Skip to main content

Table 1 Demographic and clinical characteristics of patients with pediatric inflammatory bowel disease

From: Analysis and prediction of nutritional outcome of patients with pediatric inflammatory bowel disease from Bahrain

Variables

IBD, n = 130

CD, n = 73 (56.2)

UC, n = 57 (43.8)

p value

Demographic data

    

Sex

   

0.096*

 Male

84 (64.6)

52 (71.2)

32 (56.1)

 

 Female

46 (35.4)

21 (28.8)

25 (43.9)

 

Nationality

   

1.000*

 Bahraini

112 (86.2)

63 (86.3)

49 (86.0)

 

 Non-Bahraini

18 (13.8)

10 (13.7)

8 (14.0)

 

Age at presentation (yr)

10.9 (9.1–13)

11.4 (9.7–13)

10 (7.5–12.7)

0.034†

IBD onset (Paris Classification)

   

0.035‡

 Infantile (< 2 year)

1 (0.8)

0 (0.0)

1 (1.8)

 

 Very-early onset (2 to < 6 year)

15 (11.5)

4 (5.5)

11 (19.3)

 

 Early onset (6 to < 10 year)

34 (26.2)

18 (24.7)

16 (28.1)

 

 Late onset (10 to < 18 year)

80 (61.5)

51 (69.9)

29 (50.9)

 

Post-diagnosis disease duration (yr)

4.8 (1.3–11.1)

3.2 (1.2–8.7)

7.6 (2.5–13.7)

0.017†

Clinical presentations

120 (92.3)

67 (91.8)

53 (93)

1.000*

 Diarrhea

86 (71.7)

40 (59.7)

46 (86.8)

0.001*

 Bloody diarrhea

75 (62.5)

28 (41.8)

47 (88.7)

< 0.001*

 Recurrent abdominal pain

75 (62.5)

48 (71.6)

27 (50.9)

0.024*

 Weight loss

60 (50.0)

41 (61.2)

19 (35.8)

0.010*

 Pallor

49 (40.8)

24 (35.8)

25 (47.2)

0.262*

 Anorexia

46 (38.3)

29 (43.3)

17 (32.1)

0.258*

 Vomiting

36 (30.0)

21 (31.3)

15 (28.3)

0.841*

 Arthralgia

30 (25.0)

16 (23.9)

14 (26.4)

0.833*

 Perianal disease

28 (23.3)

26 (38.8)

2 (3.8)

< 0.001*

 Fever

22 (18.3)

13 (19.4)

9 (17)

0.815*

 Constipation

18 (15.0)

14 (20.9)

4 (7.5)

0.061*

 Skin rash

12 (10.0)

8 (11.9)

5 (9.4)

0.772*

 Jaundice

6.0 (5.0)

2 (3.0)

4 (7.5)

0.404*

 Hematemesis

5 (4.2)

2 (3.0)

3 (5.7)

0.654*

 Extraintestinal manifestationsa

47 (36.2)

24 (35.3)

18 (34.0)

0.852*

Laboratory markers

    

 Hematocrit (%), (n = 127)

30.9 (26.4–36)

30.9 (25.8–37.2)

30.3 (26.6–35.7)

0.553†

 ESR (mm/h), (n = 120)

25 (15-44.8)

27 (15–46)

20 (13–44)

0.434†

 CRP (mg/dL), (n = 118)

13.9 (1.6–48.2)

34.5 (7.4–65)

3.6 (1.0-17.5)

< 0.001†

Disease activity at presentation (n = 121)

   

< 0.001‡

 Mild

30 (24.8)

26 (38.2)

4 (7.5)

 

 Moderate

45 (37.2)

17 (25.0)

28 (52.8)

 

 Severe

46 (38)

36.8 (36.8)

21 (39.6)

 

Medications used

119 (91.5)

65 (89%)

54 (94.7)

0.346*

 Prednisolone

94 (79.0)

54 (83.1)

40 (74.1)

0.263*

 Omeprazole

86 (72.3)

45 (69.2)

41 (75.9)

0.538*

 Azathioprine

85 (71.4)

54 (83.1)

31 (57.4)

0.002*

 Folic acid

85 (71.4)

46 (70.8)

31 (57.4)

1.000*

 Mesalazine

73 (61.3)

31 (47.7)

42 (77.8)

0.001*

 Iron supplementation

71 (59.7)

35 (53.8)

36 (66.7)

0.190*

 Vitamin D supplementation

55 (46.2)

34 (52.3)

21 (38.9)

0.196*

 Biological therapy

55 (46.2)

38 (58.5)

17 (31.5)

0.005*

 Calcium supplementation

42 (35.3)

25 (38.5)

17 (31.5)

0.448*

 Multivitamins

37 (31.1)

21 (32.3)

16 (29.6)

0.843*

 H2 blockers

6.0 (5.0)

1 (1.5)

5 (9.3)

0.090*

 Ursodeoxycholic acid

5.0 (4.2)

0 (0.0)

5 (9.3)

0.017*

 Fat soluble vitamins (ADEK)

4.0 (3.4)

0 (0.0)

4 (7.4)

0.040*

 Vitamin B12 supplementation

3.0 (2.5)

0 (0.0)

3 (5.6)

0.091*

 Other medicationsb

11 (9.2)

7 (9.6)

4 (7.0)

0.752*

 Exclusive enteral nutrition

8 (6.2)

6 (8.2)

2 (3.5)

0.465*

  1. Values are presented as number (%) or median (interquartile range). IBD, inflammatory bowel disease; CD, Crohn’s disease; UC, ulcerative colitis; ESR, erythrocytes sedimentation rate; CRP, C-reactive protein. aArthralgia (n = 30, 25%; four of them had arthritis), erythema nodosum (n = 12, 10%), conjunctivitis (n = 6, 4.6%), aphthous ulcers (n = 5, 3.8%), sclerosing cholangitis, overlap syndrome, autoimmune hemolytic anemia, thromboembolic manifestation (n = 2, 1.5% each), while autoimmune hepatitis, nephritis, clubbing, ankylosis spondylitis and gall bladder edema (n = 1, 0.8% each). Some patients had more than one extraintestinal manifestation. bSomatotropin (n = 4), methotrexate (n = 2), testosterone, tacrolimus, colchicine, loperamide hydrochloride, isoniazid with vitamin B6 for latent tuberculosis prophylaxis, lactulose, and hydroxyurea for sickle cell disease (n = 1 each). Some patients received more than one medication. *Fisher’s exact test, †Mann-Whitney U test, ‡Pearson’s χ2 test. Boldface indicates a statistically significant difference with p < 0.05.