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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_2899_Библиотеки_им_академика_М_И_Перельмана
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Diagnosis
History
Diagnosis is achieved through a combination of history alongside biochemical,
endoscopic,stool,andhistologicalfindings.Commonhistoryfindingsinclude:
Rectalbleeding
Diarrhoea
Increaseinbowelfrequency
Urgency,tenesmus,andincontinence
Abdominalpain(typicallycrampsrelatedtotheneedtodefecate)
Constitutionalsymptoms,e.g.fatigue
In severe disease, systemic symptoms may manifest, e.g. fever and anorexia. Weight loss is
relativelyuncommonandtypicallyoccursinlatepresentationsofextensivedisease.
Alsoaskabout:
RecenttravelhistoryregardingGIinfections
Smokinghistory:typicallyex-ornever-smokers
FamilyhistoryofIBD.
Examination
Mayhavenospecificsignsinpatientswithmildtomoderatedisease
Abdominaltenderness(especiallyduringacuteflare)
Extraintestinalmanifestations(Box32.1)
Signsofanaemia,e.g.conjunctivalpallor,koilonychia
Rectalexaminationisusuallyunnecessarysincethepatientwillneedendoscopicinvestigation
AcutesevereflareofUC:tachycardia(>90bpm)and/orpyrexia(>37.8°C).
Box32.1Extraintestinalmanifestationsofulcerativecolitis
Erythemanodosum
Pyodermagangrenosum
Uveitis
Fingerclubbing
Arthropathy:largejointarthritisandsacroiliitis
Primarysclerosingcholangitis(PSC).
Investigations
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Bedside
Pulserateandtemperature
Stoolchart—monitorbowelfrequency,stoolconsistency,andpresenceofbloodwithstool.
Bloods
FBC:lowhaemoglobin,raisedleucocytesandplatelets
CRPorESR(thelatterisrarelyperformed)
Electrolytes:forbaselinelevel
LFT: alanine aminotransferase (ALT) and alkaline phosphatase (ALP) may be ↑ if concomitant
PSC.Albuminmaybelowinmoreseveredisease
Ironstudies.
Imaging
Abdominal X-ray—to check for toxic megacolon in acute severe flare of UC (internal colon
diameter≥5.5cm)
CTifsuspectedperforation(moreseverepersistentabdominalpain,and/orsepsis).
Other
Stoolsample:
Faecalcalprotectin(FC)—markerofcoloninflammation(↑).Usefulformonitoringofdisease
activity. Not useful as a diagnostic tool, but typically used in primary care for its good
negativepredictivevalue(i.e.toexcludeinflammatoryboweldisease)
Microbiology analysis to rule out infective causes of bloody diarrhoea, especially
Clostridiumdifficile
Testforova,cysts,andparasitesdependingonthepatient’sdemographicsandtravelhistory
LowerGIendoscopy—ileo-colonoscopyorflexiblesigmoidoscopy:
Continuousinflammationvisualizedintherectumandextendingproximally(unlikeCDwhich
has‘skip’lesions)
Mucosa—loss of vascular pattern, bleeding and friability, erosions, and/or ulcers. Larger
(>5mm)and/ordeepulcersaretypicallyrepresentativeofmoreseveredisease
Biopsy—colonicandrectalbiopsiesshouldbetaken.HistologicalfeaturesofUCarelistedin
Box32.2
Flexible sigmoidoscopyispreferredinsevereactivedisease asbowel preparationmaynot
betolerated,andthereisahigherriskofperforationwithcolonoscopy.
Box32.2Histologicalfeaturesofulcerativecolitis
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Basalplasmacytosis(earliestfeature)
Cryptdistortion
Cryptabscesses
Mucosalatrophy
Absenceofgranuloma(granulomasseeninCD)
Continuous colonic involvement with clear demarcation of inflammation plus rectal
involvement.
Source:datafromMaaserC,etal(August2018)ECCO-ESGARGuidelineforDiagnosticAssessment
inIBDPart1:Initialdiagnosis,monitoringofknownIBD,detectionofcomplications.Journalof
Crohn’sandColitis13(2):144–164K.
Management
Guided by disease severity and distribution of UC. Truelove and Witts’ criteria are
predominantlyusedtoassessdiseaseseverityinacuteflares(Table32.1).
Table32.1AssessingseverityinUCflares(TrueloveandWitts’criteriamodifiedto
includeCRP)
Variable MildUC ModerateUC SevereUC
Motions/day <4 4–6 >6
Rectalbleeding Small Moderate Large
Temperature Apyrexial 37.1–37.8°C >37.8°C
Restingpulse(bpm) <70 70–90 >90
Haemoglobin(g/L) >110 105–110 <105
ESR/CRP <30 >30
Source:datafromTrueloveSC,etal(October1955)CortisoneinUlcerativeColitis.BritishMedical
Journal2(4947):1041–8.
Patienteducation
Patient to monitor symptoms and contact IBD team/nurse if they develop persistent changes in
symptoms.
Pharmacologicalmanagement
Acuteflare
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Mild–moderateUC:
For proctitis alone, topical 5-aminosalicyclic acid (5-ASA) is first line (can be combined
withtopicalsteroidsororal5-ASAforgreatereffectiveness)
Oral5-ASAincombinationwithtopical5-ASAforleft-sidedandextensivedisease
OralsteroidssuchasbudesonideMMX®(Cortiment®)orprednisoloneshouldbeconsidered
incasesrefractoryto5-ASA
Severe UC: indicationfor admissionto hospital in those patientsfulfilling Truelove and Witts’
criteria.Thismeans>6bloodystools/dayplusoneormoreofthecriteria(temperature>37.8°C,
pulserate>90bpm,haemoglobin<105g/L,CRP>30mg/L):
TreatwithIVsteroids,thromboprophylaxis,andIVrehydrationwithelectrolyte replacement
(willtypicallyrequirepotassium>60mmol/day)
Maintainhaemoglobinof>8g/dLwithtransfusion
Considermedicalrescuetherapywithinfliximaborciclosporinifnoorincompleteresponse
tosteroidbyday3.Day3criteriaare>8stools/day,or3–8stools/dayandCRP>45mg/L
Ifnoresponsetorescuetherapyafter4–7days,colectomyisrecommended.
Thromboprophylaxis
Inpatients with UC should be prescribed thromboprophylaxis given their ↑ risk of
thromboembolism,despitebloodydiarrhoea.
Chronicmanagement
Patients should remain on long-term maintenance treatment with the aim of achieving
steroidfreeremission.
Steroid-sparingtherapy:
Patients requiring steroids despite 5-ASA treatment, and with steroid-responsive disease,
shouldbecommencedonthiopurinesinthefirstinstance.Evidencesuggeststhereislittlerole
for methotrexate as monotherapy in UC, but it does still have use as a concomitant
immunomodulatorwithanti-TNFtherapy
Forthosewithactivediseasedespite5-ASAandthiopurines,orthosewithsteroid-refractory
disease, there are now a number of medical options. These include anti-TNF agents (e.g.
infliximab, adalimumab), anti-integrin therapy (vedolizumab), JAK inhibitors (tofacitinib),
andanti-IL-12p40(ustekinumab)
Specialconsiderationsforprescribingsteroid-sparingtreatmentsarelistedinTable32.2.
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Table32.2Prescribingthiopurines,anti-TNFagents,vedolizumab,andtofacitinib
Thiopurines Anti-TNF Vedoli-
zumab
Tofacitinib
Before
starting
Checkthiopurine
methyltransferase
(TMPT)levels
CheckbaselineFBC,
U&E,LFT
Checkserologyfor:
HepatitisB/C,HIV.
Vaccinate/treatif
appropriate
Checkserologyfor:
HepatitisB/C,HIV,varicellazostervirus(VZV)
AlsoperformTBtestingasper
localguidelines.Vaccinate/treat
ifappropriate
No
specific
checks
Checkserologyfor:
HepatitisB/C,Epstein–Barr
virus,HIV,VZV
Vaccinate/treatifappropriate
Checkfastinglipids
Shinglesvaccineifpossible
ConsiderriskofDVTand
pulmonaryembolism(PE).
Usealternativeagentif
possibleifadditionalVTE
risks
Monitoring FBCandLFTevery
otherweekfor1month,
Checkanti-TNFtroughlevels
ifincompleteorlossof
response,andatleastevery6–
12monthsinstablepatients
No
specific
monitoring
Checkfastinglipidsat8
weeks
CheckFBCandLFTat4
and8weeks,andthenevery
3months
Cautions Patientshouldhavealow
thresholdforseeking
medicalattentionifthey
developfever/infection
Patientshouldhavealow
thresholdforseekingmedical
attentioniftheydevelop
fever/infection
No
specific
cautions
Patientshouldhavealow
thresholdforseeking
medicalattentionifthey
developfever,shingles,or
symptomsofDVT/PE
Source:datafromtheBNF.
Surgicalmanagement
Subtotal colectomy withileostomymay be required after failure ofmedical treatmentor due to
complications(e.g.colonicperforation)
Subsequentcompletionproctectomyandpermanentileostomy,orformationofileo-analpouch,isa
decisiontobetakenafterfullrecoveryfromsubtotalcolectomy.
Psychosocialconsiderations
Livingwithsymptomsof↑bowelfrequencyandurgency:
Feelingsofsocialembarrassment
Adolescentsat↑riskofsocialisolationanddepression
Psychologicalimpactofstomaformation
Directpatientstostomaspecialistnursesandsupportgroupstohelpwiththeabovepoints.
Complications
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Strictures
Fibrosis
Toxiccolonicdilatation
Bowelperforation
↑riskofcolorectalcancer
Thromboembolism.
Monitoringandfollow-up
Mostpatientswillrequirelong-termmaintenancetreatment,usuallywith5-ASA/mesalazine
FollowupwithIBDteamatintervalsappropriatefordiseaseactivity.Thiswillincludeareview
ofsymptoms,seruminflammatorymarkers,±faecalcalprotectin±endoscopicassessment
Patientsonthiopurinesoranti-TNFagentsshouldhavetheirdruglevelsmonitored.
Endoscopy
If patientsare asymptomaticatfollow-upbuthaveabnormalinflammatorymarkersand/orfaecal
calprotectin,considerendoscopytoassessforactivedisease
Monitor mucosal healing with endoscopy or faecal calprotectin 3–6 months after commencing
treatmentinpatientswhoimproveclinicallywithpharmacologicaltreatment
Ifnewsymptoms,poorresponsetotreatment,orsevererelapse,repeatendoscopy
Surveillancecolonoscopyshouldbecarriedout(between5-yearlyandannually,dependingonrisk
stratification)dueto↑riskofcolorectalcancerassociatedwithUC.Surveillanceshouldbemore
frequentinpatientswithconcurrentPSC.
Specialconsiderations
Pregnancy
Fertilityisunaffectedbywell-controlledUC
Patientsconceivingduringinactivediseasehavesimilarriskofrelapsetonon-pregnantpatients
For the majority of UC medications there is no evidence of harm during pregnancy and
breastfeeding, although pregnancy must be avoided if the patient is taking methotrexate or
tofacitinib
Investigation during pregnancy should always be considered carefully and discussed with the
patient. There is no evidence of harm with flexible sigmoidoscopy, although this is avoided if
possible,particularlyinthefirsttrimestergiventhenaturalfrequencyofmiscarriageinthisstage
ofpregnancy.MRIistypicallyonlyperformedinthesecondandthirdtrimesters.
Furtherreading
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1.Wilkinson IB,RaineT,WilesK, etal. (2017). Ulcerativecolitis. In: OxfordHandbook of Clinical
Medicine, 10th ed (pp. 262–3). Oxford: Oxford University Press. Available at:
https://doi.org/10.1093/med/9780199689903.003.0006
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Part5
Hepatobiliary
Acuteliverfailure
Alcohol-relatedliverdisease
Alcoholusedisorders
Livercirrhosis
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Chapter33
Acuteliverfailure
Guideline: EuropeanAssociationfortheStudyoftheLiver(EASLClinical
Practical Guidelines on the management of acute(fulminant) liver failure):
https://www.journal-of-hepatology.eu/article/S0168-8278(16)30708-5/fulltext
OUPdisclaimer:OxfordUniversity Press makesno representation, express
or implied, that the drugdosagesarecorrectand thatthe recommendations
are an exclusive or mandatory course of care. All health professionals
readingthistexthavearesponsibilitytoevaluateitsappropriatenessandtake
theindividualneedsofthepatientintoaccount.
Localtrustguidelines:pleaserefertoyourlocalguidelinesasnecessary.
Overview
Acute liver failure (ALF) refers to an acute episode of liver dysfunction in a patient
without previously diagnosed liver disease, resulting in coagulopathy and hepatic
encephalopathy (HE). ALF typically begins with an acute liver injury, suggested by
derangedliverfunctionandcoagulopathy.
Diagnosis
ThediagnosisofALFisdependenton:
Acuteliverinjury—a2–3×increaseintransaminases(ALTandaspartateaminotransferase(AST))
—andimpairedliverfunctionevidencedbyjaundiceandcoagulopathy
ThepresenceofHE.
Coagulopathy is defined as INR >1.5 and/or prolonged PT. Depending on the time of
onset of HE from the time jaundice was noted, ALF can be further divided into
hyperacute (7 days), acute (8–28days), andsubacute(5–12weeks).The timeframecan
helptosuggestthepotentialcauseofALF(Table33.1).
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HEisnecessaryforadiagnosisofALF.Itsabsenceinthepresenceofnewlyderanged
liverfunctionandcoagulopathysuggestsanacuteliverinjury,butnotALF.
History
A focused history will help make a prompt diagnosis of ALF and give clues to the
aetiology, guiding management and allowing prognostication. Ask about onset of
symptomsandsignssuggestiveofliverdysfunctionsuchas:
Jaundice
Confusion
Atraumatic/spontaneousbleeding
Generalmalaise
Nauseaorvomiting
Abdominalswelling(ascitesismoretypicalofchronicliverdiseasebutcanoccurinBudd–Chiari
syndrome)
Rightupperquadrant(RUQ)pain.
Takeathoroughsocialhistory,includingforeigntravel,occupation,alcoholuse,anddrug
use. Besureto ask aboutregularand acutemedications, includingover-the-counterand
herbalmedications!HEcanbesubtlesoithelpstohaveacollateralhistory.Considerthe
timeframeofsymptomsasthismayprovideacluetothediagnosis(Table33.1).
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