1. The document provides an overview of the history and development of cardiac catheterization, from the first experiments on horses in 1844 to the techniques used today.
2. It describes the key principles and procedures for performing cardiac catheterization studies, including patient preparation, accessing venous routes, transducer setup, pressure measurements, and oxygen saturation assessments to detect shunts.
3. The document emphasizes the importance of collecting all hemodynamic data in a steady state and maintaining standards to ensure accurate measurements and interpretations.
2. OBJECTIVES…
Overview of history and development
How to perform a study tailored to answer
specific clinical question
Gain better understanding of role of as a
diagnostic tool in specific situations
2
3. CLAUDE BERNARD
1844: France
1st RHC on horse
Inserted glass tubes via
jugular vein and carotid
artery
Measured temperature
in both ventricles
Later measured
intracardiac pressures
too
3Nossaman BD et al. H/o RHC: 100 years of experimentation and methodology development. Cardiol Rev 2010;18:94-101.
4. WERNER FORSSMANN
1929; Germany
Self catheterization
using urethral catheter
Used lt. anticubital
vein RV; (X-RAY)
Against medical ethics
4
Meyer JA. W Forssmann and catheterisation of the heart, 1929.
Ann Thorac Surg 1990;49:497-9
6. INTRODUCTION
Advent of non-invasive modalities (ECHO,
MRI): Cardiac catheterization reduced
Gold standard: For assessment of cardiac
hemodynamics
Resolves discrepancy b/w c/fs+ non-invasive
measurements
6
7. INTRODUCTION CONT…
Through review of clinical history, physical
exam, ECG, CXR, ECHO, MRI(+/-) before
patient enters cath lab
Why is study performed?
If results are not going to alter course of
management: Best not to perform
Have clear idea as what is the data one wishes
to seek
Wild goose chase: More questions than
answers 7
8. CONDUCT OF CATHETERIZATION STUDY
Adherence to standard protocols
Due attention to pressure recordings and
saturation assessments
Flexibility: Each case is different
8
9. PATIENT PREPARATION
Parents informed of indication and risks of
procedure
Retrospective and prospective data:
Serious adverse event: 1.1%
Mortality: 0.05%
Hoeper M et al. Complications of RHC procedures in patients with PH in experienced centers. J Am Coll Cardiol 2006;48: 2546-52
9
10. PATIENT PREPARATION CONT…
MC complications:
Access site hematoma
Vagal reaction
Pneumothorax
Arrhythmias
Quote individual/ departmental complications
10
11. PATIENT PREPARATION
Rule out anemia, infections, thrombocytopenia
Electrolyte/ metabolic disturbances
Dehydration
Digoxin toxicity
Coagulopathy
Safe in patients with INR <3.5 undergoing
RHC via IJV or anti cubital veins
Ranu H et al. A retrospective review to evaluate the safety of RHC via IJV in assessment of PH.. Clin Cardiol 2010;33: 303-6
11
12. PROTOCOL
Cath profile and PAC clearance before
admission (1 day prior)
NBM: 4 hours before
Caution: OVERZELOUS FASTING PROTOCOLS
MAY LEAD TO VOLUME DEPLETION: MAKING
CHALLENGING VENOUS ACCESS
IVFs: 1/2DNS since NMB
Blood in hand
Injection Cefazolin 30mg/kg i/v 1 hr before
procedure 12
13. VENOUS ACCESS
Route of access depends on:
Operator experience
Presence of cardiac devices and indwelling catheters
Prior h/o venous cannulation and associated
complications
FV access commonly used in children or if LHC
performed concurrently
Small studies demonstrated feasibility and
safety of RHC+LHC via ACV+ radial artery
respectively
Yang CH, Guo GB, Yip HK. Bilateral cardiac catheterizations: the safety and feasibility of a superficial forearm venous and transradial arterial
approach. Int Heart J 2006;47:21–7.
Lo TS, Buch AN, Hall IR, et al. Percutaneous left and right heart catheterization in fully anticoagulated patients utilizing the radial artery and
forearm vein: a two-center experience. J Interv Cardiol 2006;19:258–63
Gilchrist IC, Kharabsheh S, Nickolaus MJ, et al. Radial approach to right heart catheterization: early experience with a promising technique.
13
14. VENOUS ACCESS CONT…
USG guided vs landmark based:
Meta-analysis available
Clear benefit of USG for IJV cannulation
Higher success rate
Fewer complications
Faster access
Hind Daniel, Calvert Neill, McWilliams Richard, et al. Ultrasonic locating devices for central venous cannulation: meta-analysis. BMJ
2003;327:361.
Data very limited: USG for FV and SCV
cannulation
14
15. VENOUS ACCESS CONT…
Balloon flotation catheters (Swan- Ganz) :
Balloon at distal end, facilitate passage through
RH
Designed to be placed without fluoroscopy,
although screening helps (marked RH
dilatation/ severe TR)
15
16. VENOUS ACCESS CONT…
Catheter inserted into RA and balloon inflated
Catheter follows direction of blood flow towards
PAs
Advancing further should allow performer to
obtain PCWP
Important to avoid leaving balloon inflated for
longer than necessary : Risk of pulmonary
infarction/ rupture
16
17. CATHETERIZATION FROM FV
Commonly performed using multipurpose end
hole catheter using direct fluoroscopy
Requires greater manipulation than balloon
flotation catheters to navigate through RH:
Guide wire may be required to improve
steerability
MP catheters can be used to
cross directly into LA in patients
with PFO for direct pressure
17
18. PROCEDURE
Before starting: Confirm pressure transducers
are zeroed, leveled, appropriately calibrated
Establishment of “zero” value: Concept of
making hydrostatic measurements with fluid
filled systems relative to a reference value,
usually atmospheric pressure (760mm Hg),
then examining change from that value
18
19. PROCEDURE
Transducer should be placed at appropriate
level
For every 1cm above/ below LA the catheter is
referenced, the pressure measurement is
underestimated/ overestimated by??
0.74mmHg
19
21. THE CONCEPT OF PHLEBOSTATIC AXIS
Correct reference point
Midpoint b/w anterior
and posterior surfaces
of chest at 4th ICS
Essential that level of
stopcock of transducer
be at this level
All transducers must
be at this level
21
22. PRINCIPALS TO BE ADHERED TO DURING CATH
STUDY
Data to be obtained in a steady state
Essential to maintain decorum in a quiet and
calm environment
Appropriate sedation needed in case of agitated
child
Watch for over sedation: Respiratory
depression, consequently changes in sats
22
23. PRINCIPALS TO BE ADHERED TO DURING CATH
STUDY
Obtain entire data in………..??
Withdrawal pressures and saturations better
than ingoing
If sample can’t be obtained from a site due to
ventricular premature complex: Skip site until
rest of run completed
Complete hemodynamic data must be obtained
before angiograms
Obtain pressures and oxymetry samples as
close in time as possible
23
24. PRINCIPALS TO BE ADHERED TO DURING CATH
STUDY
Repeated measurements : More accurate
Record catheter course
Sat syringes not to be overheparinized, sample
gets diluted; just quote inner lining of syringe
Remove air bubbles: PO2 rises
24
25. PRINCIPALS TO BE ADHERED TO DURING CATH
STUDY
Glass syringes: Gold standard
Plastic syringes: Porous, fall in PO2
Metabolism of WBCs: Tends to fall in PO2
Measure sats <5 mins (if delay: Transfer in ice
<30 mins)
25
26. USE DEDICATED OXYMETRY MACHINE
Should be in lab
Measures directly o2 saturation using
spectrophotometry to correctly quantify oxy,
deoxy, carboxy and methHb and total Hb
Do not use ABG machines: WHY???
O2 saturation results derived from o2
dissociation curves, using PO2 values: Affected
by many factors ( Adult or fetal Hb, temp, ph,
CO2, 2,3-DPG levels)
26
27. THE ACTUAL MEASUREMENTS FOR SHUNTS
• Place catheter in PA (Swan Ganz) and pigtail in Ao
• Measure PA and Ao pressures
• Take o2 sat in PA+ Ao blood
• Enter LV by retrograde crossing of Ao valve
• Advance PA catheter to PCWP position
• Measure simultaneously LV-PCWP pressures
27
28. THE ACTUAL MEASUREMENTS FOR SHUNTS
CONT…
• Pull back from PCWP to PA
• Pull back from PA to RV for PS and record RV
pressure. Take RV sample for O2 sats
• Record simultaneous LV-RV pressure
• Pull back from RV to Rato screen for tricuspid
stenosis and record RA pressure. Take RA sample
• Take SVC+IVC samples for O2 saturations
• Pull back from LV to aorta for AS
28
29. NORMAL PRESSURE VALUES OF VARIOUS
HEART CHAMBERS
CHAMBER AVERAGE PRESSURE
RA 6/5/3
RV 25/4
PA 25/9/15
PCWP 9
LA 10/12/8
LV 130/8
Ao 130/70/85
29
30. DO MAKE A NOTE
Mean RA pressure=RVEDP
RVSP=Peak PA pressure
PA diastolic pressure=Mean PCWP=Mean LA
pressure= LVEDP
LVSP=Ao pressure
Presence of gradients across these chambers
indicates obstruction to blood flow
30
31. RIGHT ATRIAL PRESSURES
A: Atrial systole, just
after P wave
C: RV contraction/ TV
closure
V: Filling of RA against
closed TV valve
X: Atrial relaxation
Y: Opening of TV in
early diastole
31
32. RV PRESSURE
A rapid upstroke
during isovolumetric
contraction
A plateau during
systolic ejection
A decline to near zero
during isovolumetric
relaxation
A slow rise to the end
diastolic pressure
during diastolic filling
32
33. PA PRESSURE
PA systolic pressure=
RVSP (<30mm Hg)
Mean pressure< 20mm
Hg
PA diastolic pressure
begins with dicrotic
notch caused by valve
closure, and the diastolic
pressure is typically no
more than 2-3 mm Hg
higher than the wedge
pressure
33
34. PCWP
Is usually a good
reflection of LA and
LVEDP because of
absence of valves in
pulmonary circulation
It has the characteristic
a and v wave
appearance of an atrial
tracing
34
35. SATURATIONS
Site Average Range
SVC 74% 67-83%
IVC 78% 65-87%
RA 75% 65-87%
RV 75% 67-84%
PA 75% 67-84%
LA 95% 92-98%
LV 95% 92-98%
FA 95% 92-98%
35
38. WHEN IS IT UTILISED?
Discrepancy b/w physical and non-invasive
findings
Time of device closure
Assessment of shunt operability in patients
with severe PAH with borderline findings
38
39. SHUNT DETECTION
Oximetric run used
Past: Indicator dye (Indocyanine green) used
Detected very small lt rt shunt missed by
oxymetry
No longer used
Presence of unexplained arterial desaturation
(FA SaO2<95%) or unexpectedly high O2
content in PA (SaO2>80%): Raises suspicion of
rt lt or a lt rt shunt respectively
Follow this by a complete oximetry run 39
40. OXIMETRY RUN
Full oximetry run
involves taking serial
samples at following
locations:
Lt+ rt. PA
MPA
RVOT
RV mid
RV tricuspid valve or
apex
RA low or near TV
RA high
SVC low (near RA
junction)
SVC high (near
innominate vein junction)
IVC high ( just at/ below
diaphragm)
IVC low L4-5
LV
Ao (diatal to ductus
insertion)
40
41. DETECTION OF LEFT TO RIGHT SHUNT BY
OXIMETRY
41
Antman et al, AJC 80; Barrat et al, JLCM 57, Freed et al, BHJ 79
42. CAUSES OF STEP UP AT ATRIAL LEVEL??
ASD
PAPVC
VSD with TR
RSOV RA
LV RA shunt
Cor AV Fistula RA
42
43. CAUSES OF STEP UP AT VENTRICULAR LEVEL??
VSD
RSOV RV
Low ASD
Cor AV Fistula RA
PDA with PR
AVSD
43
44. CAUSES OF STEP UP AT GREAT VESSEL LEVEL??
Patent Ductus Arteriosus
Aorto-pulmonary Window
Outlet VSD
Coronary origin from pulmonary artery
44
45. LIMITATIONS
Steady state may not be present: Patient
agitation/ Arrhythmias
Lacks sensitivity: Small shunts may be missed
In conditions of high level of systemic blood
flow, mixed venous o2 sats tends to be higher
than normal and interchamber variablility would
be reduced equalization of arterial and venous
blood 45
46. UNDERSTANDING THE FICK’S PRINCIPAL
Total uptake/release of a substance by an
organ is the product of the bld flow to the organ
and the AV concentration difference of the
substance
46
47. PULMONARY BLOOD FLOW
Lung as an organ and O2 as substance: Bld
flow to lung will be:
Qp (L/min) =O2 consumption(VO2)/ AV O2
difference
=VO2/ PV O2 content-PA O2 content
47
48. PBF
If PV can’t be entered
See systemic arterial O2 content
≥95% <95
Use this value Determine if rt lt shunt
+nt –nt
Use 98% value Use observed systemic
arterial saturation value 48
49. SYSTEMIC BLOOD FLOW
Using body as an organ and O2 as substance:
Bld flow to body will be:
Qs= o2 consumption(VO2)/ SA02-MVO2
In presence of shunt lesions, MVO2 is to be
measured in chamber immediately proximal to
shunt
49
50. CALCULATION OF QS IN PRESENCE OF LT->RT
SHUNT
50
Grossman & Baim’s, 8th edition (FLAMM’S FORMULA)
51. SHUNT QUANTIFICATION
Absolute terms (L/min)=Qp-Qs
Relative terms (ratio)=Qp/Qs
Ratio advantageous as it takes out unreliable
variables like VO2
Qp/Qs=(SAO2-MVO2)/ (PVO2-PAO2)
51
52. QP/QS
1: No shunt
<1: Rtlt shunt
1-1.5: Small lt rt shunt (in absence of PAH;
would not need closure)
1.5-2: Intermediate lt rt shunts (may be
closed if risk of closure low)
>2: Large lt rt shunt (Needs closure)
52
53. CALCULATION OF BIDIRECTIONAL SHUNT
Effective bld flow: Flow that would exist in
absence of any lt—>rt or rt lt shunt
Qeff= O2 consumption/ (PVO2-MVO2)
Lt rt: Qp-Qeff
Rt lt: Qs-Qeff
53
54. SHUNT OPERABILITY
Large shunts: High PAH due to increased flow
Anatomic changes takes place in pul.
vasculature
Reversible initially, later ir-reversible
As PVRI increases> 6-8 Wood U: Poor
operative outcome
In these cases: If PAH irreversible; Sx tends to
transform these from Eisenmenger’s syndrome
to one analogous to idiopathic PAH
54
55. SHUNT OPERABILITY CONT…
Compared to idiopathic PAH; pts. with ES have
much better prognosis with 40% expected to
survive till 25 yoa
Assessment of operability is not an “ all or
none” phenomenon
Clinical and non invasive parameters too are
considered
55
56. CLINICAL & NON INVASIVE FINDINGS TO ASSESS
SHUNT OPERABILITY
56
Vijaylaxmi: Cardiac Catheterization From Pediatric to Geneatric: 1st edition
57. HEMODYNAMIC ASSESSMENT OF SHUNT
OPERABILITY
Favorable outcomes:
Baseline Qp/Qs >1.5-2
PVRI <6Wood U
PVR:SVR <0.3 without vasoreactive test
Age <1 year (Most imp.)
57
58. TECHNIQUES TO ASSESS OPERABILITY
Lung biopsy
Exposure to vasodilator
Temporary balloon occlusion of defect
58
59. 01. LUNG BIOPSY
Gold standard
Heath Edward classification Grade 4-6:
Irreversible
Invasive
Associated with morbidity
Not available at all centers
Some studies have questioned reliability
59
61. 02. EXPOSURE TO VASODILATOR
100% O2
NO (+/- O2)
Tolazoline
Adenosine
Epoprostenol
Used to assess pulmonary reactivity in cath
labs
61
62. PROCEDURE
Pt. adequately sedated
Obtain baseline rt/lt heart studies (PVRI,SVRI,
Qp, Qs)
100% o2 X 10 mins
Repeat rt/lt heart studies (recalculate Qp, Qs,
PVRI, SVRI)
If NO used: 20-80ppm by NO ventilator
62
63. TIPS FOR CALCULATION
O2 consumption remains constant
Post O2 inhalation: Dissolved O2 must be taken
into account in calculating O2 content
Failure to take into consideration the dissolved
O2 may make an inoperable case appear
operable
In pts with a positive response , there is a fall in
the diastolic and mean PA pressures without a
fall/rise in Ao pressure/ CO
63
64. PRESENCE OF ALL OF THESE INDICATES
FAVOURABLE OUTCOME FOLLOWING SURGERY
Decrease of 20% in PVRI
Decrease of 20% in PVR: SVR ratio
Final PVRI <6Woods U/m2
Final ratio of PVR: SVR <0.3
64
65. 03. TEMPORARY BALLOON OCCLUSION
Occlusion abolishes lt rt shunt
Operable pts: Drop in PA pressure
Inoperable pts: No drop in PA pressure; actual
rise in PA pressure with/without a fall in Ao
pressure
Best studied in PDAs and sometimes in ASDs
Technically difficult in VSDs
65
66. PDA BALLOON OCCLUSION
10 mins occlusion
A 25% fall in PA pressures or 50% fall in ratio
b/w pulmonary and Ao diastolic pressures
A fall in PA pressure with a > 20 mm Hg
systolic, diastolic and mean pressure difference
b/w PA and FA during balloon occlusion
66
67. ASD BALLOON OCCLUSION
15 mins
+ve response: Mean reduction in pulmonary
pressure of ≥25% after balloon occlusion
compared to basal levels, without a fall in
systemic pressure or an increase in VEDP
67
71. A. FICK METHOD OF CO ESTIMATION
Gold standard
Fick’s principal
In the absence of shunts:
Qp=Qs=CO
Also useful in patients with TR where
thermodilution method is unreliable
2 main variables:
O2 consumption (VO2)
AVO2 71
72. 01. O2 CONSUMPTION (VO2)
Earlier methods: Rarely used
Douglas bag/ polarography method/ paramagnetic
method
Cumbersome/ specialized equipments/ experienced
personnel
Only means of getting accurate VO2
Children: La Farge- Miettinen tables
72
73. LA FARGE- MIETTINEN TABLES: BOYS
73Vijaylaxmi: Cardiac Catheterization From Pediatric to Geneatric: 1st edition
74. LA FARGE- MIETTINEN TABLES: GIRLS
74Vijaylaxmi: Cardiac Catheterization From Pediatric to Geneatric: 1st edition
75. 02. AV O2 DIFFERENCE
O2 content
= O2 bound to Hb+ Dissolved O2
= 1.36mlx Hbx saturation+ 0.003mlxPaO2
In pts on RA: Content of dissolved O2 low:
Hence ignored (= 1.36x Hb(g/L)X 10X (AO2-
MVO2)
If breathing with FiO2 >50%: Take dissolved O2
too (Imp when shunt operability in severe PAH
cases is assessed) 75
76. BEFORE STARTING THE CASE, DO HAVE THESE
HANDY
Hb level
Ht +Wt for BSA calculation
HR, age, sex: For VO2
76
77. LIMITATIONS OF THE FICK PRINCIPAL
Use of assumed VO2 value (Errors of 10-25%
can creep in)
Inability to obtain steady state under certain
circumstances (samples to be obtained
simultaneously)
Do not use this method in: Significant MR, AR
77
78. B. THERMODILUTION METHOD OF CO
ESTIMATION
Values correlate well to Fick method
Involves determining the extent and rate of
thermal changes in blood stream following
injection of fixed vol of cold NS
Temperature time curve obtained: Area gives
CO
78
79. METHOD
Distal tip of Swan Ganz catheter placed in PA,
proximal port in RA
10 ml NS bolus injected rapidly in proximal port at
a constant rate
Resultant change in temperature in liquid
measured by thermistor mounted at the distal end
of catheter
Result displayed on computer
Repeated 3 times
3 recordings should be within 15-20% of each
other, otherwise repeat procedure 79
80. LIMITATIONS OF THERMODILUTION METHOD
Do not use in:
Severe TR
Low CO states (overestimates CO)
Intracardiac shunts
Marked respiratory variation
Cardiac arrhythmias
80
81. C. ANGIOGRAPHIC METHOD OF CO ESTIMATION
CO=SV X HR
SV= EDV- ESV
By tracing LV ED and ES images of a high
quality ventriculogram, EDV and ESV can be
calculated
Inherent inaccuracies of calibrating
angiographic volumes: Rarely used clinically
Only use: Calculation of stenotic valve areas in
pts with significant AR or MR
81
83. RESISTANCE MEASUREMENT
Ohm’s law??
R=V/I
Resistance= Δ Pressure/ Flow
SVR= Mean Ao Pre – Mean RA pre/ Qs
Wood units(mm Hg/L/min)
X 80: dynes/sec/cm-5
Normal SVR: 8-20 Wood U (700-1,66
dynes/sec/cm-5)
83
84. RESISTANCE MEASUREMENT CONT…
PVR= Mean PA pre- Mean LA (or PCWP) pre/
Qp
Normal PVR: 20-130dynes/sec/cm-5(.25-1.6W
U)
PVRI
= Mean PA- Mean PCWP/ CI
= Mean PA- Mean PCWP/Qp/BSA
= (Mean PA- Mean PCWP/ Qp) x BSA
= PVR X BSA 84
87. ANGIOGRAMS
Should be performed after all hemodynamic
and oximetry data have been obtained
In pts with elevated LVEDP/ PCWP (>25
mmHg), avoid angiograms or perform only it
has been reduced to safe levels with NTG/ lasix
87
88. PRIOR TO PERFORMING ANGIOGRAMS, ALWAYS
DO:
Confirm catheter type
Ensure catheter is not entrapped and no air
bubble
Perform a test injection to confirm that
catheter has not migrated
Confirm contrast volume, flow rates and
injection pressures
88
89. COMMONLY USED RADIOLOGICAL VIEWS
89Vijaylaxmi: Cardiac Catheterization From Pediatric to Geneatric: 1st edition
91. 01. ERRORS IN PRESSURE RECORDING
Errors at zero level, balancing, calibration of
transducers
Clots or kinks in system
Loose connections/ defective transducers
Use of multi hole catheter for withdrawal
gradients
Systolic pressure amplification in periphery
Use of computer derived mean values in
patients with marked respiratory variation
91
92. 02. ERRORS IN SAMPLING
Obtaining samples in different physiologic
states ( arrhythmias, acidosis,
hypoventilation)
Partial wedging of catheter (PA)
Non representative sampling (PVs)
92
93. 03. ERRORS IN OXIMETRY
Diluted samples (saline/ heparin)
Air bubble in syringe
Delay in sample sending
Using ABG samples to estimate O2 sats
Using non standardized equipment
93
94. 04. ERRORS IN CALCULATION
Assumed VO2
Assumed PV saturation
Failure to account for dissolved O2 during
O2 study
Flows corrected for BSA by dividing instead
of multiplying
Errors in identifying the mixing chamber
correctly and using O2 sats from wrong
chamber
94