SPECIAL ARTICLES
Epidural Catheter Design
History, Innovations, and Clinical Implications
Roulhac D. Toledano, M.D., Ph.D., Lawrence C. Tsen, M.D.
ABSTRACT
F
Laureate of the Faculty of Medicine, University of Paris Faculty of Medicine, Paris, France), Barnet E. Bonar, M.D.4
(1894–1937; Department of Pediatrics, Rush Medical College, Chicago, Illinois; Member of the American Academy
of Pediatrics, Salt Lake City, Utah), and William R. Meeker,
M.D. (1889–1955; Head of Section on Anesthesia, Division of Surgery, Mayo Clinic, Rochester, Minnesota), among
others, also advocated the caudal approach for epidural
anesthesia.
The Spanish surgeon Fidel Pagés Miravé, M.D. (1886–
1923; Medical Commandant, Department of Surgery,
Emergency Military Hospital of Madrid, Madrid, Spain)
reported the first single-shot thoracolumbar epidural anesthesia in 1921.5 Within a decade, the Italian surgeon Achille
M. Dogliotti, M.D. (1897–1966; Professor, Department of
Clinical Surgery, University of Turin, Turin, Italy) described
a reproducible loss-of-resistance technique to identify the
epidural space.6 Contemporaneously, the Argentine surgeon
Alberto Gutiérrez, M.D. (1892–1945; Chief of Surgery,
Hospital Español, Buenos Aires, Argentina; Extraordinary
Professor, University of Buenos Aires School of Medicine,
Buenos Aires, Argentina) described the “sign of the drop”
method for identification of the space.7 Charles B. Odom,
M.D.8 (1909–1988; Director of Surgical Services, Charity
Hospital, New Orleans, Louisiana), John R. Harger, M.D.,
F.A.C.S.9 (1876–1956; Professor, Department of Surgery,
University of Illinois; Attending Surgeon, Cook County
Hospital, Chicago, Illinois), and John Abajian, Jr., M.D.10
(1921–1996; Captain, Medical Corps, Army of the United
States; Professor, Chief of the Division of Anesthesiology,
Department of Surgery, University of Vermont College of
Medicine, Burlington, Vermont) popularized the single-shot
ROM its origins as a modified ureteral catheter, the
epidural catheter has evolved into versions made with
silk, rubber, plastic, and coiled stainless steel. These changes
resulted from a growing recognition that particular design
elements could potentially influence catheter performance.
This article reviews the history of epidural catheter design,
focusing on how modifications in the materials used, tip
design, and orifice number and arrangement may have
affected analgesic and anesthetic outcomes, and provides a
summary of the comparative studies that evaluate the clinical performance of distinct epidural catheter design features.
History
The most consistent entry into the epidural space for the
administration of anesthesia occurred at the turn of the 20th
century when the French physicians Jean A. Sicard, M.D.
(1872–1929; Professor, Department of Pathology, Necker
Hospital; Laboratory of Professors Raymond and Brissaud,
Salpêtrière Hospital, Paris, France) and Fernand Cathelin,
M.D. (1873–1945; Department of Surgery, University of
Paris Faculty of Medicine, Paris, France) independently introduced single-shot epidural blocks via the caudal approach
for neurologic and genitourinary procedures, respectively
(table 1).1 Within a few years, German physicians Walter
Stoeckel, M.D. (1871–1961; Honorary Professor, Department of Gynecology, Berlin Charité, Berlin, Germany) and
Arthur Läwen, M.D. (1876–1958; Professor, Department of
Surgery, University of Leipzig Faculty of Medicine, Leipzig,
Germany) applied this technique for obstetric deliveries and
surgical procedures to the perineum.2 During the 1920s,
Gaston Labat, M.D.3 (1876–1934; Laureate of the Faculty
of Sciences, University of Montpelier, Montpelier, France;
Submitted for publication July 8, 2013. Accepted for publication February 7, 2014. From the Department of Anesthesiology, SUNY Downstate Medical Center, Lutheran Medical Center, Brooklyn, New York (R.D.T.); and Department of Anesthesiology, Perioperative and Pain
Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts (L.C.T.).
Copyright © 2014, the American Society of Anesthesiologists, Inc. Lippincott Williams & Wilkins. Anesthesiology 2014; 121:9–17
Anesthesiology, V 121 • No 1
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July 2014
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Epidural catheters have evolved during the past several decades, as clinicians and manufacturers have sought to influence the
quality of analgesia and anesthesia and reduce the incidence of catheter-related complications. This evolution has allowed
a transformation from single-shot to continuous-infusion techniques and resulted in easier passage into the epidural space,
more extensive medication distribution, and ultimately, improved patient satisfaction. Particular catheter features, including
the materials used, tip design, and orifice number and arrangement, have been associated with specific outcomes and provide
direction for future development. (ANESTHESIOLOGY 2014; 121:9-17)
Epidural Catheter Design
Table 1. Pioneers of Continuous Epidural Techniques
Timeline
1901
1910
1921
1923
Pioneer(s)
1931
1931
Achille Dogliotti
Eugene Aburel
1930
1938
1940
1941
1942
1944
Charles Odom; John Harger; John Abajian
Peter Graffagnino; Louis Seyler
William Lemmon
Samuel Manalan
Robert Hingson; Waldo Edwards; James
Southworth
Charles Adams; John Lundy; Thomas
Seldon
Edward Tuohy
1944
1947
James Southworth; Robert Hingson
Manuel Martinez Curbelo
1942
Independently introduced single-shot caudal blocks
Advocated caudal blocks for pelvic and obstetric surgeries
Introduced single-shot thoracolumbar approach to epidural analgesia
Advocated caudal approach for epidural anesthesia
Described the “hanging drop” method for identification of the epidural
space
Described loss-of-resistance technique to identify the epidural space
Introduced a continuous catheter technique to block the lumboaortic
plexus during early stage of labor
Early practitioners of epidural anesthesia in North America
Applied single-shot epidural anesthesia in obstetrics
Introduced a continuous spinal technique via a malleable needle
Used catheter technique for labor analgesia
Modified the malleable Lemmon needle; pioneered an approach to
continuous caudal analgesia in obstetrics
Advocated continuous caudal technique for peripartum analgesia
Introduced the ureteral catheter for continuous spinal anesthesia;
modified the Huber needle for epidural use
Attempted a modified continuous lumbar epidural technique
Introduced continuous lumbar epidural anesthesia with ureteral catheters
had originally developed the malleable spinal needle, made
of German silver, to provide continuous spinal anesthesia.15
Hingson and Edwards16 described inserting a 19-gauge malleable stainless steel needle into the sacral canal and attaching the hub to a Luer-Lock syringe via a four-foot length
of rubber tubing. The authors reported occasional complications, such as needle breakage, and warned of the theoretical possibility of undetected needle migration into the
subarachnoid space.
Edward B. Tuohy, M.D., M.S. (1908–1959; Major,
Medical Corps, Army of the United States; Chief of Anesthesia and Operative Section, Percy Jones General Hospital, Battle Creek, Michigan; Consultant, Mayo Clinic,
Rochester, Minnesota; Professor, Department of Anesthesiology, Georgetown University Medical Center, Washington, D.C.) introduced the ureteral catheter for continuous
spinal anesthesia in the early 1940s, thereby eliminating
some of the drawbacks associated with the malleable needle. In his early works, he described threading a gradated,
round-tipped nylon ureteral catheter through a 15-gauge
Barker needle at the level of the lower lumbar vertebrae and connecting a rubber adapter or, alternatively, a
22-gauge needle to the free end for dosing.17 Tuohy18 cautioned that catheters should be properly sterilized and, in
the absence of any obvious breaks or cracks, reused not
more than 10 times.
Several other investigators introduced the catheter as
an alternative to an indwelling needle for continuous caudal anesthesia. Samuel A. Manalan, M.D. (1912–1990;
Department of Obstetrics and Gynecology, Indiana
University School of Medicine, Indianapolis, Indiana)
thoracolumbar epidural technique in the United States. In
1938, clinicians at the Louisiana State University Medical
Center reported the first application of this technique to the
obstetric population.11
A number of innovations attempted to prolong
single-shot epidural procedures. In 1931, Eugen B. Aburel,
M.D. (1899–1975; Professor, Department of Obstetrics
and Gynecology, University of Medicine and Pharmacy,
Iasi, Romania) introduced a continuous lumboaortic plexus
block with a silk ureteral catheter to alleviate labor pain.12
Clinicians at the Mayo Clinic had previously reported using
ureteral catheters for alternative purposes, including for the
treatment of hydrocephalus.13 Aburel’s combination of a
continuous lumboaortic block for the first stage of labor and
a single-shot caudal for the second stage yielded unreliable
results and was abandoned as more promising continuous
techniques evolved.14
Robert A. Hingson, M.D., Sc.D. (1913–1996; Chief of
Anesthesiology, U.S. Marine Hospital, Staten Island, New
York; Director of Anesthesia, Lying-In Hospital, Philadelphia, Pennsylvania; Professor, Department of Anesthesiology, Western Reserve University School of Medicine,
Cleveland, Ohio) and Waldo B. Edwards, M.D. (1905–
1981; Chief of Obstetrics, U.S. Marine Hospital, Stapleton,
Staten Island, New York), both affiliated with the United
States Public Health Service during the Second World War,
pioneered an approach to continuous caudal analgesia for
the obstetric population in 1942 with the use of a modified
Lemmon needle. William T. Lemmon, M.D. (1896–1974;
Junior Faculty Member, Department of Anatomy, Jefferson
Medical College and Hospital, Philadelphia, Pennsylvania)
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1930
Jean Sicard; Fernand Cathelin
Arthur Läwen; Walter Stoeckel
Fidel Pagés Miravé
Gaston Labat; Barnet Bonar; William
Meeker
Alberto Gutiérrez
Novel Development
SPECIAL ARTICLES
Tuohy needles and small, gradated number 3.5-French ureteral catheters that curved as they exited the needle.12 He
advocated continuous epidural anesthesia for a broad range
of surgeries, from the neck to the lower extremity. Charles
E. Flowers, Jr., M.D. (1920–1999; Instructor, Department
of Obstetrics and Gynecology, Johns Hopkins University
and Hospital, Baltimore, Maryland) and Louis M. Hellman,
M.D. (1908–1990; Professor, Department of Obstetrics and
Gynecology, State University of New York College of Medicine; Director of Obstetrics and Gynecology, Kings County
Hospital, Brooklyn, New York), both at Johns Hopkins University at the time, collaborated with Hingson to apply Martinez Curbelo’s technique to the obstetric population. They
threaded plastic tubing in lieu of a ureteral catheter through
a blunt-tipped 16-gauge Tuohy needle at the level of the second lumbar interspace to provide analgesia or anesthesia for
vaginal or cesarean delivery.24
In the late 1940s, John G. Cleland, M.D., C.M., M.Sc.,
F.A.C.S. (1898–1980; Clinical Instructor, Department of
Obstetrics and Gynecology, University of Oregon Medical
School, Portland, Oregon) devised an alternative method of
pain relief in the obstetric population with a dual continuous
lumbar and caudal epidural technique.25 With the goal of
selectively blocking pain at different stages of labor, he placed
one number 3.5-French ureteral x-ray catheter between the
second and third lumbar vertebrae and a second “soft-nosed”
number 3.5-French catheter in the caudal canal. The caudal catheter, autoclaved in the straightened position to prevent kinking or curling, was placed at the same time as the
lumbar catheter but was activated only when the parturient
reached the second stage of labor.
By the second half of the 20th century, the practice of
epidural analgesia had gained popularity in North America.
In 1951, Oral B. Crawford, Jr., M.D. (1921–2008; Department of Anesthesiology, St. John’s Hospital, Springfield,
Missouri) and colleagues reported more than 600 cases of
thoracic epidural anesthesia.26 Similarly, in 1953, F. Paul
Ansbro, M.D. (1899–1977; Assistant Clinical Professor,
Department of Anesthesiology, St. Catherine’s and Adelphi
Hospitals, Brooklyn, New York) and colleagues reported
success with more than 1000 single-shot and continuous
epidural anesthetics for a variety of surgeries, including
gastrectomies, thyroidectomies, and kidney and chest
surgeries.27
Obstetric anesthesia also gained momentum as epidural
techniques became more widespread. John J. Bonica, M.D.
(1917–1994; Professor and Chairman, Department of Anesthesiology, University of Washington School of Medicine,
Seattle, Washington) organized one of the first 24-h labor
anesthesia wards in the late 1940s,28 and published his classic textbook, Principles and Practice of Obstetric Analgesia and
Anesthesia, 2 decades later.29 Philip R. Bromage, M.B., B.S.,
F.F.A.R.C.S, F.R.C.P. (1920–2013; Professor and Chairman, Department of Anesthesia, McGill University, Montreal, Canada; Professor, Departments of Anesthesiology and
* The French scale (or gauge) system was devised by JosephFrédéric-Benoît Charrière, a 19th-century Parisian maker of surgical
instruments, who defined the “diameter times 3” relationship, meaning the external diameter of a catheter in millimeters multiplied by
three results in the French gauge.20 As an example, a catheter with a
3-mm external diameter is a French size of 9. An increasing French
size corresponds to a larger external diameter. The measurement is
most commonly abbreviated as Fr, but Ga, FR, F, CH, or Ch (for its
inventor) are also used.
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presented the catheter technique in a preliminary report
in 1940.19 He described threading a number 4-French*
ureteral catheter through a 14-gauge needle into the sacral
canal.20 Nylon ureteral catheters, which were more easily
sterilized, replaced silk catheters during the course of his
pilot study due to a case of meningitis that was attributed
to the latter.
R. Charles Adams, M.D. (1906–1956; Faculty Member, Head of Section on Anesthesia and Intravenous
Therapy, Mayo Clinic, Rochester, Minnesota), John S.
Lundy, M.D. (1894–1973; Professor, Head of Section
on Anesthesia, Mayo Clinic, Rochester, Minnesota), and
Thomas H. Seldon, M.D. (1905–1991; Faculty Member,
Mayo Clinic, Rochester, Minnesota) also contributed to
the advancement of the epidural catheter technique in the
early 1940s.21 Their continuous caudal technique for peripartum analgesia involved threading a woven silk or nylon
number 5-French ureteral catheter through a 13-gauge
Love-Barker needle at the level of the third sacral foramen. Catheter curling, tearing, cracking, and improper
sterilization were among the complications associated with
this technique.
With the collaboration of the surgeon James L. Southworth, M.D. (1913–1970; Assistant Surgeon, U.S. Marine
Hospital, Stapleton, Staten Island, New York), Hingson22
modified the continuous technique again in 1944, this time
introducing a blunt-tipped silk ureteral catheter into the
lumbar epidural space via a large Barker needle. However,
a high incidence of paresthesias, inadequate analgesia, unilateral blockade, and intravascular cannulation forced the
collaborators to devise a new approach. Familiar with the
work by Francis R. Irving, M.D.23 (1896–1959; Clinical
Professor, Department of Obstetrics and Gynecology, Syracuse University College of Medicine, Syracuse, New York)
in the field of continuous caudal anesthesia, Southworth
and Hingson attempted placing the Barker needle over an
18-gauge hubless Irving needle to facilitate catheter insertion, but abandoned this approach in favor of a continuous
epidural technique with a malleable 19-gauge spinal needle
inserted at the T12-L1 interspace. Innovations in spinal
and epidural catheterization, however, soon superseded this
technique.
Shortly after visiting the Mayo Clinic in 1946, Cuban
anesthesiologist Manuel Martinez Curbelo, M.D. (1906–
1962; Department of Anesthesiology, Hospital Municipal de
la Habana, Havana, Cuba) adapted Tuohy’s continuous subarachnoid technique for the epidural space, using 16-gauge
Epidural Catheter Design
Obstetrics and Gynecology, Duke University Medical Center, Durham, North Carolina), who advanced the concept
of providing regional analgesia as a complement to general
anesthesia, introduced his classic text Epidural Analgesia in
1978.30 Broader commercial availability of epidural catheters, the first report of intrathecal opioid efficacy, and the
formation of pain services also occurred in the 1970s. The
acceptance and proliferation of analgesic and anesthetic
applications for the epidural catheter prompted further
innovations in catheter materials and designs.
Catheter Design Innovations and Clinical
Implications
During the past few decades, a number of innovations in
the design and manufacture of epidural catheters have been
made, including changes in the materials used, tip design,
and orifice location and number. Comparative studies that
evaluate the clinical performance of these distinct epidural
catheter design features have been performed; however, a
number of factors should be acknowledged when interpreting their results.
First, most of the catheters discussed were approved under
the 510(k) program of the Medical Device Amendment to the
Federal Food, Drug, and Cosmetic (FD&C) Act.† Enacted
in 1976, this program allows a device that exhibits “substantial equivalence to a legally marketed device” to be marketed
without independent demonstrations of safety and effectiveness. As a consequence, robust, blinded assessments of the
altered epidural catheter design feature likely did not occur
during the approval process, with claims regarding the efficacy of a design modification being the result of internal,
manufacturer-conducted investigations. Second, many of the
published investigations were nonrandomized, open-labeled
trials performed at a time when industry support and relevant
conflicts of interest were not routinely disclosed. It is possible that bias in conducting the research, interpreting the
findings, or publishing the results may have occurred. Finally,
some of the studies evaluating epidural catheter modifications were small in number and did not disclose whether
anatomic approaches to the epidural space (e.g., midline vs.
paramedian), methods used to identify the epidural space
(e.g., loss-of-resistance, hanging drop, and many more), and
the experience of persons placing the technique were standardized; these may have confounded the results. With an
appreciation of these potential study limitations, the epidural
catheter design features may be reviewed.
Innovations in Catheter Materials
The materials used in the production of catheters directly
affect the length at which coiling occurs,31 deformability
to force,32 intrinsic bending stiffness, and tensile strength.
† Available at: http://www.fda.gov/medicaldevices/deviceregulationandguidance/guidancedocuments/ucm282958.htm. Accessed January
13, 2014.
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These properties, in turn, may influence clinical outcomes,
such as analgesic spread, paresthesias, intravascular cannulation, kinking, breakage, and migration. During the past several decades, materials have evolved to improve the flexibility
and reduce the complications associated with catheters.
Ureteral catheters used initially for cerebrospinal fluid
drainage and then adapted for continuous spinal and epidural techniques were made of various materials. In the
1930s, woven natural silk catheters with gum elastic interior
walls were widely available.33 However, during the Second
World War when silk became scarce, ureteral catheters of
nylon, a synthetic polymer, became more common. Early
prototypes were flexible at body temperature, required cold
sterilization, and were equipped with red rubber adapters to connect with syringes. By 1942, autoclavable silk
and nylon catheters impregnated with a woven gum coating for improved longevity and elasticity replaced previously imported products. Lacquered nylon number 3.5- or
4-French ureteral catheters used for epidural techniques were
available in radiopaque and nonradiopaque versions, with or
without centimeter gradations.
Advances in the plastics industry eventually led to the
development of catheters that better withstood the sterilization process. Polyethylene, a widely available plastic, is easily
deformed during the autoclaving process and at body temperature. Polyvinylchloride catheters, available in bulk in the
1960s, proved more resistant to kinking and easier to place
than polyethylene versions; however, the intrinsic stiffness
of polyvinylchloride may have contributed to a higher incidence of tissue trauma, intravascular cannulation, and dural
punctures. Polyvinylchloride tubing was cut, marked with
centimeter gradations, and sterilized by autoclaving by individual anesthesia providers.34
Nylon, a polyamide, largely replaced polyvinylchloride
because of its improved tissue inertness, transparency, and
tensile strength. The high melting point of nylon confers an
ability to withstand the sterilization process and retain its
shape at body temperature. Nylon is sufficiently flexible to
stretch rather than buckle or break, yet rigid enough to thread
easily. Many currently available catheters are nylon blends.
Teflon® (E.I. du Pont de Nemours and Company, Wilmington, DE), a brand name for polytetrafluoroethylene,
emerged in the manufacture of epidural catheters in the
1970s. Polytetrafluoroethylene has an extremely low coefficient of friction that facilitates catheter placement, a high
melting point, which minimizes thermolability, and greater
tensile strength than polyvinylchloride or polyethylene.
However, the stiffness of Teflon® catheters may contribute
to displacement from the epidural space, kinking or fracture,
venous cannulation, and paresthesias. A comparative study
of central venous catheters indicated that Teflon® catheters
were up to 10 times stiffer than silicone elastomer, polyvinylchloride, and polyurethane catheters; reducing the diameter
of Teflon® catheters to limit their stiffness results in sizes that
are not clinically viable.35
SPECIAL ARTICLES
of paresthesias and intravascular cannulations. Many commercially available catheters are made of nylon blends with
intermediate bending stiffness, which facilitates threading
and increases the likelihood of successful insertion.37 Other
nylon and polyurethane catheters have an inner stainless
steel wire coil to impart rigidity, with fewer coils in the distal
tip to impart flexibility; how this more flexible tip influences
threading ease or failure has not been fully investigated.
The rigidity of catheter materials also seems to influence
the incidence of paresthesias. Soft-tipped, flexible catheters
are believed to result in fewer paresthesias because they curl
up or change course as they brush against nerve roots or
other obstacles in the epidural space.38 Catheter materials
that soften at body temperature, such as polyurethane, have
been observed to reduce the paresthesia rate;39 however, this
is unlikely to be important during the initial placement due
to the time required for temperature equilibration. A number
of studies demonstrate a significantly lower incidence of paresthesias with springwound polyurethane versus non–wirereinforced catheters (table 2). In a study of 222 attempts at
epidural placement in 200 parturients randomized to receive
continuous epidural analgesia, Banwell et al.40 reported
an incidence of paresthesias of 3 of 112 with a single endhole springwound polyurethane catheter compared with
39 of 110 with a blunt-tipped, multiorifice nylon catheter
(P < 0.0001); the catheters were likely 19- and 20-gauge,
respectively (actual gauge not provided), based on the products being produced by the companies.
Slight modifications in the materials of non–wirereinforced catheters by a single manufacturer seem to have a
negligible impact on the incidence of paresthesias. In a prospective cohort-controlled study of 188 patients receiving either a
20-gauge polyamide or a 20-gauge polyurethane–polyamide
Clinical Implications of Catheter Materials
The materials used in the manufacture of catheters have
been observed to have some effect on clinical performance,
including ease of placement and removal and the incidence
Table 2.
The Incidence of Paresthesias and Intravascular Cannulation with Various Epidural Catheters
Paresthesia
Intravascular
Cannulation
2.7%
0%
Concord/Portex® (blunt-tip, nylon
with three lateral holes)
20-gauge B Braun Perifix Standard
(polyamide)
35.5%
10%
21.3%
8.9%
20-gauge B Braun Perifix New (combined polyamide–polyurethane)
19-gauge Arrow FlexTip Plus®
(open-tip, polyurethane)
19-gauge Hakko catheter (open-tip,
polyethylene)
16.7%
3.2%
NA
0.67%
NA
5.3%
Study
Banwell et al.40
Bouman et al.39
Terasako et al.42
Catheter
Arrow FlexTip Plus® (open-tip,
polyurethane)
Comment
Prospective, randomized, unblinded study
(n = 200 parturients). Epidural catheter
gauge not provided.
Prospective, open, cohort-controlled study
(n = 188 patients). The incidence of paresthesias increased to 37.8% (standard)
and 32.6% (new), respectively, on direct
questioning by the observer. The study
was inadequately powered to detect a
difference in intravascular cannulation
between the two groups.
Prospective, randomized, study (n = 300
parturients).
Arrow FlexTip Plus® (Teleflex®, Durham, NC, formerly Arrow International, Reading, PA); Concord/Portex® (Smiths Medical, St. Paul, MN).
NA = not assessed.
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Wire-reinforced catheters, manufactured in the United
States by Teleflex® (Durham, NC; formerly Arrow International, Reading, PA), B. Braun Medical Inc. (Bethlehem, PA),
and Epimed (Johnstown, NY) represent the most recent technological advance in epidural catheter design. The inner wire
coil is designed to provide sufficient columnar strength for insertion, lumen patency, and kink resistance,36 and is surrounded
by either a polyurethane or nylon-blend catheter, depending on
the manufacturer. The technique by which the outer coating
is attached to the inner stainless steel spring also varies with
the manufacturer; some use a “tipping” process in which the
proximal and distal ends alone are melded together, whereas
others secure the entire length of the coil to the surrounding
material in a proprietary extrusion process. Wire-reinforced
catheters are all designed with fewer coils in the distal tip,
which reportedly confers greater flexibility to minimize paresthesias and perforations of the dura and epidural vessels,31 and
with distal and proximal flashback windows for visualization
of cerebrospinal fluid or blood. Adult versions are 19-gauge in
diameter (designed for use with a 17-gauge epidural needle)
and are available in either single end-hole (i.e., open-tipped)
or closed-tipped, multiorifice versions, with or without a stylet.
The catheter bodies are radiopaque; however, one manufacturer
considers its catheter “magnetic-resonance-conditional” based
on nonclinical testing, which allows for use under specific conditions (i.e., a static magnetic field of 3-Tesla or less, a maximum spatial gradient magnetic field of 720-Gauss/centimeter
or less, and a transmit/receive radio frequency head coil).
Epidural Catheter Design
demonstrated the greatest tensile strength. One nylon catheter demonstrated slightly less tensile strength, with another
nylon catheter demonstrating significantly less. The materials with the lowest tensile strength were polyethylene and
Teflon®. Interestingly, all catheters demonstrated less tensile
strength under traction from a steel hemostat, with polyurethane and polyethylene catheters exhibiting the least. These
findings suggest that the use of a stainless steel hemostat or
similar instruments should not be used to extract epidural
catheters that are difficult to remove.
Ateş et al.44 reported similar high tensile strength with
polyurethane catheters compared with clear nylon and radiopaque nylon catheters in their blinded, controlled study on
intact and traumatized catheters by three different manufacturers. Specifically, nontraumatized polyurethane catheters
stretched more than 300% of their original length without
breaking, whereas all other catheter specimens broke before
the elongation limit of the tensile testing machine was
reached. Of note, some clinicians have characterized the elasticity associated with the wire-reinforced polyurethane catheter as a disadvantage; the distal tip may remain immobile
and allow the proximal portion to stretch until breaking.45 In
the event of entrapment of wire-reinforced catheters, some
clinicians have indicated that removal may be facilitated by
placing the patient in the lateral decubitus position or in
the original insertion position, reattempting removal in 30
to 60 min, or applying gentle, continuous traction. Alternatively, threading a stylet into the catheter or injecting saline
into a soft springwound catheter has also been observed to
assist in extracting a “trapped” catheter.46
Other investigators have observed diminished tensile
strength of wire-reinforced versus non–wire-reinforced catheters and of springwound polyurethane catheters exposed
to higher temperatures. Asai et al.47 performed an ex vivo
study on the degree of stretching, the force required to snap,
and the site of breakage of four 19-gauge catheters made
by different manufacturers. The springwound polyurethane
Table 3. The Incidence of Complications in Studies Comparing Uniport and Multiport Epidural Catheters
Study
Michael et al.58
Collier and Gatt59
Catheter
Nylon uniport Portex®
Nylon multiport Portex®
Nylon uniport Portex®
Nylon multiport Portex®
D’Angelo et al.60
Nylon uniport Braun
Nylon multiport Braun
Jaime et al.61
Springwound uniport Arrow®
Nylon multiport Portex®
Paresthesia
Intravascular
Cannulation
Inadequate
Analgesia
12.2%
8.5%
28%
17.3%
5.7%
10.5%
4.0%
7.7%
32.7%
13.7%
32%
11.5%
41%
42%
7.0%
6.5%
31.8%
21.2%
6%
11.2%
1.1%
5.7%
3.3%
4.4%
Comment
Prospective, randomized, singleblind study (n = 802 patients).
Prospective, randomized,
single-blind study (n = 200
parturients). Terminated early
(n = 102) due to high incidence of inadequate analgesia
in uniport group.
Prospective, randomized,
unblinded study (n = 500
parturients).
Prospective, quality assurance
study (n = 1,352 parturients
uniport; n = 1,260 parturients
multiport).
Arrow® (Teleflex®, Durham, NC, formerly Arrow International, Reading, PA); Concord/Portex® (Smiths Medical, St. Paul, MN).
Anesthesiology 2014; 121:9-17
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catheter, Bouman et al.39 reported no significant difference
between the incidence of paresthesias between the two catheters (21.3 vs. 16.7%; P = 0.42). Overall, evidence suggests
that paresthesias occur less frequently with springwound
polyurethane catheters compared with non–wire-reinforced
nylon and polyamide–polyurethane blend catheters. Studies
comparing springwound catheters from different manufacturers, each of which has a different material surrounding the
inner wire coil, are currently lacking.
Catheter materials can also influence the incidence of
intravascular cannulation. Collectively, softer, single end-hole
catheters and, specifically, flexible wire-reinforced polyurethane catheters have been observed to have a lower incidence
of intravascular cannulation compared with conventional
catheters (table 3).41 Terasako et al.42 randomized 300
patients to receive either a 19-gauge wire-reinforced polyurethane open-tipped or a 19-gauge polyethylene open-tipped
catheter and found a statistically significant lower incidence
of intravascular cannulation in the former group (1 of 150
vs. 8 of 150). In a 1998 study, Banwell et al.40 randomized
200 parturients requesting continuous epidural analgesia to
receive either a nylon catheter or a wire-reinforced polyurethane catheter and reported 11 of 110 episodes of venous
cannulation in the former group and no cases in the latter
(P = 0.0007). As in the case of paresthesias, slight changes
in the materials of non–wire-reinforced catheters by a single
manufacturer seem to have a negligible impact on the incidence of epidural vein cannulation.
Catheter breakage also seems to be related to the
mechanical properties of materials used. However, comparative studies on the tensile strength of wire-reinforced versus
non–wire-reinforced catheters have resulted in conflicting
findings. Nishio et al.43 undertook a comparative study on
the tensile strength of seven different 19-gauge epidural
catheters under traction from both a stainless steel hemostat and a rubber-sleeved hemostat. When stretched with
a rubber-sleeved hemostat, catheters made of polyurethane
SPECIAL ARTICLES
Department of Anaesthesia, Queen Elizabeth Hospital, Barbados, West Indies) subsequently developed an open-ended,
blunt-tip catheter with a lateral hole 3 mm from the tip.34
Catheters with two lateral orifices on opposing sides, one at
5 mm and a second at 12 mm from the closed tip, and later,
with three orifices followed.54
Limited data preclude a robust assessment of whether the
position and number of catheter ports significantly affect the
spread of analgesia, incidence of paresthesias and intravascular cannulation, and potential for a multicompartmental
blockade. Some studies suggest that single-orifice, open-end
catheters reliably detect intravascular and subarachnoid
placements and limit infusions to one anatomic site. Multiorifice, closed-tipped catheters, when compared with single
end-hole catheters, have been observed to result in improved
injectate distribution,55 greater likelihood that aspiration of
cerebrospinal fluid or blood can occur from one of the orifices in the event of a misplaced catheter, and diminished
likelihood of orifice blockage by a clot or adjacent tissue.
Furthermore, the blunt-tipped multiport catheter is potentially less traumatic, reducing the likelihood of intravascular
cannulation. However, a multiport catheter can result in a
multicompartment block56 and preferential efflux from a
single or all ports based on the rate and pressure of injectate delivery.57 As a result of the preferential efflux, rapid
manual boluses are likely to recruit all ports, including the
distal port, for injectate delivery; theoretically, this may be
a reason why a distal port that has migrated into a vascular,
subarachnoid, or subdural location may go unnoticed during a slower, continuous infusion.
A number of studies have compared single- and multiorifice catheters to determine the optimal number and positioning of ports (table 3). A single-blind, randomized study
in 802 parturients found a significantly higher incidence of
inadequate analgesia with open-end, uniport (32.7%) versus
closed-end, multiport (13.7%) nylon catheters (P < 0.001).58
Although not reaching statistical significance, intravascular cannulation occurred more frequently in the closed-end
group (10.5 vs. 5.7%), but open-end catheters were reportedly more difficult to place. In a randomized, single-blind
study of smooth-tipped, open-end uniport versus closed-end,
multiport (8, 12, 16 mm from tip) nylon catheters, Collier
and Gatt59 planned to enroll 200 obstetric patients but were
forced to abandon the study after 102 patients had been
assessed due to the incidence of unsatisfactory block in the
uniport (32%, 16 of 50 patients) versus multiport (11.5%, 6
of 52 patients) group (P = 0.016). Ultimately, all patients with
unsatisfactory analgesia in the uniport group developed an
adequate block after catheter adjustments and redosing. The
overall rate of intravascular cannulation was low in both the
uniport (4%) and multiport (8%) groups. Pain or paresthesia
on insertion did not reach statistical significance between the
terminal (28%) and lateral orifice (17%) catheters.
In a randomized, nonblinded study on an 18-gauge multiport (three lateral ports) versus a uniport (single distal hole)
Innovations and Clinical Implications
in Catheter Tip Design
In 1962, J. Alfred Lee, M.R.C.S., L.R.C.P., M.M.S.A.,
F.F.A.R.C.S, D.A. (1906–1989; Senior Consultant Anaesthetist, Southend University Hospital, Westcliff-on-Sea,
Essex, United Kingdom) introduced a closed-tipped, flexible nylon catheter with a lateral opening 1 cm from the tip,
designed to facilitate insertion and minimize tissue trauma.53
A catheter with two lateral orifices for a more reliable spread
of local anesthetics soon followed, but was prone to kinking. Basil S. Skinner, M.D. (1917–1993; Chairman of the
Anesthesiology 2014; 121:9-17
15
R. D. Toledano and L. C. Tsen
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catheter stretched significantly more (P < 0.001) and
snapped at a significantly lower weight (P < 0.01) than the
three conventional non–wire-reinforced nylon catheters.
In comparing the tensile strength of similarly designed
19- and 20-gauge springwound polyurethane catheters at
22° and 37°C (“room” vs. “body” temperature), Tsui and
Finucane48 found a slightly reduced tensile strength of all
catheter samples at the higher temperature, with no significant differences between the two catheters at the two temperatures studied. The authors found that the mean fracture
force required to break either of these catheters at 37°C
was 1.98 and 1.99 kg; this was greater than both the previously reported mean force required to remove an epidural
catheter from a patient (0.17 to 0.32 kg) and the maximum
withdrawal force (1.17 kg). They concluded that these catheters were therefore unlikely to fracture under normal clinical circumstances.
Catheter occlusion, kinking, and/or knotting may be
associated with a number of factors, including the port configuration, depth of insertion, method of catheter fixation
to the skin, and, in the case of wire-reinforced catheters, the
method of attaching the inner wire coil to the surrounding
coating; however, one implicated cause has been the materials used to manufacture catheters. In the late 1990s, slight
alterations in the manufacturing materials used in Portex®
(Smiths Medical, St. Paul, MN) catheters were associated
with a globally reported high incidence of occluded catheters.49 Reinforced catheters, such as the BD Ribflex catheter
(Becton, Dickinson and Company, Franklin Lakes, NJ) with
internal longitudinal ribs throughout its length, introduced
in the 1990s, and, more recently, wire-reinforced catheters
have been observed to confer kink resistance, better flow
characteristics, and improved patency when compared with
non–wire-reinforced versions.50 Knotting of the epidural
catheter is a rare complication (with an estimated incidence
of 0.0015% and rate of one in 20,000 to 30,000)51 that can
lead to reinstrumentation, replacement, difficult removal,
and breakage. Limiting the amount of catheter threaded into
the epidural space may reduce the risk of this complication.
Reports regarding neurologic sequelae from retained portions of broken catheters have been uncommon, suggesting
that surgical removal is likely not warranted in the asymptomatic patient.52
Epidural Catheter Design
Illinois) for their assistance in obtaining primary information
sources.
Support was provided solely from institutional and/or
departmental sources.
nylon epidural catheter in 487 laboring patients, D’Angelo
et al.60 demonstrated that the multiport catheter had less
inadequate analgesia (21.2 vs. 31.8%, respectively, P <
0.05) and reduced need for catheter manipulation (44.2 vs.
31.4%, respectively, P < 0.05). The incidence of catheter
replacement, intravascular cannulation, and paresthesia on
insertion was similar in both groups. One uniport catheter
was inadvertently placed intrathecally.
To date, few published studies have compared traditional
multiport catheters and newer wire-reinforced catheters in
terms of analgesic efficacy or the incidence of complications. In a prospective quality assurance study, Jaime et al.61
compared clinical complications in 2,612 obstetric patients
who received epidural analgesia with either a 20-gauge
closed-tipped, multiport (three lateral ports) nylon catheter
or a 19-gauge open-end, uniport springwound polyurethane
catheter. The incidence of unsatisfactory block was similar in both the groups (nylon catheter 4.4%, 55 of 1,260
patients versus springwound polyurethane catheter 3.3%, 45
of 1,352 patients), but the incidence of paresthesias, venous
cannulation, and reinsertion related to venipuncture was significantly higher in the patients who received the non–wirereinforced nylon catheters.
Until recently, a comparative study on flexible,
wire-reinforced nylon or polyurethane catheters that differed
in the number of holes at the tip had not been undertaken.
However, a prospective, single-blind, randomized, controlled trial conducted in 2009 by Spiegel et al.62 investigated the success of labor analgesia, the number of episodes
of breakthrough pain requiring supplemental medicine, and
the occurrence of complications, such as paresthesias and
intravascular and intrathecal catheters, in 493 parturients
who received either a single end-hole wire-reinforced polyurethane catheter or a multiorifice wire-reinforced nylon
catheter. The authors found no statistically significant difference in outcomes between the two groups and postulated
that the flexibility afforded by the wire coil may eliminate
any of the potential advantages of the multiport design.
Competing Interests
Neither author has participated in studies of catheters either
funded by or with materials supplied by industry. In addition, neither author has received previous research support from epidural catheter manufacturers, participated in
funded trials, received travel support, or consulted for companies that manufacture epidural catheters.
Address correspondence to Dr. Tsen: Department of Anesthesiology, Perioperative and Pain Medicine, Brigham
and Women’s Hospital, Harvard Medical School, 75 Francis Street, Boston, Massachusetts 02115. ltsen@zeus.bwh.
harvard.edu. Information on purchasing reprints may be
found at www.anesthesiology.org or on the masthead page
at the beginning of this issue. ANESTHESIOLOGY’s articles are
made freely accessible to all readers, for personal use only,
6 months from the cover date of the issue.
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Epidural catheter material and tip design seem to affect the
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SPECIAL ARTICLES
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