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New	Zealand	Obstetric	Doppler	Guideline,	NZMFMN	,	revised	September	2014,	Page	1																				
	
NEW	ZEALAND	OBSTETRIC	DOPPLER	GUIDELINE	
	
	
This	is	a	New	Zealand	guideline	for	the	performance	of	obstetric	Doppler	examinations.	The	guideline	incorporates	detailed	notes	
on	correct	Doppler	technique,	interpretation	and	reference	charts	for	each	of	commonly	used	obstetric	Doppler	examinations.	All	
health	practitioners	involved	in	the	performance	and	interpretation	of	obstetric	ultrasound	examinations	are	encouraged	to	use	
this	document	and	incorporate	the	principles	and	reference	values	into	their	clinical	practice.		
	
Unaltered	copies	of	this	guideline	may	be	freely	reproduced	and	distributed.	
	
Contributors:	Martin	Necas,	Dr	Emma	Parry,	Professor	Lesley	McCowan
New	Zealand	Obstetric	Doppler	Guideline,	NZMFMN	,	revised	September	2014,	Page	2																				
Which	Doppler	Test	When?		
	
SGA	or	IUGR Umbilical	artery	PI
+	
	Mean	uterine	artery	PI		
at	time	of	diagnossi	(once)
Umbilical	artery	PI	raised Add	MCA	PI	+	CPR
Same	day	referral	
to	specialist
Add	MCA	PI	+	CPR
Specialist	review	
now
Absent	or	reversed		
end-diastolic	flow	
Normal	>	34	weeks Add	MCA	PI	+	CPR
Normal	<	34	weeks
Specialist	review	
in	1-2	weeks
At	risk	of	early	onset	maternal	
hypertensive	disorder	or	SGA
Mean	uterine	artery	PI	at		
20	or	24	weeks	
Suspected	fetal	anaemia MCA	PSV
MCDA	Twins No	evidence	of	TTTS
Both	twins:
UA	PI	from	16	weeks	+	
MCA	PSV	from	24	weeks
Both	twins:
UA	PI	,	MCA	PI,	MCA	PSV,	DV	PI
TTTS
New	Zealand	Obstetric	Doppler	Guideline,	NZMFMN	,	revised	September	2014,	Page	3																				
Umbilical	Artery	Pulsatility	Index	(UA	PI)		
Indications:		
§ Suspected	or	known	small	for	gestational	age	(SGA)	fetus	
§ The	estimated	fetal	weight	on	the	GROW	chart	is	<10
th
	percentile	
§ The	estimated	fetal	weight	on	the	GROW	chart	is	dropping	percentiles	by	≥30%	
§ The	abdominal	circumference	on	the	population	scan	chart	is	<	5
th
	percentile	
§ Discrepancy	(≥30%)between	the	head	and	abdominal	circumference	percentile	with	lower	AC	percentile	
§ Maternal	hypertensive	disorders	e.g.	preeclampsia	
§ Decreased	fetal	movements	
Not	indicated:		
§ Routine	screening	of	normal	pregnancies	with	no	maternal	or	fetal	risk	factors	
How	to	perform	the	test:	
§ Perform	assessment	during	fetal	quiescence	
§ Always	keep	TIb<0.5	if	possible	or	at	least	<1	by	reducing	the	acoustic	output	power	
§ Identify	a	free	loop	of	umbilical	cord	on	color	Doppler	
§ Use	high	color	PRF	to	avoid	aliasing	and	conservative	gain	to	avoid	color	bleeding	
§ Position	the	sample	volume	in	a	portion	of	the	cord	coursing	parallel	to	Doppler	beam		
§ Avoid	sampling	in	such	a	way	that	the	Doppler	beam	is	directed	towards	fetal	eyes	
§ Optimise	the	spectral	Doppler	baseline,	PRF	and	sweep	speed	to	get	a	large	waveform	
§ If	the	EDV	is	near	the	baseline,	ensure	wall	filter	is	sufficiently	low	to	display	EDV	
§ If	the	PI	is	within	normal	range,	only	sample	one	of	the	umbilical	arteries	
§ If	the	PI	is	abnormal,	sample	both	umbilical	arteries	and	use	the	more	normal	(lower)	value	
§ If	the	end-diastolic	flow	is	absent	or	reversed,	comment	on	this	finding	in	the	report		
How	to	interpret	the	test:	
§ >95
th
	percentile	is	abnormal	
Common	pitfalls:	
§ Poor	Doppler	angle	and	poor	optimisation	leading	to	fuzzy	waveform	which	is	hard	to	measure	
§ End-diastolic	flow	is	not	visualised	due	to	high	filter	setting	
§ End-diastole	is	not	well	visualised	when	EDV	is	near	baseline	because	of	venous	contamination	-	
readjust	sampling	to	avoid	capturing	adjacent	UV	
Reference:	Ebbing,	C.,	Rasmussen,	S.,	&	Kiserud,	T.	Middle	cerebral	artery	blood	flow	velocities	
and	pulsatility	index	and	the	cerebroplacental	pulsatility	ratio:	longitudinal	reference	ranges	
and	terms	for	serial	measurements.	Ultrasound	Obstet	Gynecol,	2007.	30(3):	p.	287-96.
New	Zealand	Obstetric	Doppler	Guideline,	NZMFMN	,	revised	September	2014,	Page	4																				
	
	
Middle	Cerebral	Artery	Pulsatility	Index	(MCA	PI)		
Indications:	
§ SGA	with	abnormal	UA	PI	at	any	gestational	age	
§ SGA	with	normal	UA	PI	after	34	weeks	gestational	age	
§ MCDA	twin	gestation	with	TTTS	
How	to	perform	the	test:	
§ Perform	assessment	during	fetal	quiescence	
§ Always	keep	TIb<0.5	if	possible	or	at	least	<1	by	reducing	the	acoustic	output	power	
§ Start	with	the	BPD	view	
§ Move	caudally	to	visualise	the	butterfly	shape	of	suprasellar	cisterns	and	the	sphenoid	
§ Use	the	coronal	suture/sphenoidal	fontanelle	as	an	acoustic	window	
§ Use	high	definition	(write)	zoom	
§ Activate	color	Doppler	to	visualise	the	MCA	
§ Assess	the	MCA	which	is	closer	to	the	transducer		
§ Move	anteriorly	and	angle	back	to	align	the	MCA	flow	direction	with	the	Doppler	beam		
§ Position	a	small	(0.5-1mm)	sample	volume	2mm	beyond	from	the	MCA	origin	
§ Optimise	the	spectral	Doppler	baseline	and	PRF	to	get	a	large	waveform	
How	to	interpret	the	test:	
§ <5
th
	percentile	is	abnormal	
Common	pitfalls:	
§ Poor	Doppler	angle	and	poor	optimisation	leading	to	fuzzy	waveform	which	is	hard	to	measure	
§ Gate	too	close	to	MCA	origin	where	multidirectional	contamination	from	ACA	and	PCoA	occurs	
§ Sample	positioned	too	peripherally	in	the	MCA	where	velocities	fall		
§ PCA	misidentified	as	MCA	
§ Poor	visualisation	due	to	inadequate	zoom	
Reference:	Ebbing,	C.,	Rasmussen,	S.,	&	Kiserud,	T.	Middle	cerebral	artery	blood	flow	velocities	
and	pulsatility	index	and	the	cerebroplacental	pulsatility	ratio:	longitudinal	reference	ranges	
and	terms	for	serial	measurements.	Ultrasound	Obstet	Gynecol,	2007.	30(3):	p.	287-96.
New	Zealand	Obstetric	Doppler	Guideline,	NZMFMN	,	revised	September	2014,	Page	5																				
	
	
Cerebroplacental	Ratio	(CPR)		
Indications:		
§ If	MCA	PI	assessment	was	performed,	the	CPR	should	be	calculated	and	recorded	
How	to	calculate	CPR:		
§ The	CPR	is	defined	the	ratio	of	MCA	PI	and	UA	PI	
How	to	interpret	the	test:	
§ <5
th
	percentile	is	abnormal	
§ Note:	It	can	be	helpful	to	plot	the	MCA	and	CPR	results	on	serial	assessments	to		
determine	the	trend	
	
Reference:	Ebbing,	C.,	Rasmussen,	S.,	&	Kiserud,	T.	Middle	cerebral	artery	blood	flow	velocities	
and	pulsatility	index	and	the	cerebroplacental	pulsatility	ratio:	longitudinal	reference	ranges	
and	terms	for	serial	measurements.	Ultrasound	Obstet	Gynecol,	2007.	30(3):	p.	287-96.
New	Zealand	Obstetric	Doppler	Guideline,	NZMFMN	,	revised	September	2014,	Page	6																				
Ductus	Venosus	Pulsatility	Index	(DV	PI)		
Indications:		
§ Markedly	raised	UA	PI	(>>95
th
	)	and	reduced	MCA	PI	in	preterm	SGA	
§ MCDA	twin	gestation	with	TTTS	or	selective	IUGR	
How	to	perform	the	test:		
§ Perform	assessment	during	fetal	quiescence	
§ Always	keep	TIb<0.5	if	possible	or	at	least	<1	by	reducing	the	acoustic	output	power		
§ Sagittal	and	transverse	approaches	are	acceptable	as	long	as	Doppler	angle	is	0-60	degrees	
§ Activate	color	Doppler	to	identify	DV	at	the	end	of	UV	
§ Enlarge	the	image	
§ 0.5-1mm	gate	placed	in	the	inlet	of	DV	
§ Set	wall	filter	low,	sweep	speed	high	
§ Optimise	the	spectral	Doppler	baseline	and	PRF	to	get	a	large	waveform	
§ If	PI>95
th
	percentile,	assess	umbilical	vein	for	pulsatility	
How	to	interpret	the	test:	
§ >95
th
	percentile	is	abnormal	
Common	Pitfalls	
§ Color	PRF	too	low	and	gain	too	high	leading	to	difficulty	in	DV	identification	amongst	other	vessels		
§ Sample	size	too	large,	leading	to	contamination	from	other	vessels	
§ Sample	not	placed	at	the	inlet	of	the	DV	
§ Adjacent	hepatic	vein	or	celiac	axis	misidentified	as	DV	
§ Poor	Doppler	angle	and	poor	optimisation	leading	to	fuzzy	waveform	which	is	hard	to	measure	
§ Fetal	breathing	activity	may	result	in	false	impression	of	absent	A	wave	
Reference:	Kessler,	J.,	Rasmussen,	S.,	Hnson,	M.,	&	Kiserud,	T.	Longitudinal	reference	ranges	for	ductus	
venosus	flow	velocities	and	waveform	indices.	Ultrasound	Obstet	Gynecol,	2006.	28:	890-898.
New	Zealand	Obstetric	Doppler	Guideline,	NZMFMN	,	revised	September	2014,	Page	7																				
MCA	Peak	Systolic	Velocity	(MCA	PSV)	
Indications:	
§ Maternal-fetal	isoimmunisation	
§ Any	suspicion	of	fetal	anaemia	
§ Unexplained	hydrops	
§ MCDA	twins	>24	weeks	gestational	age	
§ MCDA	twins	with	known	or	suspected	of	TTTS	or	TAPS	
How	to	do	perform	the	test:	
§ Perform	assessment	during	fetal	quiescence	
§ Always	keep	TIb<0.5	if	possible	or	at	least	<1	by	reducing	the	acoustic	output	power	when	required	
§ Start	with	the	BPD	view	
§ Move	caudally	to	visualise	the	butterfly	shape	of	suprasellar	cisterns	and	the	sphenoid	
§ Use	the	coronal	suture/sphenoidal	fontanelle	as	an	acoustic	window	
§ Use	high	definition	(write)	zoom	
§ Activate	color	Doppler	to	visualise	the	MCA	and	assess	the	MCA	which	is	closer	to	the	transducer		
§ Move	anteriorly	and	angle	back	to	align	the	MCA	flow	direction	with	the	Doppler	beam	
§ Ideal	interrogation	angle	is	0	degrees	but	30	degrees	or	less	is	acceptable	
§ Position	a	small	(0.5-1mm)	sample	volume	2	mm	beyond	from	the	MCA	origin	
§ Optimise	the	spectral	Doppler	baseline	and	PRF	to	get	a	large	waveform	
§ If	the	Doppler	angle	is	not	zero,	angle	correction	must	be	used	
§ If	PSV>1.5	multiples	of	the	median	(MoM),	obtain	3	high	quality	samples	and	use	the	highest	value	
How	to	interpret	the	test:	
§ >1.5MoM	is	abnormal	
Common	Pitfalls:	
§ Poor	Doppler	angle	and	poor	optimisation	leading	to	fuzzy	waveform	which	is	hard	to	measure	
§ Gate	too	close	to	MCA	origin	where	multidirectional	contamination	from	ACA	and	PCoA	occurs	
§ Sample	positioned	too	peripherally	in	the	MCA	where	velocities	fall	
§ PCA	misidentified	as	MCA	
§ Failure	to	angle-correct	at	angles	other	than	0	leading	to	underestimation	of	PSV	
§ Poor	visualisation	due	to	inadequate	zoom	 References:		
Mari,	G.	Noninvasive	Diagnosis	by	Doppler	ultrasonography	of	fetal	anemia	due	to	maternal	red-cell	alloimmunization.	N	Engl	J	Med	2000;	342:9-14,	p	9-14.	
Mari,	G.	Middle	cerebral	artery	peak	systolic	velocity	for	the	diagnosis	of	fetal	anemia:	the	untold	story.	Ultrasound	Obstet	Gynecol	2005	Apr;25(4):323-30.
New	Zealand	Obstetric	Doppler	Guideline,	NZMFMN	,	revised	September	2014,	Page	8																				
Mean	uterine	Artery	Pulsatility	Index	
Indications:		
§ Screen	patients	at	high	risk	of	early	preeclampsia	or	early	SGA	at	20	or	24	weeks	
§ If	abnormal	at	20	weeks,	repeat	at	24	weeks		
§ Early	onset	IUGR	
§ Current	hypertensive	disorder	in	pregnancy	
§ Full	assessment	of	suspected	SGA	pregnancy	
How	to	perform	the	test:	
§ Locate	the	maternal	anterior	superior	iliac	spine	and	angle	medially		
§ Alternatively	visualize	the	external	iliac	artery	(EIA)	
§ The	uterine	artery	is	typically	seen	crossing	the	EIA	anteriorly	
§ Select	a	portion	of	the	uterine	artery	which	courses	at	a	favourable	Doppler	angle	0-60	degrees	
§ Optimise	the	spectral	Doppler	baseline	and	PRF	to	get	a	large	waveform	
§ Measure	the	right	and	left	PI	and	calculate	the	mean	value	
How	to	interpret	the	test:	
§ >95
th
	percentile	is	abnormal	
§ Bilateral	notching	after	24	weeks	is	abnormal	
Common	Pitfalls:	
§ Failure	to	identify	the	uterine	artery	by	not	scanning	inferiorly	enough		
	
Reference:	
Gomez	O.,	et	al.	Reference	ranges	for	uterine	mean	pulsatility	index	at	11-
41	weeks	of	gestation.	Ultrasound	Obstet	Gynecol	2008;	32:	128-132.
New	Zealand	Obstetric	Doppler	Guideline,	NZMFMN	,	revised	September	2014,	Page	9																				
Quick	Reference	Tables	
	
	 Umbilical	Artery	PI	v
	 	 MCA	PI	v
	 	
	
Cerebroplacental	Ratio	
(CPR)	v
	
	 Mean	Uterine	Artery	PI	ö
	
	 	 	 	 	 CPR	=	MCA	PI/UA	PI	 	 Mean	PI=(RT	PI	+	LT	PI)/2	
	 >95
th
	percentile	is	abnormal	 	 <5
th
	percentile	is	abnormal	 	 <5
th
	percentile	is	abnormal	 	 >95
th
	percentile	is	abnormal	
	 	 	 	 	 	 	 	
Gestation	
Weeks	
50
th
		
percentile	
95
th
		
percentile	
	 50
th
	
percentile	
5th		
percentile	
	 50
th
	
percentile	
5th		
percentile	
	 50
th
	
percentile	
95th		
percentile	
18	 	 	 	 	 	 	 	 	 	 1.20	 1.79	
19	 1.25Ô
	 1.63Ô
	 	 	 	 	 	 	 	 1.15	 1.70	
20	 1.22Ô
	 1.59Ô
	 	 	 	 	 	 	 	 1.10	 1.61	
21	 1.15	 1.46	 	 	 	 	 	 	 	 1.05	 1.54	
22	 1.13	 1.43	 	 	 	 	 	 	 	 1.00	 1.47	
23	 1.10	 1.40	 	 	 	 	 	 	 	 0.96	 1.41	
24	 1.08	 1.38	 	 1.86	 1.38	 	 1.74	 1.16	 	 0.93	 1.35	
25	 1.06	 1.35	 	 1.94	 1.44	 	 1.85	 1.24	 	 0.89	 1.30	
26	 1.04	 1.33	 	 2.01	 1.50	 	 1.95	 1.32	 	 0.86	 1.25	
27	 1.02	 1.31	 	 2.06	 1.55	 	 2.05	 1.40	 	 0.84	 1.21	
28	 1.00	 1.28	 	 2.11	 1.58	 	 2.14	 1.47	 	 0.81	 1.17	
29	 0.98	 1.26	 	 2.15	 1.61	 	 2.21	 1.53	 	 0.79	 1.13	
30	 0.96	 1.24	 	 2.16	 1.62	 	 2.28	 1.58	 	 0.77	 1.10	
31	 0.94	 1.21	 	 2.16	 1.62	 	 2.32	 1.62	 	 0.75	 1.06	
32	 0.92	 1.19	 	 2.14	 1.61	 	 2.35	 1.64	 	 0.73	 1.04	
33	 0.90	 1.16	 	 2.10	 1.58	 	 2.36	 1.65	 	 0.71	 1.01	
34	 0.88	 1.14	 	 2.04	 1.53	 	 2.35	 1.63	 	 0.70	 0.99	
35	 0.86	 1.11	 	 1.96	 1.47	 	 2.32	 1.60	 	 0.69	 0.97	
36	 0.84	 1.09	 	 1.86	 1.39	 	 2.27	 1.55	 	 0.68	 0.95	
37	 0.81	 1.06	 	 1.75	 1.30	 	 2.19	 1.48	 	 0.67	 0.94	
38	 0.79	 1.03	 	 1.63	 1.20	 	 2.09	 1.40	 	 0.66	 0.92	
39	 0.77	 1.00	 	 1.49	 1.10	 	 1.97	 1.29	 	 0.65	 0.91	
40	 0.75Ô
	 1.07Ô
	 	 1.29ø
	 1.02ø
	 	 1.80ø
	 1.24ø
	 	 0.65	 0.90	
References:		
Ô	
Acharya	G,	et	al.	Reference	ranges	for	serial	measurements	of	blood	velocity	and	pulsatility	index	at	the	intra-abdominal	portion,	and	fetal	and			
				placental	ends	of	umbilical	artery.	Ultrasound	Obstet	Gynecol	2005;	26:162-169.
v
Ebbing,	C.,	Rasmussen,	S.,	&	Kiserud,	T.	Middle	cerebral	artery	blood	flow	velocities	and	pulsatility	index	and	the	cerebroplacental	pulsatility			
				ratio:	longitudinal	reference	ranges	and	terms	for	serial	measurements.	Ultrasound	Obstet	Gynecol,	2007.	30(3):	p.	287-96.	
ø
		Baschat	AA,	Gembruch	U.	The	cerebroplacental	Doppler	ratio	revisited.	Ultrasound	Obstet	Gynecol	2003;	21:124-127.	
ö	
Gomez	O,	et	al.	Reference	ranges	for	uterine	mean	pulsatility	index	at	11-41	weeks	of	gestation.	Ultrasound	Obstet	Gynecol	2008;	32:	128-132.
New	Zealand	Obstetric	Doppler	Guideline,	NZMFMN	,	revised	September	2014,	Page	10																				
Obstetric	Doppler	reference	charts
New	Zealand	Obstetric	Doppler	Guideline,	NZMFMN	,	revised	September	2014,	Page	11																				
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
Reference:	Ebbing,	C.,	Rasmussen,	S.,	&	Kiserud,	T.	Middle	cerebral	artery	blood	flow	velocities	and	pulsatility	index	and	the	cerebroplacental	pulsatility	ratio:		
longitudinal	reference	ranges	and	terms	for	serial	measurements.	Ultrasound	Obstet	Gynecol,	2007.	30(3):	p.	287-96.
New	Zealand	Obstetric	Doppler	Guideline,	NZMFMN	,	revised	September	2014,	Page	12																				
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
Reference:	Ebbing,	C.,	Rasmussen,	S.,	&	Kiserud,	T.	Middle	cerebral	artery	blood	flow	velocities	and	pulsatility	index	and	the	cerebroplacental	pulsatility:	
longitudinal	reference	ranges	and	terms	for	serial	measurements.	Ultrasound	Obstet	Gynecol,	2007.	30(3):	p.	287-96.
New	Zealand	Obstetric	Doppler	Guideline,	NZMFMN	,	revised	September	2014,	Page	13																				
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
Reference:	Ebbing,	C.,	Rasmussen,	S.,	&	Kiserud,	T.	Middle	cerebral	artery	blood	flow	velocities	and	pulsatility	index	and	the	cerebroplacental	pulsatiliy	ratio:		
longitudinal	reference	ranges	and	terms	for	serial	measurements.	Ultrasound	Obstet	Gynecol,	2007.	30(3):	p.	287-96.
New	Zealand	Obstetric	Doppler	Guideline,	NZMFMN	,	revised	September	2014,	Page	14																				
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
Reference:	Gomez	O.,	et	al.	Reference	ranges	for	uterine	mean	pulsatility	index	at	11-41	weeks	of	gestation.	Ultrasound	Obstet	Gynecol	2008;	32:	128-132.
New	Zealand	Obstetric	Doppler	Guideline,	NZMFMN	,	revised	September	2014,	Page	15																				
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
Reference:	Kessler,	J.,	Rasmussen,	S.,	Hnson,	M.,	&	Kiserud,	T.	Longitudinal	reference	ranges	for	ductus	venosus	flow	velocities	and	waveform	indices.	Ultrasound	Obstet	Gynecol,	2006.	28:	890-898.
New	Zealand	Obstetric	Doppler	Guideline,	NZMFMN	,	revised	September	2014,	Page	16																				
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
	
References:	Mari,	G.	Noninvasive	Diagnosis	by	Doppler	ultrasonography	of	fetal	anemia	due	to	maternal	red-cell	alloimmunization.	N	Engl	J	Med	2000;	342:9-14,	p	9-14.	
Mari,	G.	Middle	cerebral	artery	peak	systolic	velocity	for	the	diagnosis	of	fetal	anemia:	the	untold	story.	Ultrasound	Obstet	Gynecol	2005	Apr;25(4):323-30.

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