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Patient Demographics Referred by:

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Presentation on theme: "Patient Demographics Referred by:"— Presentation transcript:

1 Patient Demographics Referred by:
ILD MDM Toolkit Patient Demographics Referred by: History of Presenting Complaint Referral diagnosis: Background: Medications: Social History: Exposures: Family History: Three Clinical Slide Format - Royal Alfred Hospital, Sydney

2 Patient Demographics Prior Investigation: Prior Management: Date FEV1
FVC DLCO KCO TLC Date 6MWT distance Distance (m) SpO2 initial SpO2 lowest Three Clinical Slide Format - Royal Alfred Hospital, Sydney Slide 2

3 Patient Demographics Clinical Diagnosis: Management Plan:
Three Clinical Slide Format - Royal Alfred Hospital, Sydney Slide 3

4 Common diagnostic terms Acronym
Consensus diagnosis Research terminology Diagnostic confidence Differential diagnosis Disease behaviour Suggested management & therapeutic goal Common diagnostic terms Acronym Idiopathic pulmonary fibrosis IPF Non-specific interstitial pneumonitis NSIP Cryptogenic organising pneumonia COP Desquamative interstitial pneumonia DIP Respiratory bronchiolitis-interstitial lung disease RB-ILD Pleuro-parenchymal fibroelastosis PPFE Lymphoid interstitial pneumonia LIP Acute interstitial pneumonia AIP Unclassifiable interstitial pneumonia, [state if provisional] Connective tissue disease related interstitial lung disease, [include histological subtype & connective tissue disease] CTD-ILD Hypersensitivity pneumonitis [acute, chronic] [A/C]HP Eosinophilic pneumonia [acute, chronic] [A/C]EP Langerhans cell histiocytosis LCH Pulmonary lymphangioleiomyomatosis PLAM Common diagnostic terms (cont.) Acronym Sarcoidosis, [specify organ involvement] Dust induced disease, [specify dust] Drug induced lung disease, [specify drug] Pulmonary vasculitis, [specify subtype] Pulmonary alveolar proteinosis Primary pulmonary haemosiderosis Primary alveolar microlithiasis Diagnostic confidence Likelihood Confident ≥90% Provisional, high confidence 70-89% Provisional, low confidence 51-69% Unclassifiable ILD ≤50% Disease behaviour Reversible and self-limited Reversible disease with risk of progression Stable with residual disease Progressive, irreversible disease with potential for stabilization Progressive, irreversible disease despite therapy Notes – no title for disease behaviour Diagnostic terms go over the page - Research terminology Acronym Interstitial pneumonia with autoimmune features IPAF Combined pulmonary fibrosis and emphysema CPFE Familial ILD Smoking related ILD Suggested Therapeutic Goal Achieve regression Maintain status Slow progression Palliative/best supportive care Three Clinical Slide Format - Royal Alfred Hospital, Sydney Slide 4

5 CURRENT CLINICAL TRIALS AND RESEARCH
Project name 1 2 3 4 Agent Duration Comparator Key inclusion criteria Key exclusion criteria Primary endpoint Number participants sought Screened Enrolled Notes Contact person Three Clinical Slide Format - Royal Alfred Hospital, Sydney Slide 5


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