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CARDIOVASCULAR JOURNAL OF AFRICA • Volume 30, No 1, January/February 2019

AFRICA

63

variables that correlatewith right heart haemodynamics, including

an estimate of right ventricular systolic pressure (RVSP), and can

simultaneously uncover functional and morphological cardiac

sequelae of PH, and assist in the identification of possible

cardiac causes of PH.

The Doppler echo estimation of RVSP (Fig. 3A) is based on

the peak velocity of the jet of tricuspid regurgitation (TR). TR

velocity can be obtained by either a duplex imaging from the

right ventricular inflow view, parasternal short-axis view at the

basal level, para-apical four-chamber view, apical four-chamber

view, or even the subcostal view. The TR maximal instantaneous

gradient (TR MIG) is frequently automatically calculated and

displayed on the screen (Fig. 3A) when the maximal TR velocity

is measured. Otherwise it is easily calculated using the simplified

Bernoulli equation:

12

TR MIG

=

4 (TR velocity)²

Fig. 2.

Chest X-ray and electrocardiogram in pulmonary

hypertension in sub-Saharan Africa. (A) Postero-

anterior chest X-ray in a 51-year-old HIV-positive

patient on antiretroviral therapy and with a past history

of diabetes and one episode of TB, who presented

with dyspnoea. CXR showing no signs of chronic lung

disease, but combined heart enlargement and hilar

pulmonary artery prominence. (B) ECG of a different

patient showing sinus tachycardia, right atrial enlarge-

ment, right ventricular hypertrophy and strain, and

right-axis deviation of the QRS complex. Courtesy of

the PAPUCO investigators group.

A

B

Step 1: clinical examination

Symptoms, signs and

medical history suggestive

of PH

Clinical examination

supportive of PH

Step 2: chest X-ray

and ECG

Search for other causes,

e.g. TB, PCP, COPD, LHD,

malignancy

Chest X-ray and ECG

supportive of PH

Step 4:

CTPA,

V/Q scan

Step 3: Doppler echo

Group 5

Multifactorial

e.g. endo-

myocardial

fibrosis, sickle

cell disease

Group 4

CTEPH

Group 2

PH due to left

heart disease:

e.g. mitral

stenosis

due to RHD,

hypertensive

heart failure,

valvular disease,

coronary artery

disease

Group 3

PH due to lung

disease:

e.g. COPD,

post-TB

bronchiectasis,

interstitial lung

disease

Step 4: liver-

function test,

HRCT

Group 1

Pulmonary

arterial

hypertension

(PAH): e.g.

HIV-PAH,

schistosomiasis,

drugs/toxins

Step 4: HIV

testing, urine

screen, abdominal

US, drug screen

Step 4: consider common

causes of PH in Africa

Doppler echo

supportive of PH

YES

YES

YES

NO

NO

NO

Probably less

common

Fig. 1.

Diagnostic algorithm to diagnose pulmonary hyperten-

sion due to left heart disease in low-resource settings,

as evidenced from the PAPUCO study. PH, pulmo-

nary hypertension; TB, tuberculosis; PCP, pneumo-

cystis pneumonia; COPD, chronic obstructive pulmo-

nary disease; LHD, left heart disease; Doppler echo,

Doppler echocardiography; US, ultrasound; LFT, liver-

function tests; HRCT, high-resolution computerised

tomography; CTEPH, chronic thromboembolic pulmo-

nary hypertension; CTPA, CT pulmonary angiography;

V/Q, ventilation/perfusion lung scan.