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Types and Control of Bleeding in Surgery

The document discusses types of bleeding, categorizing them based on source, nature of the vessel, timing, volume, speed, degree, and type of intervention. It explains the hemostasis process and the coagulation cascade, detailing intrinsic and extrinsic pathways. Additionally, it outlines various methods to control bleeding, including mechanical, chemical, and thermal approaches.

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0% found this document useful (0 votes)
3 views12 pages

Types and Control of Bleeding in Surgery

The document discusses types of bleeding, categorizing them based on source, nature of the vessel, timing, volume, speed, degree, and type of intervention. It explains the hemostasis process and the coagulation cascade, detailing intrinsic and extrinsic pathways. Additionally, it outlines various methods to control bleeding, including mechanical, chemical, and thermal approaches.

Uploaded by

Jai Bhargava
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© All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd

ORAL & MAXILLOFACIAL SURGERY 1

Paper – I (Physiology)

Explain types of bleeding. Describe the intrinsic and extrinsic pathways and
methods to control bleeding. (10 marks)

ANSWER

CONTENTS/ SYNOPSIS
Introduction
Types of bleeding
1. Basis: source of bleeding
2. Basis: nature of bleeding vessel
3. Basis: time of hemorrhage
4. Basis: volume of blood loss
5. Basis: speed of blood loss
6. Basis: degree of hemorrhage
7. Basis: type of intervention
Etiology
Hemostasis
Coagulation cascade
1. Intrinsic and Extrinsic pathway
Methods to control bleeding
1. Mechanical
2. Chemical
a. Local agents
b. Systemic agents
3. Thermal
References

INTRODUCTION

• Bleeding or haemorrhage denotes the escape of blood from a blood vessel.


• Any damage to the vasculature leads to the outflow of blood
• Loss of blood due to any reason beyond a certain point is potentially life
threatening and may lead to exsanguination (blood loss to a degree sufficient
to cause death

TYPES OF BLEEDING
• Bleeding or haemorrhage can be classified in many ways:
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Basis: source of bleeding


i) External/ Revealed Hemorrhage: When bleeding is revealed and seen
outside, e.g. epistaxis.
ii) Internal/ Concealed Hemorrhage: Bleeding is concealed and not seen
outside, e.g. intracranial hematoma. Concealed hemorrhage may become
revealed as in haemetemesis or melaena in peptic ulcer bleed

Basis: nature of bleeding vessel


i) Arterial Hemorrhage: Bright red in color; blood emitted as a jet with each
heartbeat → difficult to control.
ii) Venous Hemorrhage: Dark red in color; steady and copious blood flow,
color becomes darker with oxygen desaturation → Usually easy to control.
iii) Capillary Hemorrhage: Bright red in color. Generalized ooze of blood
instead of blood flow → Easy to control

Basis: time of hemorrhage


i) Primary Hemorrhage:
▪ Occurs at the time of trauma or surgery
▪ Cause: injury to vessels
▪ Maybe arterial, venous or capillary
ii) Reactionary Hemorrhage:
▪ Occurs within 24 hours of trauma or operation.
▪ Cause: slippage of ligature, clot dislodgement, cessation of reflex
vasospasm
▪ Bleeding starts when there is rise in blood pressure
iii) Secondary Hemorrhage:
▪ Occurs after 7 – 14 days of trauma or operation.
▪ Cause: sloughing of vessel due to infection, pressure necrosis or
malignancy

Basis: volume of blood loss


i) Mild Hemorrhage: Blood loss ≤ 500 mL.
ii) Moderate Hemorrhage: Blood loss 500 – 1000 mL.
iii) Severe Hemorrhage: Blood loss ≥ 1 L.

Basis: speed of blood loss


i) Acute Hemorrhage: Massive bleeding in short span of time.
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Paper – I (Physiology)

ii) Chronic Hemorrhage: Slow bleeding small in quantity for long time.

Basis: degree of hemorrhage


i) Class I: Up to 15% blood volume loss
ii) Class II: Between 15 – 30% blood volume loss
iii) Class III: Between 30 – 40% blood volume loss
iv) Class IV: More than 40% blood volume loss

Basis: type of intervention


i) Surgical Haemorrhage: is the result of injury and amenable to surgical control,
or from angioembolism.
ii) Non-Surgical Haemorrhage: is general ooze from all raw surface due to
coagulopathy, it cannot be stopped by surgical means, require correction
coagulation abnormalities.

ETIOLOGY
• Trauma.
• Infections.
• Congenital malformations.
• Surgical (intraoperative/postoperative).
• Due to systemic diseases (viral infection, scurvy, allergy).
• Abnormalities in clotting factor (hemophilia A, multiple myeloma).
• Abnormalities in platelets (leukemia, ITP, thrombocytosis, thrombocytopenia).

HEMOSTASIS
• Mechanism of cessation of extravasation of blood.
• Four steps:
o Injured blood vessel undergoes constriction due to spasm.
o Activation of platelets and formation of platelet plug→ primary
hemostasis.
o Activation of clotting mechanism and formation of clot → secondary
hemostasis.
o Fibrous organization of clot or retraction of clot.

COAGULATION CASCADE

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• Activation of clotting process in plasma that results in formation of fibrin which


strengthens the primary hemostatic plug.
• Completed in several minutes and is important in bleeding from larger vessels.
• Procoagulants: substances promote clotting ; anticoagulants : prevent clotting
• There is a complex interaction of various factors of coagulation in the
formation of a clot.

Coagulation Mechanism
• Series of 4 reactions:
o Reaction 1:
▪ Intrinsic or contact phase of coagulation.
▪ Factors VIII, IX, XI, XII along with calcium and plasma proteins
take part.
▪ Partial thromboplastin time screens this.
o Reaction 2:
▪ Extrinsic pathway for initiation of coagulation.
▪ Release of tissue thromboplastin from injured tissues.
▪ Protease complex formed between factor VII, calcium and tissue
thromboplastin, which activates factor X.
▪ Prothrombin time screens this.
o Reaction 3:
▪ Factor X is activated by proteases generated in the previous two
reactions.
o Reaction 4:
▪ Prothrombin is converted into thrombin in presence of factor V,
calcium and phospholipids.
▪ Main role of thrombin is conversion of fibrinogen into fibrin.
▪ It also activates factor V, VIII and XIII and helps in platelet
aggregation and secretion.

Intrinsic and Extrinsic pathway

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METHODS OF ACHIEVING HEMOSTASIS


1. Mechanical Methods
o Pressure.
o Hemostat.
o Sutures and Ligation.
o Surgical staples and ligating clips
o Transcatheter arterial embolization
2. Chemical Methods
o Local Agents:
▪ Adrenaline.
▪ Thrombin.
▪ Surgicel.
▪ Oxycel.
▪ Surgicel Fibrillar.
▪ Gelatine Sponge.
▪ Microfibrillar Collagen.
▪ Fibrous Glue.

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▪ Styptics and Astringents.


▪ Alginic Acid.
▪ Natural Collagen Sponge.
▪ Bone Wax.
▪ Ostene.
o Systemic Agents:
▪ Ethamsylate
▪ Tranexamic acid
▪ Whole Blood.
▪ Platelet Rich Plasma.
▪ Fresh Frozen Plasma.
▪ Cryoprecipitate.
3. Thermal Agents
o Cautery.
o Electrocautery.
o Cryosurgery.
o Lasers.

Mechanical methods
Pressure
• Immediate measure for capillary or venous bleeding.
• Firm pressure should be applied over the bleeding site using either fingers or
gauze for at least 5 minutes.
• This would control most hemorrhages by counteracting the hydrostatic
pressure of the bleeding vessel.

Haemostat
• Application of haemostat at the bleeding point helps in direct occlusion of the
bleeding vessel

Sutures and ligation


• Severed blood vessels may be tied with ligatures.
• A ligature replaces the hemostat as a permanent method of effective
hemostasis.
• For large pulsatile artery, a trans – fixation suture to prevent slipping is
indicated.

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• Non – resorbable sutures such as silk and polyethylene are used as they
evoke less tissue reaction

Surgical staples and ligating clips


• Staples → sterile and disposable
• steel and titanium staples available
• Ligating clips→ quick and easy
• decrease foreign body reaction
• various sizes
• expensive compared to sutures.

Trans catheter arterial embolization


• Restricts tumors blood supply .
• Arterial embolization preferentially interrupts tumors blood supply and stalls
growth until neovascularization
• Used to control bleeding in Hemangiomas

Chemical methods
Local Agents:
Adrenaline
• Topical application of adrenaline brings about vasoconstriction of bleeding
capillaries.
• Available in ampoule, which is applied with the help of gauze.
• Concentration of 1:1000 is used for hemostasis over the oozing site.

Thrombin
• Helps in converting fibrinogen into fibrous clot.

Surgicel
• Oxidized cellulose polymer obtained by dissolving pure alpha- cellulose in an
alkaline solution.
• Acts by forming acid products from partial dissolution that coagulates the
plasma proteins to form a black or brown sticky gelatinous clot.
• Applied surgicel resorbs from the site in 4 to 8 weeks.
• Disadvantage : surgicel clot is not formed by normal physiological mechanism.

Surgicel fibrillar
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• Modified surgicel or oxidised regenerated cellulose in layers that can be


adapted to irregular surfaces and inaccessible areas.
• Complete resorption occurs in 2 weeks.

Gelatine sponge or gelfoam or surgifoam:


• Formed from purified pork skin gelatin.
• Completely absorbable material.
• Has the capacity to absorb 45 times its weight in blood.
• Resorbs completely in 4 to 6 weeks.

Oxycel
• Oxidized cellulose polymer product.
• This absorbable hemostatic material is manufactured by controlled oxidation of
cellulose using nitrous dioxide.
• Cellulosic acid present in it has affinity for hemoglobin which leads to the
formation of artificial clot.
• Should be applied on the dry surface as the acid formed during the wetting
process inactivates the thrombin.
• The platelets plug into its meshwork like surface & helps in clot formation.

Microfibrillar collagen (avitene)


• Collagen derived from bovine skin cause contact activation in addition to direct
platelet aggregation.
• Absorption time is 3 months.

Fibrin glue
• Biological adhesive which contains thrombin, fibrinogen, factor XIII, aprotinin.
• Thrombin converts fibrinogen to unstable fibrin clot, factor XIII stabilizes the
clot and aprotinin prevents its degradation.

Styptics & astringents


• Precipitates protein & arrests bleeding.
• Commonly used styptics & astringents are Monsel’s solution containing ferric
subsulfate & tannic acid.
• Thrombin & gelatin sponge are now widely used.

Alginic acid
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• Placed over the bleeding sites


• Forms protective film over the bleeding site→ film compresses the capillaries
& stabilizes the blood clot.

Natural collagen sponge


• White sponge material
• fully absorbable
• stimulates the platelet aggregation
• Activates coagulation factors XI & XIII.

Fibrin sponge
• Obtained from bovine material.
• Chemically treated to avoid allergic reactions.
• Applied on the bleeding site especially in post extraction socket.
• Fully absorbed by the tissues within 4-6 weeks.

Ostene
• water soluble bone hemostatic agent
• alkylene oxide copolymers
• no incidence of adverse response in the cortical defect site, medullary cavity
or the surrounding tissue.

Bone Wax
• Sterilized, non – absorbable mix of waxes.
• Consists of seven parts by weight of wax (white bees wax, paraffin wax & an
isopropyl ester of palmitic acid), two parts of olive oil and one part of phenol.
• Indicated in cases of bleeding from the bone or from chipped edges of bone.
• Bone wax is softened with the fingers to desired consistency & then applied
over the bleeding site.
• Its hemostatic mechanism is through mechanical obstruction of the osseous
cavity containing the bleeding vessels.

Botroclot Haemocoagulase
• A proteolytic enzyme from venom of South American viper, Bothrops atorox,
• plasma clotting agent for fibrinogen
• Indications: Topical capillary bleeding & tissue oozing
• Hastens coagulation through multiple actions
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• Promotes cosmetically elegant, scarless wound healing


• Arrests bleeding in cuts and wounds, Surgical incisions, Skin Grafting (Donor
& Receptor areas), Dental Extractions
• Dosage: Apply 5 to 10 drops or sufficient quantity to cover the wound
completely.

Systemic Agents:
Ethamsylate
• Hemostatic mechanism is due to activation of thromboplastin formation on
damaged vessel walls and decrease prostacyclin 2 synthesis and facilitates
platelet aggregation.
• Ethamsylate reduces capillary bleeding in the presence of normal number of
platelets.
• It acts by correcting abnormal platelet adhesion.
• exerts antihyaluronidase action,improves capillary [Link],not stabilize
fibrin(not an antifibrinolytic)
• Indications: used in prevention and treatment of capillary bleeding in
menorrhagia, epistaxis, hematuria after tooth extraction
• Efficacy is unsubstantiated
• adverse effects like rash are common and blood pressure falls only after IV
injection.
• Dose: 250-500 mg TDS orally

Tranexamic acid
• Tranexamic acid 4.8% oral rinse is an antifibrinolytic agent that stabilizes clots
and facilitates clot formation by competitively inhibiting plasminogen, the
enzyme responsible for activating plasmin.
• It can also be useful as a prophylactic mouthwash in patients who are on
anticoagulant medications which require oral surgery.
• It can be used preoperatively, intraoperatively, or postoperatively to manage
bleeding.
• popular as a post-operative hemostatic mouthwash.

Whole Blood
• Fresh whole blood refers to blood that is administered within 24 hours of its
donation.
• Whole blood transfusion indicated when there is excessive blood loss.
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• Contains all factors for coagulation


• Must be checked for HIV, hepatitis B, C viruses.

Platelet Rich Plasma


• Platelets can be collected from donated whole blood.
• Platelet concentrates are viable for 3 days when stored at room temperature.
• Must be infused quickly via short i.v. tranfusion set
• One unit raises platelet count by approx 7,000 to 10,000 cells per cu mm.

Fresh Frozen Plasma


• Unit of fresh frozen plasma is collected from one donor and contains all
coagulation factors.
• Stored at -30°C
• should be infused within 2 hours once defrosted.

Cryoprecipitate
• Stored at -30°C.
• Each bag is derived from single donor and is not treated to inactivate viruses.
• Associated with a substantial risk of viral transmission.

Thermal agents
Heat achieves hemostasis by denaturation of proteins.
Cautery
• Heat is transmitted from instrument by conduction directly to the tissues.
• Electrocautery has replaced direct heat application.
• Dental burnisher like instrument can be directly heated over flame and applied
directly to the bleeding point.

Electrocautery
• Most widely used.
• Electrocautery can be applied directly to bleeding point.
• Cautery point is touched to the hemostat, causing sealing of vessel through
action of heat
• Causes tissue destruction producing burning smell and smoke during
application
• Advantages
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o Permits any degree of hemorrhage control.


o Provides clear and improved view.
o Increases efficiency.
o Reduces chair side time.
o Gives pressureless cutting.

Cryosurgery
• Temperature ranging from -20°C to -180°C are used.
• Tissues, capillaries, small arterioles and venules undergo cryogenic necrosis.
• Caused by dehydration and denaturation of lipid molecules.
• specially used to treat superficial hemangiomas.

Lasers
• Lasers usually result in bloodless surgery.
• Effectively coagulate the small blood vessels during cutting of tissues.

REFERENCES

1. Malik NA, Textbook of oral and maxillofacial surgery. 3rd Ed. (2012). New Delhi
: Jaypee Brothers Medical Publishers (P) Ltd.
2. Shenoy A, Shenoy R. Manipal manual of Surgery, 4 th Edition. 2014. CBS
Publishers & Distributors
3. Peterson. Peterson's Principles of Oral and Maxillofacial Surgery. Shelton, CT:
People's Medical Pub. House-USA, 2012.
4. Behrens AM, Sikorski MJ, Kofinas P. Hemostatic strategies for traumatic and
surgical bleeding. J Biomed Mater Res A. 2014; 102 (11): 4182–4194.
5. McBee WL, Koerner KR. Review of hemostatic agents used in dentistry. Dent
Today. 2005; 24 (3): 62-5

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