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MS.MUTHU RAJATHI, M.SC (N)
ASST., PROFESSOR
DEPARTMENT OF MEDICAL SURGICAL NURSING
GANGA INSTITUTE OF HEALTH SCIENCES
COIMBATORE
ULCERATIVE COLITIS
INTRODUCTION
• Belongs to the wide spread category of inflammatory
bowel disease.
• Only pathological, endoscopical changes differs it
from crohn’s disease.
• Course of remitting and relapsing disease.
CROHNS
DISEASE
ULCERATIVE
COLITIS
INFLAMMATORY BOWEL DISEASE
SIGNIFICANT ANATOMY & PHYSIOLOGY
SIGNIFICANT ANATOMY & PHYSIOLOGY
Last part of the GI tract.
The large intestine is about 5 feet long in adults.
Absorbs water and any remaining nutrients from
partially digested food passed from the small
intestine.
The large intestine changes waste from liquid to a
solid matter called stool.
The rectum is located between the lower, or
sigmoid, colon and the anus
Ulcerative colitis affects only the large intestine part.
DEFINITION
INFLAMMATION IRRITATION ULCERATION
CHRONIC INFLAMMATORY DISEASE.
“INFLAMMATION, IRRITATION AND
ULCERATIONS LINING THE WALL OF THE LARGE
INTESTINE .”
DEFINITION
Chronic inflammatory disease in the inner lining of
the intestine which leads to ulceration and bleeding
in the intestinal tissue.
“Ulcerative colitis is a chronic inflammatory
condition characterized by relapsing and remitting
episodes of inflammation limited to the mucosal
layer of the colon”.
DEFINITION
Is an inflammatory bowel disease (IBD)
marked by gastrointestinal (GI) mucosal
inflammation due to altered microbiota,
increased intestinal permeability, and
immune system dysfunction.
FEATURES OF ULCERATIVE COLITIS
 MACROSCOPIC CHANGES
 Continuous inflammation
 Reddened & Inflamed intestinal mucosa
 Evidence of inflammatory polyps
 MICROSCOPIC CHANGES
 Alterations in the crypt architecture
 Crypt abscess
 Goblet cell depletion
 Inflammatory infiltrations in the lamina proporia
INCIDENCE AND PREVALENCE
• AGE : most common in 15 – 30 yrs of age; people
above 60 yrs are also in the risk category.
• Gender : both the gender are equally affected.
• Family history of ulcerative colitis
• Statistics : 6.02 per 100000 population in India.
• Personal Habits : Smoking & Alcoholism not
influencing the prevalence of the disease.
CLASSIFICATION
ULCERATIVE PROCTITIS
Inflammation in the rectum.
PROCTOSIGMOIDITIS
Inflammation in the rectum
along with sigmoid colon.
CLASSIFICATION
DISTAL PROCTITIS
Inflammation beyond the rectum
and as far proximally as the
splenic fixture.
PANULCERATIVE COLITIS
Inflammation of the entire
colon.
CAUSES AND RISK FACTORS
Environmental
factors
Immune
factors
Genetic
suscepti
bility
CAUSES AND RISK FACTORS –
Auto immune reaction
Immune
response
Autoimmune
reaction towards
intestinal mucosa
Fight against
Viral and bacterial
infection in the
intestinal mucosa
Inflammatory
process
Does not stop once
the infection
resolves which
causes intestinal
mucosal damage
CAUSES AND RISK FACTORS –
Genetic factors
Genetic
composition
Family history of
ulcerative colitis
Susceptible genes
increases the risk of
ulcerative colitis
CAUSES AND RISK FACTORS –
Environmental factor
E
N
V
I
R
O
N
M
E
N
T
A
L
F
A
C
T
O
R
S
Antibiotics
NSAIDs
Oral contraceptives
Certain foods
Stress
Emotional distress
Poor dietary pattern
Smoking
PATHOPHYSIOLOGY
Due to any cause
Mucosal cell
damage
Inflammation &
desquamation of
the colonic
epithelium
Edematous of
intestinal mucosa
Vascular pattern
impairment
Chronic tissue
injury
Bleeding
Excessive loss of
body fluids
Shock
GRADING OF ULCERATIVE COLITIS –
Truelove & witt Criteria
CRITERIA MILD MODERATE SEVERE
BOWEL
MOVEMENTS
Less than 4
episodes
4 – 6 episodes More than 8
episodes
BLOOD IN
STOOL
Minimal Mild to severe Visible blood
PYREXIA No No Yes
ANEMIA No No Yes
ESR Less than 30 30 More than 30
PULSE >
90bPM
No No Yes
CLINICAL MANIFESTATIONS
Warning Symptoms
Chronic Diarrhea
Blood in Stools
Abnormal weight loss
Tenesmus
Abdominal pain
CLINICAL MANIFESTATIONS
Fever
Dehydration
Abdominal tenderness
Abdominal distention
Abdominal mass
Tachycardia
Hypotension
Fatigue
Passage of
mucopurulent
exudates
Nocturnal
defecationVomiting
Signs of dehydration
CLINICAL MANIFESTATIONS –
Extra intestinal symptoms
Skin :
Erythema nodosum
Pyoderma gangrenosum
Gall bladder :
Cholelithiasis
Sclerosing cholangitis
Joints :
Spondylitis
Sacroillitis
Peripheral arthritis
Liver :
steatosis
Mouth :
Stomatitis
Aphthous ulcer
Circulation :
Phlebitis
Kidneys:
Nephrolithiasis
UTI
Eyes :
Episcleritis
Uveitis
DIAGNOSTIC EVALUATION –
Physical examination
• Abdominal tenderness
• Bowel sounds
• Abdominal distention
• Signs of toxic shock
• Signs of bleeding
DIAGNOSTIC EVALUATION
Complete blood profile
Complete metabolic
profile
Inflammatory markers
Stool assays
Serological series
Leukocytosis
Anemia
Thrombocytosis
DIAGNOSTIC EVALUATION
Complete blood profile
Complete metabolic
profile
Inflammatory markers
Stool assays
Serological series
Hypo
albuminemia
Hypo
magnesemia
Hypokalemia
Elevated ALP
DIAGNOSTIC EVALUATION
Complete blood profile
Complete metabolic
profile
Inflammatory markers
Stool assays
Serological series
Elevated ESR &
CRP
Fecal
calprotectin – to
identify the
mucosal healing.
DIAGNOSTIC EVALUATION
Complete blood profile
Complete metabolic
profile
Inflammatory markers
Stool assays
Serological series
Fecal ,
Blood
Ova and
parasites
Viral load
Bacterial culture
Leukocytes
DIAGNOSTIC EVALUATION
Complete blood profile
Complete metabolic
profile
Inflammatory markers
Stool assays
Serological series
P – ANCA
Serological
marker.
Positive in 60 –
80% patients
Identifies the
early need for
surgery.
DIAGNOSTIC EVALUATION –
Plain abdominal X Ray
• Useful in fulminant or severe colitis.
• Due to the thickening of colonic wall, thumb printing
appearance will be visible.
• In toxic mega colon, the bowel dilatation with loss of
haustral markings.
Thumb printing appearance Mega colon
DIAGNOSTIC EVALUATION –
Barium Enema
• Useful ulcerative colitis, polyps and masses.
• Appears as granular and shortened colon.
DIAGNOSTIC EVALUATION – CT scan
• Shows colonic wall thickening.
DIAGNOSTIC EVALUATION –
Colonoscopy
• Shows,
– Mucosal inflammation
– Loss of vascular pattern
– Inflammatory Pseudopolyps
– Contact bleeding
– Superficial ulceration
DIAGNOSTIC EVALUATION –
Colonoscopy
• Shows,
– Mucosal inflammation
– Loss of vascular pattern
– Inflammatory Pseudopolyps
– Contact bleeding
– Superficial ulceration
DIAGNOSTIC EVALUATION –
Flexible sigmoidoscopy
MANAGEMENT
Induction of remission
Maintenance of
remission
Prevention of
complications
MANAGEMENT – pharmacolgical therapy
5 - Aminosalicytes
Corticosteroids
Thiopurine
Cyclosporine
Biological therapy
Eg : Sulfasalazine,
Mesalamine
Exhibitis results in
remission induction and
maintainance.
Sulfasalazine
suppositries is a prefered
therapy for rectal
ulcerations.
MANAGEMENT – pharmacolgical therapy
5 - Aminosalicytes
Corticosteroids
Thiopurine
Cyclosporine
Biological therapy
Eg : methylprednisolone,
hydrocortisone,
Budesonide (new)
Used in acute treatment
of moderate to severe
colitis.
40 – 60mg/day
Rectally administered
steroid enemas for flares of
symptoms.
MANAGEMENT – pharmacolgical therapy
5 - Aminosalicytes
Corticosteroids
Thiopurine
Cyclosporine
Biological therapy
Eg : Azathioprine 2 -
2.5mg/kg/day
6 mercaptopurine 1-
1.5mg/kg/day
Effective for
maintenance of remission.
Very slow onset of
action.
MANAGEMENT – pharmacolgical therapy
5 - Aminosalicytes
Corticosteroids
Thiopurine
Cyclosporine
Biological therapy
Effective for severe
ulcerative colitis.
Dose : 2-4mg/kg/day
Continuous infusion.
MANAGEMENT – pharmacological therapy
5 - Aminosalicytes
Corticosteroids
Thiopurine
Cyclosporine
Biological therapy
ANTI TNF :
Its an IGG monoclonal
antibody directed against TNF.
It is a less toxic
alternative to cyclosporine for
patients with severe ,steroid
refractory disease
Effective for both
induction and maintenance of
remission.
PREPARATIONS –
Infliximab - induction
of remission:
5 mg/kg IV at weeks 0, 2,6.
Maintenance: 5 mg/kg IV every
8 weeks
MANAGEMENT – SURGICAL THERAPY
PROCTOCOLECTOMY WITH END ILEOSTOMY
MANAGEMENT – SURGICAL THERAPY
RESTORATIVE PROCTOCOLECTOMY WITH
ILEO ANAL POUCH
MANAGEMENT – SURGICAL THERAPY
PAN PROCTOCOLECTOMY
MANAGEMENT – Nutritional therapy
Lactose
free diet
Low
fiber
diet
Low
salt
diet
Low fat
diet
High
caloric
diet
MANAGEMENT – Nutritional therapy
• low residue , high protein, high caloric diet
• Vitamin supplements
• Iron replacement
• IV fluids
• Avoid milk
• Avoid cold foods and smoking
• TPN nutrition
COMPLICATIONS
osteoporosis
Colon
cancer
Toxic
megacolon
Primary
sclerosing
cholangitis
Malnutrition
Vitamin &
Mineral
deficiency
NURSING MANAGEMENT
• Diarrhea related to inflammation of the bowel mucosa as evidenced
by increased bowel sounds.
• Fluid volume deficit related to loss of body fluids secondary to
diarrhea and rectal bleeding as evidenced by signs of dehydration.
• Imbalanced nutrition less than body requirement related to fear
that eating may cause diarrhea as evidenced by reluctant to eat
• Impaired anal skin integrity related to repeated episodes of
diarrhea as evidenced by redness in the anal skin.
• Risk for shock related to profuse bleeding.
• Risk for exacerbation related to poor adherence with the
therapeutic regimen.
REFERENCE
• LEWIS , TEXTBOOK OF MEDICAL SURGICAL NURSING
• BRUNNER & SUDDHARTH’S , TEXTBOOK OF MEDICAL SURGICAL
NURSING
• JOYCE.M.BLACK, TEXTBOOK OF MEDICAL SURGICAL NURSING
• ANTONY.S , BOOK OF ANATOMY & PHYSIOLOGY
• WWW. GASTRICASSOCIATION.COM
• WWW. PUBMEDINDIA.COM
• www. Crohnscolitis.foundation.org
ULCERATIVE COLITIS

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ULCERATIVE COLITIS

  • 1. MS.MUTHU RAJATHI, M.SC (N) ASST., PROFESSOR DEPARTMENT OF MEDICAL SURGICAL NURSING GANGA INSTITUTE OF HEALTH SCIENCES COIMBATORE
  • 3. INTRODUCTION • Belongs to the wide spread category of inflammatory bowel disease. • Only pathological, endoscopical changes differs it from crohn’s disease. • Course of remitting and relapsing disease. CROHNS DISEASE ULCERATIVE COLITIS INFLAMMATORY BOWEL DISEASE
  • 5. SIGNIFICANT ANATOMY & PHYSIOLOGY Last part of the GI tract. The large intestine is about 5 feet long in adults. Absorbs water and any remaining nutrients from partially digested food passed from the small intestine. The large intestine changes waste from liquid to a solid matter called stool. The rectum is located between the lower, or sigmoid, colon and the anus Ulcerative colitis affects only the large intestine part.
  • 6. DEFINITION INFLAMMATION IRRITATION ULCERATION CHRONIC INFLAMMATORY DISEASE. “INFLAMMATION, IRRITATION AND ULCERATIONS LINING THE WALL OF THE LARGE INTESTINE .”
  • 7. DEFINITION Chronic inflammatory disease in the inner lining of the intestine which leads to ulceration and bleeding in the intestinal tissue. “Ulcerative colitis is a chronic inflammatory condition characterized by relapsing and remitting episodes of inflammation limited to the mucosal layer of the colon”.
  • 8. DEFINITION Is an inflammatory bowel disease (IBD) marked by gastrointestinal (GI) mucosal inflammation due to altered microbiota, increased intestinal permeability, and immune system dysfunction.
  • 9. FEATURES OF ULCERATIVE COLITIS  MACROSCOPIC CHANGES  Continuous inflammation  Reddened & Inflamed intestinal mucosa  Evidence of inflammatory polyps  MICROSCOPIC CHANGES  Alterations in the crypt architecture  Crypt abscess  Goblet cell depletion  Inflammatory infiltrations in the lamina proporia
  • 10. INCIDENCE AND PREVALENCE • AGE : most common in 15 – 30 yrs of age; people above 60 yrs are also in the risk category. • Gender : both the gender are equally affected. • Family history of ulcerative colitis • Statistics : 6.02 per 100000 population in India. • Personal Habits : Smoking & Alcoholism not influencing the prevalence of the disease.
  • 11. CLASSIFICATION ULCERATIVE PROCTITIS Inflammation in the rectum. PROCTOSIGMOIDITIS Inflammation in the rectum along with sigmoid colon.
  • 12. CLASSIFICATION DISTAL PROCTITIS Inflammation beyond the rectum and as far proximally as the splenic fixture. PANULCERATIVE COLITIS Inflammation of the entire colon.
  • 13. CAUSES AND RISK FACTORS Environmental factors Immune factors Genetic suscepti bility
  • 14. CAUSES AND RISK FACTORS – Auto immune reaction Immune response Autoimmune reaction towards intestinal mucosa Fight against Viral and bacterial infection in the intestinal mucosa Inflammatory process Does not stop once the infection resolves which causes intestinal mucosal damage
  • 15. CAUSES AND RISK FACTORS – Genetic factors Genetic composition Family history of ulcerative colitis Susceptible genes increases the risk of ulcerative colitis
  • 16. CAUSES AND RISK FACTORS – Environmental factor E N V I R O N M E N T A L F A C T O R S Antibiotics NSAIDs Oral contraceptives Certain foods Stress Emotional distress Poor dietary pattern Smoking
  • 17. PATHOPHYSIOLOGY Due to any cause Mucosal cell damage Inflammation & desquamation of the colonic epithelium Edematous of intestinal mucosa Vascular pattern impairment Chronic tissue injury Bleeding Excessive loss of body fluids Shock
  • 18. GRADING OF ULCERATIVE COLITIS – Truelove & witt Criteria CRITERIA MILD MODERATE SEVERE BOWEL MOVEMENTS Less than 4 episodes 4 – 6 episodes More than 8 episodes BLOOD IN STOOL Minimal Mild to severe Visible blood PYREXIA No No Yes ANEMIA No No Yes ESR Less than 30 30 More than 30 PULSE > 90bPM No No Yes
  • 19. CLINICAL MANIFESTATIONS Warning Symptoms Chronic Diarrhea Blood in Stools Abnormal weight loss Tenesmus Abdominal pain
  • 20. CLINICAL MANIFESTATIONS Fever Dehydration Abdominal tenderness Abdominal distention Abdominal mass Tachycardia Hypotension Fatigue Passage of mucopurulent exudates Nocturnal defecationVomiting Signs of dehydration
  • 21. CLINICAL MANIFESTATIONS – Extra intestinal symptoms Skin : Erythema nodosum Pyoderma gangrenosum Gall bladder : Cholelithiasis Sclerosing cholangitis Joints : Spondylitis Sacroillitis Peripheral arthritis Liver : steatosis Mouth : Stomatitis Aphthous ulcer Circulation : Phlebitis Kidneys: Nephrolithiasis UTI Eyes : Episcleritis Uveitis
  • 22. DIAGNOSTIC EVALUATION – Physical examination • Abdominal tenderness • Bowel sounds • Abdominal distention • Signs of toxic shock • Signs of bleeding
  • 23. DIAGNOSTIC EVALUATION Complete blood profile Complete metabolic profile Inflammatory markers Stool assays Serological series Leukocytosis Anemia Thrombocytosis
  • 24. DIAGNOSTIC EVALUATION Complete blood profile Complete metabolic profile Inflammatory markers Stool assays Serological series Hypo albuminemia Hypo magnesemia Hypokalemia Elevated ALP
  • 25. DIAGNOSTIC EVALUATION Complete blood profile Complete metabolic profile Inflammatory markers Stool assays Serological series Elevated ESR & CRP Fecal calprotectin – to identify the mucosal healing.
  • 26. DIAGNOSTIC EVALUATION Complete blood profile Complete metabolic profile Inflammatory markers Stool assays Serological series Fecal , Blood Ova and parasites Viral load Bacterial culture Leukocytes
  • 27. DIAGNOSTIC EVALUATION Complete blood profile Complete metabolic profile Inflammatory markers Stool assays Serological series P – ANCA Serological marker. Positive in 60 – 80% patients Identifies the early need for surgery.
  • 28. DIAGNOSTIC EVALUATION – Plain abdominal X Ray • Useful in fulminant or severe colitis. • Due to the thickening of colonic wall, thumb printing appearance will be visible. • In toxic mega colon, the bowel dilatation with loss of haustral markings. Thumb printing appearance Mega colon
  • 29. DIAGNOSTIC EVALUATION – Barium Enema • Useful ulcerative colitis, polyps and masses. • Appears as granular and shortened colon.
  • 30. DIAGNOSTIC EVALUATION – CT scan • Shows colonic wall thickening.
  • 31. DIAGNOSTIC EVALUATION – Colonoscopy • Shows, – Mucosal inflammation – Loss of vascular pattern – Inflammatory Pseudopolyps – Contact bleeding – Superficial ulceration
  • 32. DIAGNOSTIC EVALUATION – Colonoscopy • Shows, – Mucosal inflammation – Loss of vascular pattern – Inflammatory Pseudopolyps – Contact bleeding – Superficial ulceration
  • 34. MANAGEMENT Induction of remission Maintenance of remission Prevention of complications
  • 35. MANAGEMENT – pharmacolgical therapy 5 - Aminosalicytes Corticosteroids Thiopurine Cyclosporine Biological therapy Eg : Sulfasalazine, Mesalamine Exhibitis results in remission induction and maintainance. Sulfasalazine suppositries is a prefered therapy for rectal ulcerations.
  • 36. MANAGEMENT – pharmacolgical therapy 5 - Aminosalicytes Corticosteroids Thiopurine Cyclosporine Biological therapy Eg : methylprednisolone, hydrocortisone, Budesonide (new) Used in acute treatment of moderate to severe colitis. 40 – 60mg/day Rectally administered steroid enemas for flares of symptoms.
  • 37. MANAGEMENT – pharmacolgical therapy 5 - Aminosalicytes Corticosteroids Thiopurine Cyclosporine Biological therapy Eg : Azathioprine 2 - 2.5mg/kg/day 6 mercaptopurine 1- 1.5mg/kg/day Effective for maintenance of remission. Very slow onset of action.
  • 38. MANAGEMENT – pharmacolgical therapy 5 - Aminosalicytes Corticosteroids Thiopurine Cyclosporine Biological therapy Effective for severe ulcerative colitis. Dose : 2-4mg/kg/day Continuous infusion.
  • 39. MANAGEMENT – pharmacological therapy 5 - Aminosalicytes Corticosteroids Thiopurine Cyclosporine Biological therapy ANTI TNF : Its an IGG monoclonal antibody directed against TNF. It is a less toxic alternative to cyclosporine for patients with severe ,steroid refractory disease Effective for both induction and maintenance of remission. PREPARATIONS – Infliximab - induction of remission: 5 mg/kg IV at weeks 0, 2,6. Maintenance: 5 mg/kg IV every 8 weeks
  • 40. MANAGEMENT – SURGICAL THERAPY PROCTOCOLECTOMY WITH END ILEOSTOMY
  • 41. MANAGEMENT – SURGICAL THERAPY RESTORATIVE PROCTOCOLECTOMY WITH ILEO ANAL POUCH
  • 42. MANAGEMENT – SURGICAL THERAPY PAN PROCTOCOLECTOMY
  • 43. MANAGEMENT – Nutritional therapy Lactose free diet Low fiber diet Low salt diet Low fat diet High caloric diet
  • 44. MANAGEMENT – Nutritional therapy • low residue , high protein, high caloric diet • Vitamin supplements • Iron replacement • IV fluids • Avoid milk • Avoid cold foods and smoking • TPN nutrition
  • 46. NURSING MANAGEMENT • Diarrhea related to inflammation of the bowel mucosa as evidenced by increased bowel sounds. • Fluid volume deficit related to loss of body fluids secondary to diarrhea and rectal bleeding as evidenced by signs of dehydration. • Imbalanced nutrition less than body requirement related to fear that eating may cause diarrhea as evidenced by reluctant to eat • Impaired anal skin integrity related to repeated episodes of diarrhea as evidenced by redness in the anal skin. • Risk for shock related to profuse bleeding. • Risk for exacerbation related to poor adherence with the therapeutic regimen.
  • 47. REFERENCE • LEWIS , TEXTBOOK OF MEDICAL SURGICAL NURSING • BRUNNER & SUDDHARTH’S , TEXTBOOK OF MEDICAL SURGICAL NURSING • JOYCE.M.BLACK, TEXTBOOK OF MEDICAL SURGICAL NURSING • ANTONY.S , BOOK OF ANATOMY & PHYSIOLOGY • WWW. GASTRICASSOCIATION.COM • WWW. PUBMEDINDIA.COM • www. Crohnscolitis.foundation.org