Core principles
- Consider suitability for home haemo/PD and review tx listing
status
- Customise dialysis regime to patient.
- Ensure adequate volume control as a key primary priority
- Bloods: Reflect on trends, rather than individual results.
- Dialysate: avoid positive sodium balance, positive calcium, high K
gradients. Avoid dialysate Mg <1, K <2, Ca2+ <1.5.
- Aim for your targets, but within the context of that patient, and
not at the expense of personalised care.
Volume First
A Volume first
approach, major CV contributor. Light on evidence, but compelling.
Extending treatment time or frequency is an effective way to address
volume control and tolerance of dialysis sessions, with less
dialysis-related morbidity and mortality
notes
- BP should be normal throughout, high post HD BP ?wet
- Can take ~3 months to get to a first dry weight – persistence is
key
- Early tapering of BP meds may help hit dry weight by avoiding
hypotension (?evidence?)
- Hypotension/cramps = refill capacity. Does not necessarily mean at
dry weight
- BP normalisation can lag weeks after ECF volume normalisation
(allegedly ?evidence)
Adequacy
URR: ((Pre urea-post urea)*100)/Pre-urea
- Underestimates due to ignoring urea clearance during UF and intra HD
urea generation
- Target 70%. Mostly a Fn of Time and Qb in that order.
Single Pool Kt/V
Accounts of size by using TBW in formula
Urea Clearance(K)*Time(T)/Vd of Urea (55% TBW in men, 50% in
women)
Target 1.4, min 1.2
Equilibrated Kt/V
HEMO study
HEMO
1846 patients 3*week HD
Primary outcome: death
Secondary outcome: hospitalization for cardiac causes or death
from any cause, first hospitalization for infection or death from any
cause, first 15 percent decrease in the serum albumin level or death
from any cause, and all hospitalizations not related to vascular
access
Results: No difference between high dose (Kt/v 1.7, URR 75) vs
low (Kt/V 1.16, URR 66). No difference between high flux and low
flux.
Anaemia & Iron
Has its own page here
HD Prescription tips
- Lower temps = may have greater tolerability and possibly CV/Neuro
outcomes in selected patients,
- Qb 300-500, Qd 500-800
- Initiation: 2hr Qb200 Qd500 ,3hr Qb250 Qd500 ,4hrs Qb300 Qd800.
- Never use a 0/1 K+ bath (if its even an option) – too much K flux
unless you really really need to lower it
- Post Tx: avoid hypotension (assoc. with increase risk of acute
rejection)
- Acidaemic: Check ionised Calcium – the incoming bicarb load will
drop the iCa - >seizures etc
MyTEMP
MyTEMP
- cluster randomised Canadian trial, 36’5c Vs 0.5c less than body
temp.
- Pragmatic and excellently done, healthy budget and embedded in
care
- The primary composite outcome was CV-related death or hospital
admission with MI, stroke, CCF during the 4-year trial period
- 15413 patients, 4.3 million HD sessions
- mean dialysate temperature was 35·8°C in the cooler dialysate group
and 36·4°C
- mean drop in intradialytic sys BP 26·6 mm Hg in the cool HD vs 27·1
mm Hg in the standard temperature group (mean difference –0·5 mm Hg, 99%
CI –1·4 to 0·4; p=0·14)
Severe Uraemia
- Pericarditis is a clinical diagnosis
- Rx:* Daily HD, no anticoagulation
- Check for pericardial effusion
- Chest pain – improves leaning forward, friction rub, distant heart
sounds. Fever/sob. BP low. Tachycardic.
- ECG: Diffuse ST & T wave elevation – not
typically coronary territory. electrical alternans = pericardiocentesis.
Trop leak.
- JVP: Kussmaul’s sign is a paradoxical rise in
jugular venous pressure (JVP) on inspiration
- Pulsus paradoxus: aka exaggerated respiratory
variation
- Inflate 30mmHg above pulse. Note first intermittent Korotkoff
sounds. (higher systemic BP occurring during expiration). Slowly deflate
cuff until highest BP with continuous beat. The delta is the pulsus
paradoxus. >10mmHg suggest tamponade.
- CXR: Increased cardiac silhouette
- ECHO: Effusion in 50% of uraemic pericarditis.
Repeat echo to ensure resolution 3-5 days.
- D.Dx: Infectious/inflammation(SLE/vasculitis),
neoplastic, meds(hydralazine)
Bicarb
Bicarb target : > 22 – 28
Notes
- Total carbon dioxide [CO2], generally 1–1.5 mEq/L higher than the
serum bicarbonate concentration, is actually what is measured in all
epidemiologic studies
- High and low bicarb associated
with poorer outcomes (<20), sicker patients eat less protein,
resulting in less acid generation.
- European Best Practice Guidelines suggest maintaining midweek
predialysis serum bicarbonate at 20–22 mEq/L
- Low or high values tend to return to baseline, only 3 month mean
values tend to stick around, so a single abnormal reading is unlikely to
be significant. Regression to the mean.
- Rapid increase in blood BIC/PH: hypercapnia, arrythmia, haemodynamic
instability, possibly immune dysfunction/infection, electrolyte ( drop
in Calcium, K+ driven by PH)
Sources: KDOQI , excellent
review in JASN and summary
in KI.
Vaccinations
HEP B – 1/3 don’t respond. At 1 year, only about ~64% have
adequate Ab protection
- HBVAXPRO 40 micrograms at 0, 1 and 6 months by IM
injection. Not in buttocks – go deltoid – better response.
- Fendrix -20micrograms at 0,1,2 and 6 months
- Engerix B -40 micrograms at 0,1,2 and 6 months
Check anti-Hbs antibodies 1-2 months after course.
- Responder: >100mIU/ml .
- Partial response: 10-100mIU/ml. Give booster (once)
and recheck in 1-2 months.
- Non response: <10mIU/ml. Repeat entire course
once only. If still <10mIU/ml, then patient is a ‘non responder’ and
move on. If level 10-100mIU/ml then treat as partial response.
- If non response, check for ABsag and either proceed as acute
infection if + or “vulnerable”
- HBIG postexposure prophylaxis for any known or likely parenteral
exposure to HBsAg positive blood is available.
- Once established, annual check with a booster if <100mIu/ml.
Notes:
- Better immune response and high rates of conversion if given before
ESKD
- If started on normal dose pre HD but transitioning to HD during
vaccine course, increase to the double dose (40mg) once on HD
- Ab tires >10 are still protective
Other Vaccines
- Annual inactivated influenza
- Pneumococcal: Regime varies depending on history and PCV13/PPSV23:
See table 2 and table 3 of the appendix of CDC document here
- Green
book
- COVID probably