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HYPOVOLEMIC SHOCK University of Medicine and Pharmacy, Iasi

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Presentation on theme: "HYPOVOLEMIC SHOCK University of Medicine and Pharmacy, Iasi"— Presentation transcript:

1 HYPOVOLEMIC SHOCK University of Medicine and Pharmacy, Iasi
School of Medicine ANESTHESIA and INTENSIVE CARE Conf. Dr. Ioana Grigoras MEDICINE 4th year English Program Suport de curs HYPOVOLEMIC SHOCK

2 HYPOVOLEMIC SHOCK DEFINITION Hemorrhagic shock
syndrom characterized by decreased circulating blood volume (hypovolemia), which results in reduction of effective tissue perfusion pressure and generalized cellular dysfunctions. Forms: Hemorrhagic shock Non-hemorrhagic hypovolemic shock

3 HYPOVOLEMIC SHOCK CAUSES: Hemorrhagic: Non-hemorrahagic:
External blood loss (wounds) Exteriorization of internal bleeding (hematemesis, melena, epistaxis, hemoptysis,etc.) Internal bleeding (hemothorax, hemoperitoneum,etc. ) Traumatic shock Non-hemorrahagic: Digestive losses (vomiting, diarrhea, nasogastric suction, billiary, digestive fistula, etc ) Renal losses (diabetes mellitus, polyuria caused by diuretics overdose, osmotic substances, polyuric phase of acute renal failure, etc.) Skin losses (intense physical effort, overheated enviroment, burns, etc.) Third space losses (peritonites, intestinal oclussion, pancreatits, ascitis pleural effusions, etc.)

4 PATHOPHYSIOLOGY Primary pathophysiological event
(reduction of ventricular filling volumes and pressures) compensatory phenomena macrocirculatory reaction time decompensatory phenomena microcirculatory reaction

5 PATHOPHYSIOLOGY Hypodynamic shock: Macrocirculatory reaction:
sympatho-adrenergic + humoral reaction (ADH, cortizol, SRAA) EFFECTS: centralisation of the circulation (compensatory effect) worsening of tisular hypoperfusion (decompensatory effect) Microcirculatory reaction: Alterations of capillary exchanges EFFECTS: transcapilary filling (compensatory effect) capilary leak (decompensatory effect) Maldistribution of blood flow EFFECTS: preferential renal blood flow towards medular region (cortical vasoconstriction) Abnormal peripheral oxygen extraction EFFECTS: early - increased (compensatory effect) late - decreased (decompensatory effect) Rheologic changes EFFECTS: ↑ blood viscosity,  blood flow, CID Endhotelial modifications EFFECTS: morpho-functional modifications proinflamatory and procoagulatory status, altered permeability

6 HYPOVOLEMIC SHOCK CLINICAL SIGNS: Intense thirst Tachycardia Tachypnea
Positive orthostatic test Small pulse wave hTA (blood hypotension) Agitation, anxiety , confusion, coma Oliguria Cold extremities Profuse sweating Collapsed peripheral veins Delayed return of color to the nail bed + History of hemorrhagic or non-hemorrhagic losses

7 CLASSIFICATION OF HYPOVOLEMIC SHOCK
Class II Class III Class IV Blood loss- ml < 750ml ml ml >2000ml Blood loss-% <15% 15-30% 30-40% >40% Pulse rate <100/min < 100/min /min >140/min BP N   Pulse wave amplitude Capillary refill + Respiratory rate 14-20/min 20-30/min 30-40/min >40/min Urinary output >30ml/oră Oliguria Oligoanuria Anuria Mental status Mild anxiety Anxiety Confused Lethargy

8 DIFFERENTIAL DIAGNOSIS WITH OTHER FORMS OF SHOCK
HR BP CO CVP PAOP SVR Da-vO2 SvO2 Hypovolemic shock Cardiogenic shock  Septic shock ↑ N  N N

9 ABBREVIATIONS: HR – heart rate BP – arterial blood pressure
CO – cardiac output CVP –central venous pressure PAOP – pulmonary artery occlusion pressure SVR – systemic vascular resistance Da-v O2 – oxygen arterial-venous difference SvO2 – mixed venous blood oxygen saturation

10 HYPOVOLEMIC SHOCK TREATMENT PRINCIPLES
Initial treatment of shock states Causative treatment – STOP losses Volume repletion Inotropic therapy Vasomotor therapy

11 TREATMENT OF HYPOVOLEMIC SHOCK
Causative treatment – STOP losses essential role surgical treatment (when appropriate) emergency surgery for ongoing hemorrhage

12 TREATMENT OF HYPOVOLEMIC SHOCK
volume replacement Vascular access site Solutions for volume replacement Rhythm of administration

13 TREATMENT OF HYPOVOLEMIC SHOCK
Volume replacement – SITE of VASCULAR ACCESS Peripheral vascular access Multiple access (2-4 veins) Large peripheral catheters External jugular vein Advantages: Short time of instalation Requires basic knowledge and simple matherials Minor complications (hematomas, cutaneous seroma, etc.) Disadvantages: The diameter of peripheral catheter must be adapted for peripheral veins dimensions Vascular access can be lost (restless patient, during transportation); must be changed at hours; no catecholamines administration (except in emergency for a short time period,until a central venous access is available) Central venous access After peripheral vascular access is established and volume replacement is initiated Reliable and long lasting venous access (7-10 days) Allows CVP measuring and guiding of treatment Allows the administration of catecholamines and hypertonic substances Risk of complication (at instalation – pneumothorax, cervical or mediastinal hematoma, cardiac dysrhytmias; during utilization – infection, gas embolism)

14 TREATMENT OF HYPOVOLEMIC SHOCK
Volume replacement - Solutions for volume replacement Isotonic crystalloid solutions Hypertonic crystalloid solutions Colloid solutions Whole blood and red blood cells Fresh-frozen plasma Platelets

15 TREATMENT OF HYPOVOLEMIC SHOCK
Solutions for volume replacement -Isotonic crystalloid solutions Normal saline (NaCl 0,9 %), Ringer solution, lactated Ringer solutions Advantages: easy available cheap reduced risks Disadvantages: Small volume effect (out of 1000ml infused solution – ml remains intravascullarly, the rest is distributed to the interstitial space) short duration of volume effect risk of interstitial edema, metabolic hyperchloremic acidosis -Hypertonic crystalloid solutions hypertonic saline (NaCl 7,4%) Efficient blood volume resuscitation with small solution volume (water is atracted from interstitial space ) Avoidance of fluid overload and peripheral edema may result in acute pulmonary edema

16 TREATMENT OF HYPOVOLEMIC SHOCK
Solutions for volume replacement Colloid sollutions Dextrans: Dextran 70, Dextran 40 Gelatines: Gelofusin, Haemacel, Eufusin Hetastarch: Haes, Voluven, Refortan Human albumin 5%, 20% Advantages: Good volume effect Long duration of volume effect Disadvantages: expensive risk for anaphylactic reactions interfere with blood groups determination can induce/ aggravate coagulation disorders

17 TREATMENT OF HYPOVOLEMIC SHOCK
Solution for volume replacement Blood and blood products are not volume solutions Only isogroup isoRh blood Only after restauration of intravascular volume with cristalloid /colloid solutions; For correction of oxygen transport In case of posthemorragic anemia (after volume replacement) or ongoing hemorrhage In case of massive blood transfusion – add fresh-frozen plasma and platelet concentrate

18 TREATMENT OF HYPOVOLEMIC SHOCK
Volume replacement RHYTHM OF ADMINISTRATION Rhytm of administration depends on: Ongoing losses / stopped losses Rhytm of losses – rapid (minutes, hours) or slow (days) instalation For the patient with hypotension – normal saline (2000 ml in the first minutes) after the first minutes - volume replacement continues depending on the clinical and hymodinamic parameters (BP, HR, etc..)

19 TREATMENT OF HYPOVOLEMIC SHOCK
Volume replacement – MONITORING THE TREATMENT EFFICIENCY Clinical parameters normalisation of BP, HR, pulse amplitude, skin colour and temperature, mental status, urinary output Hemodynamic parameters Normalization of CVP, PCPB, DC, RVS, so Laboratory parameters Normalization of acid-base balance, liver, renal tests, Hb şi Ht, so

20 TREATMENT OF HYPOVOLEMIC SHOCK
Inotropic support Only after volume replacement Used to improve cardiac output Dobutamine inotropic positive support peripheral arterial vasodilatation

21 TREATMENT OF HYPOVOLEMIC SHOCK
Vasopressor therapy NOT RECOMMENDED (may aggravate peripheral hypoperfusion and metabolic acidosis) EXCEPTIONS Only temporary In case of ongoing hemorrhage, which outruns the possibilities of volume replacement Only until surgical procedure stops the hemorrhage (emergency surgical treatment) Noradrenaline, dopamine, adrenaline


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