Intro Flashcards

1
Q

Principle of x ray

A
  1. represent a form of ionizing radiation
    produced by an X-ray tube.
  2. The X-ray beam is passed through the body
    where a portion of the X-rays are either
    absorbed or scattered by the internal
    structures, and the remaining X-ray is
    transmitted to a detector (e.g., film)
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2
Q

The 5 X-ray densities

A

• air is represented as black on radiograph.
• Very dense material such as, cortical bones
metal, stones or contrast material are
represented as white.
• Body tissues are varying degrees of grey,
depending on density

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3
Q

Uses of X-ray

A

• Orthopedic evaluations
• Chest or abdomen screening
• Dental examination
• Mammography
• Verification of correct placement of surgical
markers prior to invasive procedures.
• Spot film or static recording during
fluoroscopy.

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4
Q

Advantages of X-ray

A

• Good bone resolution
• Widely available
• Quick imaging

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5
Q

Disadvantages of X-ray

A

• Uses ionising radiation can cause cells mutation
and cancer
• Not suitable for soft tissues

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6
Q

Fluoroscopy

A

Live radiographic examination detecting the anatomy and
motion of internal structures(Contrast agents often used).

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7
Q

Uses of Fluoroscopy

A

• Barium Study(meal, swallow, enema, fistolography )
• Hystero-salpingo-graphy
• Angiography and interventional radiology
• Orthopedic surgery, e.g. reduction and fixation of fractures,
joint replacements.

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8
Q

DXA scan

A

It is a test that measures the density of bones.
The denser the tissue, the less X-rays pass
through.

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9
Q

use of DEXA

A

calculate the strength of bones ,
measure bone loss, helps diagnose osteoporosis
and assess whether a person’s bones are at risk
of fracture.

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10
Q

ULTRASOUND?

A

Medical Ultrasound uses ultra-high-frequency
sound waves (1 MHz to 30 MH) to produce
cross-sectional images of the body.

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11
Q

Uses of ultrasound

A
  1. Examining deep structures:

Abdominal ultrasound»»>Using convex
transducer
Obstetrical and gynaecological»»Convex and or
transvaginal probe
Echocardiography»»sector probe
Transcranial US»>sector probe

  1. Examining superficial structures:»>using linear
    probe
    Small parts ( Neck,breast, scrotal)
    Vascular Doppler
    Musculoskelatal ultrasound
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12
Q

Advantages of US over other imaging
modalities

A

• Lack of ionizing radiation, a particular
advantage in pregnancy and pediatrics
• Relatively low cost
• Wide availability
• Portability of equipment.

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13
Q

Disadvantages and limitations of US

A

• US is highly operator dependent: US
relies on the operator to produce and
interpret images at the time of
examination.
• US cannot penetrate gas or bone.
• Bowel gas may obscure structures deep in
the abdomen, such as the pancreas .

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14
Q

Doppler principle

A

Doppler ultrasound measures the movement of
the RBCs through the ultrasound beam.

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15
Q

Uses:
Doppler principle

A
  1. Detection of tissue movement
  2. Measurement of blood flow velocity and
    direction
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16
Q

Doppler Advantages

A

• Non Invasive
• Non Ionizing
• Portable
• No nephrotoxic agents
• See arterial Lumen & wall
• Assess haemodynamics
• Detect occluded Aneurysm

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17
Q

Doppler Limitations:

A

• Ca Hender
• Skin Henders : ulcers, bandages, scars
• Need patient co-operation
• Operator dependent

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18
Q

Computed tomography

A

Computed Tomography (CT) is a high-resolution technique using X-ray to
generate axial cuts of any area of the body (slices).
Images can be viewed in any anatomical plain (axial, coronal or sagittal)
also, reconstructed into three dimensional images (3D)

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19
Q

MOST COMMON INDICATIONS FOR
COMPUTED TOMOGRAPHY

A

1-Emergencies:
Head trauma as CT is the best modality in detection of acute
bleeding, skull fractures.
Stroke: differentiate ischemic from hemorrhagic stroke
Poly trauma: solid organ injury and acute hemorrhage
2- Bone fracture: the best imaging modalities
3-Complex intra-abdominal conditions: solid organ focal lesions
(hepatic, renal, spleen), intestinal obstruction, inflammatory conditions,
biliary obstruction, acute vascular conditions and different abdominal
masses
4- Chest: pneumonia (the standard imaging modality in COVID 19), lung
masses, mediastinal LNs, trauma, pneumothorax, hemothorax.

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20
Q

CONTRAINDICATIONS OF CT

A

1- Absolute contraindications: Early pregnancy, as the risk of
radiation usually outweighs diagnostic benefit.
2- Relative contraindications:
Children, since they are more radio-sensitive except when
indicated.
Renal impairment, since intravenous contrast can further injury the
kidneys, in severe cases necessitating dialysis.
Allergy to intravenous contrast media.
Pheochromocytoma patients, since intra-venous contrast may
induce hypertensive crisis

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21
Q

IMAGNETIC RESONANCE IMAGING

A

Magnetic resonance imaging is a medical imaging technique used in
radiology to form pictures of the anatomy and the physiological processes
of the body.

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22
Q

ADVANTAGES OF MRI

A

• MR image acquisition does not use X-ray or ionizing radiation. It
requires little patient preparation and is non-invasive, so patient
acceptability is high.
• MRI produces images in multiple planes with equivalent resolution
without moving the patient.
• MRI contrast agents are very well tolerated and are much less likely
than x-ray and CT contrast agents to cause allergic reactions or alter
kidney function

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23
Q

CONTRAINDICATION OF MRI:

A

1- People with implants, particularly those containing iron, —
pacemakers, vagus nerve stimulators, implantable cardioverterdefibrillators,
loop recorders, insulin pumps, cochlear implants, deep
brain stimulators, and capsules from capsule endoscopy should not
enter an MRI machine.
2- Pregnancy: Not in the 1st trimester
3- Contrast agents—patients with severe renal failure who require
dialysis may risk a rare but serious illness called nephrogenic
systemic fibrosis that may be linked to the use of certain gadoliniumcontaining
agents, such as gadodiami

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24
Q

DISADVATAGES OF MRI:

A

• Claustrophobia—people with even mild claustrophobia may
find it difficult to tolerate long scan times inside the machine.
• Noise—loud noise commonly referred to as clicking and beeping,
as well as sound intensity up to 120 decibels in certain MR
scanners, may require special ear protection.
• Keeping still for long time cannot be tolerated by many patients
• Expensive than x-ray imaging or CT scanning and not widely
available

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25
Q

1.ABRASION:

A

It is destruction of the surface epithelium of the skin without
loss of dermis integrity (Fig 1).
• It is caused by friction against rough surface e.g., roll-over
trauma

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26
Q

Treatment of ABRASION:

A

• Cleaning of the area with liberal amounts of normal saline
and antiseptic solution to remove all debris.
• Application of topical antibiotic and Vaseline gauze for 7 to 10 days when
re-epithelialization becomes complete.

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27
Q

Complications of ABRASION:

A

• Infection leads to deep tissue destruction and may leave raw area.
• Pigmentation or tattooing of the area by embedded debris.

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28
Q

INCISED WOUNDS (CUT WOUNDS):

A

These wounds are caused by sharp objects such as knives and broken
glass. Surgical wounds belong to this type.

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29
Q

Clinically INCISED WOUNDS (CUT WOUNDS):

A

Incised wounds are cleanly cut, have regular
edges, bleed profusely and may be
accompanied by cut of deeper structures such as
muscles, tendons, nerves, and blood
vessels

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30
Q

Treatment:

A

• Management should entail resuscitation of the patient if the wound is a big
one and bleeds too much.
• Management of the wound itself includes:
o Cleaning the wound by washing it liberally with normal saline and
antiseptic solution
o Repair of cut important structures such as tendons, nerves if ends are
close and re-anastomosis of important nourishing blood vessels.
o Wound is closed primarily by simple suture without drainage if clean
not contaminated or with drainage if contaminated or potentially
infected.

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31
Q

LACERATED WOUNDS:

A

These are severely damaged wounds caused by traffic road accidents or rollover
trauma.

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32
Q

Clinically of LACERATED WOUNDS:

A

• Tissues are compressed and devitalized by severity
of trauma.
• Skin has irregular edges with scanty bleeding and
dirty ischemic margins (Fig 3).
• Devitalization may occur in deeper structures
such as muscles, nerves, tendons, and blood vessels. Dirties and debris
are usually found in these wounds.
• There may be significant skin loss or degloved skin (degloving wounds)

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33
Q

Treatment of LACERATED WOUNDS:

A

o Management should start by trauma life support in patients with big
wounds or polytraumatized.
o Under general anesthesia, the wound is cleaned with liberal amounts
of normal saline and antiseptic solution.
o All devitalized tissues and muscles should be excised until the tissues
look good vascularized and bleed freshly.
o Deep important structures are repaired according to their conditions,
tendons and big vessels are repaired, nerves if they can approximate
easily are repaired, otherwise marked for later repair.
o Skin is closed with drainage, if possible, if there is significant loss of
skin and approximation of skin edges is difficult, local skin flaps or
skin grafts are used.
o In some circumstances the wound is left open for later reconstruction.

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34
Q

PENETRATING WOUNDS (STAB WOUNDS):

A

• These are wounds caused by sharp
pointed objects penetrating deeply into
the body.
• Such wounds may penetrate the visceral
cavities (peritoneum, pleura or
pericardium) and cause serious injuries to
vital organs such as the liver, spleen,
bowel, lungs or heart.

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35
Q

Clinically of PENETRATING WOUNDS (STAB WOUNDS):

A

o Patients may become shocked shortly
after injury due to internal
hemorrhage. The wound itself may
look trivial and does not bleed

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36
Q

Treatment ofPENETRATING WOUNDS (STAB WOUNDS):

A

o Management of the patient on traumatic life support bases.
o With any suspicion that the wound is extending into the visceral
cavities, the patient should be explored by laparotomy or thoracotomy
according to the site of wound.
o Arrest of bleeding and repair of damaged vital organs according to the
nature of injury, liver repair, splenectomy, bowel repair…etc.

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37
Q

PERFORATING WOUNDS:

A

• These are wounds which penetrate the body and have an inlet and an exit.
The commonest example is gunshot injuries (Fig 5).
• Such wound usually has great damage to internal organ,
partly by the penetrating object and the damage of the
surrounding tissue caused by evacuation effect and
propagated extensive heat.

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38
Q

Clinically of PERFORATING WOUNDS:

A

o The patient may become shocked, hemodynamically unstable and
require emergency resuscitation and very early surgical
exploration to stop bleeding and removal of injurious
objects or foreign body if possible.

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39
Q

CONTUSION (BRUISES)

A

• It is reddish swelling caused by
extravasations of blood into the tissue
spaces. It is usually caused by hitting by
blunt object as blow or heavy stick. Due to
disintegration of extravasated blood, the area is at first red then within few, it
becomes yellow days and later becomes
greenish and lastly fades out

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40
Q

Treatment of CONTUSION (BRUISES)

A

o In the first 24 hours cold compresses are applied to the area to induce
vasoconstriction and stop further blood extravasation
o After 24 hours, warm compresses are applied to induce vasodilation
and enhance absorption of extravasated blood.

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41
Q

HEMATOMA:

A

• It is a collection of blood in
the tissue spaces caused by
extravasation from injured
sizable vessel.
• Blood is at first fluid and
then becomes clotted
within 3-4 days and after
one week it turns fluid
again

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42
Q

Treatment of HEMATOMA:

A

o Large rapidly increasing hematoma is treated by exploring the area or
re-opening the wound, washing out the hematoma and ligating the
bleeding vessel.
o Moderate-sized hematoma may resolve by repeated aspiration under
aseptic conditions.
o Small hematoma may be left to resolve spontaneously.

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43
Q

Complications of HEMATOMA:

A
  1. Infection leading to abscess formation.
  2. Calcification forming calcified hematoma.
  3. Pressure on neighboring structures
  4. Opening into the nearby vein leading to traumatic arteriovenous fistula
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44
Q

WOUND CLEANING

A

• Thoroughly clean the wound with normal saline or antiseptic solution.
• Use a large syringe for irrigation. Attach a 16- or 19-gauge needle or soft
IV catheter to generate pressure.
• Control residual bleeding with compression, ligation, and cautery
• Dead or devitalized muscle is dark in color, soft, easily damaged; does not
contract when pinched. Dead tissue does not bleed when cut.
• Prep skin with antiseptic.

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45
Q

TETANUS PROPHYLAXIS

A

• Patient vaccinated: give booster dose if needed.
• Patient not vaccinated: give antitetanic serum and start dose of tetanus
toxoid vaccine (separate syringes, separate sites)
• Tetanus immunoglobulin (human) 250 units IM.

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46
Q

ANTIBIOTIC PROPHYLAXIS

A

• Contaminated wounds
• Penetrating wounds
• Abdominal trauma
• Compound fractures
• Lacerations greater than 5 cm
• Wounds with devitalized tissue
• High risk anatomical sites—hand, foot

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47
Q

WOUND CLOSURE

A

• Less than 6 hours from injury, cleaned properly: primary closure.
• Greater than 24 hours, contaminated or animal bite: do not close.
• Wounds not closed primarily should be packed lightly with damp gauze.
• If clean after 48 hours, delayed primary closure.
• If wound infected, pack lightly, heal by secondary intention.

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48
Q

Low COP symptoms:

A

• Easy fatigue
• Anginal pain
• Dizziness & ggiddiness
• Syncopal attack

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49
Q

Preoperative Considerations that influence the choice of anesthetic
technique:

A

1-Co-existing disease
2-Site of the surgery
3-Age of the patient
4-Preference of the patient
5-Body position of the patient during the surgery
6-Elective or emergency surgery
7-Likelihood of increased amounts or gastric contents (as in pregnancy)

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50
Q

Indication of general anesthesia:

A

❖ Extreme anxiety and fear
❖ Patient with mental or physical disability or disoriented
❖ Age (Infants and children)
❖ Prolonged procedure

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51
Q

Contraindication of general anesthesia

A

❖ Lack of adequate training by the doctor
❖ Lack of adequate equipment
❖ Lack of adequate facilities
❖ Compromised patient

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52
Q

Monitors for general anesthesia:

A

1-ECG
2-Blood pressure
3-Tempreture
4-Respiratory rate
5-Capnogram for end tidal CO2
6-Pulse oximeter for O2 saturation and pulse
7-Train of four for neuromuscular monitoring

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53
Q

Complication of general anesthesia and Postoperative care

A

➢ Anaphylaxis
Epinephrine (Adrenaline) is the only recommended medication for
treating anaphylaxis, antihistamines and steroids may also alleviate
symptoms.
➢ Hypothermia
Passive rewarming with heated blankets and warm fluids.
➢ Nerve injury
-Physical therapy
-Medication as Gabapentin, Pregabalin and Ibuprofen
➢ Nausea and vomiting
-Ensure good oxygenation and normal blood pressure
-IV fluids if dehydrated
-Medication as zofran
➢ Cardiovascular collapse
-Anticholinergic drugs for bradycardia
-Increase the venous return using gravity
-IV fluid
-Sympathomimetic drugs
➢ Respiratory depression
-Oxygen therapy
-Relieve pain
-Mechanical ventilation
➢ Sore throat
-Most cases resolve spontaneously
➢ Pain control
- Nonsteroidal anti-inflammatory drugs (NSAIDs)
- Opioids - Acetaminophen - Alpha-2 agonist
- Antidepressants - Anticonvulsant - Corticosteroids - Lidocaine

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54
Q

Indications of Spinal anesthesia

A

(1) Bone of the lower limb operations. (2) Obstetric, gynecological
operations.
(3) Urologic and rectal operations (pills and fissures).
(4) Operation of lower abdomen (appendix).

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55
Q

Contraindications of Spinal anesthesia

A

Absolute contraindications:
(1) Patient refusal. (2) Allergy to local anesthetics.
(3) Skin infection at the injection site. (4) Severe hypovolemia (shock).
(5) Coagulopathy and the use of therapeutic anticoagulant.
(6) Increased intracranial pressure (may predispose to brainstem
herniation) .

Relative contraindications:
(1) Neurological disorders. (2) Prior spine surgery and back pain.
(3) Uncooperative patient. (4) Psychosis, dementia or emotional
instability.
(5) Certain cardiac lesions e.g., Aortic stenosis

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56
Q

Preparation of the patient: as general anesthesia beside:

A

*History: Exclude history of back problems.
*Physical examination: Especially examination of the back for
dermatologic conditions, kyphoscoliosis or surgical scar. Palpation of
lumbar interspaces
*Investigation: Especially bleeding time, clotting time, Prothrombin Time
(PT) and Partial Thromboplastin Time (PTT).
*Premedication: Preoperative visit may allay fear, and pharmacologic
premedication can allow smooth block.

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57
Q

Complications of spinal and epidural anesthesia

A

(1) Hypotension: (especially with spinal anesthesia): Reflect
venodilatation with decreased venous return and cardiac output
Prophylaxis: Adequate hydration (10-15 ml/kg of crystalloid) before
induction of spinal and epidural anesthesia.
Treatment: - Rapid I.V fluid.
-Head down tilt 5-10 degrees after fixation of local anesthetic level.
-Vassopressor: as Ephedrine (α and ß agonist) 5-10 mg i.v. in incremental
doses.

(2) High spinal anesthesia:
Occur with spinal anesthesia manifested by severe hypotension,
bradycardia and respiratory insufficiency or apnea.
Treatment:
1-Support of the airway: -100% oxygen by simple face mask.
- Intubation and mechanical ventilation may be needed.

2-Support of circulation:
- Head down positioning
- I.V fluid
- Ephedrine (5-10 mg i.v) to treat hypotension.
- Atropine i.v to treat bradycardia.
- Inotropes as adrenaline (5-10 µg) in hypotension.

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58
Q

Complications of spinal and epidural anesthesia(other’s)

A

(3) Nerve injury:
During placement of a needle, it can come in direct contact with the nerve
roots. The nerve injuries lead to persistent paresthesia that resolve without
treatment within weeks or months.
(4) Vascular injury:
Injury to blood vessels result in hematoma due to continued bleeding from
the epidural venous plexus. This complication is reported in patients with
coagulopathy or has been taking anticoagulants, but it may occur in
patients with no apparent risk factors.
(5) Meningitis: The incidence of meningitis has fallen dramatically with
the use of disposable needles and trays.
6) Urinary retention:
Blockade of S2-S4 is associated with loss of bladder tone and inhibition of
the voiding reflex. It may require intermittent catheterization.
(7) Backache:
Needle penetration can cause hyperemia, local tissue irritation, and reflex
spasm of muscles. Backache may be also reflecting ligament strain due to
profound skeletal muscle relaxation and surgical positioning.
(8) Headache (postdural puncture headache):
It is believed to be due to decreased CSF pressure resulting from leakage
of CSF through the needle hole in the dura. This exerts downward traction
on the structures of the central nervous system and on the blood vessels
that are attached to both the dura and the brainstem.
Risk factors: -Young females - Using large gauge needle

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59
Q

Character of post dural puncture headache:

A

-It is frontal or occipital.
-Associated with nausea and vomiting.
-The headache is postural in nature, worse in the upright position.
-Beginning within 6-12 hours after lumbar puncture.
-Associated with diplopia and tinnitus.

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60
Q

Treatment of postdural puncture headache:

A

-Aggressive hydration. -Soft diet and stool softeners.
-Analgesics and bed rest. -Caffeine (300-500mg) oral once or twice
daily.

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61
Q

Uses for infiltrative anesthetics are as follows:

A

1-Subcutaneous infiltration (IV placement, superficial biopsy, suturing).
2-Submucosal infiltration (dental procedures, laceration repairs).
3-Wound infiltration (postoperative pain control at incision site).
4-Intraarticular injections (postsurgical pain control, arthritic joint pain
control).
5-Infiltrative nerve blocks (ankle block, scalp block, digit block).

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62
Q

Most common drugs used in local anesthetic infiltration:

A

Drug Onset Maximum dose Duration
Lidocaine Rapid 4.5 mg/kg 120 min
Bupivacaine Slow 2.5 mg/kg 4 hours

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63
Q

Complications associated with local anesthesia:

A

1- Pain on injection: Can be due to aggressive insertion of the needle,
damaging soft tissues, blood vessels, nerves.
To prevent: use topical
anesthetic application and using a smaller-gauge needle.
2- Needle fracture: In most cases, needle fracture happened due to
unexpected motion of the patient or assistants.
3- Lack of effect: may be due to anatomical variants, pathological and
psychological factors, and poor technique.
4-Prolongation of anesthesia and various sensory disorders:
paresthesia, or neuralgia. Avoiding high concentration of anesthetic agent
is recommended.
5-Hematoma: due to venous or arterial laceration.
To prevent hematoma
formation : aspiration before injection , using a short needle and a
minimum number of needle penetrations into tissues. When swelling forms
immediately after injection, localized pressure should be applied.
6-Edema: Swelling of tissues can be due to trauma during injection,
infection, allergy, hemorrhage, and injection of irritating solutions. It`s
managed as a hematoma.
7-Infection: is rare since the usage of disposable needles.
To prevent
infection: The area to be penetrated should be cleaned with a topical
antiseptic prior to insertion of the needle. The local anesthetic should not
be injected through the infected area. Antibiotics should be prescribed.

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64
Q

Natural suture materials

A

A. Catgut: natural absorbable suture material (made from the submucosa
of bovine intestine) is absorbable suture material, but
the resorption time is highly variable. It stimulates a
considerable inflammatory reaction and tends to
potentiate infections.
B. Silk: a natural nonabsorbable suture material and
is an animal protein but is relatively inert in human
tissue and is a non-absorbable suture material.
• It has a favorable handling characteristic.
• It is unsuitable for suturing arteries to plastic grafts or for insertion of
prosthetic cardiac valves.
• Silk sutures are multifilament, providing mechanical immune barriers
for bacteria.

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65
Q

Synthetic non-absorbable sutures

A

generally inert polymers that retain
strength. However, their handling characteristics are not as good as those of silk,
and they must usually be knotted at least four times, resulting in increased
amounts of retained foreign material.
• Multifilament plastic sutures may also become infected and migrate to
the surface like silk sutures.
• Monofilament plastics will not harbor bacteria. Nylon monofilament is
extremely nonreactive, but it is difficult to tie. Monofilament
polypropylene is intermediate in these propertie.
Vascular anastomoses rely indefinitely on the strength of sutures; therefore, use
of absorbable sutures may lead to aneurysm formation.

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66
Q

Synthetic absorbable sutures

A

strong, have predictable rates of loss of
tensile strength, incite a minimal inflammatory reaction, and have special
usefulness in gastrointestinal, urologic, and gynecologic operations that
are contaminated.
• Polyglycolic acid and polyglactin retain tensile strength longer in
gastrointestinal anastomoses.
• Polydioxanone sulfate and polyglycolate are monofilament and lose
about half their strength in 50 days, thus solving the problem of premature
breakage in fascial closures.
• Poliglecaprone monofilament synthetic
sutures have faster reabsorption, retaining
50% tensile strength at 7 days and 0% at 21
days. This suture is suitable for low-load
soft tissue approximation but is not intended
for fascial closure.

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67
Q

Stainless steel

A

wire is inert and maintains
strength for a long time. It is difficult to tie
and may have to be removed late postoperatively because of pain. It does
not harbor bacteria, and it can be left in granulating wounds, when
necessary, and will be covered by granulation tissue without causing
abscesses.

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68
Q

SUTURES SUBSTITUTES

A
  1. Staples, whether for internal use or skin closure, are mainly steel-tantalum
    alloys that incite a minimal tissue reaction. The technique of staple placement
    is different from that of sutures, but the same basic rules pertain.
    • There are no real differences in the healing that follows
    sutured or stapled closures. Stapling devices tend to
    minimize errors in technique (Fig 17).
  2. Surgical glues or tissue adhesives are now established
    as safe and effective for the repair of small skin incisions.
    The most common forms are cyanoacrylate-based glues.
  3. Tissue adhesives (Steri-strips) are often less painful
    than sutures or staples, and the seal can serve as the
    wound dressing as well (Fig 18).
    • Size of suture “bite” and interval between bites should be equal in length,
    proportional to thickness of tissue being approximated.
    • Suture is a foreign body: use minimal size, amount of suture necessary to
    close wound.
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69
Q

Basics of wound closure

A
  1. Good approximation of wound edges is important to
    proper wound closure technique (Fig 19).
  2. The placement of deep sutures subcutaneously to approximate the skin
    edges.
    • When placing deep sutures, absorbables (e.g.,
    gut, Dexon, Vicryl, Monocryl) are typically used. The knot is
    buried.
    • All deep sutures serve to eliminate the dead space and relieve
    tension from the wound surface (Fig 20).
  3. Achieve hemostasis prior to wound closure to avoid
    future complications such as hematoma.
  4. Use atraumatic skin-handling technique with
    instruments such as skin hooks and small forceps.
    Typically, a cutting needle is the needle of choice.
  5. For wound closure in the head and neck region,
    small 5-0 or 6-0 sutures of nonabsorbable Prolene.
  6. Take great care to avoid tension during closure.
  7. Ensure that wound edges are not only aligned but are also
    everted (Fig 21). Eversion of all skin edges avoids unnecessary
    depression of the resultant scar.
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70
Q

Suturing techniques

A

o Surgical suture material
o Needle holder (Fig 22)
o Tissue forceps (Fig 23)
o Stitch scissor (Fig 24)
o Drapes
o Antiseptics
o Anesthetics
o Artery forceps

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71
Q

SUTURE MATERIALS

A

Non-absorbable
– Use when possible
– Braided suture not ideal for contaminated wounds
Absorbable
– Degrades, loses tensile strength within 60 days
– Option when not possible for patient to return or for
children for whom suture removal may be difficult

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72
Q

Types of wound suturing

A
  1. Interrupted sutures
  2. Simple running suture
  3. Vertical mattress suture
  4. Horizontal mattress suture
  5. Subcuticular suture
  6. Purse string suture
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73
Q

Perioperative

A

is a term used to
describe the entire span of surgery,
including what occurs before, during,
and after the actual operation.

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74
Q

Phases of perioperative care

A
  1. Preoperative: begins with the decision to perform
    surgery and continues until the client has reached the
    operating area.
    2 .Intraoperative: includes the entire
    duration of the surgical procedure, until
    transfer of the client to the recovery area.
  2. Postoperative: begins with admission to the recovery area and
    continues until the client receives a follow up evaluation at home, or is
    discharged to a rehabilitation unit.
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75
Q

Goal of preoperative assessment

A
  1. Assess the fitness for anesthesia.
  2. Optimizing patient physical condition for anesthesia and surgery.
  3. Arrange further investigations, consultations and treatments for
    patients not yet optimized
  4. Allay fear and anxiety.
  5. Establishment of preoperative fasting.
  6. Premedication.
  7. Provide appropriate information to the patient and obtain consent.
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76
Q

I. History

A

• History of present illness and reason for surgery
• Past medical history
• Medical conditions (acute and chronic)
• Previous hospitalization and surgeries
• History of any past problem with anesthesia
• Allergies
• Substance use: alcohol, tobacco, street drugs
• Family history: Hereditary diseases and Anesthetic history.
• Review of system
• Drug history

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77
Q

Drug history

A

Antihypertensive
ACEI May be associated with severe hypotension during induction.
B blocker -ve inotropic effect additive with anesthetic agents.
Ca blocker Decrease AV conduction and excitability.

Digoxin Toxicity enhanced by hypokalemia (should be corrected) pre

Diuretics
Can cause hypokalemia may potentiate Ms Relaxant

Anticonvulsant
MAOIs React with opioid (pethidine) causing coma or convulsion
Tricyclic A.D Inhibit metabolism of catech. Increase likehood of arrhythmia

Antibiotics
Aminoglycoside Potentiate effect of NM Blockers

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78
Q

History of smoking

A

• Vascular disease of peripheral, coronary and cerebral
circulation
• lung carcinoma.
• Effect of nicotine ..tachycardia and HPT
• Increase in CO hemoglobin decrease O2 delivery to the
tissues.
• Six fold increase in postoperative respiratory morbidity
• Should be stopped 6 weeks or at least 12 hrs before surgery

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79
Q

➢General examination

A

• Nutritional state
• Fluid balance.
• Condition of skin and mucus m.(anaemia –perfusion-jaundice )
• Temperature

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80
Q

➢Cardiovascular examination

A

• Presence of dyspnea, fatigue, chest pain.
• Peripheral pulse (rate, rhythm, volume).
• Neck veins
• Carotid bruits
• Heart sounds
• Lower Limb edema

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81
Q

➢Respiratory examination

A

• Presence of cyanosis ( peripheral or central).
• Presence of cough
• Presence of tachypnoea
• Tracheal shift
• Auscultation of all the lung fields

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82
Q

➢Nervous system

A

• Documentation of the level of consciousness
• Documentation of any cranial or peripheral nerve lesions

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83
Q

➢Skeletal system

A

• Documentation of any skeletal muscles dysfunction or syndromes

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84
Q

➢Airway examination

A

• Teeth exam. ( dentures, loose teeth, protruding upper incisors)
• Prediction of difficult airway (for ventilation or endotracheal intubation)

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85
Q

➢CBC

A

• Major surgery requiring group and screen or cross and match
• Male>50 years.
• All adult female.
• Bloody surgery.
•History of anemia.
•Haemoglobinopathy.
• CVD

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86
Q

➢Urine analysis

A

• Routine for all patients

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87
Q

➢FBS

A

•History of diabetes,
•Patients on steroid therapy

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88
Q

➢Renal function test (urea, creatinine ,electrolytes)

A

•All pts > 65 years
• +ve urinalysis
•Patient with renal or liver diseases
• Diabetic patients
• Malnutrition
• Dehydrated patients
•Patients on diuretics
•Antihypertensive
•Steroid drugs
•Pituitary or adrenal disease
•Vascular disease
•Digoxin , diuretic, or other drug therapies affecting electrolytes

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89
Q

➢Liver function test

A

•History of liver disease
•Previous hepatitis
• Malnutrition
•Alcoholism

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90
Q

➢Coagulation profile (INR, aPTT )

A

•History of bleeding disorder
•Liver disease
•Drug abuse
•Anticoagulant therapy

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91
Q

➢ECG

A

•All patients > 50 years
•Smoker>45 years
•History of CVD and DM
•History of Pulmonary disease
•History of medication active on CVS or diuretics

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92
Q

➢Chest X-ray

A

•All patients > 60 years
•Any possibility of cardiovascular and/or pulmonary disease
•Thyroid enlargement (thoracic inlet x-ray)

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93
Q

➢ Pulmonary Function test & arterial blood gases

A

•All COPD and asthmatic pts
•Patients scheduled for elective thoracotomy.

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94
Q

➢Pregnancy (HCG)

A

•Women of reproductive age

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95
Q

Go for surgery if

A

•Pt is fit for anesthesia.
•Pt is in the optimal
physical condition.
•Pt is in the almost possible
Correction.
•Pt is in high emergency
Situation.
•There is a legal consent.
•Pt is not fit for anesthesia.
•Pt is not in the optimal
physical condition.
•Pt is not in the almost possible
Correction.
•Pt is not in high emergency
Situation.
•There is no legal consent.===
Determine the degree of fitness
and the anesthetic risk by ASA
grading

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96
Q

Postpone surgery if

A

•Pt is not fit for anesthesia.
•Pt is not in the optimal
physical condition.
•Pt is not in the almost possible
Correction.
•Pt is not in high emergency
Situation.
•There is no legal consent.
Determine the degree of fitness
and the anesthetic risk by ASA
grading===
Cardiac, pulmonary consultation
Or any other measures to optimize
Physical condition of the pt

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97
Q

Pre-Operative Optimization(Medications )

A

Pre -operative medications to consider
Pre -operative medications to stop
Pre -operative medications to adjust

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98
Q

Pre-Operative Optimization(Diseases )

A

• Hypertension
• Coronary Artery Disease
• Respiratory Diseases
• Aspiration
• Fasting Guidelines
• Hematological Disorders
• Endocrine Disorders
• Obesity and Obstructive Sleep Apnea

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99
Q

➢Pre -operative medications to consider:

A

• Risk of GE reflux: sodium citrate and/or ranitidine and/or metoclopramide 30
min-1 h prior to surgery
• Risk of infective endocarditis: antibiotics
• Risk of adrenal suppression: steroid coverage
• Anxiety: consider benzodiazepines
• COPD, asthma: bronchodilators
• Coronary artery disease risk factors: nitroglycerin and -blockers

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100
Q

➢Pre -operative medications to stop:

A

❖Oral antihyperglycemics: do not take on morning of surgery
❖ACEI and angiotensin receptor blockers: do not take on the day of
surgery (controversial – they increase the risk of hypotension postinduction
but have not been shown to increase mortality or adverse
outcomes; therefore, some people hold and some do not)
❖Warfarin : (consider bridging with heparin).
❖ASA and NSAIDs : In patients undergoing non-cardiac surgery, starting or
continuing low-dose ASA in the perioperative period does not appear to
protect against post-operative MI or death, but increases the risk of
major bleeding
❖Herbal supplements: stop one week prior to elective surgery .

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101
Q

➢Pre -operative medications to adjust:

A

Insulin (consider insulin/dextrose infusion or holding dose)
Prednisone
Bronchodilators

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102
Q

Hypertension

A

• BP <180/110 is not an independent risk factor for perioperative
cardiovascular complications
• Target systolic blood pressure <180 mmhg, diastolic blood pressure
<110 mmhg
• Assess for end-organ damage and treat accordingly

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103
Q

Coronary Artery Disease

A

➢At least 60 day should elapse after a MI before a noncardiac surgery in the
absence of a coronary intervention
• This period carries an increased risk of re-infarction/death
➢Mortality with perioperative MI is 20-50%
➢Perioperative -blockers
• May decrease cardiac events and mortality (but increases risk of
perioperative strokes)
• Continue -blocker if patient is routinely taking it prior to surgery
• Consider initiation of -blocker in:
• Patients with CAD or indication for -blocker
• Intermediate or high risk surgery, especially vascular surgery

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104
Q

Risk factor assessment of Noncardiac Surgical Procedures

A

Higher&raquo_space;• Emergent major operations, especially elderly
• Aortic and other noncarotid major vascular surgery (endovascular and nonendovascular)

• Prolonged surgery associated with large fluid shift and/or blood loss
Intermediate» • Major thoracic surgery
• Major abdominal surgery
• Carotid endarterectomy surgery
• Head/neck surgery
• Orthopedic surgery
• Prostate surgery
Lower» • Eye, skin, and superficial surgery
• Endoscopic procedures

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105
Q

Respiratory Diseases (1)
Smoking

A

• Adverse effects: altered mucus secretion and clearance, decreased small
airway calibre, altered oxygen carrying capacity, increased airway reactivity,
and altered immune response
• Abstain at least 8 wk pre-operatively if possible
• If unable, abstaining even 24 h pre-operatively has been shown to increase
oxygen availability to tissues

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106
Q

Respiratory Diseases (2)
Asthma

A

Asthma
• Increased risk of bronchospasm from intubation
• Administration of short course (up to 1 wk) pre-operative corticosteroids
and inhaled 2-agonists decreases the risk of bronchospasm and does not
increase the risk of infection or delay wound healing
• Avoid non-selective -blockers due to risk of bronchospasm (cardioselective -
blockers (metoprolol, Atenolol) do not increase risk in the short-term)
• Delay elective surgery for poorly controlled asthma (increased cough or
sputum production, active Wheezing)
• Ideally, delay elective surgery by a minimum of 6 wk if patient develops URTI

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107
Q

Respiratory Diseases (3)
COPD

A

• Anesthesia, surgery (especially abdominal surgery, in particular upper
abdominal surgery) and pain Predispose the patient to atelectasis,
bronchospasm, pneumonia, prolonged need for mechanical Ventilation, and
respiratory failure
• Pre-operative ABG is needed for all COPD stage II and III patients to assess
baseline respiratory Acidosis and plan post-operative management of
hypercapnea
• Cancel/delay elective surgery for acute exacerbation

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108
Q

Predisposing Risk Factors for Pulmonary Complications

A
  1. Upper respiratory tract infection: cough, dyspnea
  2. Age >60 years
  3. COPD
  4. American Society of Anesthesiologists Class 2
  5. Functionally dependent
  6. Congestive heart failure
  7. Serum albumin <3.5 g/dL
  8. FEV1<2 L
  9. MVV <50% of predicted
  10. PEF <100 L or 50% predicted value
  11. PCO245 mmHg
  12. PO250 mmHg
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109
Q

Aspiration
➢Increased risk of aspiration with:

A

•Decreased level of conscious (drugs/alcohol, head injury, CNS pathology, trauma/shock)
•Delayed gastric emptying (non-fasted within 8 h, diabetes, narcotics)
•Decreased sphincter competence (GERD, hiatus hernia, nasogastric tube, pregnancy,
obesity)
•Increased abdominal pressure (pregnancy, obesity, bowel obstruction, acute abdomen)
•Unprotected airway (laryngeal mask vs. endotracheal tube )

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110
Q

Aspiration
➢Management

A

• Manage risk factors if possible
• Utilize protected airway (i.e. Endotracheal tube)
• Reduce gastric volume and acidity
• Delay inhibiting airway reflexes with muscular relaxants
• Employ rapid sequence induction

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111
Q

Fasting Guidelines

A

Fasting Guidelines Prior to Surgery :
Before elective procedures, the minimum duration of fasting should be:
• 8 h after a meal that includes meat, fried or fatty foods
• 6 h after a light meal (such as toast or crackers) or after ingestion of
infant formula or non-human milk
• 4 h after ingestion of breast milk
• 2 h after clear fluids (water, black coffee, tea, carbonated beverages,
juice without pulp)

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112
Q

Hematological Disorders

A

deficiency, ITP, liver disease)
➢Evaluate hemoglobin, hematocrit and coagulation proles when indicated .
➢Anemia:
Pre -operative treatments to increase hemoglobin (PO or IV iron
supplementation, erythropoietin or pre-admission blood collection in
certain populations)
➢Coagulopathies
• Discontinue or modify anticoagulation therapies (warfarin, clopidogrel,
ASA, apixaban, dabigatran) in advance of elective surgeries
• Administration of reversal agents if necessary: vitamin K, FFP, prothrombin
complex concentrate, recombinant activated factor VII

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113
Q

Endocrine Disorders (1)
Diabetes mellitus (DM)

A

• Clarify type 1 vs. Type 2
• Clarify treatment – oral anti-hyperglycemics and/or insulin
• Assess glucose control with history and Hba1c; well controlled diabetics have more
stable glucose levels intraoperatively
• End organ damage: be aware of damage to cardiovascular, renal, and central,
peripheral and autonomic nervous systems
• Preoperative guidelines for DM:
1. Verify target blood glucose concentration with frequent glucose monitoring: <180
mg/dl in critical patients, <140 mg/dl in stable patients)
2. Use insulin therapy to maintain glycemic goals
3. Hold biguanides, -glucosidase inhibitors, thiazolidinediones, sulfonylureas and GLP1
agonists on the morning of surgery
4. Consider cancelling nonemergency procedures if patient presents with metabolic
abnormalities (DKA, HHS, etc.) Or glucose reading above 400 mg/dl

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114
Q

Endocrine Disorders (2)

A

Hyperthyroidism and hypothyroidism
Hyperthyroidism : can experience sudden release of thyroid hormone
(thyroid storm) if not treated or well-controlled pre-operatively.
Treatment : -blockers and pre-operative prophylaxis

Adrenocortical insufficiency (Addison’s, exogenous steroid use)
Consider intraoperative steroid supp

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115
Q

Obesity and Obstructive Sleep Apnea(OSA)

A

• Severity of OSA may be determined from sleep studies and level of
pressure prescribed for home CPAP device
• Both obesity and OSA independently increase risk of difficult
ventilation, intubation and post-operative respiratory complications

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116
Q

Total testing process (TTP)

A

It is a set of steps of laboratory testing, beginning from the test
requested by the clinician to the interpretation of the results.

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117
Q

The TTP is
typically divided into the following three phases

A

I)Pre-analytical
• Selection of tests
• Test request
• Patient identification & preparation
• Specimen identification
• Sample collection and labeling procedures
• Sample transportation
• Sample receipt and preparation for analysis
II) Analytical
• Selection of analytical method and device.
• Quality control
• Performance of analysis.
III) Post analytical
- Result transcription & reporting
- Interpretation of results.

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118
Q

Test selection:

A

selection of the appropriate investigation for each patient
is a must so as to provide the patient with the best possible medical service, with minimal side-effects on the patient and at an appropriate cost
to the health

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119
Q

Request a laboratory service

A

The communication link between the clinician and clinical laboratory is
the laboratory request form (LRF)

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120
Q

ISO15189, LRF should include:

A

1) At least 2 unique patient identifiers (full name, date of birth, national
ID number, hospital file number…)
2) Sex
3) Date and time of collection (where supplied)
4) Date and time of receipt in Laboratory
5) Type of Specimen (e.g., blood, urine, body fluid)
6) Person collecting the sample.
7) Clinical status of patient (e.g., fasting), where required.
8) Specimen characteristics which may provide information relevant to
interpretation of results (e.g., hemolysis)
9) Informed consent where required by legislation.
10) The name of the requesting clinician.
11) Adequate clinical information, which is essential for proper
result interpretation (e.g., clinical diagnosis, cause of admission,.)

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121
Q

Examples for lab tests that can be ordered as STAT:

A

-Cardiac enzymes (CKMB, troponins)
-Electrolytes: Na, K, Cl.
-Complete Blood picture (CBC)

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122
Q

Patient identification:

A

Confirmed positive identification of a patient is a must before sampling.
Failure of proper patient identification may results in mix up of lab
results with grave medical consequences.

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123
Q

Sampling:

A

1) Blood specimens:
• Venous: the easiest sample to obtain. The commonest site is the
veins of antecubital fossa. Phlebotomy is a technique to acquire a
venous blood sample.
• Arterial: arterial blood is used to measure arterial blood gases, like
oxygen, CO2, and pH.
• Capillary: capillary blood is mostly used in the pediatric patient’s
group and for bedside tests where there is no need for a large amount
of blood. The common sites are the fingertips and heel.
2) Urine, stool, sputum, nasal discharge.
3) Ascitic, synovial, pleural, and cerebrospinal fluids.
4) Seminal and prostatic fluids.
5) Bronchoalveolar lavage, tissues for culture.
6) Swabs for nasopharynx, oral cavity, vagina, and wounds.
7) Any unknown collection of fluid and abscess.
8) Bone marrow

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124
Q

General rules before sampling:

A

1) The appropriate container is ready: tube, urine collection container,
heparinized syringe for blood gases, etc.
2) Proper labelling of the sample container with full patient data (full
name, hospital number, ward, ….), type of sample (blood, body
fluid,…), and the required tests. In clinical laboratories, where
information system is applied, barcoded label with the previous date in
addition to unique sample number is used for labelling the samples.
3) The clinician/nurses must ensure proper patient preparation
prerequisites before sampling (e.g., fasting patient, 2 hours after drug
therapy in case of therapeutic drug monitoring, etc.). Clinical
pathologists provide the clinician with these data.
4) The appropriate transport container is available: ice on a chilled
container, and courier to transport the sample promptly, etc.

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125
Q

Types of blood containers used for sampling

A

• Light blue capped tubes: contain Na citrate as an anticoagulant.
Used for coagulation testing (PT, PTT and coagulation factor assay).

• Red capped tubes: empty tubes without adding any anticoagulant
material which are used in serology and some routine samples.

• Yellow capped tubes: contain a clot activator which cause blood
to clot quickly and serum gel separator that separates blood cells
from serum, allowing the clear serum to be removed easily for
testing after centrifugation. Used for the same purposes as the red
capped tubes but not for PCR testing.

• Green capped tubes: contain Na or lithium heparin. Used for
cytogenetic analysis sampling.
• Purple capped tubes: contain EDTA as an anticoagulant. Used for
CBC, reticulocyte counting, and for HbA1c estimation.

• Grey capped tubes: contain K oxalate as an anticoagulant and Na
fluoride, which acts as sample preservative, that preserve glucose in
whole blood by inhibition of glycolysis by the red cells, which would
subsequently cause false-low glucose level. Used for glucose testing
(figure 3)

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126
Q

Phlebotomy (Venipuncture) Procedure:

A
  1. Ensure proper patient preparation (e.g., fasting before sampling;
    8 hours for fasting blood glucose and 12 hours for serum lipid
    profile).
  2. Put on gloves.
  3. Position the patient properly.
  4. Apply a tourniquet just above the venipuncture site and ask the
    patient to make a fist without vigorous hand pumping. Select a
    suitable vein for puncture.
  5. Clean the skin with 70% alcohol and allowed to dry spontaneously.
  6. Withdraw blood from an antecubital vein or other visible veins in
    the forearm.
  7. Enter the skin with the needle at approximately a 20-30-degree
    angle or less to the arm, with the bevel of the needle up. Insert the
    needle smoothly and fairly rapid to minimize patient discomfort.
  8. Venipuncture is done by means of either an evacuated tube or a
    syringe.
    ▪ If evacuated tube is used for blood collection, the vacuum
    controls the amount of blood which enters the tube.
    ▪ If a syringe is used for blood collection, the piston of the
    syringe should be withdrawn slowly and no attempt made to
    withdraw blood faster than the vein is filling. Haemolysis can
    be avoided or minimized by withdrawing the blood slowly.
  9. Release it as soon as the blood begins to flow into the syringe /
    vacutainer tube.
  10. After obtaining the blood, remove the needle and then press a
    sterile swab over the puncture site for a minute or two. Then cover
    the puncture site with a small adhesive dressing.
  11. Anticoagulated specimens must be mixed gently by inverting the
    containers several times.
  12. Needle disposal: place needle, together with the used swab and any
    other dressings, in a puncture-resistant container, for disposal.
    Don’t try to recover the needle.
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127
Q

Post-phlebotomy Procedure:

A

• Check the patient’s identity and sample barcoded label again and
make sure that it corresponds to the details on the LRF.
• The specimen tubes must be set upright in a holder or rack and
placed -
in a carrier together with the request forms for transport to the
laboratory.

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128
Q

Causes of errors related to sample collection procedure: Pre-collection:

A

• Failure to adhere to proper patient preparation according to the
requested test (e.g., fasting blood glucose is requested but dietary
supplement was administrated within 8 hours).
• Failure to adhere to proper timing in sampling (e.g., cortisol AM/PM,
therapeutic drug monitoring, and fertility hormones)
• Vigorous activity before sample collection affect results of some tests
(e.g., CK, protein in urine)

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129
Q

Causes of errors related to sample collection procedure: During collection:

A

• Prolonged tourniquet pressure results in haemo-concentration.
• Excessive negative pressure when drawing blood into syringe results
in hemolysis.
• Using incorrect type of tube for blood collection ( e.g., EDTA tube for
liver enzymes test

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130
Q

Causes of errors related to sample collection procedure: Handling of specimen:

A

• Insufficient or excess anticoagulant
• Inadequate mixing of blood with anticoagulant.
• Error in patient and/or specimen identification results in mix up of
results
• Inadequate specimen storage conditions affect the result of some tests
(e.g., light cause breakdown of bilirubin)
• Delay in transport to laboratory affects the result of some tests (e.g.,
culture of fastidious organisms)

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131
Q

Sample transport:

A

Specimens should always be placed upright in the plastic biohazard
transport container. LRFs are transported separate from samples (don’t
place them in the same container with samples so as not to be contaminated
by any possible sample spills).

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132
Q

Performance of analysis: some examples of tests performed in each:

A

1) Microbiology: Urine culture, culture for tuberculosis.
2) Immunology: Anti-Nuclear anti body testing, Epstein Barr virus
serology.
3) Chemistry: kidney & liver function tests, and hormones testing.
4) Hematology: Complete blood counts, and prothrombin time.

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133
Q

Laboratory test panels:

A

Test panels are groups of tests that are routinely ordered to determine the
status of a major body organs. The tests are usually performed on a blood
sample

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134
Q

Examples of common chemistry panels include:

A

1- Liver Panel (also called Hepatic Function tests) – used to screen,
detect, evaluate, and monitor acute and chronic liver inflammation
(hepatitis), liver disease and/or damage. It includes Total ,direct bilirubin,
total protein, albumin, and liver enzymes [AST, ALT, and Alkaline
phosphatase enzyme ( ALP)].
2- Renal Panel (also called Kidney Function tests) – contains tests such
as creatinine, urea, uric acid , estimated glomerular filtration rate (eGFR)
to evaluate kidney function.
3- Thyroid Function Panel – used to evaluate thyroid gland function,
diagnose thyroid disorders, and follow up of treatment. It includes TSH,
FreeT4, Free T3, T4, T3.

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135
Q

Results transcription and reporting:

A

• Patient identifiers (full name, age, sex, hospital number).
• Requester name
• Date and time of analysis.
• Test name, result, measuring unite, and reference interval.
• Result interpretation (where required and appropriate).
• Name of Clinical pathologist who released the report and date of
release.

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136
Q

Test result interpretation:

A

1) Is it normal?
2) Is it significantly different from any previous results?
3) Is it consistent with the clinical findings?

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137
Q

Is it normal?

A

Comparison of a patient’s laboratory test result versus a reference or
“normal” range is an important aspect of medical decision making.

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138
Q

Examples for some laboratory critical results:

A
  • White blood cell count (WBCs) <2 x109
    /L & >30 x109
    /L.
  • Platelets <20 x109
    /L & >1000 x109
    /L.
  • Hemoglobin <5 g/dl & >20 g/dl
  • Bilirubin (newborn) >15 mg/dl.
  • Sodium < 120 mmol/L & ˃150 mmol/L.
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139
Q

I) Pre-analytical phase:

A

Pre-analytical phase issues are related to patient’s interaction, specimen
collection, sample receiving and its transport. It includes the following
ethical issues:
A) Respect for persons:
- Consent must be understood by the patient.
- The patient’s right to refuse to get tests done should be appreciated.
- Confidentiality
B) Beneficence:
- All tests performed/referred must benefit to patient.
- Collection of samples should be done as per universally
recommended precautions so as to protect the patient and the
healthcare worker.
- The additional samples should not be drawn from the patient without
informing and getting the permission from Institutional ethics
committee.
- The specimens should be well-labeled with minimum two unique
identifiers.
- Transportation of samples should be done to protect the integrity of
the sample.
C) Justice:
No preference should be given to some patients in order to facilitate
or accelerate the collection procedure at the cost of others.

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140
Q

II) Analytical phase:

A

A) Respect for persons:
- After collection, patients have the right to refuse to have their
specimens examined.
- Confidential information
B) Beneficence:
The aim is to provide the best possible result to the patients. This is
accomplished via good laboratory practices which should involve the
establishment of quality assurance program including quality control
analysis, proficiency testing and accreditation of laboratory.
C) Justice:
- All patient samples are treated equally.
- Develop operating procedures for STAT samples.
- All specimens are analyzed accurately and in a timely manner.

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141
Q

III) Post analytical phase:

A

A) Respect for persons:
- Specimens will not be used beyond the testing prescribed by a
clinician.
- Maintain the confidentiality of results.
B) Beneficence:
- Reporting of results by qualified persons
- Reports should be understandable and interpretable.
- Notifying for errors and correction
C) Justice:
- Consistent reporting for all patients.
- Avoid withholding of results because of financial causes

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142
Q

Respect for persons:

A

We must respect patient and their self-respect. It is
an obligation to respect the decisions made by people concerning their own
samples.

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143
Q

Beneficence:

A

The goal is to maximize benefits and minimize harms,
Everyone must be fair and correct in all their actions to prevent harm.

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144
Q

Justice:

A

Basically, we have an obligation to treat all people equally, fairly

145
Q

Ethical practice in laboratory medicine

A

good technical
practice accompanied by proper attitudes and behavior. In deciding
what is proper, reference is often made to moral values adhered to
the community and to standards of professional practice.

146
Q

SCINTIGRAPHY (NUCLEAR MEDICINE)

A

Scintigraphy, also known as a gamma scan, is a diagnostic test
in nuclear medicine, where radioisotopes attached to drugs that travel
to a specific organ or tissue (radiopharmaceuticals) and taken internally then the emitted gamma radiation is captured by external detectors
(gamma cameras) to form two-dimensional images in a similar process
to the capture of x-ray images.

147
Q

Precautions with Scintigraphy

A

1- Pregnancy (suspected or confirmed). If the patient is known or
suspected to be pregnant, a clinical decision is necessary to weigh the
benefits against the possible harm of carrying out any procedure.
2-Breast –feeding: The patient should stop and milk expressed and
discarded when possible for 24 h and at least for 4 h post
radiopharmaceutical administration.

148
Q

The main advantages of scintigraphy are:

A

**High sensitivity
**Functional information is provided as well as anatomical
information.

149
Q

Limitations and disadvantages of scintigraphy

A

• Use of ionizing radiation
• Cost of equipment
• Extra care required in handling radioactive materials and long period
required for isolation of patient after examination.

150
Q

Classification of Poisons. According to their nature:

A

-solid, liquid, or gases.

151
Q

Classification of Poisons. According to their natural sources:

A

plants, animals, minerals, and
synthetics.

152
Q

Classification of Poisons. According to the site of action:

A

a) Poisons that have local action: Corrosives (act only when
come in contact with tissue).
b) Poisons that have remote action: most poisons (act only after
being absorption).
c) Poisons that have both local & remote action: heavy metals.

153
Q

Classification of Poisons. According to the selective organ toxicity:

A

hepato toxin,
nephro toxin, cardiac toxin.

154
Q

Mode of poisoning:

A

It may be suicidal, accidental or homicidal.
Ideal homicidal poison should be tasteless, odorless, colorless, highly and
rapidly fatal. Suicidal patients need psychiatric evaluation.

155
Q

Factors affecting (modifying) the action of the poison:
1

A

1)Dose: ↑ Dose →↑ toxic effect except with vomiting.
2) State of the poisons:
➢ Increased concentration →↑ effect.
➢ Form: gas > liquid >fine powder > coarse powder in their effect and
rapidity of the onset of action.
➢ Increased solubility →↑ effect.
➢ Route: IV > inhalation >IM >SC >oral >MM >intact skin in the
rapidity of the onset of action.
3) State of the stomach:
➢ Empty or full stomach:
• Empty stomach → more rapid & serious action.
• Full stomach → delayed absorption & action.
➢ Nature of food:
• Fatty food → delay absorption except in fat soluble substances
such as phosphorus.
➢ Gastric acidity:
• In cases of achlorhydria → cyanide salt is not fatal.
4) Age of the patient:
Extremes of age are more affected than adults.
5) Health of the patient:
➢ ↑ Health → ↓ the effect of the poison.
➢ Liver & /or kidney diseases → ↓ metabolism & /or absorption of the
poison → prolonged & serious effect.

156
Q

Factors affecting (modifying) the action of the poison:
2

A

6) Tolerance & habit:
Patient with addicting drugs (opium, cocaine, alcohol) can withstand
high doses without serious effect.
7) Abnormal response to the drug:
➢ Hypersensitivity: (immunological response) in which severe
allergic reactions can result from a small harmless dose of a certain
drug to certain individuals (e.g., anaphylaxis occurred with
penicillin).
➢ Personal idiosyncrasy:
It may be of genetic origin in which an abnormal response occurs to
the usual therapeutic dose of a certain drug (e.g., liver damage that
occurs in persons received valproic acid, hemolysis that occur in
patients with G6PD deficiency when they receive any oxidant as
fava beans).
➢ Drug abuse: It is the use of a drug for non-medical purposes, or
persistent or sporadic drug use inconsistent with acceptable medical
practice.
➢ Drug Dependence includes:
A. Drug addiction (physical & psychological dependence)
B. Drug habituation (psychological dependence)

157
Q

Drug Addiction

A

Definition: It is a state of chronic intoxication produced by repeated
use of the drug which affects the individual`s psychological, mental,
and physical state and characterized by:
1. Tolerance: a tendency to increase the dose frequently to produce
the same effect as there is progressive diminish effect on repetition
of the same dose.
2. Physical & psychological dependence: An overpowering desire
(craving) or compulsion to continue taking the drug and to obtain it
by any mean in order to reach personal satisfaction (psychological
dependence) and prevent a characteristic and specific group of
symptoms termed withdrawal or abstinence syndrome.
3. Withdrawal syndrome (abstinence syndrome): A serious
characteristic and specific group of symptoms occur on withdrawal
of the drug and disappear immediately on administration of the drug.
4. Detrimental effects on both addict and society.

158
Q

Physical manifestation of addicting drugs

A

A. General physical characters:
• Moral & Mood changes: Mood swings, Anger and Depression, Lying, stealing,
cheating.
• Mental changes: Poor judgment, Lapses in memory and amnesia.
• Loss of appetite & weight loss except cannabis (bulimia & craving for sweets)
• Infection due to unsterile injection (e.g., Infective endocarditis, septic emboli to
lungs & organs, Tetanus, malaria, TB, Hepatitis, Nephritis, AIDS, Bacterial &
fungal pneumonia)
B. Others:
• In opiates addiction: Pulmonary edema (Heroin), Cerebral edema, transverse
myelitis, CVS, and marrow depression.
• In cocaine addiction: sexual perversion & nymphomania in females.
• In amphetamine addiction: hallucinations, irritability, mood swings, paranoia.

159
Q

Psychological dependence

A

➢ Definition: A desire but without compulsion to take the drug to
produce pleasure or to avoid discomfort.
➢ There is no tolerance, physical dependence, withdrawal syndrome
or detrimental effects (e.g., tea, coffee).

160
Q

Drug interaction:

A

Definition: an interaction between a drug and another substance that
prevents the drug from performing as expected.

161
Q

Types of drug interaction:

A

a) Synergistic: it is of two types:
• Summation: drugs are full agonists act at the same receptor (e.g.,
barbiturate with benzodiazepine).
• Potentiation: one drug makes the other drug/s more potent (e.g.,
barbiturates or benzodiazepines with a muscle relaxant → more
CNS depression).
b) Antagonistic: when one drug diminishes or completely abolishes
the action of another drug (e.g., the action of morphine is abolished
by its competitive antagonist naloxone).

162
Q

Levels of drug interaction:

A

a) At the sites of absorption:
Drug interaction may ↓ or ↑ absorption (e.g., prolonged use of
antibiotics → ↓ absorption of digitalis as they kill bacterial flora
which enhance digitalis absorption).
b) Distribution:
Drugs with plasma protein binding sites (e.g., warfarin and
salicylates can compete with each other).
Competition at receptor sites (e.g., naloxone and morphine).
c) Metabolism:
It is mainly by P450 enzyme system. Induction or inhibition of
this enzyme can shorten or lengthen the duration of action of
drugs metabolized by this enzyme system.
d) Excretion:
Alkalization of urine enhances excretion of salicylates.

163
Q

Fate of the poison in our body:

A

It may be one of the followings:
➢ Metabolism then excretion as a metabolite.
➢ Excretion as a parent drug via the kidney.

164
Q

General Approach to the Poisoned Patient:

A

I) Emergency stabilization.
By maintaining vital signs ABCD
Airway, Breathing, Circulation, and CNS Depression.
II) Proper clinical evaluation.
History, clinical examination, laboratory tests, and differential
diagnosis.
III) Reduction of further absorption (Decontamination)
GIT, skin, Eyes
IV) Elimination of the absorbed poison
• Repeated dose activated charcoal.
• Alteration of urine pH & diuresis.
• Hemodialysis.
• Hemoperfusion.
V) Antidotal therapy.
VI) Supportive & symptomatic therapy.

165
Q

Causes of toxic airway obstruction

A

• Toxic coma: may cause posterior displacement of the tongue (1st
cause of death in impaired conscious level)
• Foreign bodies aspiration (e.g., Button batteries, seeds as nut meg,
castor oil seeds)
• Mucosal swelling: hypersensitivity or corrosive irritation, or smoke
inhalation
• ↑↑ Secretions: organophosphorus insecticides.

166
Q

Symptoms and signs of airway obstruction

A

• Dyspnea
• Dysphonia
• Air hunger
• Hoarseness of voice
• Cyanosis
• Tachypnea
• Intercostal retraction

167
Q

Treatment of airway obstruction

A

• Prevent the tongue from falling back by pulling the tongue forward,
supporting the jaw or oropharyngeal or nasopharyngeal airway.
• Frequent suction of secretions.
• Removal of any foreign body.
• Cuffed endotracheal tube in comatose patient with lost gag reflex to
prevent aspiration.
• Tracheostomy in acute upper airway obstruction as angioneurotic
edema.

168
Q

Maintain breathing and oxygenation:

A

• O2 inhalation by nasal cannula or mask.
• Artificial ventilation if failure of spontaneous respiration is present
as in cases of respiratory muscle paralysis (e.g., botulism) or
continuous fits (strychnine), or sustained spasm (antipsychotics).

169
Q

Toxic causes of hypotension and shock:

A

• Excessive fluid loss: arsenic.
• Depression of myocardial contractility: tricyclic antidepressants.
• Post- arteriolar dilatation: iron.
• Hypoxia: carbon monoxide, cyanide.

170
Q

Treatment Assessment of Circulation: (pulse-blood pressure-ECG)

A

• It depends on central venous pressure (CVP):
• Normal values vary between 4 and 12 cmH2O (CVP is 2 to 6 mm
Hg). If low
• Fluid replacement therapy.
• Vasopressor drugs as dopamine and noradrenaline.
• Cardiotonic as digoxin.
• Treatment of the cause and correction of complications
as metabolic acidosis.

171
Q

Toxic causes of arrhythmias:

A

digitalis, theophylline, phenytoin,
antiarrhythmics, electrolyte imbalance.

172
Q

Acute alteration of mental status is of 2 types:

A

• Qualitative abnormality: decreased content of consciousness:
confusion, delirium, dementia, psychosis.
• Quantitative abnormality: decreased level of consciousness:
lethargy, stupor and coma

173
Q

Drugs that alter the content of consciousness (qualitative
impairment):

A
  1. Anticholinergics as atropine.
  2. Withdrawal syndromes as with alcohol and sedative
    hypnotics.
  3. Drugs causing encephalopathy as lead and arsenic.
  4. Hallucinogenic and designer drugs
174
Q

Clinical picture (confusion and delirium):
Qualitative abnormality:

A
  1. In- alertness: the patient can’t repeat 5 digits.
  2. Disorientation of persons, time and place.
  3. Loss of short-term memory.
  4. Delusions, illusions or hallucinations.
  5. Dementia: 1, 2 are usually not present.
175
Q

Qualitative abnormality:Treatment

A

Treatment of the cause.
2. Benzodiazepines &/ or major tranquilizers in severe cases.

176
Q

➢ Causes of coma

A

• Traumatic. (concussion &compression)
• Medical as diabetic comas, cerebrovascular accidents, hepatic
encephalopathy.
• Toxic causes as:
❖ CNS depressants as alcohol and sedative- hypnotics.
❖ Hypoxic causes as carbon monoxide, organophosphates.
❖ Heavy metals.
❖ Narcotics.
❖ Causes of hypoglycemia as oral hypoglycemic toxicity.
❖ Causes of acid- base disorders as iron and salicylates.

177
Q

Quantitative abnormalities:Treatment

A

• Stabilization, patent airway, O2 therapy, i.v line.
• All comatose patients should be given a triad of naloxone,
Dextrose 50 or 25% & thiamine (Coma Cocktail) due to:
1) Most of the toxicological comas are due to opiate
overdose, hypoglycemia or Wernicke’s encephalopathy of
alcoholics
2) This triad is highly diagnostic as no response to any of
them can exclude their causes, while, the response to one
of them is extremely diagnostic.
Single dose of any of them is not harmful to the patient not
responding to the triad.
➢ Dose:
Naloxone: 0.4 – 2 mg IV.
Dextrose: 100 ml of 50% solution in adults or 1gm /kg of
25% solution in children.
Thiamine: 100 mg IV.
• Treatment of the cause.
• Supportive measures are very important to minimize
complications in comatose (see symptomatic & supportive
therapy).

178
Q

Approach to diagnose a poisoned case
(History taking:)

A

Personal history, complaint, analysis of the complaint (including name
of the toxic substance, amount, route of exposure, time of ingestion,
symptoms following ingestion) and past history (See toxicological
sheet).

179
Q

Approach to diagnose a poisoned case
2. Clinical examination:

A

• Assessment of the patient’s level of consciousness using
Reed’s classification.
• Assessment of the patients’ vital signs: pulse, blood pressure,
respiratory rate, temperature.
• Examination of other systems:
a) Auscultation of the chest &heart
b) Proper neurological examination
c) Palpation of the abdomen

180
Q

Approach to diagnose a poisoned case
3. Investigations:

A

• Routine investigations: [complete blood count, liver function tests,
renal function tests, arterial blood gases (ABG), electrocardiogram
(ECG), random blood sugar (RBS)].
• Specific investigations:
a) Qualitative: toxicological drug screen in urine (e.g., drug
abuse kits), confirmed by HPLC & GCMS in legal situations.
b) Quantitative: drug level in the blood (e.g., paracetamol,
pseudocholinesterase enzyme in organophosphorus
insecticide).
• Others:
a) Abdominal erect x-ray: e.g., Body packer.
b) Chest x-ray: e.g., kerosene toxicity.

181
Q

Approach to diagnose a poisoned case
4. Differential diagnosis:

A

To differentiate the toxicological case from other medical cases (e.g.,
differentiate the toxic coma from traumatic coma or medical coma as
hypoglycemic coma, renal or hepatic coma).

182
Q

Conscious level:

A

gait, behavior, and movements in moving
child.

183
Q

Conscious level assessment through either through

A

A. Clinical assessment as
1. Alert and oriented about time, place and person in older child or active
and playing in small infants OR
2. The child either delirious, confused, stuporous or comatose
B. The Glasgow Coma Scale has been adapted to assess the level
of consciousness for children.

184
Q

In this scoring system

A

three areas of brain function should be
considered: speech (4 scores), eye opining (5 scores), and motor
response (6 scores)

185
Q

Built:

A

normal (average), underbuilt, or overbuilt.

186
Q

Abnormal: gx

A

► Fascial expression
► Position in bed (Decubitus)
► Colors (Complexions)
► Odors
► Sounds.

187
Q

Abnormal fascial features

A

• Toxic, dehydrated, wasted or edematous.
• Mongol in Dawn syndrome
• Mongoloid features as in thalassemia and racial.
• Wiseman face: As in marasmus
o In which there is loss of buccal pad of fat which is the last one
to disappear as it is brown fat (not easily dissolved).
• Cretin face: in congenital hypothyroidism in which coarse fascial
features

188
Q

dehydrated, wasted or edematous

A

Toxic,

189
Q

Dawn syndrome

A

Mongol

190
Q

thalassemia and racial.

A

Mongoloid features

191
Q

In which there is loss of buccal pad of fat which is the last one
to disappear as it is brown fat (not easily dissolved).

A

Wiseman face

192
Q

congenital hypothyroidism in which coarse fascial
features

A

Cretin face

193
Q

Abnormal positions in bed

A

• Orthopneic position:
o In heart failure:
o Due to lung congestion with defective gas exchange
• Opisthotonos position:
o In meningitis → There is hyperextended neck, arching of the
back & flexion of the lower limbs to relax paravertebral muscle
& relieve the back pain.
• Squatting position:
o In Fallot tetralogy and most cases of CCHD with
↓↓ pulmonary blood flow
o An acquired condition to ↑↑ VR to the lungs for more oxygenation
• Tripod position:
o In bronchial asthma, and acute epiglottitis
o The child is sitting on three part of the body and leaning
forwards to increase work of accessory muscles of respiration.

194
Q

o In heart failure:
o Due to lung congestion with defective gas exchange
[Position]

A

• Orthopneic position:

195
Q

o In meningitis → There is hyperextended neck, arching of the
back & flexion of the lower limbs to relax paravertebral muscle
& relieve the back pain
[Position]

A

• Opisthotonos position:

196
Q

o In Fallot tetralogy and most cases of CCHD with
↓↓ pulmonary blood flow
o An acquired condition to ↑↑ VR to the lungs for more oxygenation
[Position]

A

• Squatting position:

197
Q

o In bronchial asthma, and acute epiglottitis
o The child is sitting on three part of the body and leaning
forwards to increase work of accessory muscles of respiration.
[Position]

A

• Tripod position:

198
Q

The odors may originate

A

breath, urine, stool, sputum, vomitus,
skin, or vagina.

199
Q

Abnormal odor

A

Of the body
▪ Acetone odor due to
ketones in DKA
▪ Fishy smell due to toxic
chemicals as in CRF
▪ Kerosene smell in
kerosene poisoning

Of the mouth
▪ Bad odor (halitosis): due to:
o Gingivitis & dental caries
o Chronic tonsilitis
o Suppurative lung diseases.
▪ Rotten apple (fetor
hepaticus): in hepatic failure

Of urine
▪ Acetone odor:
in DKA.
▪ Bad odor in
UTI

200
Q

ketones in DKA [odro]

A

Acetone odor

201
Q

toxic
chemicals as in CRF
[Odor]

A

Fishy smell

202
Q

kerosene poisoning
[odor]

A

Kerosene smell

203
Q

o Gingivitis & dental caries
o Chronic tonsilitis
o Suppurative lung diseases.
[Odor]

A

▪ Bad odor (halitosis):

204
Q

in hepatic failure
[odor]

A

▪ Rotten apple

205
Q

Abnormal sounds

A

Snoring/// Inspiratory, low pitched, irregular ==Oropharyngeal
obstruction

Stridor //Inspiratory, sometimes an expiratory
component===
Larynx/ trachea
obstruction

Rattling //Insp. / Exp., may be felt by placing hands
over the chest ==
Secretions in the
airways

Wheezing// Whistling or musical sound,
predominantly expiratory ==
Lower airway
obstruction

Grunting// Expiratory, expiration against a partially
closed glottis==
Lung consolidation

206
Q

Inspiratory, low pitched, irregular[character ]

A

Snoring

207
Q

Cause
Oropharyngeal
obstruction

A

Snoring

208
Q

character Inspiratory, sometimes an expiratory
component

A

Stridor

209
Q

Cause
Larynx/ trachea
obstruction

A

Stridor

210
Q

character Insp. / Exp., may be felt by placing hands
over the chest

A

Rattling

211
Q

Cause
Secretions in the
airways

A

Rattling

212
Q

character Whistling or musical sound,
predominantly expiratory

A

Wheezing

213
Q

Cause
Lower airway
obstruction

A

Wheezing

214
Q

character Expiratory, expiration against a partially
closed glottis

A

Grunting

215
Q

Cause
Lung consolidation

A

Grunting

216
Q

Abnormal colors (complexions)

A

❖ Pallor
❖ Cyanosis
❖ Jaundice:

217
Q

Pallor

A

Def,: is an unusual paleness of the skin and mucous membrane.

218
Q

The best sites for examination of pallor are:

A

o Mucous membranes of the mouth, tongue & inner sides of the lips by
gentle pressure.
o Inner membranes of the lower eye lids
o Hands→ palms, palm creases (become evident on stretching of the
fingers) and fingernails.

219
Q

Clinically: Pallor

A

pallor may be graded as mild to moderate and severe.
o In mild to moderate pallor, there is paleness of the mucosae but pink
palmar creases.
o In severe pallor, the palmar creases become faint and pale.

220
Q

Causes of pallor:

A

o ↓↓ in RBCs number: anemic causes……..
o ↓↓ in blood flow and oxygen: shock, hypoxia, vagal stimulation,
hypothermia, or fear
o ↑↑ skin’s thickness: as in edema and myxedema
o Abnormal amount of melanin in the skin: normally pale or so dark.

221
Q

Cyanosis

A

• Definition: bluish discoloration of the skin and mucous membrane
due to the presence of reduced Hb in the blood (at least 5 gm/dl of
reduced hemoglobin)

222
Q

Types of cyanosis

A

Central cyanosis: cyanosis of mucosae and extremities.
▪ Impaired pulmonary function:
o Alveolar hypoventilation,
▪ Cardiac shunts:
o Cyanotic congenital heart diseases …….
o Pulmonary AV fistulas
▪ CNS causes:
o Central respiratory failure
▪ Hemoglobin abnormalities
o Methemoglobinemia
o Carboxy-hemoglobinemia
➢ Peripheral cyanosis: cyanosis in extremities but not the mucosae.
Due to poor peripheral circulation resulting in increased 02 extraction
from blood as in:
▪ Cold exposure, congestive heart failure
▪ Arterial obstruction (Raynaud phenomenon, emboli)

223
Q

➢ Central cyanosis:

A

▪ Impaired pulmonary function:
o Alveolar hypoventilation,
▪ Cardiac shunts:
o Cyanotic congenital heart diseases …….
o Pulmonary AV fistulas
▪ CNS causes:
o Central respiratory failure
▪ Hemoglobin abnormalities
o Methemoglobinemia
o Carboxy-hemoglobinemia

224
Q

Peripheral cyanosis:

A

cyanosis in extremities but not the mucosae.
Due to poor peripheral circulation resulting in increased 02 extraction
from blood as in:
▪ Cold exposure, congestive heart failure
▪ Arterial obstruction (Raynaud phenomenon, emboli)

225
Q

➢ Differential cyanosis:

A
  1. The hands are blue, but feet are pink. (Coarctation of aorta with
    TGA)
  2. Alternatively, the hands are pink, but the feet are blue.
    (PDA with reversed shunt due to pulmonary hypertension)
226
Q

❖ Jaundice:

A

• Definition: is the yellowish discoloration of skin and mucosal
membranes.

227
Q

Etiology: of jaundice either in NB or in children.

A

o Jaundice is clinically apparent at serum bilirubin levels > 2 mg/dl in
older children and > 5 mg/dL in neonates.

228
Q

We examine the jaundice by

A

blanching of the skin.

229
Q

• Jaundice examined in:

A

o Sclera
o Mouth: in the palate and under surface of tongue
o Skin especially tip of nose, palms, and soles (in neonates)

230
Q

• Evaluation of Extent of Hyperbilirubinemia in New-born

A

(Kramer’s index) depending on the clinical scoring system:
1. Face and neck: around 5 mg/dL
2. Upper trunk: 6 - 10 mg/dL
3. Lower trunk and thighs: 10 - 15 mg/dL
4. Legs: 15 – 18 (< 20) mg/dL
5. Palms and soles: ≥ 20 mg/dL

231
Q

Skull Examination for:

A

Size
Shape
Sutures
Swellings
Fontanels
Craniotabes
Hair examination

232
Q

Size of the skull:

A

microcephaly or macrocephaly

233
Q

Swelling in the scalp

A

o Caput succedaneum (crosses the suture lines) or
o Cephalohematoma (does not cross suture lines) or
o Subgaleal hematoma: loose fluctuating swelling cover all the skull.
o Others as: abscess, hemangioma, encephalocele, tumor

234
Q

• Sutures: Palpate the sutures for:

A

• Premature closure (craniosynostosis) or
• Widely separated may occur in:
– Mongol
– Achondroplasia
– Cretinism - Rickets
– Osteogenesis imperfecta. - Hydrocephalus, Prematurity

235
Q

• Shape of the skull:

A

o Microcephaly: due to premature closure of all sutures or
o Macrocephaly due to …..
o Trigonocephaly:
Pointed skull due to closure of metopic suture.
o Brachycephaly:
Anterior-posterior flattened skull (square and short) due to premature closure of
coronal suture e.g., Down syndrome.
o Plagiocephaly:
Skewing of skull due to premature unilateral fusion of coronal or lambdoid
suture. It may be a flattened occiput which is postural in infancy.
o Scaphocephaly:
Anteroposterior elongated skull due to premature fusion of sagittal suture. The
parietal eminences are usually absent.
o Oxycephaly (tower skull):
Elongation of the skull like a tower due to premature closure of multiple sutures.

236
Q

Pointed skull due to closure of metopic suture.

A

Trigonocephaly:

237
Q

Anterior-posterior flattened skull (square and short) due to premature closure of
coronal suture e.g., Down syndrome.

A

Brachycephaly:

238
Q

Skewing of skull due to premature unilateral fusion of coronal or lambdoid
suture. It may be a flattened occiput which is postural in infancy.

A

Plagiocephaly:

239
Q

Anteroposterior elongated skull due to premature fusion of sagittal suture. The
parietal eminences are usually absent.

A

Scaphocephaly:

240
Q

Elongation of the skull like a tower due to premature closure of multiple sutures.

A

Oxycephaly (tower skull):

241
Q

Fontanels:

A

the areas in between 3-4 skull bones meetings

242
Q

• The fontanels should be examined by

A

inspection and palpation while
the infant is calm and held in both supine and upright positions.

243
Q

o The newborn normally has 6 fontanels

A

✓ One posterior.
✓ Two sphenoids.
✓ Two mastoids.
✓ One anterior.

244
Q

o The triangular (lambda) posterior fontanel:

A

✓ Located at the junction of the occipital and two parietal bones.
✓ Its size at birth equal to the tip of the baby little finger (0.5 cm).
✓ Closes at age of 6 - 8 weeks (2 months).

245
Q

o The diamond shaped anterior fontanel:

A

✓ Located at the junction of the two parietal and two frontal bones.
✓ It is the most prominent and important fontanel.
✓ It measures 2.5 x 2.5 cm at birth in a full-term baby.
✓ Closes gradually at the age of 18 ± 6 months (12 - 24 month)
o Palpate to decide:
✓ If the fontanel is bulging or depressed (without crying) or
✓ Pulsatile (as in meningitis, encephalitis or hydrocephalus)
o Causes of delayed closure of anterior fontanelles: MACRO
✓ Mongol
✓ Achondroplasia
✓ Cretinism
✓ Rickets
✓ Osteogenesis imperfecta – Hydrocephalus

246
Q

• Craniotabes

A

o Skull bones yield under pressure like ping - pong or egg shell
crackling sensations due to thinning of both layers of the skull and
weakness of the trabeculae in-between → weak support → yield
under pressure.
o May be normal in new-born especially premature.
o Detected by pressing over occipital or parietal bone while
putting the 2 thumbs over the forehead and the other fingers
are fanned over the skull.
o Disappear by the end of 1st year esp. in rickets.

247
Q

o Causes of craniotabes are:

A

✓ Rickets (parietal bone mainly)
✓ Osteogenesis imperfecta (frontal bone mainly)
✓ Hydrocephalus (all bones of skull)

248
Q

❖ Hair examination:

A

• Fine silky hair as in Dawn syndrome.
• Blond hair: in phenylketonuria
• Coarse: brittle, and easily removable as in kwashiorkor.
• Flag sign: means alternating horizontal bands of normal coloration
with:
o Hypopigmentation of the hair (in kwashiorkor) or
o Hyperpigmentation: in high dose methotrexate cycles.
• Low anterior hair line:
o An apparently ↓↓ distance between the hairline and the
glabella = low by 3.5 cm than normal as in cretinism
• Low posterior hair line means that the posterior hair line is below
5th cervical spinous process as in turner syndrome.

249
Q

Eye examination

A
  1. Eye ball size:
  2. Placement of the eye:
  3. Eye slant:
    ▪ Upward eye
  4. Eyelid/ eye lash:
  5. Eye brow and eye lashes
  6. Conjunctiva/ Cornea/ Sclera
250
Q
  1. Eye ball size:
A

o Prominent (exophthalmos)
✓ Unilateral proptosis: as in orbital cellulitis (most common)
✓ Bilateral proptosis: as in neuroblastoma, leukemia, thyrotoxicosis.
✓ Can be measured by Ophthalmometer or by a ruler.
o Sunken (enophthalmos) an in Horner syndrome, dehydration
o Small (microphthalmos) as in TORCH infection.

251
Q

orbital cellulitis
size:

A

✓ Unilateral proptosis

252
Q

in neuroblastoma, leukemia, thyrotoxicosis.
✓ Can be measured by Ophthalmometer or by a ruler.
size:

A

Bilateral proptosis:

253
Q

in Horner syndrome, dehydration
size:

A

Sunken (enophthalmos)

254
Q

in TORCH infection.
size:

A

Small (microphthalmos)

255
Q
  1. Placement of the eye:
A

▪ Hypotelorism: the eyes too closely placed may be seen in
trisomy 13 and holoprosencephaly (even single eye).
▪ Hypertelorism: too widely spaced eye may be seen
in Down syndrome, cretinism, thalassemia, Turner.

256
Q

the eyes too closely placed may be seen in
trisomy 13 and holoprosencephaly (even single eye).Placement of the eye:

A

Hypotelorism:

257
Q

too widely spaced eye may be seen
in Down syndrome, cretinism, thalassemia, Turner.
Placement of the eye:

A

Hypertelorism:

258
Q
  1. Eye slant:
A

▪ Upward eye slant (mongoloid):
o The outer canthus is higher than the inner canthus.
o As in Dawn syndrome.
▪ Antimongoloid slant:
o The inner canthus is higher than the outer canthus.
o As in Turner, Noonan syndrome, …
▪ Epicanthic folds:
o Are folds of skin which project from the upper lid over the medial
epicanthus.
o fo example: Down syndrome or racial.

259
Q

o The outer canthus is higher than the inner canthus.
o As in Dawn syndrome.
Eye slant:

A

Upward eye slant (mongoloid):

260
Q

The inner canthus is higher than the outer canthus.
o As in Turner, Noonan syndrome, …
Eye slant:

A

Antimongoloid slant:

261
Q

Are folds of skin which project from the upper lid over the medial
epicanthus.
o fo example: Down syndrome or racial.
Eye slant:

A

Epicanthic folds:

262
Q

Eyelid/ eye lash:

A

▪ Oedema or swollen eye lid: as in
o Allergic (red, itchy, and usually without discharge)
o Acute nephritis, nephrotic syndrome, …
o Pertussis or IMN in which there is puffy eye lids.
o Conjunctivitis (pink eye) (painful and tender ± yellowish discharge
o Chalazion or stye
• Position:
Normally, the upper eyelids cover 1-2 mm
of upper corneoscleral junction.
o Ptosis of the eyelids can be congenital or acquired.
o May be unilateral or bilateral. It may be partial or complete.
o As in Horner syndrome, botulism, myasthenia gravis

263
Q

o Allergic (red, itchy, and usually without discharge)
o Acute nephritis, nephrotic syndrome, …
o Pertussis or IMN in which there is puffy eye lids.
o Conjunctivitis (pink eye) (painful and tender ± yellowish discharge
o Chalazion or stye
Eyelid/ eye lash:

A

Oedema or swollen eye lid

264
Q

Eye brow and eye lashes

A

• Thinning and loss of the outer 1/3 of eye brow as
o Familial or artificial.
o Vitamin & mineral deficiency (esp. vitamin A and zinc)
o Hypothyroidism
• Fused eye brow (Unibrow or Synophrys) as in Cornea de Lange
syndrome
• Long and curly eyelashes:
o Familial, single gene mutation or as a part of syndrome
o Acquired as severe malnutrition, TB, …

265
Q

o Familial or artificial.
o Vitamin & mineral deficiency (esp. vitamin A and zinc)
o Hypothyroidism
Eye brow and eye lashes

A

Thinning and loss of the outer 1/3 of eye brow

266
Q

(Unibrow or Synophrys) as in Cornea de Lange
syndrome
Eye brow and eye lashes

A

Fused eye brow

267
Q

o Familial, single gene mutation or as a part of syndrome
o Acquired as severe malnutrition, TB,
Eye brow and eye lashes

A

Long and curly eyelashes:

268
Q

Abnormal color of conjunctiva/sclera

A

• Pallor
• Jaundice
• Hemorrhages: trauma, scurvy, pertussis, or hemorrhagic disorders.

269
Q

• Blue sclera:

A

o As in IDA, Marfan syndrome, Osteogenesis imperfecta, & Congenital
glaucoma.
o Due to thinning and transparency of the collagen fibers of the sclera
that allow visualization of the underlying uvea

270
Q

Dryness and ulceration of the cornea

A

(keratomalacia) as in vitamin
A Def.

271
Q

Kayser-Fleischer ring

A

is a brownish ring around the cornea (Wilson
dis.)

272
Q

Pupils:

A

assess the pupil size, symmetry, and reaction of the pupil to
light.

273
Q

Legal classification of wounds:

A

1- Slight or simple wound: not serious, heals in less than 20 days, no
permanent infirmity.
2- Dangerous wound: wound is serious, heals in more than 20 days, and
may leave permanent infirmity.
3- Fatal wound: causes death immediately or sometime after injury.

274
Q

Medicolegal classification:

A

1- Blunt trauma:
- Abrasions
- Bruises (Contusions).
- Contused (Lacerated) wounds.
2- Sharp trauma:
- Cut (Incised) wounds.
- Stab wounds

275
Q

Abrasions

A

Destruction of superficial layers of skin

276
Q

Causal instrument:Abrasions

A

Rough blunt object e.g., fingernail, teeth, tire of car

277
Q

Types of abrasions:

A

1- Sliding abrasions: classified into:
a- Scratches: due to blunt object with pointed end passing across the
skin and moving the surface layers in front of it e.g., fingernail,
fork…etc.
b- Grazes: when a rough object comes in contact with a wider surface
of skin. e.g., dragging abrasion after motor car accident.
2- Pressure abrasions: they occur when an object is stamped on the skin
e.g., ligature mark, motor car tire, teeth marks (bite).

278
Q

due to blunt object with pointed end passing across the
skin and moving the surface layers in front of it e.g., fingernail,
fork…etc.

A

Scratches:

279
Q

when a rough object comes in contact with a wider surface
of skin. e.g., dragging abrasion after motor car accident.

A

Grazes:

280
Q

they occur when an object is stamped on the skin
e.g., ligature mark, motor car tire, teeth marks (bite).

A

Pressure abrasions:

281
Q

Medicolegal importance: Abrasions

A

1- Sign of resistance or struggle.
2- Type of crime:
a) Throttling: semilunar fingernail abrasions on skin of
victim’s neck.
b) Strangulation & hanging: ligature mark on skin of neck.
c) Smothering: semilunar fingernail abrasions around mouth &
nostrils.
d) Rape: semilunar fingernail abrasions on the skin of inner aspect of
thigh, on her wrists to prevent her from defensing, around mouth to
prevent her from shouting.
3- Identification of assailant
a) Fingernail abrasions tell if assailant is right or left-handed or if he
had a missing finger.
b) In case of hanging or strangulation, we can identify a suspected rope
from the pattern of ligature marks.
c) We can identify assailant’s teeth from a human bite on the body of
the victim.
4- Age of abrasion (time passed between infliction of wound and death)
abrasion is covered with soft scab for 2 days then covered with dry scab
for 3 days then the scab separates after 7 days leaving red surface.
5- Differentiation between contusion & hypostasis: Abrasions are present
around contusion only.
6- Differentiation between incised and contused wounds: abrasions are
usually present at the edges of contused wound only.
7- Site: abrasions always occur at the same site of injury.

282
Q

semilunar fingernail abrasions on skin of
victim’s neck.

A

Throttling: Abrasions

283
Q

ligature mark on skin of neck.

A

Strangulation & hanging Abrasions

284
Q

semilunar fingernail abrasions around mouth &
nostrils.

A

Smothering: Abrasions

285
Q

semilunar fingernail abrasions on the skin of inner aspect of
thigh, on her wrists to prevent her from defensing, around mouth to
prevent her from shouting

A

Rape: Abrasions

286
Q

Age of abrasion

A

abrasion is covered with soft scab for 2 days then covered with dry scab
for 3 days then the scab separates after 7 days leaving red surface.

287
Q

Site: Abrasions

A

abrasions always occur at the same site of injury

288
Q

Identification of assailant

A

a) Fingernail abrasions tell if assailant is right or left-handed or if he
had a missing finger.
b) In case of hanging or strangulation, we can identify a suspected rope
from the pattern of ligature marks.
c) We can identify assailant’s teeth from a human bite on the body of
the victim.

289
Q

Contusions

A

It is an extravasation of blood into the tissues due to rupture
of blood vessels

290
Q

Causal instrument:Contusions

A

Blunt object e.g., stick or big stone

291
Q

Medicolegal importance: Contusions

A

1- Sign of resistance or struggle.
2- Type of crime:
a) Throttling: subcutaneous bruises are found in the neck.
b) Strangulation & hanging: bruises are present in the deeper tissue of
neck.
c) Smothering: bruises are found around mouth and nostrils.
d) Rape: bruises are present around mouth, on the wrists and on the
inner aspect of thighs.
3-Identification of causal instrument: bruise usually takes the shape
of causal instrument e.g.
1) Stick → elongated bruise.
2) Human bite → two curved rows of abrasions in an
elliptical form with underlying bruises.
3) Animal bite → two parallel rows of abrasions not
meeting each other.
4-Age of bruises (time passed between infliction of wound and death):
recent bruise is red in color due to (oxy Hb) then changed into blue
due to (reduced Hb), then to green due to (biliverdin), then changed
to yellow due to (bilirubin) each change takes 2-3 days, then color
disappears after 2 weeks.
5- Differentiation between incised wound and contused wound:
bruises are present at edges of contused wound only.
6- Site: bruises usually occur at the site of injury, but it may shift under
the effect of gravity e.g. bruises in temple may sink down over cheek.

292
Q

The factors that modify the shape & degree of bruises:

A

1) Type of tissue: bruises develop more easily in soft, vascular, lax tissue
e.g., eye lid but if the skin is strongly supported by fibrous tissue or if
the muscle tone is good, bruising is less or even absent.
2) Age: infants (delicate skin) & old people (poorly supported blood
vessels) bruise more easily than adults.
3) Sex: female bruises more easily (because they have more subcutaneous
fat).
4) Color of skin: white person shows bruises more obviously than dark
person.
5) Natural disease: persons suffering from hypertension, vitamins
deficiency, liver damage → blood vessels become unhealthy and show
more bruises.
6) Shape: usually take the shape of causal instrument
7) Site: bruises shift down under the effect of gravity e.g., deep bruise in
the hip fasciae may sink down and appears at the knee

293
Q

Abrasions of Antemortem

A

▪ Red in color
▪ Underlying bruise
▪ Healing or sepsis
▪ Vital reaction e.g.:
- Small hemorrhage
- Fibrin threads
- Infiltration with
polymorpho-nuclear
leucocytes

294
Q

Postmortem
Of Abrasions

A

Vice versa

295
Q

Antemortem Bruises

A

▪ May be of any size.
▪ Accompanied by
swelling.
▪ May show color
changes.
▪ Blood is clotted in
tissues.

296
Q

Postmortem
Bruises

A

▪ Small
▪ No swelling
▪ No color changes.
▪ Amount of blood in
meshes of tissue is very
slight.

297
Q

Contused wound (lacerated wound)

A

Tearing or splitting of tissue

298
Q

Causal instrument: Contused

A

Heavy blunt object e.g., heavy stick or big stone

299
Q

Incised wound (cut wound)

A

Drawing edge of sharp instrument along surface of skin

300
Q

Causal instrument:Incised

A

Sharp object e.g., knife or broken glass

301
Q

Edges Contused

A

Irregular & lacerated

302
Q

Hair at edges Contused

A

Crushed

303
Q

Bleeding Contused

A

Slight because blood
Vessels are crushed

304
Q

Sepsis Contused

A

Common: because
more tissue damage at
edges and causal
instrument is usually
infected

305
Q

Abrasion &
bruises
:Contused

A

Usually present at
edges

306
Q

Bridging of
tissues across
edgesContused

A

present

307
Q

Shape Contused

A

Irregular

308
Q

Healing Contused

A

Take longer time to
heal & leaving
extensive scar

309
Q

Edges Incised

A

Sharp & regular

310
Q

Hair at edges Incised

A

Sharply cut

311
Q

Bleeding Incised

A

Free because blood
vessels are sharply cut

312
Q

Sepsis Incised

A

Unusual: minimal tissue
damage at edges and
bleeding washes out any
bacteria carried into the
wound

313
Q

Abrasion &
bruises Incised

A

absent

314
Q

Examination of
floor
Incised

A

Clean

315
Q

Bridging of
tissues across
edges Incised

A

absent

316
Q

Shape Incised

A

Linear or spindle shaped

317
Q

Healing Incised

A

Leave thin scar

318
Q

Stab wound

A

Forcing sharp pointed
instrument into the body

319
Q

Edges Stab

A

Sharply cut & regular

320
Q

Hair Stab

A

Sharply cut

321
Q

Relation between
length & depth Stab

A

Depth > length

322
Q

Dangerous Stab

A

Very dangerous because
may injure deep organs
and introduce sepsis

323
Q

Relation between
wound & size or
shape of causal
instrument =
(identification of
weapon) Stab

A

1) Wound has one sharppointed
angle → in case of
single sharp bladed
instrument C >
2) wound has two sharppointed
angles → in case
of double sharp bladed
instrument < >
3) length of wound is little
smaller than breadth of
blade because skin is
elastic. But it may be
larger if the weapon is
withdrawing or by its
lateral movement.
4) Broken tip of weapon
may be present inside
wound → help
identification of weapon

324
Q

Fabricated wound (Fictitious wound)

A
  • May be a desire for revenge.
  • Self-inflicted wound, not suicidal.
  • In areas within the reach of hand e.g., in case of right-handed people
    occur in left arm.
  • Harmless, superficial, parallel cuts.
  • No corresponding tear or blood stain in clothes.
325
Q

Characters of antemortem wound:

A
  • Gaping edges.
  • Swollen and hyperemic edges.
    Blood clot (bruise) infiltrates the edges (not washable under the tap and
    may show color changes).
  • Vital reactions (healing or sepsis).
  • Microscopical examination will show infiltration by polymorphnuclear
    leucocytes and fibrin threads.
    In the postmortem wound, the above-mentioned characters are
    absent.
326
Q

Causes of death:

A
  1. Neurogenic shock due to reflex vagal cardiac inhibition.
  2. Hemorrhage from carotid arteries and jugular veins.
  3. Chocking: trachea is opened, and blood may be inhaled.
  4. Mechanical asphyxia: - in cases of complete division of trachea, the soft
    parts of the neck fall in and close the air way to cause death from
    mechanical asphyxia.
  5. Venous air embolism
  6. Delayed death
    - Sepsis
    - Infection of larynx, oedema of glottis
    - Bronchopneumonia
327
Q

Liver:

A

Liver is bulky and friable organ; blow on abdomen may cause
lacerations of liver. These lacerations may be shallow & split capsule
especially over right lobe of liver or severe & separate right and left lobes
of liver with severe bleeding inside peritoneal cavity.

328
Q

Spleen:

A

Malaria and schistosomiasis render the spleen larger and more
friable. The minimal trauma in these cases may cause severe rupture of
spleen.

329
Q

Kidneys:

A

The injury of kidney is uncommon because they are protected
in their situation alongside the spine. They may be penetrated by stab
wound or may be lacerated after running over accident that may cause
partial or complete rupture of renal artery

330
Q

Intestine:

A

to differentiate between traumatic rupture and pathological
rupture of the intestine

331
Q

Capillary Hemangioma:

A

• The tumor may date since birth or may appear immediately after.
It is purple in color birth mark or port wine nevus.
• Although it may appear anywhere in the skin, the
commonest sites are the face and neck. The tumor
is flat and not raised above the surface (Fig 1).
• Spontaneous regression may occur, and the tumor
may disappear within months or years.
• X-ray therapy or C02 snow applied to the nevus
every month may cause partial or complete
cure.

332
Q

Treatment of Capillary Hemangioma

A

X-ray therapy or C02 snow applied to the nevus
every month may cause partial or complete
cure.

333
Q

commonest sites of Capillary Hemangioma

A

the face and neck

334
Q

Cavernous Hemangioma:

A

• The tumor consists of dilated vascular spaces and thus it
bleeds easily on injury. The face, lips and tongue are
common sites of affection. It may occur in the internal
organs such as the liver and intestine where it may
cause anemia, thrombocytopenia or it may rupture
giving internal hemorrhage.
• The tumor is raised above the surface, soft and compressible and
may be lobulated It is usually bluish in color, but the center may
be red (Fig 2).
• Surgical excision if possible is the best line of treatment.
• X-ray therapy, surface or interstitial irradiation by radium and
repeated electrocoagulation by diathermy may lead to a cure.

335
Q

Treatment od Cavernous Hemangioma

A

• Surgical excision if possible is the best line of treatment.
• X-ray therapy, surface or interstitial irradiation by radium and
repeated electrocoagulation by diathermy may lead to a cure.

336
Q

common sites of Cavernous Hemangioma

A

The face, lips and tongue and others the liver and intestine

337
Q

common sites of SEBACEOUS CYSTS

A

the scalp, the face, the neck and the scrotum
#Multiple
cysts are common in the scalp and the scrotum.

338
Q

Clinically:
SEBACEOUS CYSTS

A

• The cyst is not usually tense; it is attached to the skin in the
center, where the mouth of the
gland may be seen as a punctum.
• It is freely mobile over the
underlying structures.
• The cyst contains a greasy, thick,
greyish material with a
characteristic odor, but it does not
contain hair. On pressure the contents may come out and the
cyst evacuates, to fill again in a short period (Fig 3).

339
Q

Complications:
SEBACEOUS CYSTS

A

1) Infection to form an abscess.
2) Rarely ulceration and fungation (sometimes it resembles a
carcinoma and is then called Cock’s peculiar tumor.
4) Malignant change is rare.
5) Multiple sebaceous cysts of the scalp may by pressure effects lead
to baldness

340
Q

Treatment:
SEBACEOUS CYSTS

A

• Complete surgical excision. If any part of the wall is left the
cyst recurs. If infected it is drained first and when the
inflammation subsides, complete excision is performed.

341
Q

Lipoma

A

Lipoma is a common tumour composed of adult fat
cells. It has a well-formed (Fig 4), capsule, from
which it can be easily shelled out at operation.
Strands of fibrous tissue passing from the capsule
divide the tumour into lobules.

342
Q

The stromal tissue is usually minimal in amounts
but occasionally the fibrous element is well
marked, and the tumour may be referred to as a

A

fibrolipoma.

343
Q

The stromal tissue is usually not vascular, some cases show
angiomatous formations, and it is then called

A

angiolipoma,

344
Q

Examples of this condition
are fatty deposition of lipoma

A

Cushing’s syndrome, cretinism and
alcoholics.

345
Q

Dercum’s disease

A

painful false lipomas are found in fatty women
near the menopause (lipoma dolorosa). The thighs are usually
affected.

346
Q

Complications: Lipoma

A

o Calcification.
o Infection.
o Malignant changes into a liposarcoma (Common in lipomas
of the shoulder region and retroperitoneal).
o A submucus lipoma of the intestine may predispose to
intussusception.
o A subthecal lipoma, although rare may compress the cord
causing paraplegia.

347
Q

A subcutaneous lipoma

A

in consistency, pseudocystic and
pseudofluctuant. Its surface is lobulated, and it has a slippery
margin. It is freely mobile over the deep fascia and due to its
attachment to the skin by multiple fibrous strands, when it is moved
it is dimpled at many points.

348
Q

Subfascial lipoma:

A

May feel firm in consistency and it is not usually
lobulated therefore it is difficult to diagnose.

349
Q

Uncommon lipomata:

A

may be intermuscular, subperiosteal,
subserous, submucous and retroperotonial. Subsynovial lipoma
(lipoma arborescens) occurs in joints. A subperiosteal lipoma is
usually seen in the skull and it causes depression of the bone
underlying it.

350
Q

Treatment: lipoma

A

Excision by incising the capsule and shelling it out. A
retroperitoneal lipoma is liable to recur and it is considered by some
to be a liposarcoma from the start.

351
Q

Dermoid cysts

A

A dermoid cyst is a benign cutaneous developmental anomaly
that arises from the entrapment of ectodermal elements along
the lines of embryonic closure.

352
Q

Etiology
Of Dermoid cysts

A

• Dermoid cysts are true hamartomas. They occur due to the
abnormal sequestration and inclusion of the surface ectoderm
along the lines of skin fusion during embryologic
development.

353
Q

Histopathology
Of Dermoid cysts

A

• Dermoid cyst on histology shows a well-defined wall lined by
stratified squamous epithelium and a lumen that may be filled
with mature adnexal structures of mesodermal origin, such as
hair follicles and shafts, sebaceous and eccrine glands.

354
Q

Clinically
Dermoid cysts

A

• In the majority of cases, dermoid cysts occur in the head and
neck region, although they may be found anywhere on the
body.
• In the head and neck region, dermoid cysts can most
commonly be seen in the frontal, occipital, and supraorbital
areas, with the outer third of the
eyebrow being the most frequently
affected region (Fig 5).
• A lower lid dermoid cyst may be
evident as a painless, gradually
enlarging swelling of the lower lid.
Dermoid cysts in the medial canthal
area may present as masses
adherent to lacrimal canaliculi.
• Dermoid cysts are typically present as a pale, flesh-colored,
pearly, dome-shaped, firm, deep-seated, subcutaneous nodule.
They are usually asymptomatic, non-pulsatile, and noncompressible.

355
Q

Diagnosis
Of Dermoid cysts

A
  1. Ultrasound will show a well-defined homogenous and
    hypoechoic cystic lesion.
  2. Fistulography was done preoperatively in some cases to rule
    out the involvement of a deep tract in a dermoid cyst.
  3. Consultation with a neurosurgeon is highly recommended for
    dermoid cyst complicated by intracranial or intraspinal
    extension.
356
Q

Differential Diagnosis of Dermoid cysts

A
  1. Epidermoid cyst
  2. Encephalocele
  3. Lipoma
  4. Meningioma
  5. Neurofibroma
  6. Teratoma
  7. Lymphoma
  8. Subcutaneous abscess
  9. Lymphatic malformation
    10.Thyroglossal duct cyst
357
Q

Treatment of Dermoid cysts

A

• Dermoid cysts usually tend to grow slowly, further having the
potential to cause bony deformities, intracranial extension, or
intraspinal extension.
• The presence of intracranial extension or intraspinal extension
can further lead to meningitis or develop into an abscess.
Because most dermoid cysts grow over time, complete surgical
excision without disruption of the cyst wall by an experienced
surgeon is recommended before the development of such
complications.

358
Q

Complications of Dermoid cysts

A

Dermoid cysts that have intracranial or intraspinal extension may lead to
meningitis, abscess, or cause local mass effect. Aspiration and biopsies of
dermoid cysts have the potential to cause infection, further leading to
osteomyelitis, meningitis, or cerebral abscess.