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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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Specialconsiderations
Contrast-inducedAKI
ThisisdefinedasAKIoccurringwithin48hoursofapatientreceivingiodinatedcontrast.
As such, the following may be considered when managing a patient at high risk of
contrast-inducedAKI:
Discusspatientsathighriskofcontrast-inducedAKIwithanephrologisttoassessthebenefitsand
risksofproposedimaging,butdonotdelayemergencyimaging
Unenhancedoralternativescanningtechniquesinpatientswithriskfactors
Considerwithholdingnephrotoxicmedicationspreandpostscan
Encourageoralhydrationpreandpostscan
Volume expansionwith IV normal saline or isotonic sodium bicarbonate at 1mL/kg/hour for 12
hourspreandpostprocedureifthepatientishighrisk,e.g.eGFR<30mL/min/1.73m2,theyhavea
renaltransplant,alargevolumeofcontrastisduetobeused,orthecontrastwillbeinjectedintraarteriallywithfirst-passrenalexposure.
Furtherreading
1.HertzbergD, RydénL,Pickering JW,etal. (2017). Acutekidneyinjury—an overview ofdiagnostic
methodsandclinicalmanagement.ClinKidneyJ.10:323–31.
2.Steddon S,AshmanN,ChesserA,etal.(2014).Acutekidneyinjury(AKI).In:OxfordHandbookof
Nephrologyand Hypertension,2nded(pp. 87–190).Oxford:OxfordUniversity Press. Availableat:
https://doi.org/10.1093/med/9780199651610.003.0002
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Chapter47
Chronickidneydisease
Guidelines: NICE NG203 (Chronic kidney disease: assessment and
management): https://www.nice.org.uk/guidance/ng203 UK Kidney
Association (Anaemia of chronic kidney disease):
https://ukkidney.org/sites/renal.org/files/Updated-130220-Anaemia-ofChronic-Kidney-Disease-1-1.pdf
UK Kidney Association (Sodium-glucose co-transporter-2 (SGLT-2)
inhibition in adults with kidney disease):
https://ukkidney.org/sites/renal.org/files/UKKA%20guideline_SGLT2i%20in%20adults%20with%20kidney%20disease%20v1%2018.10.21.pdf
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
Chronic kidney disease (CKD) refers to an abnormality of renal function or structure,
present for >3 months. The underlying cause of CKD should be established to ensure
optimalmanagement.
Terminology
eGFR: this refers to estimated glomerular filtration rate, which is the standardized result
calculatedbylaboratorieswhenaserumcreatininelevelisrequested
GFR category: this refers to the internationally approved GFR categories of CKD which are
explainedinFig.47.1.
Diagnosis
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History/diagnosticcriteria
The causes of CKD are broad and the symptoms may be non-specific. Diagnoses that
increasetheriskofCKDinclude:
Diabetesmellitus(DM)
Hypertension
PreviousAKIinthelast3years
Cardiovasculardisease
Structuralrenaltractdisease,recurrentrenalcalculi,orprostatichypertrophy
Multisystemdiseasewithpotentialforrenalinvolvement,e.g.systemiclupuserythematosus
Gout
Familyhistoryofend-stagekidney disease(GFRcategoryG5)or hereditarykidney disease,e.g.
polycystickidneydisease
Incidentalfindingofhaematuriaorproteinuria.
AllpatientswiththeseriskfactorsshouldbetestedforCKDatpresentation.
Patients on nephrotoxic drugs (e.g.ciclosporin, tacrolimus, lithium, NSAIDs) should
havetheireGFRmonitoredatleastannually.
CKDisclassifiedaccordingtoeGFRandACR(Fig.47.1):
↑ACRand↓eGFRareindependentlyassociatedwithadverseoutcomes
Interpret the eGFR with caution at extremes of muscle mass (↓ muscle mass leads to
overestimationoftheeGFRandtheconverseistrueof↑musclemass)
PatientswithDM,CKD,orsuspicionofCKDshouldbemonitoredforproteinuria
UseurineACRtodetectproteinuria(>3mg/mmol):
IfinitialACRis3–70mg/mmol,confirmwithanearlymorningsample
IfinitialACRis>70mg/mmol,arepeatsampleisnotrequired
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Fig.47.1ClassificationofCKDandriskofadverseoutcome.
ReprintedwithpermissionfromKidneyDisease:ImprovingGlobalOutcomes(KDIGO)CKDWork
Group.KDIGO2012ClinicalPracticeGuidelinefortheEvaluationandManagementofChronicKidney
Disease.Kidneyinter.,Suppl.2013;3:1–150.
Examination
Thepatientmayhaveexaminationfindingsrelatedto theunderlyingcause,signsrelated
tomanagement,orstigmataofcomplicationsofCKD:
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Signsrelatedtotheunderlyingcause:
Polycystic kidney disease (MR, bilateral palpable flank masses with hepatomegaly if liver
cysts)
Obstructiveuropathy(palpable,distendedbladder)
Signsrelatedtomanagement:
Cushingoidfromsteroids
Peritonealdialysiscatheter
Fistulaorvascularaccessrouteforhaemodialysis
Parathyroidectomyscar;abdominalscarorpalpabletransplantedkidneyfromtransplant
Signsrelatedtocomplications:
Anaemia:pallor,angularstomatitis,koilonychia
Fluidstatus:signsofperipheralorpulmonaryoedema
Uraemia: excoriations, Lindsay’s nails (proximal half of the nail appears white while the
distalhalfappearsreddishbrownwithasharpdemarcationbetweenthehalves)
Cachexiaormalnutrition.
Investigations
Bedside
Bloodpressure
Urine(urinalysis,MC&S,ACR,BenceJonesprotein).
Ifproteinuriaisfoundincidentallyonurinalysis,calculateeGFRandcheckurineACR:
Persistent microscopic haematuria (1+ or greater) should raise a suspicion ofurinary tract
malignancyandbefollowedupannually.
Bloods
SeeTable47.1.
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Table47.1RationaleforbloodsfordiagnosisandassessmentofCKD
Test Rationale
FBC AnaemiaiscommoninCKD.Screen6–12-monthly
Ironstudiesandhaematinics;testsforhaemolysis;
serumelectrophoresisandfreelightchains
Importantinthedifferentiationofthecauseofanaemia
AnaemiashouldbeinvestigatedifHb<110g/L,orifthe
patientissymptomatic
CKDshouldalwaysbeconsideredasapossiblecauseof
anaemiawheneGFR<60mL/min/1.73m
2
Creatinineandurea Fordiagnosisandmonitoring
LFT ALPmaybe↑inrenalosteodystrophy
HbA1c DiabetesisariskfactorforCKD
Calcium,phosphate,vitaminD,PTH,andcalcidiol IdentifiesmineraldisturbancesandvitaminDandPTH
derangement
C-reactiveprotein Assessesforinflammation
ANA,ANCA,anti-glomerularbasementmembrane,
complement
AssessesforautoimmunecausesofCKD
Imaging
Considerrenalultrasoundif:
Symptomsofobstructiveuropathy
Macroscopic,orpersistentmicroscopic,haematuria
AcceleratedprogressionofCKD:
DecreaseineGFRof≥25%andachangeinGFRcategorywithin12monthsOR
SustaineddecreaseineGFRof15mL/min/1.73m2peryear
Familyhistoryofpolycystickidneydiseaseandaged>20years
eGFR<30mL/min/1.73m
2
Renalbiopsyisconsiderednecessary:
Progressivedisease,nephroticsyndrome,systemicdisease,AKInotimproving.
Management
Patienteducation
Patients should be prepared for the possibilityof needingrenal replacement therapy in
progressiveCKD.
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Lifestyleandsimpleinterventions
Exercise
Achieveahealthyweight
Stopsmoking
All patients should receive dietaryadvice aboutpotassium, phosphate, salt,and calorie intake.
Patients with GFR category G4–5 should be seen by a specialist renal dietician to receive
individualizedinformationandsupportondietaryphosphateandproteinmanagement.
Pharmacologicalmanagement
General
ReviewpotentiallynephrotoxicmedicationandavoidNSAIDs
Statintherapy, e.g.atorvastatin20mgOD, andlow-dose aspirin(75mgOD) inall patientswith
CKD
Offer annual influenza and 23-valent polysaccharide pneumococcal vaccination with a booster
every5years
1
GiveavitaminDsupplement(cholecalciferol)ifdeficient.
Bloodpressurecontrol
UseanACEinhibitor,ARB,ordirectrenininhibitortocontrolbloodpressureinpatientswithany
ofthefollowing:
CKD,hypertension,andACR≥30mg/mmol
CKD,diabetes,andACR≥3mg/mmol
CKDandACR≥70mg/mmol
Bloodpressuretargets:
<140mmHgsystolic,<90mmHgdiastolic
IfdiabeticORACR≥70mg/mmol,usetarget<130mmHgsystolic,<80mmHgdiastolic
If patientsdo notfallintoanyof thesecategories, followstandard hypertensionguidelines (see
Chapter6)
Monitor eGFR and potassium before starting, 1–2 weeks after starting, and after each dose
increase
Donotusethesemedicationsifpre-treatmentpotassium>5mmol/L
Stopmedicationsifpotassium>6mmol/L.
Electrolyteimbalances
Hyperphosphataemia in patients with GFR category G4–5 should be managed with phosphate
binderssuchascalciumacetate,1tabletwitheverymeal
ConsidersodiumbicarbonateifGFRcategoryG4–5andserumbicarbonate<20mmol/L.
SGLT2inhibitors
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StartanSGLT2inhibitor,e.g.dapagliflozin10mg,ifACR≥25
Ifcommenced,patientsshouldbemonitoredforhypovolemiaandworseningofeGFR
Advisethatthemedicationshouldbeheldifthepatientfeelsunwell,becomesdehydrated,orhas
reducedfoodintake.ThisisduetotheriskofeuglycaemicDKA.
Psychosocialconsiderations
Anxiety,depression,andfatiguearecommon.
Complications
Acute-on-chronickidneydisease
Cardiovasculardisease:
↑mortality associatedwithworsening renalfunctionis largelysecondarytocardiovascular
disease
Anaemia:
If eGFRis <60mL/min/1.73m2, CKD maybethe cause but othercauses of anaemia should
alsobeconsidered
Treat iron deficiency; oral iron supplements are usually sufficient if the patient is not on
dialysis
Offererythropoietinstimulatingagentsifthepatientislikelytobenefitintermsofqualityof
lifeandphysicalfunction
Avoidbloodtransfusion,particularlyiftransplantationisatreatmentoption,duetotheriskof
allosensitization
Renalmineralandbonedisorder:
Disturbance in vitamin D, calcium, PTH, and phosphate metabolism due to dysregulated
homeostasis
Peripheralneuropathyandmyopathy(duetouraemia)
Malignancy:
The exact cause is unknown, but end-stage kidney disease patients may have an ↑ risk of
malignancy,particularlyrenalandthyroid
Renalreplacementtherapy:
Dialysisortransplantation.
Monitoringandfollow-up
MonitorCKDwitheGFRandACRatleastannually:
Monitormultipletimesayearifhighriskorveryhighrisk(Fig.47.1)
ScreenforanaemiaatleastannuallyinpatientswithGFRcategoryG3and atleastbiannuallyin
patientswithGFRcategoryG4–5notondialysis
Monitor serum potassium 2–4 times a year.2 Also check before starting an ACE inhibitor, 1–2
weekslaterandaftereverydosechange
Monitorcalcium,phosphate,ALP,PTH,and25-hydroxyvitaminD(calcidiol)levelsifGFRG4–5.
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Specialistrenalreferral
ReferifCKDwith:
eGFRreduction≥25%causingachangeineGFRcategoryinthelastyear
eGFRfalling≥15mL/min/1.73m2peryear
ACR≥70mg/mmol(unlesssecondarytodiabetes)
ACR≥30mg/mmolwithhaematuria
Resistanthypertension(poorlycontrolledonatleastfourantihypertensivemedications)
Rareorgeneticcause
Suspectedrenalarterystenosis.
Specialisturologyreferral
ReferifCKDwith:
Renaloutflowobstruction
Specialconsiderations
Pregnancyandbreastfeeding
Many drugs may not be suitable for use in pregnancy and breastfeeding, while others
requiredoseadjustment.SeeTable47.2.
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Table47.2SummaryofsafetyofdrugsusedinCKDinpregnancyandbreastfeeding
Drug Safeinpregnancy? Safeinbreastfeeding?
Angiotensin-2receptor
antagonistsandACE
inhibitors
Avoidinpregnancyunlessessential Informationislimited;notrecommendedin
breastfeeding
SGLT2inhibitors Avoid Avoid
Statins Avoidinpregnancy(discontinue3
monthspriortoattemptingto
conceive)
Manufactureradvisestoavoid;noinformation
available
Antiplateletmedication
(aspirin)
Usedoseswithcautionduringthird
trimester
Avoidanalgesicdosesifpossiblein
lastfewweeks
Avoid;possibleriskofReye’ssyndrome
VitaminDsupplement
(cholecalciferol)
Highdosesteratogenicinanimalsbut
therapeuticdosesunlikelytobe
harmful
Cautionwithhighdoses;maycause
hypercalcaemiaininfant—monitorserum
calciumconcentration
Vaccinations Inactivatedvaccinesnotknowntobe
harmful
Inactivatedvaccinesnotknowntobeharmful
Hepaticandrenalimpairment
Be aware thatmost drugs willneed dose adjustmentinaccordancewiththe severityof
impairment.TheRenalDrugHandbook/Databaseisakeyresourceforsafeprescribingin
CKD;mosthospitalswillhavethis,usuallyviathepharmacyortherenalteam.
Furtherreading
1. NICE Clinical Knowledge Summaries (2021). Chronic kidney disease: background. Available at:
https://cks.nice.org.uk/chronic-kidney-disease#!background
2.TheRenalDrugDatabase.Availableat:https://renaldrugdatabase.com
3.KDIGO(2012).2012ClinicalPracticeGuidelinefortheevaluationandmanagementofchronickidney
disease.Availableat:https://kdigo.org/wp-content/uploads/2017/02/KDIGO_2012_CKD_GL.pdf
1NICEClinicalKnowledgeSummaries.Immunizations– pneumococcal:summary. 2016.Available at:
https://cks.nice.org.uk/immunizations-pneumococcal#!topicSummary
2UKKidneyAssociation.Clinicalpracticeguidelines:treatmentofacutehyperkalaemiainadults.2020.
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