ch03: sutures and suturing - clinical judeclinicaljude-5thyear.yolasite.com/resources/sutures &...
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Goals
A surgical suture is one that approximates theadjacent cut surfaces or compresses blood vesselsto stop bleeding. Suturing is performed to
1. Provide an adequate tension of wound clo-sure without dead space but loose enough toobviate tissue ischemia and necrosis
2. Maintain hemostasis3. Permit primary-intention healing4. Provide support for tissue margins until they
have healed and the support is no longerneeded
5. Reduce postoperative pain6. Prevent bone exposure resulting in delayed
healing and unnecessary resorption7. Permit proper flap position
Suture Material
Surgical sutures have been used to close woundssince prehistoric times (50,000–30,000 BC) gaveus the first written description of their use datingback as early as 4,000 BC (Macht and Krizek,1978). Many materials have been used through-out the centuries, such as gold, silver, hemp, fas-cia, hair, linen, and bark. Yet none have providedall of the desired characteristics.
Qualities of the Ideal Suture MaterialThe following qualities of the ideal suture mater-ial are compiled from Postlethwait (1971), Varmaand colleagues (1974), and Ethicon (1985):
1. Pliability, for ease of handling2. Knot security3. Sterilizability4. Appropriate elasticity5. Nonreactivity6. Adequate tensile strength for wound healing7. Chemical biodegradability as opposed to
foreign body breakdown
With the possible exception of coated Vicryl(Ethicon, Somerville, New Jersey), none of thesutures available today meet these criteria. Table3-1 lists the various materials—natural, synthet-ic, absorbable (digested by body enzymes orhydrolyzed), and nonabsorbable—available forperiodontal use.
Use
1. Silk and synthetic sutures are employed mostoften.
2. Gut sutures are used only when retrieval isdifficult when securing grafts and in youngerpatients. The limited physical characteris-tics of gut sutures do not warrant their rou-tine use.
3. When using gut (plain or chromic) sutures,it is often advantageous to soak the packagein warm water for a half-hour and to pullgently but firmly on the suture whenopened. This will remove the kinks andstraighten the suture. Finally, lubricating thesuture lightly with petrolatum or sterile bonewax will prevent brittleness. Note: This is notnecessary with Ethicon sutures.
4. Monofilament sutures are recommendedfor bone augmentation procedures to pre-vent “wicking,” reduce the inflammatoryresponse, and permit longer retention(10–14 days).
5. Gore-Tex (Flagstaff, Arizona) and coatedVicryl sutures are recommended for guidedtissue regeneration procedures.
Material Choice
The choice of materials depends on the following:
1. Surgical Procedurea. Plastic procedures
Suture Site 4-0 to 6-0Needle Size P-3*Material Chromic gut, silk,
monofilamentb. Regeneration
Suture Site 3-0 to 5-0Needle Size P-3; RT-16†
Material Gore-Tex, Vicrylc. Apically positioned flaps
Suture Site 4-0Needle Size J-1; FS2; P-3Material silk
d. Periosteal suturingSuture Site 4-0 or 5-0Needle Size J-1; P-3Material silk
e. ExtractionsSuture Site 3-0 or 4-0Needle Size FS-2; X-1Material silk
2. Biocompatibility‡
3. Clinical experience and preference4. Quality and thickness of tissue5. Rate of absorption versus time for tissue
healing
Table 3-2 outlines the charateristics and applica-tions of resorbable and nonresorbable sutures.
Note: Because silk is a multifilament material that“wicks,” it is not the material of choice when anysterile materials are used (eg, implants, bonegrafts, guided tissue regeneration, or guided boneregeneration) or in the presence of infection (Sil-verstein and Kurtzman, 2005). The ideal materialfor these procedures is expanded polytetrafluo-roethylene (ePTFE).
Knots and Knot Tying
“Suture security is the ability of the knot andmaterial to maintain tissue approximation duringthe healing process” (Thacker and colleagues,1975). Failure is generally the result of untyingowing to knot slippage or breakage. Since the knotstrength is always less than the tensile strength ofthe material, when force is applied, the site of dis-ruption is always the knot (Worsfield, 1961;Thacker and colleagues, 1975). This is becauseshear forces produced in the knot lead to breakage.
Knot slippage or security is a function of thecoefficient of friction within the knot (Price,1948; Hermann, 1971). This is determined by thenature of the material, suture diameter, and typeof knot. Monofilament and coated sutures(Teflon, silicon) have a low coefficient of frictionand a high degree of slippage; braided and twist-ed sutures such as uncoated Dacron and catgut
3
Sutures and Suturing
*Small needles (P-3) are more difficult to negotiate the
posterior interproximal areas.†Gore-Tex.
‡These recommendations are not for microsurgical
procedures.
Cohen_015-028_03.qxd 11/16/06 8:23 PM Page 15
16 Basics
Tabl
e 3-
1Su
ture
s an
d Su
turi
ng
Sutu
re T
ensi
le
Tis
sue
Kn
ot T
ensi
le
Sutu
reTy
pes
Raw
Mat
eria
lA
bsor
ptio
nSt
ren
gth
Rea
ctio
nSt
ren
gth
Indi
cati
ons
Eas
e of
Han
dlin
g
Surg
ical
gu
tP
lain
Col
lage
n f
rom
hea
lthy
D
iges
ted
by b
ody
+
Mod
erat
e +
++
Rap
idly
hea
ling
Abs
orba
ble;
shou
ld n
ot b
e u
sed
mam
mal
sen
zym
es w
ith
in
(lea
st)
++
++
mu
cosa
wh
ere
exte
nde
d ap
prox
imat
ion
70 d
Avo
id s
utu
re
ofti
ssu
es u
nde
r st
ress
is r
equ
ired
rem
oval
Sh
ould
not
be
use
d in
pat
ien
ts
wit
h k
now
n s
ensi
tivi
ties
or
alle
rgie
s to
col
lage
n o
r ch
rom
ium
Surg
ical
gu
tC
hro
mic
Col
lage
n f
rom
hea
lthy
D
iges
ted
by b
ody
+M
oder
ate
but
less
++
+A
s ab
ove;
slow
er
mam
mal
s tr
eate
den
zym
es w
ith
in
than
pla
in g
ut
abso
rpti
onw
ith
ch
rom
ic s
alts
90 d
++
++
Coa
ted
Vic
ryl
Bra
ided
C
opol
ymer
of
lact
ide
Hyd
roly
sis
++
+M
ild
++
Sube
pith
elia
l +
++
(pol
ygla
ctin
910
)C
oate
dan
d gl
ycol
ide
coat
ed
56–7
0 d
++
mu
cosa
l su
rfac
esw
ith
pol
ygla
ctin
370
V
esse
l lig
atio
n
and
calc
ium
ste
arat
eA
ll ty
pes
ofge
ner
al c
losu
reD
exon
B
raid
edH
omop
olym
er o
fSl
ow h
ydro
lysi
s af
ter
++
+M
ild+
+Su
bepi
thel
ial
++
++
(pol
ygly
colic
aci
d)C
oate
dgl
ycol
ic a
cid
coat
ed
60–9
0 d
++
sutu
res
wit
h p
olax
amer
188
Mu
cosa
l su
rfac
esV
esse
l lig
atio
nP
DS
(pol
ydio
xan
one)
Mon
ofila
men
tPo
lyes
ter
Slow
hyd
roly
sis
++
++
Slig
ht
++
Abs
orba
ble
sutu
re
++
Bra
ided
poly
mer
180–
210
d+
wit
h e
xten
ded
wou
nd
supp
ort
Surg
ical
silk
Mon
ofila
men
tN
atu
ral p
rote
in f
iber
U
sual
ly c
ann
ot b
e +
+M
oder
ate
+M
uco
sal s
urf
aces
++
++
Bra
ided
ofra
w s
ilk t
reat
ed
fou
nd
afte
r 2
yr+
++
+(l
east
)Sh
ould
not
be
use
d in
pat
ien
tsw
ith
sili
con
pro
tein
w
ith
kn
own
sen
siti
viti
es o
ror
wax
alle
rgie
s to
silk
Nyl
on D
ura
lon
Eth
ilon
Mon
ofila
men
tLo
ng-
chai
n a
liph
atic
D
egra
des
at a
rat
e +
++
Ext
rem
ely
++
Skin
clo
sure
++
poly
mer
sof
15–2
0%/y
rlo
w 0
- +
Nyl
on 6
or
nylo
n 6
.6N
ylon
Du
ralo
n
Bra
ided
Poly
amid
e po
lym
erD
egra
des
at a
rat
e +
++
Ext
rem
ely
++
Skin
clo
sure
++
++
Sueg
ilon
of15
–20%
/yr
low
0-
+M
uco
sal s
urf
aces
Poly
este
r M
ersi
len
e B
raid
edPo
lyes
ter,
Poly
ethy
len
e,N
onab
sorb
able
++
+M
inim
al +
++
+C
ardi
ovas
cula
r,+
++
Dac
ron
Eth
ibon
dTe
reph
thal
ate
coat
ed
plas
tic,
gen
eral
N
one
know
nw
ith
pol
ybu
tila
tesu
rger
yPe
olen
e M
onof
ilam
ent
Poly
mer
of
prop
ylen
eN
onab
sorb
able
++
+M
inim
al+
+
+G
ener
al,p
last
ic,
++
(pol
ypro
pyle
ne)
tran
sien
t ac
ute
ca
rdio
vasc
ula
r,re
acti
onsk
in s
urg
ery
Gor
e-Te
xM
onof
ilam
ent
Exp
ande
d N
onab
sorb
able
++
+E
xtre
mel
y +
+A
ll ty
pes
ofso
ft
++
++
poly
tetr
aflu
oroe
thyl
ene
low
tiss
ue
appr
oxi-
Not
kn
own
(eP
TFE
)m
atio
n a
nd
card
iova
scu
lar
surg
ery
Mon
ocry
l M
onof
ilam
ent
Polig
leca
pron
e 25
Hyd
roly
sis
90–1
20 d
++
++
Min
imal
++
++
Soft
tis
sue
++
+(p
olig
leca
pron
e 25
)C
opol
ymer
of
glyc
olid
e cl
osu
reA
bsor
babl
e;sh
ould
not
be
use
d an
d ca
prol
acto
ne
wh
ere
exte
nde
d ap
prox
imat
ion
of
tiss
ues
un
der
stre
ss is
req
uir
ed
Cohen_015-028_03.qxd 11/16/06 8:23 PM Page 16
Sutures and Suturing 17
Tabl
e 3-
2C
hara
cter
isti
cs a
nd
App
licat
ion
s of
Res
orba
ble
and
Non
reso
rbab
le S
utu
res
Sutu
re
Dis
cipl
ine
Ten
sile
Str
engt
h Ty
pe o
fNee
dle
Dia
met
er o
fM
ater
ial
Type
ofM
ater
ial
Rec
omm
ende
d G
ener
al a
nd
Spec
ific
Te
chn
iqu
eU
sed
Req
uir
emen
tsR
ecom
men
ded
Rec
omm
ende
dR
ecom
men
ded
Kn
otSi
tuat
ion
s U
sed
Inte
rru
pted
Pe
riod
onto
logy
,den
tal
Min
imal
to
3 / 8re
vers
e cu
ttin
g,4-
0C
hro
mic
gu
t,si
lk
Slip
kn
otIn
terp
roxi
mal
su
turi
ng
sutu
reim
plan
t an
d or
al s
urg
ery
mod
erat
eta
pere
dpo
lyte
traf
luor
oeth
ylen
e (P
TFE
)1 / 2
or 5 / 8
reve
rse
4-0
Poly
este
r “c
olor
”br
aide
d,Su
rgeo
n’s
knot
cutt
ing,
tap
ered
poly
prop
ylen
e,m
onof
ilam
ent
nylo
n5-
0C
hro
mic
gu
t,gu
tSl
ip k
not
*Fl
aps
not
un
der
ten
sion
Tape
r-cu
t5-
0Po
lyes
ter
“col
or”
brai
ded,
Surg
eon’
s kn
otpo
lypr
opyl
ene,
mon
ofila
men
t ny
lon
Figu
re e
igh
t Pe
riod
onto
logy
an
d de
nta
l M
inim
al t
o 3 / 8
reve
rse
cutt
ing,
4-0
Ch
rom
ic g
ut,
gut,
silk
,Sl
ip k
not
Pri
mar
y lin
gual
of
man
dibu
lar
mol
ar
sutu
reim
plan
t su
rger
y,m
oder
ate
tape
r-cu
tP
TFE
regi
onex
trac
tion
sit
esSl
ing
sutu
rePe
riod
onto
logy
,den
tal
Mod
erat
e3 / 8
reve
rse
cutt
ing,
4-0
Ch
rom
ic g
ut,
silk
,PT
FESl
ip k
not
Use
d w
hen
a f
lap
has
bee
n e
leva
ted
on
impl
ant
and
oral
su
rger
yta
per-
cut
only
on
e si
deH
oriz
onta
l D
enta
l im
plan
t an
d or
al
Hig
h3 / 8
reve
rse
cutt
ing,
3-0
Poly
glyc
olic
aci
d (P
GA
)Su
rgeo
n’s
knot
Use
d in
an
teri
or m
andi
ble
or p
oste
rior
m
attr
ess
surg
ery
tape
r-cu
tre
gion
to
resi
st m
usc
le p
ull
sutu
reV
erti
cal
4-0
Ch
rom
ic,g
ut,
silk
Slip
kn
otU
sed
to r
esis
t m
usc
le p
ull,
clos
ely
adap
t m
attr
ess
flap
s to
bon
e an
d ei
ther
tee
th o
r su
ture
den
tal i
mpl
ants
Can
als
o be
use
d to
api
cally
or
coro
nal
ly
posi
tion
fla
ps3-
0P
GA
Surg
eon’
s kn
otU
sed
to r
esis
t m
usc
le p
ull,
clos
ely
adap
t fl
aps
to b
one
and
eith
er t
eeth
or
den
tal i
mpl
ants
Can
als
o be
use
d to
api
cally
or
coro
nal
ly
posi
tion
fla
ps3-
0Si
lkSl
ip k
not
Use
d to
res
ist
mu
scle
pu
ll,cl
osel
y ad
apt
flap
s to
bon
e an
d ei
ther
tee
th o
r de
nta
l im
plan
tsC
an a
lso
be u
sed
to a
pica
lly o
r co
ron
ally
po
siti
on f
laps
Ver
tica
l slin
g Pe
riod
onto
logy
,den
tal
Hig
h3 / 8
reve
rse
cutt
ing,
3-0
PG
ASu
rgeo
n’s
knot
Use
d to
res
ist
mu
scle
pu
ll,cl
osel
y ad
apt
mat
tres
s im
plan
t an
d or
al s
urg
ery,
tape
r-cu
tfl
aps
to b
one,
rege
ner
ativ
e ba
rrie
rs,
sutu
rees
peci
ally
wh
en
and
den
tal i
mpl
ants
,alo
ng
wit
h
perf
orm
ing
guid
ed t
issu
e m
ain
tain
ing
appr
oxim
atio
n o
ffl
ap
and
bon
e re
gen
erat
ive
edge
ste
chn
iqu
es4-
0Si
lkSl
ip k
not
Use
d to
res
ist
mu
scle
pu
ll,cl
osel
y ad
apt
flap
s to
bon
e,re
gen
erat
ive
barr
iers
,an
d de
nta
l im
plan
ts,a
lon
g w
ith
mai
n-
tain
ing
appr
oxim
atio
n o
ffl
ap e
dges
Con
tin
uou
s Pe
riod
onto
logy
,den
tal
Hig
h3 / 8
reve
rse
cutt
ing,
3-0
PG
ASu
rgeo
n’s
knot
Use
d pr
imar
ily in
ede
ntu
lou
s ar
eas
such
in
depe
nde
nt
impl
ant
and
oral
su
rger
yta
per-
cut
as m
andi
bula
r an
teri
or o
r po
ster
ior
slin
g su
ture
regi
on t
o re
sist
mu
scle
pu
ll4-
0Si
lkSl
ip k
not
Use
d of
ten
in d
enta
l im
plan
t an
d bo
ne
augm
enta
tion
pro
cedu
res
and
in
hype
rpla
stic
/fib
rou
s ri
dge
redu
ctio
n
for
den
ture
sta
bilit
y
*Res
tric
ted
area
s su
ch a
s bu
ccal
ves
tibu
le m
axill
ary
mol
ars
or m
uco
gin
giva
l su
rger
y (e
g,so
ft t
issu
e gr
afts
).(S
ilver
stei
n L
,199
9)
Cohen_015-028_03.qxd 11/16/06 8:23 PM Page 17
have greater knot security because of their highcoefficient of friction (Taylor, 1938).
It is interesting to note that basic suture silk,although extremely user friendly, is distinctlyinferior in terms of strength and knot securitycompared with other materials (Hermann, 1971).It also shows a high degree of tissue reaction(Postlethwait, 1968; Taylor, 1978), and the addi-tion of wax or silicon to reduce the tissue reactionand prevent wicking further diminishes knotsecurity (Hermann, 1971).
Knot selection is the last of the variables andthe one over which surgeons have the most influ-ence. Knot security has been found to vary great-ly among clinicians, and even the security ofknots tied by the same clinician varies at differenttimes (Hermann, 1971).
A sutured knot has three components (Fig-ure 3-1) (Thacker and colleagues, 1975):
1. The loop created by the knot (Figure 3-1A)2. The knot itself, which is composed of a num-
ber of tight “throws” (Figure 3-1B;); eachthrow represents a weave of the two strands
3. The ears, which are the cut ends of the suture
In Figure 3-2, we see the four knots mostcommonly used in periodontal surgery. In astudy, Thacker (1975) found that the granny knotwas the least secure, always requiring morethrows or ties to achieve the same knot strengthas the square or surgical knot. For materials witha high degree of slippage (monofilament or coat-ed sutures), flat and square throws were recom-mended, with all additional throws being squared.Cutting the ears of the suture too short is con-traindicated when slippage is great because theknot will come untied if the slippage exceeds thelength of the ears. Loosely tied knots were shownto have the highest degree of slippage, whereas intight knots, slippage was not a significant factor.
Principles of Suturing
Ethicon (1985) recommends the following prin-ciples for knot tying:
1. The completed knot must be tight, firm, andtied so that slippage will not occur.
2. To avoid wicking of bacteria, knots shouldnot be placed in incision lines.
3. Knots should be small and the ends cut short(2–3 mm).
4. Avoid excessive tension to finer-gauge mate-rials because breakage may occur.
5. Avoid using a jerking motion, which maybreak the suture.
6. Avoid crushing or crimping of suture mate-rials by not using hemostats or needle hold-ers on them except on the free end for tying.
7. Do not tie the suture too tightly because tis-sue necrosis may occur. Knot tension shouldnot produce tissue blanching.
8. Maintain adequate traction on one endwhile tying to avoid loosening the first loop.
9. The surgeons knot and square knot strength,although generally not needing more thantwo throws, will have increased strength withan additional throw.
10. Granny knots and coated and monofilamentsutures require additional throws for knotsecurity and to prevent slippage. CoatedVicryl will hold with four throws—two fullsquare knots.
Sutures should be removed as atraumatical-ly and cleanly as possible. Ethicon (1985) recom-
mends the following principles for sutureremoval:
1. The area should be swabbed with hydrogenperoxide for removal of encrusted necroticdebris, blood, and serum from about thesutures.
2. A sharp suture scissors should be used to cutthe loops of individual or continuous suturesabout the teeth. It is often helpful to use a no.23 explorer to help lift the sutures if they arewithin the sulcus or in close opposition tothe tissue. This will avoid tissue damage andunnecessary pain.
18 Basics
FIGURE 3-1. Knot anatomy. A, Various knot components prior to completion. B, Completed knot anatomy.
FIGURE 3-2. Suturing knots.
Cohen_015-028_03.qxd 11/16/06 8:23 PM Page 18
Sutures and Suturing 19
3. A cotton pliers is now used to remove thesutures. The location of the knots should benoted so that they can be removed first. Thiswill prevent unnecessary entrapment underthe flap.
Note: Sutures should be removed in 7 to 10 days toprevent epithelialization or wicking about the suture.
Surgical NeedlesMost surgical needles are fabricated from heat-treated steel and possess a microsilicon finish todiminish tissue drag and a tip that is extremelysharp and has undergone electropolishing(Ethicon, 1985). The surgical needle has a basicdesign composed of three parts (Figure 3-3):
1. The eye which is press-fitted or swaged (eye-less) permits the suture and needle to act asa single unit to decrease trauma.
2. The body which is the widest point of needleand is also referred to as the grasping area. Thebody comes in a number of shapes (round,oval, rectangular, trapezoid, or side flattened).
3. The point which runs from the tip of themaximum cross-sectional area of the body.The point also comes in a number of differ-ent shapes (conventional cutting, reversecutting, side cutting, taper cut, taper, blunt)(Figure 3-4).
4. The chord length is the straight line distancebetween the point of a curved needle and theswage.
5. The radius is the distance measured from thecenter of the circle to the body of the needleif the curvature of the needle was continuedto make a full circle.
Needle Holder SelectionEthicon (1985) gives the following pointers forselecting a needle holder:
1. Use an approximate size for the given needle.The smaller the needle, the smaller the nee-dle holder required.
2. The needle should be grasped one-quarter tohalf the distance from the swaged area to thepoint, as shown in Figure 3-5.
3. The tips of the jaws of the needle holdershould meet before the remaining portionsof the jaws.
4. The needle should be placed securely in the tipsof the jaws and should not rock, twist, or turn.
5. Do not overclose the needle holder. Itshould close only to the first or secondrachet. This will avoid damaging or notch-ing the needle.
6. Pass the needle holder so that it is alwaysdirected by the surgeon’s thumb.
7. Do not use digital pressure on the tissue; thismay puncture a glove.
Placement of Needle in TissueEthicon (1985) gives the following principles forplacing the needle in tissue:
1. Force should always be applied in the direc-tion that follows the curvature of the needle.
2. Suturing should always be from movable tononmovable tissue.
3. Avoid excessive tissue bites with small needlesbecause it will be difficult to retrieve them.
4. Use only sharp needles with minimal force.Replace dull needles.
5. Grasp the needle in the body one-quarter tohalf the length from the swaged area. Do nothold the swaged area; this may bend or breakthe needle. Do not grasp the point areabecause damage or notching may result (seeFigure 3-5).a. Prior to suturing, the needle holder is
repositioned to the forward half of theneedle with a few millimeters of the tip,as shown in Figure 3-5.
6. The needle should always penetrate the tis-sue at right angles.a. Never force the needle through the tissue.
7. Avoid retrieving the needle from the tissueby the tip. This will damage or dull the nee-dle. Attempt to grasp the body as far back as possible.
9. An adequate tissue bite (≥ 2–3 mm) isrequired to prevent the flap from tearing.
Suturing Techniques
Different suturing techniques may employ eitherperiosteal or nonperiosteal suture placement:
1. Interrupteda. Figure eightb. Circumferential director loopc. Mattress—vertical or horizontald. Intrapapillary
2. Continuousa. Papillary slingb. Vertical mattressc. Locking
The choice of technique is generally made onthe basis of a combination of the individual oper-ator’s preference, educational background, andskill level, as well as surgical requirements.
Periosteal Suturing
Periosteal suturing generally requires a highdegree of dexterity in both flap management andsuture placement. Small needles (P-3), finesutures (4-0 to 6-0), and proper needle holdersare a basic requirement. Periosteal suturing per-mits precise flap placement and stabilization.
TechniqueThe five steps here are used in periosteal suturing(Chaiken, 1977) and are seen in Figure 3-6:
FIGURE 3-3. Needle anatomy. Needles are described by their arc. Most periodontal surgical needles are ofthree-eighths or one-half curvature. Different components of the needle are described.
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FIGURE 3-4. Cutting needles. Both outline and cross-sectional views of the various forms of cutting needle are shown. Conventionalcutting and reverse cutting are also shown.
FIGURE 3-5. Correct handling of suture needles. A, Needle holder holding a suture needle just anterior tothe curvature; correct position; A', suture needle undamaged. B, Suture needle held incorrectly at tip; B', tipof suture needle damaged. C, Suture needle held incorrectly behind curvature; C', needle bent as a result.
A A'
B B'
C C'
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1. Penetration: The needle point is positionedperpendicular (90°) to the tissue surface andunderlying bone. It is then inserted com-pletely through the tissue until the bone isengaged. This is as opposed to the usual 30°needle insertion angle (see Figure 3-6A).
2. Rotation: The body of the needle is nowrotated about the needle point in the direc-tion opposite to that in which the needle isintended to travel. The needle point is held
tightly against the bone so as not to damageor dull the needle point (see Figure 3-6B).
3. Glide: The needle point is now permitted toglide against the bone for only a short dis-tance. Care must be taken not to lift or dam-age the periosteum (see Figure 3-6C).
4. Rotation: As the needle glides against thebone, it is rotated about the body, followingits circumferenced outline. In this way, theneedle will not be pushed through the tissue,
resulting in lifting or tearing of the perios-teum (see Figure 3-6, D and E).
5. Exit: The final stage of gliding and rotation isneedle exit. The needle is made to exit thetissue through the gentle application of pres-sure from above, thus allowing the tip topierce the tissue. If digital pressure is to beused, care must be used to avoid personalinjury (see Figure 3-6F).
1
2
FIGURE 3-6. Periosteal suturing. A, Needle penetration; needle point is perpendicular to bone. B, Rotation of needle body about point.C,D, The needle is moved along the bone below the periostum. E, Rotation about needle body permitting point to exit periosteum andtissue. F, Completed periosteal suture.
A
D E F
B C
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Interrupted Sutures
IndicationsInterrupted sutures are most often used for thefollowing:
1. Vertical incision2. Tuberosity and retromolar areas3. Bone regeneration procedures with or with-
out guided tissue regeneration4. Widman flaps, open flap curettage, unreposi-
tioned flaps, or apically positioned flaps wheremaximum interproximal coverage is required
5. Edentulous areas6. Partial- or split-thickness flaps7. Osseointegrated implants
TypesIn Figure 3-7, we see the four most commonlyused interrupted sutures:
1. Circumferential, direct, or loop (see Figure3-7A)
2. Figure eight (see Figure 3-7B)3. Vertical or horizontal mattress (see Figure
3-7C)4. Intrapapillary placement (see Figure 3-7D)
Technique
Figure Eight and Circumferential Sutures.Suturing is begun on the buccal surface 3 to 4 mmfrom the tip of the papilla to prevent tearing of thethinned papilla. The needle is first inserted intothe outer surface of the buccal flap and then eitherthrough the outer epithelialized surface (figureeight) (Figure 3-8) or the connective tissue underthe surface (circumferential) (see Figure 3-8A) ofthe lingual flap. The needle is then returned throughthe embrasure and tied buccally.
When interproximal closure is critical, thecircumferential suture will permit greater coapta-tion and tucking down of the papilla because ofthe lack of intervening suture material betweenthe tips of the papilla.
Mattress Sutures. Mattress sutures are used forgreater flap security and control; they permitmore precise flap placement, especially whencombined with periosteal stabilization. They alsoallow for good papillary stabilization and place-ment. The vertical mattress (nonperiosteal) sutureis recommended for use with bone regenerationprocedures because it permits maximum tissue clo-
sure while avoiding suture contact with the implantmaterial, thus preventing wicking. They are left for14 to 21 days (Mejias, 1983) and therefore requirea suitable material (eg, nylon, e-PTFE) that isbiologically inert and does not rapidly “wick.”
Vertical Mattress Technique. The flap is stabi-lized and a P-3 needle is inserted 7 to 10 mm api-cal to the tip of the papilla. It is passed through theperiosteum (if periosteal sutures are being used),emerging again from the epithelialized surface ofthe flap 2 to 3 mm from the tip of the papilla. Theneedle is brought through the embrasure, wherethe technique is again repeated lingually or palatal-ly. The suture is then tied buccally (Figure 3-9A).
Horizontal Mattress Technique. A P-3 needle isinserted 7 to 8 mm apical to and to one side of themidline of the papilla, emerging again 4 to 5 mmthrough the epithelialized surface on the oppos-ing side of the midline (Figure 3-9B). The suturemay or may not be brought through the perios-teum. The needle is then passed through theembrasure, and the suture, after being repeatedlingually or palatally, is tied buccally. For greaterpapillary stability and control, the double parallel
A B
FIGURE 3–7. Four interrupted sutures. A, Circumferential. B, Figure-eight. C, Vertical mattress. D, Intrapapillary.
C D
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A B
FIGURE 3-8. A, Circumferential suture. B, Figure-eight suture.
A B
FIGURE 3-9. A, Horizontal mattress suture. B, Vertical mattress suture.
A B C
FIGURE 3-10. Sling suture about adjacent tooth.
D E F
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FIGURE 3-11. Sling suture about single tooth.
A
E FD
B C
strands of this suture can be made to cross overthe three tops of the papillae. This is the doublecrossed-over suture.
Intrapapillary Placement. This technique is rec-ommended for use only with modified Widmanflaps and regeneration procedures in which there isadequate thickness of the papillary tissue.
A P-3 needle is inserted buccally 4 to 5 mmfrom the tip of the papilla and passed through thetissue, emerging from the very tip of the papilla.This is repeated lingually and tied buccally, thuspermitting exact tip-to-tip placement of the flaps(see Figure 3-7D).
Sling Suture. The sling suture is primarily usedfor a flap that has been raised on only one side ofa tooth, involving only one or two adjacent papil-lae. It is most often used in coronally and lateral-ly positioned flaps. The technique involves use ofone of the interrupted sutures, which is eitheranchored about the adjacent tooth (Figure 3-10)or slung around the tooth to hold both papillae(Figure 3-11).
Specialized Interrupted Suturing Techniques forBone Regeneration and Retromolar and Tuberos-ity Areas. Laurell Modification. Laurell modi-fied mattress suture (1993) (Figure 3-12) for coro-nal flap positioning and primary flap coverage is atechnique which, although capable of beingemployed for all regenerative techniques, is used
sion and above the first suture (Figure 3-13A2).The suture is passed through the interproximalpapilla and returned as a horizontal mattresssuture on the buccal surface and tied off.
Retromolar Suture Modification for Primary Cov-erage. This technique (Hutchenson 2005) (Fig-ure 3-14) is specially designed for gaining inti-mate tissue-tooth contact where regeneration isbeing attempted. It is employed when there is anintrabony defect distal to the last tooth on thelower teeth. It not only permits primary flap clo-sure but close approximation of the tissue on thedistal aspect of the tooth. Figure 3-14A shows adefect distal to the last tooth. The arrows on Fig-ure 3-14B indicates desired movement of flap anddotted lines indicate ideal flap position. Flap ide-ally should be positioned against distal surface oftooth with primary closure. Suture is begun onthe mesiobuccal of the terminal tooth (Figure3-14C1). The suture is passed through interprox-imal to the distal and inserted through only theundersurface of the buccal flap. The suture isbrought almost 360° around the tooth startinglingually and continuing bucally until againreaching the distal surface (Figure 3-14C2). Theneedle is passed through the undersurface of thelingual flap and tied on the buccal surface (Figure3-14C3). Figure 13-14D shows suturing havingbeen completed and primary coverage attained.
predominantly when standard interproximal inci-sions are used. Start bucally below the papilla (2–4mm) and insert the needle to and then throughthe undersurface of the lingual flap (Figure 3-12A1). The suture needle is then reinserted lin-gually 2–4 mm above the initial suture and contin-ued to and then through the buccal flap (Figure3-12A2). The suture is then brought lingually overthe coronal aspect of the flap and through the loop(Figure 3-12A3). The suture is afterwards returnedbucally and sutured (Figure 3-12A4). Figure 3-12Bshows the completed suture.
Modified Flap Suturing Technique. This tech-nique (Cortellini et al 1995) was introducedspecifically for achieving maximum interproxi-mal coverage and primary closure over intrabonydefect is treated by GTR. The modified flap tech-nique (Figure 3-13) requires the initial incisionbe made at the buccal line angles in the area ofthe interproximal defect. It is a papillary preser-vation technique. The suturing permits coronalpositioning, flap stabilization, and primary inter-proximal closure. The first suture is begun buc-cally 5–6 mm below the initial incision (Fig-ure 3-13A1). The suture is passed through thebuccal and palatal flaps. It is then reinsertedpalatally and allowed to exit the buccal flap 2 mmabove the initial placements. This is tied off andshould stabilize the body of the flap. The secondsuture is now begun 3–4 mm below the initial inci-
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FIGURE 3-12. Laurell modified mattress suture (see text). FIGURE 3-13. Modified flap suturing technique (see text).
Continuous Sutures Sling
When multiple teeth are involved, the continuoussuture is preferred.
Advantages1. Can include as many teeth as required2. Minimizes the need for multiple knots3. Simplicity4. The teeth are used to anchor the flap5. Permits precise flap placement6. Avoids the need for periosteal sutures7. Allows independent placement and tension
of buccal and lingual or palatal flaps. Buccalflaps can be positioned loosely, whereas lin-gual and palatal flaps are pulled more tightlyabout the teeth.
8. Greater distribution of forces on the flaps
DisadvantagesThe main disadvantage of continuous sutures isthat if the suture breaks, the flap may become
loose or the suture may come untied from multi-ple teeth.
TypesThe choice of continuous suture depends on theoperator’s preference. These, too, can be periostealor nonperiosteal:
1. Independent sling suture2. Mattress sutures
a. Verticalb. Horizontal
3. Continuous locking
Technique
Independent Sling SutureThe continuous sling suture (Figure 3-15),although most often begun as a continuation oftuberosity or retromolar suturing (see Figure3-15A), can also be started with a looped sutureabout the terminal papilla (buccal, lingual, orpalatal). It is then continued through the next
interproximal embrasure (see Figure 3-15B) insuch a manner that the suture is made to encirclethe neck of the tooth (see Figure 3-15C). Theneedle is then passed either over the papilla andthrough the outer epithelialized surface or under-neath and through the connective tissue under-surface of the papilla. The needle is passed againthrough the embrasure and continued anteriorly(Figure 3-15D). This procedure is repeatedthrough each successive embrasure until allpapillae have been engaged.
Note: For maximum flap control, it is best to passthe needle through the connective tissue under-surface of the papilla.
A terminal end loop (Figure 3-15E) is thenused if a single flap has been reflected or if theflaps are to be sutured independently. In thismanner, the flaps are tied against the teeth asopposed to each other.
FIGURE 3-14. Retromolar area modified suture technique (see text).
A B
C D
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Terminal End Loop. On completion of suturing,the suture is tied off against the tooth as opposedto the other flap. This is accomplished by leaving aloose loop of approximately 1 cm length of suturematerial before the last embrasure. When the lastpapilla is sutured and the needle is returnedthrough the embrasure, the terminal end loop isused to tie the final knot (Figure 3-15F–I).
Modification. When two flaps have beenreflected and after the first flap has been sutured(Figure 3-16A), it is often desirable to continueabout the distal surface of the last tooth (Figure3-16B), repeating the procedure on the opposingflap (Figure 3-16C) and then tying off in a termi-nal end loop (Figure 3-16D and E).
Alternative Procedure. This technique simulta-neously slings together both the buccal and lin-gual or palatal flaps.
INDICATIONS.1. When flap position is not critical2. When buccal periosteal sutures are used for
buccal flap position and stabilization3. When maximum closure is desired (unrepo-
sition or Widman flaps or bone regeneration)
FIGURE 3-15. Continuous sling suture with terminal end loop.
1 23
4
A
G H
E
B
I
F
C
D
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TechniqueAfter the initial buccal and lingual tie, the suture ispassed buccally about the neck of the tooth inter-dentally and through the lingual flap. It is thenagain brought interdentally through the buccalpapilla and back interdentally about the lingualsurface of the tooth to the buccal papilla. Then it isbrought about the lingual papilla and then thebuccal surface of the tooth. This alternating buc-cal-lingual suturing is continued until the suture istied off with a terminal end loop (Figure 3-17).
Vertical and Horizontal Mattress Suture. Whengreater papillary control and stability and moreprecise placement are required or to prevent flapmovement, vertical or horizontal mattress suturesare used. This is most often the case on the palate,where additional tension is often required, orwhen the papillary tissue is thin and friable.
through the remaining loop of the suture, and thesuture is pulled tightly, thus locking it. This proce-dure is continued until the final suture is tied off atthe terminal end (Figure 3-18).
Suture Removal
Sutures are used for wound stabilization andshould be removed when sufficient tissue strengthhas been achieved. This is usually between 5 and10 days, and in most instances, these sutures areremoved in 7 days.
Materials1. Scissors2. Cotton pliers3. Double-ended scaler4. Hydrogen peroxide5. Topical anesthetic6. Cotton swabs
Technique. The procedure is identical to thatpreviously described for the independent papil-lary sling suture (see Figure 3-15), except thatvertical or horizontal mattress sutures are substi-tuted for the simple papillary sling. The tech-nique is similar to that previously described forthe interrupted mattress sutures.
Locking. The continuous locking suture is indi-cated primarily for long edentulous areas,tuberosities, or retromolar areas. It has the advan-tage of avoiding the multiple knots of interruptedsutures. If the suture is broken, however, it maycompletely untie.
Technique. The procedure is simple and repeti-tive. A single interrupted suture is used to make theinitial tie. The needle is next inserted through theouter surface of the buccal flap and the underlyingsurface of the lingual flap. The needle is then passed
A
E
B C
D FIGURE 3-16. Continuous independent sling suture of indi-vidual flaps.
1
23
4
5 8
8 7 65
4
321
7 65
67
8
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FIGURE 3-17. Modification of continuous slingsuture. This technique permits simultaneous sutur-ing of both flaps.
ED
BA C
1
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3
4
5
6
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9
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2
3
4
5
6
7
89
1
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Method1. The scaler is used to remove the dressing.
The dressing should be loosened first in anapicocoronal direction. This will place thetension against the teeth and not the tissue.
2. The area is then gently swabbed with hydro-gen peroxide to move clotted blood, serum,and debris and is rinsed with warm water.
3. Topical anesthetic may be optionally applied
for reduction of patient sensitivity prior tosuture removal.
4. A sharp scissors should be used to cut theloops of the individual or continuoussutures. Note: It is often helpful to use the tipof an explorer to gently lift the suture off thetissue prior to cutting. This will avoid tissuedamage and unnecessary pain.
5. Interrupted sutures need be cut only on thefacial aspect close to the tissue.
6. Continuous sutures will require cutting bothbuccally and lingually.
7. Once the sutures are removed, the areashould again be swabbed with hydrogen per-oxide or chlorhexidine gluconate to removeany residual debris.
8. The teeth should be polished for completeremoval of debris and stain.
9. Plaque control should again be reviewed.
FIGURE 3-18. Continuous locking sutureused primarily for edentulous areas.
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