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Understanding Multiple Organ Dysfunction Syndrome

Multiple organ dysfunction syndrome (MODS) occurs when two or more organ systems are unable to function, most commonly due to sepsis. It results from an underlying condition like systemic inflammatory response syndrome. Organs may fail over time, with respiratory failure within 72 hours, hepatic failure within a week, and renal failure within two weeks. Treatment focuses on supporting failed organ systems, managing fluids and hemodynamics, and treating the underlying cause.

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0% found this document useful (0 votes)
93 views16 pages

Understanding Multiple Organ Dysfunction Syndrome

Multiple organ dysfunction syndrome (MODS) occurs when two or more organ systems are unable to function, most commonly due to sepsis. It results from an underlying condition like systemic inflammatory response syndrome. Organs may fail over time, with respiratory failure within 72 hours, hepatic failure within a week, and renal failure within two weeks. Treatment focuses on supporting failed organ systems, managing fluids and hemodynamics, and treating the underlying cause.

Uploaded by

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

MULTIP L E O R G A N

N C TI ON S Y ND RO ME
DY SF U
(MODS) MA RIE A . AB U YAN, RN
BY: JO AHNNA
MULTIPLE ORGAN DYSFUNCTION SYNDROME
PREVIOUSLY KNOWN AS MULTIPLE ORGAN FAILURE (MOF) OR MULTISYSTEM
ORGAN FAILURE (MSOF),
IS A CONDITION THAT OCCURS WHEN TWO OR MORE ORGANS OR ORGAN SYSTEMS
ARE UNABLE TO FUNCTION IN THEIR ROLE OF MAINTAINING HOMEOSTASIS.
MODS ISNT AN ILLNESS ITSELF; RATHER, ITS A MANIFESTATION OF ANOTHER
PROGRESSIVE UNDERLYING CONDITION.
THE USE OF "MULTIPLE ORGAN FAILURE" OR "MULTISYSTEM ORGAN FAILURE"
SHOULD BE AVOIDED SINCE THAT PHRASE WAS BASED UPON PHYSIOLOGICAL
PARAMETERS TO DETERMINE WHETHER OR NOT A PARTICULAR ORGAN WAS
FAILING.
CAUSES

SIRS (SYSTEMIC INFLAMMATORY RESPONSE SYNDROME)


SEPSIS- MOST COMMON CAUSE IN OPERATIVE AND NON-OPERATIVE
PATIENTS

INJURY (ACCIDENT, SURGERY)

HYPOPERFUSION

HYPERMETABOLISM
CURRENTLY, INVESTIGATORS ARE LOOKING INTO GENETIC TARGETS FOR
POSSIBLE GENE THERAPY TO PREVENT THE PROGRESSION TO MULTIPLE
ORGAN DYSFUNCTION SYNDROME.

SOME AUTHORS HAVE CONJECTURED THAT THE INACTIVATION OF THE


TRANSCRIPTION FACTORS NF-B AND AP-1 WOULD BE APPROPRIATE
TARGETS IN PREVENTING SEPSIS AND SIRS.
PATHOPHYSIOLOGY

o RESPIRATORY FAILURE IS COMMON IN THE FIRST 72 HOURS AFTER THE


ORIGINAL INSULT.

o HEPATIC FAILURE (57 DAYS)


o GASTROINTESTINAL BLEEDING(1015 DAYS)
o RENAL FAILURE (1117 DAYS)
GUT HYPOTHESIS
THE MOST POPULAR HYPOTHESIS BY DEITCH TO EXPLAIN MODS IN CRITICALLY ILL.

Due to splanchnic hypoperfusion and the subsequent mucosal ischaemia


there are structural changes and alterations in cellular function.

This results in increased gut permeability, changed immune function of the gut
and increased translocation ofbacteria.

Hepatic dysfunction leads to toxins escaping into the systemic circulation and
activating an immune response.

This results in tissue injury and organ dysfunction.


ENDOTOXIN MACROPHAGE HYPOTHESIS
GRAM-NEGATIVE INFECTIONS IN MODS PATIENTS ARE RELATIVELY COMMON,

ENDOTOXINS HAVE BEEN ADVANCED AS PRINCIPAL MEDIATOR IN THIS


DISORDER

IT IS THOUGHT THAT FOLLOWING THE INITIAL EVENT CYTOKINES ARE


PRODUCED AND RELEASED. THE PRO-INFLAMMATORY MEDIATORS ARE:
TUMOR NECROSIS FACTOR-ALPHA (TNF-), INTERLEUKIN-1, INTERLEUKIN-6,
THROMBOXANE A2, PROSTACYCLIN, PLATELET ACTIVATING FACTOR, AND
NITRIC OXIDE.
TISSUE HYPOXIA-MICROVASCULAR HYPOTHESIS

AS A RESULT OF MACRO- AND MICROVASCULAR CHANGES INSUFFICIENT


SUPPLY OF OXYGEN OCCURS. HYPOXEMIA CAUSES CELL DEATH AND ORGAN
DYSFUNCTION.
INTEGRATED HYPOTHESIS

SINCE IN MOST CASES NO PRIMARY CAUSE IS FOUND, THE CONDITION COULD


BE PART OF A COMPROMISED HOMEOSTASIS INVOLVING THE PREVIOUS
MECHANISMS.
DIAGNOSIS

THE EUROPEAN SOCIETY OF INTENSIVE CARE ORGANIZED A CONSENSUS


MEETING IN 1994 TO CREATE THE "SEPSIS-RELATED ORGAN FAILURE
ASSESSMENT (SOFA)" SCORE TO DESCRIBE AND QUANTITATE THE DEGREE OF
ORGAN DYSFUNCTION IN SIX ORGAN SYSTEMS. USING SIMILAR PHYSIOLOGIC
VARIABLES THE MULTIPLE ORGAN DYSFUNCTION SCORE WAS DEVELOPED.
FOUR CLINICAL PHASES HAVE BEEN SUGGESTED:

Stage 1the patient has increased volume requirements and mild


respiratoryalkalosis which is accompanied byoliguria, hyperglycemia and
increasedinsulinrequirements.

Stage 2the patient istachypneic,hypocapnicandhypoxemic; develops moderate


liver dysfunction and possible hematologic abnormalities.

Stage 3the patient develops shock withazotemiaandacid-basedisturbances; has


significant coagulation abnormalities.

Stage 4the patient is vasopressor dependent and oliguric or anuric; subsequently


developsischemic colitisandlactic acidosis
CLINICAL MANIFESTATIONS
EARLY FINDINGS MAY INCLUDE:
FEVER- USUALLY GREATER THAN 101F (38.3 C)
TACHYCARDIA
NARROWED PULSE PRESSURE
TACHYPNEA
DECREASED PULMONARY ART ERY PRESSURE (PAP, PAWP, AND CVP)
INCREASED CARDIAC OUTPUT
AS SIRS PROGRESSES, FINDINGS REFLECT IMPAIRED PERFUSION OF THE
TISSUES AND ORGANS SUCH AS:

DECREASED LOC

RESPIRATORY DEPRESSION

DIMINISHED BOWEL SOUNDS

JAUNDICE

OLIGURIA OR ANURIA

INCREASED PAP AND PAWP

DECREASED CARDIAC OUTPUT


DIAGNOSTIC TESTS

ABG ANALYSIS

CBC

XRAYS

MRI

CT-SCAN

ANGIOGRAPHY
TREATMENT

MEHANICAL VENTILATION AND SUPPLEMENTAL OXYGEN

HEMODYNAMIC MONITORING

FLUID INFUSION (CRYTALLOIDS AND COLLOIDS)

VASOPRESSORS

SERIAL LABORATORY VALUES

DIALYSIS

ANTIMICROBIAL AGENTS
NURSING CARE AND MANAGEMENT
MAINTAIN THE PATIENTS AIRWAY AND BREATHING WITH THE USE OF MECHANICAL
VENTILATION AND SUPPLEMENTAL OXYGEN

MONITOR VITAL SIGNS, OXYGEN SATURATION, HEMODYNAMIC PARAMETERS AND


CARDIAC RHYTHM FOR ARRHYTHMIAS.

ADMINISTER IV FLUIDS AS ORDERED.

MONITOR LABORATORY VALUES.

MONITOR INTAKE AND OUTPUT.

ADMINISTER APPROPRIATE MEDICATIONS AS ORDERED.

PROVIDE EMOTIONAL SUPPORT TO THE PATIENT AND FAMILY.

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