Wikipedia

Bristol stool scale

This is the latest accepted revision, reviewed on 22 July 2024.

The Bristol stool scale is a diagnostic medical tool designed to classify the form of human faeces into seven categories.[4] It is used in both clinical and experimental fields.[5][6][7]

Bristol stool scale
Bristol stool chart
SynonymsBristol stool chart (BSC);[1] Bristol Stool Scale (BSS); Bristol Stool Form Scale (BSFS or BSF scale);[2]
Purposeclassify type of feces (diagnostic triad for irritable bowel syndrome)[3]

It was developed at the Bristol Royal Infirmary as a clinical assessment tool in 1997,[8] and is widely used as a research tool to evaluate the effectiveness of treatments for various diseases of the bowel, as well as a clinical communication aid;[9][10] including being part of the diagnostic triad for irritable bowel syndrome.[11]

Interpretation

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The seven types of stool are:[12]

  • Type 1: Separate hard lumps, like nuts (difficult to pass)
  • Type 2: Sausage-shaped, but lumpy
  • Type 3: Like a sausage but with cracks on its surface
  • Type 4: Like a sausage or snake, smooth and soft (average stool)
  • Type 5: Soft blobs with clear cut edges
  • Type 6: Fluffy pieces with ragged edges, a mushy stool (diarrhea)
  • Type 7: Watery, no solid pieces, entirely liquid (diarrhea)

Types 1 and 2 indicate constipation, with 3 and 4 being the ideal stools as they are easy to defecate while not containing excess liquid, and 6 and 7 indicate diarrhea.[13]

In the initial study, in the population examined in this scale, the type 1 and 2 stools were more prevalent in females, while the type 5 and 6 stools were more prevalent in males; furthermore, 80% of subjects who reported rectal tenesmus (sensation of incomplete defecation) had type 7. These and other data have allowed the scale to be validated.[12] The initial research did not include a pictorial chart with this being developed at a later point.[8]

The Bristol stool scale is also very sensitive to changes in intestinal transit time caused by medications, such as antidiarrhoeal loperamide, senna, or anthraquinone with laxative effect.[14]

Uses

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Diagnosis of irritable bowel syndrome

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See also: Irritable bowel syndrome and Rome process

People with irritable bowel syndrome (IBS) typically report that they suffer with abdominal cramps and constipation. In some patients, chronic constipation is interspersed with brief episodes of diarrhoea; while a minority of patients with IBS have only diarrhoea. The presentation of symptoms is usually months or years and commonly patients consult different doctors, without great success, and doing various specialized investigations. It notices a strong correlation of the reported symptoms with stress; indeed diarrhoeal discharges are associated with emotional phenomena. IBS blood is present only if the disease is associated with haemorrhoids.[15]

Research conducted on irritable bowel syndrome in the 2000s,[16][17] faecal incontinence[18][19][20][21] and the gastrointestinal complications of HIV[22] have used the Bristol scale as a diagnostic tool easy to use, even in research which lasted for 77 months.[23]

Historically, this scale of assessment of the faeces has been recommended by the consensus group of Kaiser Permanente Medical Care Program (San Diego, California, US) for the collection of data on functional bowel disease (FBD).[15]

More recently, according to the latest revision of the Rome III Criteria, six clinical manifestations of IBS can be identified:[24][25][26][27][28]

Subtypes prevalent presentation of stool in IBS according to the Rome III Criteria[29]
1. IBS with constipation (IBS-C) – lumpy or hard stools * ≥ 25% and loose (soft) or watery stools † <25% of bowel movements. ‡
2. IBS with diarrhea (IBS-D) – loose (soft) or watery stools † ≥ 25% and lumpy or hard stools * <25% of bowel movements. ‡
3. Mixed IBS (IBS - M) – lumpy or hard stools * ≥ 25% and loose (soft) or watery stools † ≥ 25% of bowel movements. ‡
4. Untyped IBS (IBS - U) – insufficient stool abnormalities to be IBS-C, D or M ‡
* Bristol stool scale type 1–2 (Separate hard lumps like nuts or sausage-shaped);
† Bristol stool scale type 6–7 (fluffy pieces with ragged edges, soft or watery, no solid or completely liquid pieces);
‡ In the absence of the use of antidiarrhoeal or laxative.

These four identified subtypes correlate with the consistency of the stool, which can be determined by the Bristol stool scale.[15]

In 2007, the Mayo Clinic College of Medicine in Rochester, Minnesota, United States, reported a piece of epidemiological research conducted on a population of 4,196 people living in Olmsted County Minnesota, in which participants were asked to complete a questionnaire based on the Bristol stool scale.[30]

Distribution of risk factors in three groups classified according to the colonic transit and subgroups classified according to the type of feces model century[30]
Normal
colonic transit
(BSS 3–4)
(n=1662)		 Slow
colonic transit
(BSS 1–2)
(n=411)		 Fast
colonic transit
(BSS 5–7)
(n=197)
Age (mean ± s.d.; years) 62 ± 12 63 ± 13 61 ± 12
Male (%) 50 38 43
BMI (mean ± s.d.) 29.6 ± 7.5 28.2 ± 6.8 32.5 ± 9.9
SSC score (mean ± s.d.) (Somatic Symptom Checklist) 1.6 ± 0,50 1.7 ± 0.53 1.8 ± 0.57
Smoking (%) 8 7 12
Alcohol (%) 45 48 41
Cholecystectomy (%) 11 12 19
Appendectomy (%) 28 31 35
Birth control pills (% women) 3 5 3
Marital status
Married (%) 80 77 76
School level
Compulsory education (%) 5 5 7
High school/some years (%) 53 52 58
Diploma or university (%) 41 42 36
Family history
Gastric cancer (%) 16 14 15
Bowel cancer (%) 12 11 15

The research results (see table) indicate that about 1 in 5 people have a slow transit (type 1 and 2 stools), while 1 in 12 has an accelerated transit (type 5 and 6 stools). Moreover, the nature of the stool is affected by age, sex, body mass index, whether or not they had cholecystectomy and possible psychosomatic components (somatisation); there were no effects from factors such as smoking, alcohol, the level of education, a history of appendectomy or familiarity with gastrointestinal diseases, civil state, or the use of oral contraceptives.

Therapeutic evaluation

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Several investigations correlate the Bristol stool scale in response to medications or therapies, in fact, in one study was also used to titrate the dose more finely than one drug (colestyramine) in subjects with diarrhoea and faecal incontinence.[31]

In a randomised controlled study,[32] the scale is used to study the response to two laxatives: Macrogol (polyethylene glycol) and psyllium (Plantago psyllium and other species of the same genus) of 126 male and female patients for a period of 2 weeks of treatment; failing to show the most rapid response and increased efficiency of the former over the latter. In the study, they were measured as primary outcomes: the number weekly bowel movements, stool consistency according to the types of the Bristol stool scale, time to defecation, the overall effectiveness, the difficulty in defecating and stool consistency.[32]

From 2010, several studies have used the scale as a diagnostic tool validated for recognition and evaluation of response to various treatments, such as probiotics,[33][34] moxicombustion,[35] laxatives in the elderly,[36] preparing Ayurvedic poly-phytotherapy filed TLPL/AY,[37] psyllium,[38] mesalazine,[39] methylnaltrexone,[40] and oxycodone/naloxone,[41] or to assess the response to physical activity in athletes.[42]

History

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Developed and proposed for the first time in England by Stephen Lewis and Ken Heaton at the University Department of Medicine, Bristol Royal Infirmary, it was suggested by the authors as a clinical assessment tool in 1997 in the Scandinavian Journal of Gastroenterology[14] after a previous prospective study, conducted in 1992 on a sample of the population (838 men and 1,059 women), had shown an unexpected prevalence of defecation disorders related to the shape and type of stool.[43] The authors of the former paper concluded that the form of the stool is a useful surrogate measure of colon transit time. That conclusion has since been challenged as having limited validity for Types 1 and 2;[44] however, it remains in use as a research tool to evaluate the effectiveness of treatments for various diseases of the bowel, as well as a clinical communication aid.[9][10]

Versions

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The same scale has been validated in Spanish,[45][20] Brazilian Portuguese,[46] and Polish versions.[47] A version has also been designed and validated for children.[48][49] More recently, in September 2011, a modified version of the scale was validated using a criterion of self-assessment for ages six–eight years of age.[50]

A version of the scale was developed into a chart suitable for use on US television by Gary Kahan of NewYork–Presbyterian Hospital.[51]

References

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  1. ^ Amarenco G (2014). "Bristol Stool Chart: étude prospective et monocentrique de "l'introspection fécale" chez des sujets volontaires" [Bristol Stool Chart: Prospective and monocentric study of 'stools introspection' in healthy subjects]. Progrès en Urologie (in French). 24 (11): 708–13. doi:10.1016/j.purol.2014.06.008. PMID 25214452.
  2. ^ Gut Sense What Exactly Are Normal Stools?, Konstantin Monastyrsky. Accessed July 2015
  3. ^ What to know about the Bristol Stool Chart or Bristol Stool Scale.. N.p.: Dr.Hakim Saboowala, 2022.
  4. ^ Harvey S, Matthai S, King DA (27 September 2022). "How to use the Bristol Stool Chart in childhood constipation". Archives of Disease in Childhood: Education and Practice Edition. 108 (5): 335–339. doi:10.1136/archdischild-2022-324513. PMID 36167665. S2CID 252567021.
  5. ^ Koh H, Lee MJ, Kim MJ, Shin JI, Chung KS (February 2010). "Simple diagnostic approach to childhood fecal retention using the Leech score and Bristol stool form scale in medical practice". J Gastroenterol Hepatol. 25 (2): 334–8. doi:10.1111/j.1440-1746.2009.06015.x. PMID 19817956. S2CID 46258249.
  6. ^ Corsetti M, De Nardi P, Di Pietro S, Passaretti S, Testoni P, Staudacher C (December 2009). "Rectal distensibility and symptoms after stapled and Milligan-Morgan operation for hemorrhoids". J Gastrointest Surg. 13 (12): 2245–51. doi:10.1007/s11605-009-0983-7. PMID 19672663. S2CID 30157677.
  7. ^ Wang HJ, Liang XM, Yu ZL, Zhou LY, Lin SR, Geraint M (2004). "A Randomised, Controlled Comparison of Low-Dose Polyethylene Glycol 3350 plus Electrolytes with Ispaghula Husk in the Treatment of Adults with Chronic Functional Constipation". Clin Drug Investig. 24 (10): 569–76. doi:10.2165/00044011-200424100-00002. PMID 17523718. S2CID 29204976.
  8. ^ a b Lewis, Heaton (1997). "Stool form scale as a useful guide to intestinal transit time". Scand. J. Gastroenterol. 32 (9): 920–924. doi:10.3109/00365529709011203. PMID 9299672. S2CID 32196954.
  9. ^ a b Ackley BJ, Ladwig GB (2013). Nursing Diagnosis Handbook, An Evidence-Based Guide to Planning Care, 10: Nursing Diagnosis Handbook. Elsevier Health Sciences. p. 240. ISBN 9780323085496.
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  11. ^ National Collaborating Centre for Nursing and Supportive Care (February 2008). Irritable Bowel Syndrome in Adults: Diagnosis and Management of Irritable Bowel Syndrome in Primary Care (Report). NICE Clinical Guidelines. PMID 21656972. No. 61. Retrieved 17 November 2015.
  12. ^ a b Mínguez Pérez M, Benages Martínez A (May 2009). "The Bristol scale - a useful system to assess stool form?". Rev Esp Enferm Dig. 101 (5): 305–11. doi:10.4321/s1130-01082009000500001. PMID 19527075.
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  31. ^ Remes-Troche J, Ozturk R, Philips C, Stessman M, Rao S (February 2008). "Cholestyramine--a useful adjunct for the treatment of patients with fecal incontinence". Int J Colorectal Dis. 23 (2): 189–94. doi:10.1007/s00384-007-0391-y. PMID 17938939. S2CID 23544857.
  32. ^ a b Wang H, Liang X, Yu Z, Zhou L, Lin S, Geraint M (2004). "A Randomised, Controlled Comparison of Low-Dose Polyethylene Glycol 3350 plus Electrolytes with Ispaghula Husk in the Treatment of Adults with Chronic Functional Constipation". Clin Drug Investig. 24 (10): 569–76. doi:10.2165/00044011-200424100-00002. PMID 17523718. S2CID 29204976.
  33. ^ Sakai T, Makino H, Ishikawa E, Oishi K, Kushiro A (June 2011). "Fermented milk containing Lactobacillus casei strain Shirota reduces incidence of hard or lumpy stools in healthy population". Int J Food Sci Nutr. 62 (4): 423–30. doi:10.3109/09637486.2010.542408. PMID 21322768. S2CID 35206888.
  34. ^ Riezzo G, Orlando A, D'Attoma B, Guerra V, Valerio F, Lavermicocca P, De Candia S (February 2012). "Randomised clinical trial: efficacy of Lactobacillus paracasei-enriched artichokes in the treatment of patients with functional constipation - a double-blind, controlled, crossover study". Aliment Pharmacol Ther. 35 (4): 441–50. doi:10.1111/j.1365-2036.2011.04970.x. PMID 22225544. S2CID 26673737.
  35. ^ Park J, Sul J, Kang K, Shin B, Hong K, Choi S (2011). "The effectiveness of moxibustion for the treatment of functional constipation: a randomized, sham-controlled, patient blinded, pilot clinical trial". BMC Complement Altern Med. 11: 124. doi:10.1186/1472-6882-11-124. PMC 3248868. PMID 22132755.
  36. ^ Fosnes G, Lydersen S, Farup P (2011). "Effectiveness of laxatives in elderly--a cross sectional study in nursing homes". BMC Geriatr. 11: 76. doi:10.1186/1471-2318-11-76. PMC 3226585. PMID 22093137.
  37. ^ Munshi R, Bhalerao S, Rathi P, Kuber V, Nipanikar S, Kadbhane K (July 2011). "An open-label, prospective clinical study to evaluate the efficacy and safety of TLPL/AY/01/2008 in the management of functional constipation". J Ayurveda Integr Med. 2 (3): 144–52. doi:10.4103/0975-9476.85554. PMC 3193686. PMID 22022157.
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Bibliography

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