6360abefb0d6371309cc9857
Abstract
We describe 67 years
old male patient presenting with acute coronary syndrome (acute inferior ST
elevation) with complete heart block. primary percutaneous coronary
intervention decided with temporary pacemaker insertion. In view thrombus
burden lesion in proximal right coronary artery. we did thrombus aspiration by
using thrombus aspiration catheter). After successfully aspirating thrombus,
resistance felt on withdrawal of the aspiration catheter. Tip of the thrombus
aspiration catheter was broken and retained in the guide wire at the level of
proximal right coronary artery. The broken tip of thrombus aspiration catheter
was successfully retrieved percutaneously.
Keywords: Coronary Syndrome; ST
elevation; Catheter
Introduction
In ST elevation
myocardial infraction (STEMI), percutaneous coronary intervention is superior
to thrombolysis in terms of in-hospital mortality, re infarction and stroke1.
Coronary atherosclerotic plaque rupture with thrombus formation being the basic
pathophysiologic phenomenon in acute myocardial infarction, prevalence of
thrombus is very much commonly seen in STEMI compare to non-ST elevation
myocardial infarction (NSTEMI)2.
Thrombus aspiration in
patients with high thrombus burden can decrease thrombus burden, lower rates of
distal embolization, improve thrombolysis in myocardial infarction- 3 flow,
reduce the incidence of no reflow, improve microvascular perfusion and consequently
improve clinical outcomes. However, >2 dozen randomized trials have compared
the outcomes of routine thrombus aspiration with primary percutaneous coronary
intervention (PCI) alone in patients with ST- segment– elevation myocardial
infarction (STEMI) and have not shown a consistent reduction in cardiovascular
outcomes. As such, routine thrombus aspiration during primary PCI is not
recommended by guideline committees (class III, 2021 American College of
Cardiology/American Heart Association guidelines or 2017 European Society of
Cardiology guidelines)3,4.
Case Report
Male patient aged 67 years old with history of diabetes Mellitus
type II (DM), presented to emergency department of private hospital with
central chest pain increase in intensity 3 hours before arrival with history of
sweating and nausea. ECG done on arrival (Figure 1).
Figure 1: ECG at presentation of the
patient in ER in private hospital
The patient was
subsequently admitted to the intensive care unit (ICU). On arrival, vital signs
were as follows: blood pressure 90/60 mmHg, heart rate 60 beats/min and
temperature 37 °C. Physical examination revealed no pallor or jaundice, no
lower-limb edema and intact peripheral pulses. Abdominal examination showed no
organomegaly. Chest examination was unremarkable with normal breath sounds.
Cardiac examination demonstrated normal first and second heart sounds with no
added sounds or murmurs.
Because the patient’s chest pain had decreased in intensity, thrombolytic therapy was unfortunately not administered. In addition, the admitting hospital lacked percutaneous coronary intervention (PCI) capability. Consequently, conservative management was initiated, including antiplatelet therapy, anticoagulation and statin therapy. The patient remained in the ICU for one day.
On the following day,
the patient developed dizziness and recurrent episodes of shortness of breath.
He requested expert consultation and was transferred to Nabdh Al-Hayat Cardiac
Center (NCC) in Mukalla for further evaluation and management.
At NCC, reassessment
revealed significant hemodynamic deterioration. Vital signs were as follows:
blood pressure 80/50 mmHg, heart rate 40 beats/min and temperature 37°C.
Electrocardiography was performed (Figure 2). Bedside transthoracic
echocardiography demonstrated normal left-sided cardiac structure with
preserved left ventricular systolic function, no resting regional wall-motion
abnormalities and no mitral regurgitation. No mechanical complications were identified,
including ventricular septal rupture, free-wall rupture or papillary muscle
dysfunction. However, the right ventricle was dilated with global hypokinesia.
Figure 2: ECG of the patient at
presentation to NCC
Primary percutaneous
coronary intervention (PCI) was decided and the catheterization laboratory team
was immediately activated. A trans-femoral venous approach was used for
temporary pacemaker insertion, which was successfully established at a fixed
rate of 60 beats/min. An initial attempt at right radial artery puncture for
coronary angiography was unsuccessful; therefore, crossover to the right
femoral artery was performed.
Coronary angiography
was carried out using a 6-Fr diagnostic left Judkins catheter, which revealed
an atherosclerotic left coronary system. A right Judkins guiding catheter was
then used to cannulate the right coronary artery (RCA), demonstrating total occlusion
of the proximal RCA with a high thrombus burden. The occluded segment was
successfully crossed with a 0.014-inch BMW PTCA floppy guidewire. Limited
thrombus aspiration was achieved after five passes using a 6-Fr Export
aspiration catheter (Medtronic), as shown in (Figure 3). Control
angiography of the RCA after thrombus aspiration demonstrated TIMI I flow.
Subsequently, a 1.25 × 10 mm Sprinter balloon (Medtronic Inc.) was advanced
over the guidewire for balloon predilatation. Upon reaching the proximal RCA,
three radiopaque markers were visualized instead of the expected two (Figure
4). This immediately raised suspicion of device fracture. Careful
inspection of the Export catheter, which had just been withdrawn from the
guiding catheter and was lying on the table, confirmed loss of its distal tip.
This represented a precarious situation, with a thrombogenic broken catheter
fragment retained within a thrombus-laden coronary artery and loss of operator
control over the fragment.
Given the very short
distance between the distal balloon marker and the third radiopaque marker, it
was inferred that only the distal tip of the Export catheter had
fractured (Figure 5). An attempt to advance a smaller 1.0 × 10 mm
Sprinter balloon distal to the retained fragment over the original guidewire
was unsuccessful. Therefore, a second BMW PTCA guidewire was advanced into the
distal RCA. A 2.0 × 12 mm Sprinter PTCA balloon was then advanced and
positioned distal to the fractured catheter tip. The balloon was inflated to 8
atm and gently withdrawn from the mid to proximal RCA, successfully entrapping
and retrieving the broken Export catheter tip into the guiding catheter.
The entire system,
including the guiding catheter, both BMW PTCA guidewires, the balloon and the
fractured aspiration catheter tip, was removed en bloc. The guiding catheter
was flushed with heparinized saline and the retrieved broken catheter tip was
clearly identified. The RCA was subsequently re-engaged using a new JR 3.5
guiding catheter and a fresh BMW PTCA guidewire successfully crossed the
proximal RCA lesion. Predilatation was performed using a 2.0 × 12 mm Sprinter
balloon, restoring TIMI III flow. A 3.0 × 30 mm drug-eluting stent was then
deployed in the proximal RCA and inflated to 14 atm. Final angiography
demonstrated TIMI III flow with good stent expansion and no evidence of edge
dissection (Figure 6).
Figure 3: Thrombotic materials retrieved
from RCA
Figure 4: Knob
is noticed of the broken tip of export catheter (aspiration catheter) in
proximal segment of RCA
Figure 5: Shaft of aspiration export
catheter without tip
Discussion
The incidence of
broken or retained percutaneous coronary intervention (PCI) hardware in earlier
literature is approximately 0.2%5. Although significant refinement
in device design has occurred over the past decade, the increasing number and
complexity of percutaneous coronary procedures continue to be associated with
occasional intravascular hardware failure. Several reports have described
successful retrieval of fractured catheters, guidewires, balloons and both
expanded and unexpanded stents from the intracoronary circulation using various
techniques5-7. Familiarity with these retrieval methods is
essential, as no single technique is universally effective in all clinical
scenarios.
Cagdas Akgullu, et al.8 reported
a case of a trapped thrombus aspiration catheter in a coronary artery caused by
rupture of the main shaft and twisting over the guidewire; the device was
successfully removed by withdrawing the entire system. Other case reports have
described complications related to thrombus aspiration catheters, including
thrombus formation in the left main coronary artery and inadvertent coronary
endarterectomy using the Thrombuster III GR catheter9,10.
A review of 48 case
reports involving a total of 67 patients with guidewire entrapment showed that
41.8% were managed by percutaneous extraction, 43.3% required surgical
intervention and 14.9% were treated conservatively. Various percutaneous
retrieval techniques have been described, including stenting the fragment
against the vessel wall, snare loop capture, double- or triple-wire techniques,
use of a bioptome, Tornus microcatheter, deep guide catheter wedging with
balloon inflation and pigtail catheter manipulation11.
In a prior report
assessing the prevalence and outcomes of fractured PCI hardware, 12 out of
5,400 percutaneous transluminal coronary angioplasty (PTCA) procedures were
complicated by retained components, including guidewire fragments, balloon
catheters and guide catheters12. Follow-up of patients with retained
guidewire fragments revealed no clinical sequelae over a period ranging from 6
to 60 months, suggesting that management decisions should be individualized.
Not all cases of retained hardware necessitate coronary artery bypass grafting
(CABG), particularly when fragments are located in chronically occluded or
distal vessels12. Additional reports have documented successful
retrieval of an FFR wire tip using an angiographic catheter (Slip-Cath) via the
mother–child technique13, as well as balloon assisted extraction of
a fractured Export catheter14.
Retained intracoronary
hardware can act as a nidus for thrombus formation, potentially leading to
acute vessel occlusion, myocardial infarction, arrhythmias, coronary
perforation or embolic events15. Therefore, removal of the fractured
fragment is generally recommended. In our patient, the presence of a
thrombogenic milieu with thrombus formation proximal to the broken catheter
significantly increased the risk of further thrombus propagation, making prompt
retrieval of the fractured Export catheter tip imperative.
Potential causes of
retained PCI hardware include excessive torquing, forceful catheter withdrawal,
improper handling, device reuse, manufacturing defects, inadvertent advancement
of large-caliber catheters through smaller access sheaths, polymer aging or a
combination of these factors.
References