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TYPE-II DIABETES MELLITUS WITH
DIABETIC KETOACIDOSIS
 DEMOGRPHIC DETAILS:
• Name : xyz Age : 60 D.O.A : 21/04/17
• SEX : M IP.No.13108 D.O.D :24/04/17
 REASONS FOR ADMISSION:
• C/o vomitings ; 4-5 episodes
• Loose motions _ since 4 days
 History of present illness :
No similar complaints in past
 Past medication history :
• k/c/o T2 DM _since 4 years
(Stopped insulin 4 days back )
 Personal habits : alcohlic+ ,smoker +
General examination :
• O/e pt c/c TEMP : afebrile
Systemic Examination
• BP : 90/60 mmhg PR : 65 / min
• Resp : BAE+ CVS : S1+S2+
• GRBS : >600mg/dl
• PROVISIONAL DIAGNOSIS : T2DM with DKA ?
 Rx : IVF 1pint NS
Inj.Ondonsetron IV
• LABORATORY INVESTIGATIONS
 Urine ketones : ++
 Sugars : ++
 FBS : 290mg/dl

 FINAL DIAGNOSIS : TYPE 2 DIABETES MELLITUS
WITH
DIABETIC KETOACIDOSIS
 Day 1 :
Rx
 IV NS 2 pints over 30 min - 2 pints over 1 hr -300 ml over 1hr
 INJ.REGULAR INSULIN 8 U /IV/STAT
 INJ.REGULAR INSULIN 40U IN 1PINT NS @30drops/min till GRBS
250mg/dl
 INJ.CEFTRIAXONE 1g / IV / OD
 INJ.PANTOPRAZOLE 40mg / IV / OD
 INJ.ONDONSETRON 4mg / IV / OD
 Advice : monitor GRBS regularly
 Day 2 : O/e pt c/c
• BP : 100/60mmhg PR : 70/min cvs : s1+s2+
• C/o Dry tongue ,burning epigastrium
• GRBS : 220mg/dl
 Rx
 IVF 4 PINTS NS
 1 PINT RL
 INJ.REG INSULIN 10U /SC /TID
 SYP.SUCRALFATE 10ml/PO/TID
 TAB .MVT PO/OD
 INJ.NEUROKIND 1amp /IM /OD
 INJ.CEFTRIAXONE 1g/ IV /BD
 INJ.PANTAPRAZOLE 40mg /IV / OD
 Day 3 :
• O/e pt c/c
• BP : 120/90mmhg PR : 90/min
• Resp.: BAE+ CVS : s1+s2+
 GRBS : 206mg/dl
 Rx
 CST
 INJ.REGULAR INSULIN 12U /SC/TID
 INJ.METOCLOPRAMIDE 1amp/IV/ BD
 DIABETIC KETOACIDOSIS : It is an acute, major, life-threatening
complication of diabetes. DKA mainly occurs in patients with type 1 diabetes, but
it is not uncommon in some patients with type 2 diabetes
 DKA is a state of absolute or relative insulin deficiency aggravated by ensuing
hyperglycemia, dehydration, and acidosis-producing derangements in
intermediary metabolism. The most common causes are disruption of insulin
treatment, and new onset of diabetes.
 Biochemically, DKA is defined as an increase in the serum concentration of
ketones greater than 5 mEq/L, a blood glucose level greater than 250 mg/dL
(although it is usually much higher), and a blood (usually arterial) pH less than
7.3. Ketonemia and ketonuria are characteristic, as is a serum bicarbonate level of
18 mEq/L or less (less than 5 mEq/L is indicative of severe DKA).
 Goals of treatment :
 Correction of fluid loss with intravenous fluids
• (Fluid loss averages approximately 6–9 L in DKA. The goal is to replace the
total volume loss within 24–36 hours with 50% of resuscitation fluid being
administered during the first 8–12 hours.)
 Correction of hyperglycemia with insulin
 Correction of electrolyte disturbances, particularly potassium loss
 Correction of acid-base balance
 Treatment of concurrent infection, if present
 Standard treatment :
 Initial correction of fluid loss is either by isotonic sodium chloride solution or
by lactated Ringer solution.
 The recommended schedule for restoring fluids is as follows:
 Administer 1-3 L during the first hour.
 Administer 1 L during the second hour.
 Administer 1 L during the following 2 hours
 Administer 1 L every 4 hours, depending on the degree of dehydration and
central venous pressure readings
 After initial stabilization with isotonic saline, switch to half-normal saline at
200-1000 mL/h
 Insulin : Initial bolus of regular insulin of 0.1 U/kg followed by continuous
insulin infusion(0.1U/kg/hr) using infusion pump. If plasma glucose does not fall
by at least 10% in the first hour of insulin infusion rate, 0.1 U/kg bolus of insulin
can be given once more while continuing insulin infusion.
 Larger volumes of insulin may be easier in the absence of an IV infusion pump
(eg, 60 U of insulin in 500 mL of isotonic sodium chloride solution at a rate of
50 mL/h).
• PHARMACIST INTERVENTION:
 Before starting Insulin therapy, plasma potassium levels must be monitord.
Because sudden insulin administration may lead to hypokalemia and worsen
the situation.
• DRUG INTERACTION :
 ceftioxone should not be given with Ringer lactate.Calcium in ringer solution
precipitates with ceftriaxone in blood and may lead to kidney damage
 GOALS ACHEIVED :
 Patient glucose levles are under control
 Fluid loss is corrected
 Symptoms subcided
DISCHARGE MEDICATION :
 INJ.HUMAN MIXTARD 30/70
 20 units------------10 units
 Tab .METFORMIN 500mg BD /PO
 TAB .MVT OD/PO
 REVIEW AFTER 10 DAYS
 PATIENT COUNSELLING :
 Take insulin 30min before meals.Change the site of administration for every
time.
 Regularly monitor blood glucose levels
 Do not stop insulin unless doctor advice
 If you get hypoglycemic symptoms on treatment , such as tremors ,palpitations
,sweating ,immediately take some glucose rich food ( sugar water/chocolate)
Manage Type 2 Diabetes with DKA

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Manage Type 2 Diabetes with DKA

  • 1. TYPE-II DIABETES MELLITUS WITH DIABETIC KETOACIDOSIS
  • 2.  DEMOGRPHIC DETAILS: • Name : xyz Age : 60 D.O.A : 21/04/17 • SEX : M IP.No.13108 D.O.D :24/04/17  REASONS FOR ADMISSION: • C/o vomitings ; 4-5 episodes • Loose motions _ since 4 days  History of present illness : No similar complaints in past  Past medication history : • k/c/o T2 DM _since 4 years (Stopped insulin 4 days back )
  • 3.  Personal habits : alcohlic+ ,smoker + General examination : • O/e pt c/c TEMP : afebrile Systemic Examination • BP : 90/60 mmhg PR : 65 / min • Resp : BAE+ CVS : S1+S2+ • GRBS : >600mg/dl • PROVISIONAL DIAGNOSIS : T2DM with DKA ?
  • 4.  Rx : IVF 1pint NS Inj.Ondonsetron IV • LABORATORY INVESTIGATIONS  Urine ketones : ++  Sugars : ++  FBS : 290mg/dl   FINAL DIAGNOSIS : TYPE 2 DIABETES MELLITUS WITH DIABETIC KETOACIDOSIS
  • 5.  Day 1 : Rx  IV NS 2 pints over 30 min - 2 pints over 1 hr -300 ml over 1hr  INJ.REGULAR INSULIN 8 U /IV/STAT  INJ.REGULAR INSULIN 40U IN 1PINT NS @30drops/min till GRBS 250mg/dl  INJ.CEFTRIAXONE 1g / IV / OD  INJ.PANTOPRAZOLE 40mg / IV / OD  INJ.ONDONSETRON 4mg / IV / OD  Advice : monitor GRBS regularly
  • 6.  Day 2 : O/e pt c/c • BP : 100/60mmhg PR : 70/min cvs : s1+s2+ • C/o Dry tongue ,burning epigastrium • GRBS : 220mg/dl  Rx  IVF 4 PINTS NS  1 PINT RL  INJ.REG INSULIN 10U /SC /TID  SYP.SUCRALFATE 10ml/PO/TID  TAB .MVT PO/OD  INJ.NEUROKIND 1amp /IM /OD  INJ.CEFTRIAXONE 1g/ IV /BD  INJ.PANTAPRAZOLE 40mg /IV / OD
  • 7.  Day 3 : • O/e pt c/c • BP : 120/90mmhg PR : 90/min • Resp.: BAE+ CVS : s1+s2+  GRBS : 206mg/dl  Rx  CST  INJ.REGULAR INSULIN 12U /SC/TID  INJ.METOCLOPRAMIDE 1amp/IV/ BD
  • 8.  DIABETIC KETOACIDOSIS : It is an acute, major, life-threatening complication of diabetes. DKA mainly occurs in patients with type 1 diabetes, but it is not uncommon in some patients with type 2 diabetes  DKA is a state of absolute or relative insulin deficiency aggravated by ensuing hyperglycemia, dehydration, and acidosis-producing derangements in intermediary metabolism. The most common causes are disruption of insulin treatment, and new onset of diabetes.  Biochemically, DKA is defined as an increase in the serum concentration of ketones greater than 5 mEq/L, a blood glucose level greater than 250 mg/dL (although it is usually much higher), and a blood (usually arterial) pH less than 7.3. Ketonemia and ketonuria are characteristic, as is a serum bicarbonate level of 18 mEq/L or less (less than 5 mEq/L is indicative of severe DKA).
  • 9.  Goals of treatment :  Correction of fluid loss with intravenous fluids • (Fluid loss averages approximately 6–9 L in DKA. The goal is to replace the total volume loss within 24–36 hours with 50% of resuscitation fluid being administered during the first 8–12 hours.)  Correction of hyperglycemia with insulin  Correction of electrolyte disturbances, particularly potassium loss  Correction of acid-base balance  Treatment of concurrent infection, if present
  • 10.  Standard treatment :  Initial correction of fluid loss is either by isotonic sodium chloride solution or by lactated Ringer solution.  The recommended schedule for restoring fluids is as follows:  Administer 1-3 L during the first hour.  Administer 1 L during the second hour.  Administer 1 L during the following 2 hours  Administer 1 L every 4 hours, depending on the degree of dehydration and central venous pressure readings  After initial stabilization with isotonic saline, switch to half-normal saline at 200-1000 mL/h
  • 11.  Insulin : Initial bolus of regular insulin of 0.1 U/kg followed by continuous insulin infusion(0.1U/kg/hr) using infusion pump. If plasma glucose does not fall by at least 10% in the first hour of insulin infusion rate, 0.1 U/kg bolus of insulin can be given once more while continuing insulin infusion.  Larger volumes of insulin may be easier in the absence of an IV infusion pump (eg, 60 U of insulin in 500 mL of isotonic sodium chloride solution at a rate of 50 mL/h).
  • 12. • PHARMACIST INTERVENTION:  Before starting Insulin therapy, plasma potassium levels must be monitord. Because sudden insulin administration may lead to hypokalemia and worsen the situation. • DRUG INTERACTION :  ceftioxone should not be given with Ringer lactate.Calcium in ringer solution precipitates with ceftriaxone in blood and may lead to kidney damage  GOALS ACHEIVED :  Patient glucose levles are under control  Fluid loss is corrected  Symptoms subcided
  • 13. DISCHARGE MEDICATION :  INJ.HUMAN MIXTARD 30/70  20 units------------10 units  Tab .METFORMIN 500mg BD /PO  TAB .MVT OD/PO  REVIEW AFTER 10 DAYS
  • 14.  PATIENT COUNSELLING :  Take insulin 30min before meals.Change the site of administration for every time.  Regularly monitor blood glucose levels  Do not stop insulin unless doctor advice  If you get hypoglycemic symptoms on treatment , such as tremors ,palpitations ,sweating ,immediately take some glucose rich food ( sugar water/chocolate)