Mesh Implants, Pelvic Floor Surgery

TiLOOP® Patch

The titanised TiLOOP® Patch mesh implant is used for the surgical treatment of the central cystocele and rectocele defect. Thanks to its outstanding biocompatibility, it ensures excellent quality of life and shorter convalescence.

Outstanding biocompatibility  The mesh implant is titanised, very lightweight and hydrophilic and thus outstandingly biocompatible.

Excellent quality of life combined with shorter convalescence  Outstanding biocompatibility keeps inflammation rates to a minimum, prevents shrinkage and migration and ensures shorter convalescence. The implant is not recognized as a foreign body, and postoperative pain is prevented.

Globally unique technology  The nanotechnological finishing process for the covalent bonding of polypropylene and the titanium-dioxide surface is patented and thus completely unique.

Customised products  Individual mesh implants according to customer requirements complement the comprehensive, indication-specific portfolio of mesh implants. This has been made possible thanks to a special approval process for customised products.

  • Laser-cut edges
  • Large-pore structure
  • Monofilament fabric

pfm medical titanium gmbh

Höfener Straße 45

90431 Nürnberg, Germany

  • Tension-free titanised polypropylene mesh for defect-specific pelvic floor reconstruction (surgical treatment of complex cystocele and rectocele defects)
  • Material: polypropylene with covalently bonded titanised surface
  • Thickness of titanisation layer: approx. 30–50 nm
  • Fabric: knitted monofilament fibres
  • Edging: laser cut, rounded
Characteristics


extralight

light

Weight

16 g/m2

35 g/m2

Strength (DIN EN ISO 5084)

0,20 mm

0,30 mm

Pore size

≥ 1 mm

≥ 1 mm

Fibre diameter

30 dtex (65 µm)

58 dtex (90 µm)

Porosity 2D

73 %

61 %

Porosity 3D

91 %

87 %

Physiological elasticity at 16 N

23 %

20 %

Tensile strength (Grab test)

37 N

61 N

Sizes (mm)


a

b

c

small

26

35

50

medium

37

45

65

Implantation

Central pelvic floor defects without evident lateral defect can be stabilised using TiLOOP® Patch. The anterior colporrhaphy is performed in the conventional way from the neck of the bladder to the vaginal stump or to the cervix. This is followed by extensive preparation of the anterior vaginal wall. The purpose of the patch is to prevent new hernial canals from forming in cases of an existing connective tissue weakness.

The cystocele is lowered by placing transverse sutures. The TiLOOP® Patch is then attached with loose fixation using absorbable sutures and subsequent vaginal closure.

The rectocele is treated with posterior colporrhaphy in the conventional manner. The posterior wall of the vagina is prepared from the rectum. The rectocele is lowered by placing transverse sutures. The TiLOOP® Patch is then attached with loose fixation using absorbable sutures and subsequent vaginal closure.

Titanisation

Chemical vapour deposition (CVD) is a process for the metallisation of complex components while at the same time achieving strong bonds. However, as this process involves temperatures in excess of 150°C, it is not an option for many prosthetic materials which would not be shape retentive at such temperatures (e.g. polypropylene).

For that reason, the titanisation of plastic implants takes place at low temperatures using a special plasma-coating process known as PACVD (plasma-activated chemical vapour deposition).

Plasma is the term used for an excited (ionised) gas. In that stage, atoms/molecules are highly energetic. However, plasma is not hot. In everyday life, we are familiar with plasma in fluorescent tubes. The electrically charged gas components emit light as the result of their highly energetic state, but the fluorescent tube remains cold.

In the titanisation process, gaseous titanium is introduced into the coating chamber as a precursor. By adding energy in form of plasma, the precursor is split into individual ionised atoms. These ionised titanium atoms have free electrons at their surfaces.

In addition to the precursor, the plasma also excites the surfaces of the plastic implants with the result that their surfaces also have free electrons. The ionised titanium atoms come into contact with the ionised surface of the implant resulting in the formation of covalent bonds with the free electrons. Covalent bonds are seen as the strongest of chemical bonds; the titanium is thus almost permanently bonded to the plastic.

This process creates a composite material whose surface is coated with an ultra-thin, approx. 30–50 nm (1 nanometre = 1 millionth of a millimetre), highly biocompatible layer of titanium. The coating is so thin that it appears to be transparent and is also highly flexible.

Because the titanium precursor is introduced in gaseous form, it reaches all parts of the plastic implant. As the result, the entire surface, including gaps in between complex shapes, is completely and evenly titanised.

Indication

TiLOOP® mesh implants were developed for a variety of indications in urological, gynaecological and surgical patient treatment within the broad range of procedures that use surgical mesh implants.

TiLOOP® mesh implants are particularly used for supporting and strengthening of connective tissue structures and ligaments.

Rectocele and cystocele; for defect-specific pelvic floor reconstruction (surgical treatment of the central rectocele and cystocele defect).The tension-free pelvic floor mesh TiLOOP® Patch is used for the individual defect-specific reconstruction in the herniated area. It is suitable for rectoceles and cystoceles.

TiLOOP® Patch
REFWeightSizeMaterialTypePU
600048416 g/m2, extralight5 x 3,5 cmtitanized polypropylenesmall3
600048535 g/m2, light5 x 3,5 cmtitanized polypropylenesmall3
600048735 g/m2, light15 x 15 cmtitanized polypropylene 3
600051116 g/m2, extralight6,5 x 4,5 cmtitanized polypropylenemedium3
 
 
TiLOOP® Patch - Mesh Implants, Pelvic Floor Surgery
40 Years Quality and Experience

You have questions? Call our Customer Solutions team under. +49 (0)2236 9641-0