @
Divided into 2 or 3 doses (maximum daily dose, 2.25 g)
Tablets: 500, 750, 1000 mg.
Salsalate @ (oral) (Disalcid)
Pediatric dose not published; adult maintenance dose is 2 – 4 g / day.
Tablets: 500, 750 mg.
Acetaminophen $ (oral, rectal)
10 – 15 mg / kg q4 – 6h
80 mg / 0.8 mL drops
80 mg chewable tablets
160 mg / 5 mL solution
325-, 500-mg tablets
120-, 325-, 650-mg suppositories
* An exhaustive listing of available formulations for NSAIDs may be found in AHFS 
   Drug information 1994.
@ Although they are salicylates, choline magnesium trisalicylate, and salsalate do not cross-react with aspirin and may be used in patients allergic to aspirin. As many as 28% of children with asthma may be in this group of patients. Owing to an association with Reye syndrome, salicylates should be avoided in children with flu-like symptoms or chickenpox.
$ Acetaminophen is considered a member of this class of medications, even though it mainly acts centrally and it only very weaknly inhibits prostaglandin synthesis.
Acetaminophen also does not cross-react with aspirin and may be used in patients allergic to aspirin.
Adapted from Nonsteroidal Anti-inflammatory agents. In McEvoy GK, Litvak K, Welsh OH Jr, eds. AHFS Drug Information 1994. Bethesda, MD: American society of Hospital Pharmacists, 1994; Walson PD, Mortensen ME. Pharmacokinetics of common analgesics, anti-inflammatories, and antipyretics in children. Clin Pharmacokinet 1989;17:116-137, with permission.






 

Sunday 30 September 2012

Superior Labral Anteroposterior Tear

TABLE 1 Current Superior Labral Anteroposterior (SLAP) Lesion Classification with Associated Clinical Findings and Mechanisms of Injury
Type Biceps-Labral Complex Extensiona Comments
Snyder et al. [2]


    I Fraying 11-1 Could be incidental finding; more significant in young people involved in overhead activities
    II Tear with biceps extension 11-1 Most common type; association with acute traction, repetitive overhead motion, and microinstability; could be associated with type IV
    III Bucket-handle tear with intact biceps 11-1 Less severe than type IV; association with fall on outstretched arm
    IV Bucket-handle tear with biceps extension 11-1 More severe than type III because of biceps extension; could be associated with type II; association with fall on outstretched arm
Maffet et al. [15]


    V Not specified 11-5 Either a Bankart lesion with superior extension or a SLAP lesion with anterior inferior extension
    VI Anterior or posterior flap tear 11-1 Probably represents type IV or less likely type III with tear of the bucket-handle component
    VII Not specified 11-3 Type of middle glenohumeral ligament extension (avulsion or split) not specified; association with acute trauma with anterior dislocation
Resnick Db


    VIII Not specified 7-1 Similar to type IIB but with more extensive abnormalities; association with acute trauma with posterior dislocation
    IX Not specified 7-5 Global labrum abnormality; probably traumatic event
Beltran Jc


    X Not specified 11-1 + Rotator interval extension; articular side abnormalities
Morgan et al. [21]


    IIA II 11-3 Similar to type X; association with repetitive overhead motion
    IIB II 9-11 Association with infraspinatus tear
    IIC II 9-3 Association with infraspinatus tear
  • a Clock positions.
  • b Unpublished data.
  • c Presented at the annual meeting of the Radiological Society of North America, Chicago, IL, December 2000.

Sunday 19 August 2012

Cervical Spine

Classic Patterns of Cervical Radiculopathy




Abnormalities
Nerve rootInterspacePain distributionMotorSensoryReflex
C4
C3–C4
Lower neck, trapezius
NA
Cape distribution (i.e., lower neck and upper shoulder girdle)
NA
C5
C4–C5
Neck, shoulder, lateral arm
Deltoid, elbow flexion
Lateral arm
Biceps
C6
C5–C6
Neck, dorsal lateral (radial) arm, thumb
Biceps, wrist extension
Lateral forearm, thumb
Brachioradialis
C7
C6–C7
Neck, dorsal lateral forearm, middle finger
Triceps, wrist flexion
Dorsal forearm, long finger
Triceps
C8
C7-C8
Neck, medial forearm, ulnar digits
Finger flexors
Medial forearm, ulnar digits
NA
T1
C8-T1
Ulnar forearm
Finger intrinsics
Ulnar forearm
NA

NA = not applicable.
Information from references 3 and 4.
 The nerve roots exit above their correspondingly numbered vertebral body from C2-C7. C1 exits between the occiput and atlas, and C8 exits below the C7 vertebral body.
A C4-C5 disc herniation will compress the C5 nerve root
A C5-C6 disc herniation will compress the C6 nerve root
A C6-C7 disc herniation will compress the C7 nerve root
A C7-T1 disc herniation will compress the C8 nerve root
A T1-T2 disc herniation will compress the T1 nerve root

Monday 2 July 2012

MRI REPORTING CATEGORIES


 A - 3 hrs


CERVICAL  SPINE  

DORSAL SPINE

LUMBAR SPINE

BRAIN - ROUTINE

ABDOMEN -ROUTINE

PELVIS - ROUTINE

ALL CASES WITHOUT SIGNIFICANT FINDINGS



B - 6 hrs


SPINE CONTRAST

BRAIN - CONTRAST

KNEE

HIP

ANKLE

NECK

THORAX -ROUTINE

ABDOMEN ROUTINE

MRA - BRAIN

MRA - NECK NON CONTRAST

ORBIT

PNS








C - 12 hrs

BRACHIAL PLEXUS

LUMBOSACRAL PLEXUS

SHOULDER

ELBOW

WRIST

FOOT

HIP WITH CONTRAST

MRCP

PELVIS FEMALE WITHOUT CONTRAST

PELVIS MALE

UPPER LIMB

LOWER LIMB

MR FISTULOGRAM

MRA - NECK WITH CONTRAST

MRA - AORTA , ILIAC ,FEMORAL

FACE

PHARYNX

TEMPORAL BONE

INFANT BRAIN










D - 24 hrs


ABDOMEN - MASS

LIVER WITH CONTRAST

KIDNEY WITH CONTRAST

PELVIS WITH CONTRAST

WRIST WITH CONTRAST

SHOULDER ARTHROGRAM

MR SPECTROSCOPY

MRS WITH MR PERFUSION

MRA LOWER LIMBS

MRA - RENAL ANGIO

MRA - OTHER AORTIC BRANCHES

MR MAMMOGRAPHY

TEMPOROMANDIBULAR JOINT

HAND , FINGER ,TOE