Deck overview

Severe Falciparum Malaria.

18 slides · CICM Fellowship Masterclass · 2026

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CICM Fellowship Masterclass · 2026
01 / 15 · Cover
The Returned
Traveller.
Severe Falciparum Malaria
Recognition · Resuscitation · Advanced ICU Management — a case-based fellowship masterclass.
Presenter
Dr Timothy Chimunda FCICM
Clinical Director ICU · NWRH
60
min · Case
20
min · Viva
10
min · Discuss
01Cover
I · Session Overview
Severe Falciparum Malaria02 / 18
Learning
objectives.
By the end of this session you will be able to —
Distinction territory
Recognise delayed post-artesunate haemolysis in patients who appear to have recovered.
I
Recognise
Severe malaria within minutes of presentation
II
Differentiate
Uncomplicated from severe malaria — WHO criteria
III
Initiate
Evidence-based ICU management immediately
IV
Prescribe
Modern antimalarial therapy correctly
V
Manage
Multi-organ failure of falciparum malaria
VI
Avoid
Common CICM examination pitfalls
CICM Fellowship Masterclass · 2026Dr Timothy Chimunda FCICM
02Learning Objectives
II · 0200 hrs · Emergency Department
Severe Falciparum Malaria03 / 18
The patient arrives.
Chief complaint
"He doesn't make sense anymore."
— wife at triage
36 ♂
Age · Sex
Uganda
Travel
6 wks
On-site
None
Prophylaxis
Symptoms · 4 days
Fever — high, spiking
Rigors — shaking chills
Headache · Vomiting — severe, persistent
Lethargy → confusion
Initial observations
39.8°
Temp
132
HR
84/48
BP
34
RR
95%
SpO₂ RA
13
GCS
CRT 5 s — circulatory compromise. Act now.
Teaching
"Geography is the most important laboratory investigation."
CICM Fellowship Masterclass · 2026Dr Timothy Chimunda FCICM
03Patient Arrives
III · Audience Question 1
Severe Falciparum Malaria04 / 18
Immediate priorities?
01
ABCDE
Simultaneous assessment and resuscitation
02
Sepsis pathway
Activate immediately — don't wait
03
Travel history
Geography is the key diagnostic clue
04
Blood cultures
Before antibiotics
05
Thick + thin films
Request immediately — gold standard
06
Malaria RDT
Rapid antigen test
07
Lactate · ABG · Glucose
Severity markers
08
Early ICU referral
Do not delay escalation
09
Isolation
Consider VHF — Uganda exposure
Differential — febrile returned traveller
P. falciparum malaria
Uganda + no prophylaxis — most likely
Viral haemorrhagic fever
Ebola / Marburg — isolate until excluded
Dengue
NS1 antigen · rash · thrombocytopenia
Typhoid
Rose spots · relative bradycardia
Leptospirosis
Water exposure · uveitis · Weil's
Rickettsiosis
Eschar · tick exposure · serology
Bacterial meningitis
CSF · neck stiffness · photophobia
Acute HIV seroconversion
Lymphadenopathy · screen serology
CICM Fellowship Masterclass · 2026Dr Timothy Chimunda FCICM
04Immediate Priorities
IV · Laboratory results
Severe Falciparum Malaria05 / 18
Results arrive.
Hb98 g/L ↓
Platelets39 ×10⁹/L ↓↓
Creatinine186 µmol/L ↑
Bilirubin88 µmol/L ↑↑
ALTMildly ↑
Lactate5.9 mmol/L ↑↑
Glucose2.2 mmol/L ↓
pH7.22 ↓
HCO₃14 mmol/L ↓
Base excess−11
Microbiologist phones
Thick film positive — P. falciparum
Parasitaemia 7%
Audience Q2 · Interactive poll
Does this patient already meet WHO criteria for severe malaria?
CICM Fellowship Masterclass · 2026Dr Timothy Chimunda FCICM
05Results Arrive
V · WHO 2024 — know these cold
Severe Falciparum Malaria06 / 18
Severity criteria.
Examiners expect WHO criteria verbatim — not just a list of organ failures. Know the thresholds.
Neurological01
Impaired consciousness (GCS <15) · coma (<11) · seizures ≥2/24h · prostration
Respiratory02
Pulmonary oedema · ARDS · respiratory distress · SpO₂ <92% RA
Cardiovascular03
Shock · SBP <80 mmHg · impaired perfusion · CRT >3 s
Renal04
AKI · creatinine >265 µmol/L · haemoglobinuria · oliguria
Haematological05
Severe anaemia Hb <70 g/L · DIC · thrombocytopenia
Metabolic06
Glucose <2.2 · pH <7.25 · HCO₃ <15 · lactate >5
Hepatic07
Jaundice + organ dysfunction · bilirubin >50 µmol/L
Parasitological08
Hyperparasitaemia · >5% non-immune · >10% any patient
CICM Fellowship Masterclass · 2026Dr Timothy Chimunda FCICM
06WHO Severity Criteria
VI · Treatment · Audience Q3
Severe Falciparum Malaria07 / 18
Why artesunate changed everything.
First-line · Severe malaria
IV Artesunate
2.4 mg/kg at 0 h · 12 h · 24 h — then daily
Do not wait for species confirmation in severe disease.
SEAQUAMAT 2005
34.7%
quinine mortality
AQUAMAT 2010
−22.5%
mortality reduction
WHO 2024
First-line
unequivocal
Advantages over quinine
Rapid parasite clearance — kills all life-cycle stages
Lower mortality — 22.5% RRR (AQUAMAT)
Less hypoglycaemia — no insulin stimulation
Better cerebral outcomes — reduced complications
IV bioavailability in critically ill patients
Oral follow-on — artemether-lumefantrine ACT × 3 d
Examiner trap
Listing quinine as first-line for severe malaria in 2026 costs marks. Quinine is second-line only — when artesunate is unavailable.
CICM Fellowship Masterclass · 2026Dr Timothy Chimunda FCICM
07Artesunate
VII · Case progression
Severe Falciparum Malaria08 / 18
Four hours later.
0200 — Admission
GCS 13 · BP 84/48 · Temp 39.8° · Parasitaemia 7%. IV artesunate commenced. ICU admission.
0400 — +2 h
GCS 10 · increasing agitation. Noradrenaline 0.05 mcg/kg/min commenced.
0600 — +4 h
GCS falls to 8 · generalised seizure × 1. BP 78/40. Noradrenaline escalated.
0800 — +6 h
Intubated · ventilated · bilateral CXR infiltrates. FiO₂ 0.70 · PEEP 12 · P/F 110.
Cerebral malaria — pathophysiology
P. falciparum in RBCs
↓ Cytoadherence via PfEMP1
↓ Endothelial activation (ICAM-1)
↓ Microvascular obstruction
↓ Brain oedema + coma
Key teaching
Steroids are contraindicated in cerebral malaria — the SNAP trial showed increased coma duration and GI complications.
CICM Fellowship Masterclass · 2026Dr Timothy Chimunda FCICM
08Four Hours Later
VIII · ICU management
Severe Falciparum Malaria09 / 18
Multi-system organ support.
Deaths in severe malaria are caused by multi-organ failure, not parasite burden. ICU support saves the patient — the drug clears the parasite.
Lung-protective
B · Ventilation
  • · TV 6 mL/kg IBW · Plateau ≤30 cmH₂O
  • · PEEP 12 · FiO₂ to SpO₂ ≥95%
  • · Prone if P/F <150 · ECMO last resort
Vasopressor
C · Circulation
  • · Noradrenaline first-line · MAP ≥65
  • · Arterial line essential
  • · Conservative fluids — FEAST: boluses kill
Antimalarial
D · Artesunate
  • · 2.4 mg/kg · 0 h / 12 h / 24 h / daily
  • · Repeat parasitaemia 12-hourly
  • · Switch to oral ACT when tolerating
Monitoring
E · Glucose
  • · Hourly monitoring — mandatory
  • · Target 5–10 mmol/L
  • · Treat: 50 mL 50% dextrose IV stat
RRT
F · Renal
  • · K⁺ 6.2 → urgent CRRT now
  • · Early CVVHDF for AKI
  • · Avoid nephrotoxins · protect tubules
Seizures
G · Neuro
  • · IV lorazepam first-line
  • · Levetiracetam if recurrent
  • · Steroids CONTRAINDICATED — SNAP
CICM Fellowship Masterclass · 2026Dr Timothy Chimunda FCICM
09ICU Multi-Organ Support
IX · Overnight · respiratory failure
Severe Falciparum Malaria10 / 18
Ventilator data.
0.70
FiO₂
12
PEEP cmH₂O
110
P/F ratio
P/F ratio · first 24 hBerlin threshold for severe ARDS = 100
Malaria-ARDS — why
Sequestration — parasitised RBCs adhere to pulmonary endothelium → microvascular obstruction
Cytokine storm — TNF-α, IL-1, IL-6 → alveolar capillary leak
Paradox after treatment — ARDS often worsens 24–48 h post-artesunate (parasite lysis)
Conservative fluids — aggressive resus worsens oedema (FEAST)
Prone if P/F <150 for ≥12 h — standard ARDS bundle
ECMO — last resort for refractory ARDS
★ Distinction point
ARDS often worsens after artesunate initiation. This is expected — parasite lysis releases inflammatory mediators. Continue treatment; escalate respiratory support.
CICM Fellowship Masterclass · 2026Dr Timothy Chimunda FCICM
10Ventilator Data (ARDS)
X · Day 2 · Renal failure
Severe Falciparum Malaria11 / 18
Creatinine trajectory.
Creatinine µmol/LCRRT commenced Day 2
186
Day 0
298
Day 1
442
Day 2 — peak
Examiner traps
⚠ Trap 1 — Exchange transfusion
No routine role. WHO and CDC do not recommend it. Riddle 2002 meta-analysis: no mortality benefit. Candidates who advocate it lose marks.
⚠ Trap 2 — Recurrent hypoglycaemia
Parasites consume glucose · reduced gluconeogenesis · quinine stimulates insulin. Hourly glucose is mandatory.
⚠ Trap 3 — Steroids in cerebral malaria
SNAP trial (1982): dexamethasone increased coma duration and GI complications. Never use.
CICM Fellowship Masterclass · 2026Dr Timothy Chimunda FCICM
11Creatinine Trajectory
XI · Day 4 · Apparent recovery
Severe Falciparum Malaria12 / 18
The patient wakes.
0%
Parasitaemia
15
GCS
Extubated
Status
285
Creatinine
Patient says: "I feel well. Can I go home?"
★ Distinction territory
Delayed post-artesunate haemolysis.
Volunteering this in a viva impresses examiners — most candidates omit it entirely.
Timing1–3 weeks after IV artesunate completion
MechanismSpleen pits ring stages → parasitised RBCs re-enter circulation → later haemolysed
IncidenceUp to 25% with hyperparasitaemia (>10% RBCs)
FeaturesFalling Hb · jaundice · dark urine · ↑ LDH · ↑ bilirubin · ↑ reticulocytes
MonitoringWeekly FBC · LDH · bilirubin · reticulocytes × 4 weeks
ManagementSupportive — transfuse if Hb <70 g/L or symptomatic
CICM Fellowship Masterclass · 2026Dr Timothy Chimunda FCICM
12Recovery + Delayed Haem.
XIII · Critical appraisal — what does the evidence actually say?
Severe Falciparum Malaria13 / 18
The trials we quote — and their limits.
SEAQUAMAT
2005
1,461 adults (SE Asia)
Artesunate ↓ mortality 35% vs quinine (15% vs 22%)
RCT · open-label · single-region
AQUAMAT
2010
5,425 children (Africa)
Artesunate ↓ mortality 22.5% RRR (8.5% vs 10.9%)
RCT · large · external validity strong
FEAST
2011
3,141 children (Africa)
Fluid boluses ↑ 48-h mortality (RR 1.45)
RCT · resource-limited · no ICU access
Cochrane '14
2014
8 RCTs · 1,938 pts
Exchange transfusion: no mortality benefit
Meta-analysis · heterogeneous · old data
Warrell SNAP
1982
100 cerebral malaria
Dexamethasone prolonged coma, no survival benefit
Small RCT · never repeated · still cited
Bottom line
Artesunate is the only intervention with high-quality mortality evidence in severe malaria. Most other ICU practices — fluids, RRT timing, ventilation strategy, exchange transfusion — are extrapolated from sepsis/ARDS literature, not malaria-specific RCTs.
CICM Fellowship Masterclass · 2026Dr Timothy Chimunda FCICM
13Critical Appraisal · Evidence
XIV · Critical appraisal — practices worth questioning
Severe Falciparum Malaria14 / 18
Controversies & low-value practices.
Exchange transfusion
Not recommended
Practice: Sometimes offered for parasitaemia >30%
Riddle 2002 meta + WHO 2024: no mortality benefit; resource-intensive; harms (line, transfusion, delay to artesunate).
Adjunctive steroids
Contraindicated
Practice: Tempting in cerebral malaria
Warrell 1982 SNAP: prolonged coma. No subsequent RCT has reversed this — practice persists by default, not evidence.
Liberal fluid resuscitation
Harmful
Practice: Reflex sepsis-style 30 mL/kg bolus
FEAST signal + pulmonary capillary leak in malaria. Use small aliquots, lactate trends, dynamic measures.
Early CRRT
Reasonable
Practice: Initiate on AKI + acidosis or K⁺ >6
No malaria-specific trial. STARRT-AKI/AKIKI suggest no benefit to 'very early' RRT — use standard ICU triggers.
Prone + low-VT ventilation
Apply by analogy
Practice: Standard ARDS bundle if P/F <150
PROSEVA/ARMA enrolled few malaria patients — extrapolation is defensible but not RCT-proven in this population.
Primaquine for radical cure
Don't forget G6PD
Practice: P. vivax/ovale only — not falciparum
Falciparum has no hypnozoite stage — primaquine adds nothing and risks haemolysis if G6PD-deficient.
CICM Fellowship Masterclass · 2026Dr Timothy Chimunda FCICM
14Critical Appraisal · Controversies
XV · Critical appraisal — what we still don't know
Severe Falciparum Malaria15 / 18
Evidence gaps & where the field is moving.
No adult RCT in HIC ICUs
AQUAMAT/SEAQUAMAT enrolled SE Asian/African populations. Extrapolation to ventilated, RRT-supported HIC patients is implicit.
Optimal artesunate dosing
2.4 mg/kg fixed dose may under-dose obese patients and small children. Pop-PK suggests weight-banded regimens — not yet adopted.
Delayed post-artesunate haemolysis
Mechanism (pitting of once-infected RBCs) understood; predictors and prophylaxis not. No trial of prophylactic transfusion vs surveillance.
CRRT vs IHD timing
No malaria-specific data. Practice extrapolated from septic AKI trials with different physiology (haemoglobinuria, intravascular haemolysis).
Resistance surveillance
Kelch13 mutations now in East Africa (Uganda, Rwanda). Artesunate monotherapy failure rates rising — combination ACTs essential post-IV phase.
Adjunctive therapies
Statins, NO donors, sevuparin, rosiglitazone — all phase II signals, no phase III. Active area; nothing ready for the bedside.
Examiner framing
"Demonstrate that you can cite the trial, name its limitation, and defend your bedside choice when the evidence is thin."
— how distinction candidates are separated from pass candidates.
Three sentences that score
  1. "The mortality evidence rests on AQUAMAT and SEAQUAMAT — both open-label, both outside HIC ICUs."
  2. "FEAST cannot be applied verbatim to a ventilated adult, but the signal of harm from reflex bolusing is real."
  3. "For exchange transfusion and steroids, absence of benefit in available trials outweighs mechanistic appeal."
Critical appraisal isn't a separate section of the viva — it's the texture of every good answer.
CICM Fellowship Masterclass · 2026Dr Timothy Chimunda FCICM
15Critical Appraisal · Gaps
XVI · Fellowship viva — rapid-fire
Severe Falciparum Malaria16 / 18
Click each card
for the model answer.
8 stations · 90 s each
01Thick vs thin blood films+
02WHO criteria for severe malaria+
03Management of cerebral malaria+
04Why ARDS worsens after treatment+
05Management of shock+
06Delayed haemolysis+
07Exchange transfusion — not recommended+
08IV → oral transition+
CICM Fellowship Masterclass · 2026Dr Timothy Chimunda FCICM
16Viva Stations
XVII · CICM examiner pearls
Severe Falciparum Malaria17 / 18
Top 10 — what the
examiners want.
#1
Never delay artesunate
Start immediately — don't wait for species ID
#2
Films are gold standard
Thick + thin · ×3 · 12 h apart
#3
Severe = organ dysfunction
WHO criteria verbatim — not just parasitaemia
#4
Early airway control
GCS ≤8 → RSI and intubate
#5
Conservative fluids
FEAST trial — boluses increase mortality
#6
Repeat parasite counts
12-hourly until clearance confirmed
#7
Hourly glucose
Mandatory throughout ICU admission
#8
MOF = ICU syndromes
Ventilate · CRRT · vasopressors
#9
Exchange Tx — not routine
No evidence · will cost marks
#10
Delayed haemolysis
4-week monitoring post-artesunate
CICM Fellowship Masterclass · 2026Dr Timothy Chimunda FCICM
17Top 10 Pearls
XVIII · Take-home messages
Severe Falciparum Malaria18 / 18
What matters.
01
Think malaria
Every febrile returned traveller — especially sub-Saharan Africa
02
Diagnose rapidly
Thick/thin films · RDT · PCR — treat on strong clinical suspicion
03
Start artesunate immediately
Do not delay. Do not use quinine first-line.
04
Organ support saves lives
ICU management prevents death — the drug clears the parasite
05
Recovery ≠ discharge
Monitor delayed haemolysis × 4 weeks post-artesunate
Key references
AQUAMATDondorp et al. Lancet 2010;376:1647–57 — artesunate vs quinine
SEAQUAMATDondorp et al. Lancet 2005;366:717–25 — first adult evidence
WHO 2024Living guideline — current treatment recommendations
FEASTMaitland et al. NEJM 2011;364:2483–95 — fluid bolus harm
Marks et al.Br J Anaesth 2014;113(6):910–921 — managing malaria in ICU
Riddle et al.Clin Infect Dis 2002;34:1192–8 — exchange transfusion meta
Presenter
Dr Timothy Chimunda FCICM
Clinical Director ICU · NWRH  ·  Innovate Critical Care Consultancy
CICM Fellowship Masterclass · 2026Dr Timothy Chimunda FCICM
18Take-Home + References