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PRESENTED BY:
SHINY MATHEW
HEAD NURSE MMW
DIABETES MELLITES
 Diabetes mellitus is a group of metabolic disease
  results from the production of insufficient amount
  of insulin by the pancreas. Without insulin the
  body cannot utilize glucose. So creating high level
  of glucose in the blood and a low level of glucose
  absorption by the tissue.
 Type 1 diabetes -- insulin dependant diabetes
 Type2 diabetes-- Non insulin dependant diabetes
DIABETIC KETOACIDOSIS
Diabetic keto acidosis is an acute state of severe
uncontrolled diabetic that requires emergency
treatment with insulin and intravenous fluids.bio
chemically DKA is defined as an increase in the
serum concentration of ketons greater than 5
meq/l a blood glucose level of greater than 250
mg/l,blood PH less than 7.2 and HCO3 is 18meq/l
or less.
PRECIPITATING FACTORS
 Infections
 Acute stroke
 Pancreatitis
 Myocardial infarction
 Interruption of insulin
 Pregnancy
 Dietery indiscretion
 Trauma and stress
INFECTION                               MISSED INSULIN DOSE
    STRESS                                NEW-ONSET DIABETES
 EXCESS SECRETION OF
                                              INADEQUATE
GLYCOGEN AND OTHER
                                                INSULIN
COUNTER REGULATORY
     HORMONES
                                               DCREASE
INCREASED LIPOLYSIS    GLYCOGENENOLYSIS     GLUCOSE UPTAKE
 OF ADIPOSE TISSUE            AND
                       GLUCONEOGENESIS
                          BY THE LIVER       HYPERGLYCEMIA
  KETOGENESIS
                                               OSMOTIC
    KETOSIS                                    DIURESIS
                         VOMITING
   ACIDOSIS                                    POTASSIUM
                                                 LOSS

                       DEHYDRATION
LACK OF INSULIN

DECREASED UTILIZATION                         INCREASED
OF GLUCOSE BY MUSCLE,                        BREAKDOWN
FAT AND LIVER                                   OF FAT
INCREASED PRODUCTION        •ACETONE
OF GLUCOSE BY LIVER           BREATH          INCREASED
                         •POOR APPETITE      FATTY ACIDS
                             •NAUSEA
   HYPERGLYCEMIA                             INCREASED
                                               KETONE
                               •NAUSEA         BODIES
BLURRED      POLYURIA         •VOMITING
 VISION                    •ABDOMINAL PAIN      ACIDOSIS
WEAKNESS       DEHYDRATION
HEADACHE
                                             INCREASINGLY
               INCREASED THIRST                 RAPID
                 (POLYDIPSIA)                RESPIRATIONS
COMMON CLINICAL FEATURES
 Poly urea ,poly dipsia,poly phagia
 Weight loss
 Nausea and vomiting
 weakness
 Abdominal pain
 Clouding of sensorium
 Coma
 Hyper ventillation –kuss mual pattern
 Dehydration and shock
   s
LABORATORY FINDINGS
 Blood glucose greater than 14mmol/L[250 mg/l]
 Arterial pH less than 7.3
 Anion gap less than 10
 Ketone urea
 Arterial bicarbonate less than 15
 Hyper magnesimia
 Hypokalemia
 Cardiac enzymes
 Pco2-35it reflects respiratory compensation .
NURSING ASSESSMENT
 Assess skin for dehydration like poor turgour,flushing,and dry
    mucus membrances.
   Observe for cardiac changes reflecting dehydration,metabolic
    and electrolyte imbalance,tachycardia,hypotension,weak
    pulse,ECG changes including elevated P wave flattendT wave
    or inverted and prolonged QT intervals
   Assess respiratory status kussmual breathing,acctone breaths
    characteritic of metabolic acidosis
   Assess gastro intestinal symptoms like nausea vomiting
    extreme thirst,abdominal bloating,cramping,and diarrhoea
   Genito urinary symptoms-nocturia and polyuria
   Neurologic signs-
    crying,restlessness,twitching,tremers,drowsiness,lethargy,hea
    dache.
NURSING MANAGEMENT

 Stabilize the patient’s airway,breathing,circulation
 Obtain 16 gauge iv line on both site and assess cardiac
  monitoring and pulse oxymetry.
 Monitor serum glucose hourly and urine ketone
 Monitor basic electrolyte,osmolarity and venousPHevery 4
  hourly until pt is stable.
 Determine and treat any underlyingcausesof DKAeg;;
  pneumonia,UTIand MI
1.FLUID REPLACEMENT[ADULT]
 Give 1 litre of normal saline[0.9%]rapidly via No I8 gauge
    cannula if cardiac function is normal.
   Then one litre of normal saline/ hour, for 1st3 hrs for those
    individuals who are in shock .
   Then 250-500ml /hr of normal saline depending on hydration
    status until blood sugar is 14 mmol/L[250 mg/L]. blood sugar
    level<14 mmol/L 0.9%should be switched toD51/2NS or DNS
    at 125 to 250ml/hour.
   Assess blood pressure & heart rate frequently.
   Monitor intake and out put for signs of fluid overload.
   Monitor urine specific gravity to assess fluid changes.
INSULIN TREATMENT
 Regular insulin 0.1 units/kg. as an IV bolus.
 Then regular insulin infusion IV 0.14 units /kg./hour until
  blood sugar reaches 14mmol/litre ( 250mg/dl) & follow IV
  infusion protocol
 1ml regular insulin = 100units
 Start insulin infusion 6units/hr.
 Doctor’s order x solution in volume     6units x 50
 ____________________________ =          ____________
      Strength of solution                 100 units
 300
_____ = 3ml/hr. ( 6units/hr.)
100
RATE OF INFUSION ACCORDING TO SLIDING SCALE OF
                      REGULAR INSULIN
CAPILLARY BLOOD GLUCOSE IN                  UNITS OF INSULIN / HOUR
MG/DL
                  <99                                   0.5ml/hr.
  100______ 149     (5.6—8.2mmol)                        1ml/hr.
   150 ______ 199        ( 8.3_____11 )                  2ml/hr.
  200 ______ 249        ( 11.1 ____13.8 )                3ml/hr.
  250_______299         (13.9____ 16.6)                  4ml/hr.
  300_______349         ( 16.7____19.4)                  5ml/hr.
 350_______399          ( 19.5_____22.2)                 6ml/hr.
 400_______450      ( 22.3_____24.9)                     8ml/hr.
  >450                        ( > 24.9)                  10ml/hr.
ANION GAP- Substract the major measured anion from
the major measured Cations (Cl +Hco3- Na)
 • IV insulin infusion can be switched to subcutaneous
     insulin according to sliding scale.
 •   Arterial bicarbonate rises 18.
 •   Anion gap 10 up to 12 + or- 2
 •   Urine aceton 3times negative
 •   Oral intake has resumed
 •   It is important to give the first subcutaneous insulin
     approximately two hours before stopping the infusion
 •   Flush the entire IV infusion set with solution containing
     insulin & dicard the solution ,then refill it again
 •   Keep separate IV line for insulin infusion and electrolyte
     replacement
POTASSIUM REPLACEMENT
 Aims to keep serum k+ between 4 to 5meq/ L to prevent
    hyper or hypokalemea.
   If initial potassium is <3.3 Hold insulin & replace K+
   Do not give K+ direct IV, must be added to IV fluids
   If K+ is >5 do not give Kcl recheck within hour
   If k+ is 4__ 5 give Inj.kcl 20meq in each liter of fluid
   If K+ is 3__4 give Inj.kcl 30meq in each liter of fluid
   If K+ is <3     give Inj.kcl40meq in two hour & recheck
   Follow sliding scale of K+ every 6th hourly until stable
BICARBONATE REPLACEMENT
 If arterial PH <7 give 50ml of bicarbonate in 250ml of
    0.45% NSS over one hour
   Bicarbonate infusion to correct acidosis is avoided,during
    the treatment of DKA because it precipitates further
    sudden decrease in serum potassium .
   INVESTIGATION AND OUTCOME BASED EVALUATION
   Serum glucose initially and hrly until acctone disappear
   Serum potassium initially and hrly if K+ < 3 or > 5
   Electrolyte and renal function initially and then 6 hrly ..
   Serum osmolarity , VBG,cardiac enzymes ,CBC
   Urine analysis and urine culture if needed
COMPLICATION
 Premature discontinuation of Ivinsulin can result in
    prolonged DKA
   Too rapid infusion of IVF in case of severe dehydration
    can cause cerebral edema and death
   If blood glucose level falls too fast or too slow,before
    the brain has time to equilibrate,the water is pulled
    from the cerebrospinal fluid and the brain causing
    cerebraloedema and death
   Hypoxiaand leads to ARDS
   Hypoglycemia,venous and arterial thrombosis
PATIENT EDUCATION
 Instruct to take insulin or oral diabetic agent as usual
 Check blood sugar and urine sugar every 4 hrly
 Report elevated glucose and urine acctone to physician
 Usual meal plan cannot be followed substitute soft foods 6-
  8 times /day
 If any symptoms like vomiting and diarrhoe or fever
  consume liquid diet every half to one hour to prevent
  dehydration and provide calories
 Inform physician about extreme fluid loss maybe
  dangerous.
 For type 1 diabetic, iniability to retain oral fluid needs
  hospitallization to avoid DKA and possible coma
SHINY MATHEW
    MALE
MEDICAL WARD

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Diabetic ketoacidosis

  • 2. DIABETES MELLITES  Diabetes mellitus is a group of metabolic disease results from the production of insufficient amount of insulin by the pancreas. Without insulin the body cannot utilize glucose. So creating high level of glucose in the blood and a low level of glucose absorption by the tissue.  Type 1 diabetes -- insulin dependant diabetes  Type2 diabetes-- Non insulin dependant diabetes
  • 3. DIABETIC KETOACIDOSIS Diabetic keto acidosis is an acute state of severe uncontrolled diabetic that requires emergency treatment with insulin and intravenous fluids.bio chemically DKA is defined as an increase in the serum concentration of ketons greater than 5 meq/l a blood glucose level of greater than 250 mg/l,blood PH less than 7.2 and HCO3 is 18meq/l or less.
  • 4. PRECIPITATING FACTORS  Infections  Acute stroke  Pancreatitis  Myocardial infarction  Interruption of insulin  Pregnancy  Dietery indiscretion  Trauma and stress
  • 5. INFECTION MISSED INSULIN DOSE STRESS NEW-ONSET DIABETES EXCESS SECRETION OF INADEQUATE GLYCOGEN AND OTHER INSULIN COUNTER REGULATORY HORMONES DCREASE INCREASED LIPOLYSIS GLYCOGENENOLYSIS GLUCOSE UPTAKE OF ADIPOSE TISSUE AND GLUCONEOGENESIS BY THE LIVER HYPERGLYCEMIA KETOGENESIS OSMOTIC KETOSIS DIURESIS VOMITING ACIDOSIS POTASSIUM LOSS DEHYDRATION
  • 6. LACK OF INSULIN DECREASED UTILIZATION INCREASED OF GLUCOSE BY MUSCLE, BREAKDOWN FAT AND LIVER OF FAT INCREASED PRODUCTION •ACETONE OF GLUCOSE BY LIVER BREATH INCREASED •POOR APPETITE FATTY ACIDS •NAUSEA HYPERGLYCEMIA INCREASED KETONE •NAUSEA BODIES BLURRED POLYURIA •VOMITING VISION •ABDOMINAL PAIN ACIDOSIS WEAKNESS DEHYDRATION HEADACHE INCREASINGLY INCREASED THIRST RAPID (POLYDIPSIA) RESPIRATIONS
  • 7. COMMON CLINICAL FEATURES  Poly urea ,poly dipsia,poly phagia  Weight loss  Nausea and vomiting  weakness  Abdominal pain  Clouding of sensorium  Coma  Hyper ventillation –kuss mual pattern  Dehydration and shock  s
  • 8. LABORATORY FINDINGS  Blood glucose greater than 14mmol/L[250 mg/l]  Arterial pH less than 7.3  Anion gap less than 10  Ketone urea  Arterial bicarbonate less than 15  Hyper magnesimia  Hypokalemia  Cardiac enzymes  Pco2-35it reflects respiratory compensation .
  • 9. NURSING ASSESSMENT  Assess skin for dehydration like poor turgour,flushing,and dry mucus membrances.  Observe for cardiac changes reflecting dehydration,metabolic and electrolyte imbalance,tachycardia,hypotension,weak pulse,ECG changes including elevated P wave flattendT wave or inverted and prolonged QT intervals  Assess respiratory status kussmual breathing,acctone breaths characteritic of metabolic acidosis  Assess gastro intestinal symptoms like nausea vomiting extreme thirst,abdominal bloating,cramping,and diarrhoea  Genito urinary symptoms-nocturia and polyuria  Neurologic signs- crying,restlessness,twitching,tremers,drowsiness,lethargy,hea dache.
  • 10. NURSING MANAGEMENT  Stabilize the patient’s airway,breathing,circulation  Obtain 16 gauge iv line on both site and assess cardiac monitoring and pulse oxymetry.  Monitor serum glucose hourly and urine ketone  Monitor basic electrolyte,osmolarity and venousPHevery 4 hourly until pt is stable.  Determine and treat any underlyingcausesof DKAeg;; pneumonia,UTIand MI
  • 11. 1.FLUID REPLACEMENT[ADULT]  Give 1 litre of normal saline[0.9%]rapidly via No I8 gauge cannula if cardiac function is normal.  Then one litre of normal saline/ hour, for 1st3 hrs for those individuals who are in shock .  Then 250-500ml /hr of normal saline depending on hydration status until blood sugar is 14 mmol/L[250 mg/L]. blood sugar level<14 mmol/L 0.9%should be switched toD51/2NS or DNS at 125 to 250ml/hour.  Assess blood pressure & heart rate frequently.  Monitor intake and out put for signs of fluid overload.  Monitor urine specific gravity to assess fluid changes.
  • 12. INSULIN TREATMENT  Regular insulin 0.1 units/kg. as an IV bolus.  Then regular insulin infusion IV 0.14 units /kg./hour until blood sugar reaches 14mmol/litre ( 250mg/dl) & follow IV infusion protocol  1ml regular insulin = 100units  Start insulin infusion 6units/hr.  Doctor’s order x solution in volume 6units x 50 ____________________________ = ____________ Strength of solution 100 units 300 _____ = 3ml/hr. ( 6units/hr.) 100
  • 13. RATE OF INFUSION ACCORDING TO SLIDING SCALE OF REGULAR INSULIN CAPILLARY BLOOD GLUCOSE IN UNITS OF INSULIN / HOUR MG/DL <99 0.5ml/hr. 100______ 149 (5.6—8.2mmol) 1ml/hr. 150 ______ 199 ( 8.3_____11 ) 2ml/hr. 200 ______ 249 ( 11.1 ____13.8 ) 3ml/hr. 250_______299 (13.9____ 16.6) 4ml/hr. 300_______349 ( 16.7____19.4) 5ml/hr. 350_______399 ( 19.5_____22.2) 6ml/hr. 400_______450 ( 22.3_____24.9) 8ml/hr. >450 ( > 24.9) 10ml/hr.
  • 14. ANION GAP- Substract the major measured anion from the major measured Cations (Cl +Hco3- Na) • IV insulin infusion can be switched to subcutaneous insulin according to sliding scale. • Arterial bicarbonate rises 18. • Anion gap 10 up to 12 + or- 2 • Urine aceton 3times negative • Oral intake has resumed • It is important to give the first subcutaneous insulin approximately two hours before stopping the infusion • Flush the entire IV infusion set with solution containing insulin & dicard the solution ,then refill it again • Keep separate IV line for insulin infusion and electrolyte replacement
  • 15. POTASSIUM REPLACEMENT  Aims to keep serum k+ between 4 to 5meq/ L to prevent hyper or hypokalemea.  If initial potassium is <3.3 Hold insulin & replace K+  Do not give K+ direct IV, must be added to IV fluids  If K+ is >5 do not give Kcl recheck within hour  If k+ is 4__ 5 give Inj.kcl 20meq in each liter of fluid  If K+ is 3__4 give Inj.kcl 30meq in each liter of fluid  If K+ is <3 give Inj.kcl40meq in two hour & recheck  Follow sliding scale of K+ every 6th hourly until stable
  • 16. BICARBONATE REPLACEMENT  If arterial PH <7 give 50ml of bicarbonate in 250ml of 0.45% NSS over one hour  Bicarbonate infusion to correct acidosis is avoided,during the treatment of DKA because it precipitates further sudden decrease in serum potassium .  INVESTIGATION AND OUTCOME BASED EVALUATION  Serum glucose initially and hrly until acctone disappear  Serum potassium initially and hrly if K+ < 3 or > 5  Electrolyte and renal function initially and then 6 hrly ..  Serum osmolarity , VBG,cardiac enzymes ,CBC  Urine analysis and urine culture if needed
  • 17. COMPLICATION  Premature discontinuation of Ivinsulin can result in prolonged DKA  Too rapid infusion of IVF in case of severe dehydration can cause cerebral edema and death  If blood glucose level falls too fast or too slow,before the brain has time to equilibrate,the water is pulled from the cerebrospinal fluid and the brain causing cerebraloedema and death  Hypoxiaand leads to ARDS  Hypoglycemia,venous and arterial thrombosis
  • 18. PATIENT EDUCATION  Instruct to take insulin or oral diabetic agent as usual  Check blood sugar and urine sugar every 4 hrly  Report elevated glucose and urine acctone to physician  Usual meal plan cannot be followed substitute soft foods 6- 8 times /day  If any symptoms like vomiting and diarrhoe or fever consume liquid diet every half to one hour to prevent dehydration and provide calories  Inform physician about extreme fluid loss maybe dangerous.  For type 1 diabetic, iniability to retain oral fluid needs hospitallization to avoid DKA and possible coma
  • 19. SHINY MATHEW MALE MEDICAL WARD