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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_6023_Библиотеки_им_академика_М_И_Перельмана.pdf
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- •Foreword 1
- •Foreword 2
- •Preface
- •Contents
- •Abbreviations
- •1.1.1 Pre-Jules Gonin Era
- •1.1.2 Post-Jules Gonin Era
- •2.3 Poiseuille Equation
- •1.6 Summary
- •2.1 Bernoulli’s Principle
- •2.4.1 Surface Tension
- •2.4.2 Interfacial Tension
- •2.5 Boyle’s Law
- •2.6 Fick’s Diffusion Law
- •2.7 Other Physical Principles
- •2.8 Summary
- •3.2.1 Density
- •3.2.2 Buoyancy
- •3.2.3 Interfacial Tension
- •3.2.4 Viscosity
- •3.3 Gases
- •3.3.2 Pneumatic Retinopexy
- •3.3.4 Gas Injection Techniques
- •3.3.6 Precautions After Intravitreal Gas Injection
- •3.4 Silicone Oil
- •3.4.2 Silicone Oil Usage Rate
- •3.5 Heavy Liquid
- •3.6 Summary
- •4.1 Doctor-Patient Interaction
- •4.3.1 Local Anesthesia
- •4.3.2 General Anesthesia
- •4.4 Summary
- •5.1.1 Instrument Diameter
- •5.1.2 Trocar-Cannula System
- •5.1.3 Vitrectomy Machine
- •5.2 Basic Steps
- •5.3.3 Posterior Vitreous Detachment (PVD)
- •5.4 Summary
- •6.3.2 Lincoff’s Rules
- •6.5.2 Subretinal Fluid Drainage
- •6.5.3 Scleral Encircling
- •6.6.1 Persistent Subretinal Fluid
- •6.6.2 Recurrent Retinal Detachment
- •6.6.3 Elevated Intraocular Pressure
- •6.6.4 Anterior Segment Ischemia
- •6.6.6 Extraocular Muscle Dysfunction
- •6.6.7 Refractive Changes
- •6.7 Summary
- •7.3.1 Cutting Central Vitreous
- •7.3.2 Confirming or Creating Posterior Vitreous Detachment
- •7.3.5 Removing Peripheral Vitreous
- •7.3.7 Sealing Retinal Breaks
- •7.3.9 Adjusting Intraocular Pressure
- •7.6.1 Pathological Basis
- •7.6.2 Surgical Principles
- •7.6.3 Surgical Strategies
- •7.9.1 360° Laser Encircling
- •7.9.2 Scleral Buckling
- •7.11 Summary
- •8.1.1 Retinal Proliferative Changes
- •8.1.2 Vitreous Status
- •8.5.1 Segmentation Technique
- •8.5.2 Delamination Technique
- •8.5.3 En Bloc Technique
- •8.6.1 Staining Agents
- •8.6.2 Tamponades
- •8.7.1 Corneal Edema
- •8.7.2 Lens Opacity
- •8.7.3 Pupillary Constriction
- •8.7.4 Iatrogenic Retinal Tears
- •8.7.5 Intraoperative Bleeding
- •8.8.1 Elevated Intraocular Pressure
- •8.8.3 Lens Opacity
- •8.8.5 Anterior Hyaloidal Fibrovascular Proliferation
- •8.8.6 Intraocular Fibrin Syndrome
- •8.8.7 Vitreous Hemorrhage
- •8.9 Summary
- •9.1 Clinical Characteristics
- •9.4.1 Surgical Timing
- •9.4.2 Prognostic Factors
- •9.5 Standard Surgical Steps
- •9.6.1 Triamcinolone Acetonide (TA)
- •9.6.2 Indocyanine Green (ICG)
- •9.6.3 Brilliant Blue G (BBG)
- •9.7.1 Preparation
- •9.7.2 Flap Initiation Methods
- •9.8 Complications
- •9.8.1 Intraoperative Complications
- •9.8.2 Postoperative Complications
- •9.9 Summary
- •10.2.1 Classification
- •10.4 Routine Surgical Procedures
- •10.5.1 Commonly Used Dyes
- •11.1.1.2 Glial Cells
- •11.1.1.3 Macrophages
- •11.1.3 Extracellular Matrix Remodeling
- •11.1.4 Susceptibility Genes
- •11.2.1 Clinical Manifestations
- •11.2.1.1 Characteristic Retinal Changes
- •10.6.2 Flap Initiation Techniques
- •10.6.4 ILM Flap Techniques
- •10.7 Complications
- •10.8 Summary
- •11.1 Etiology
- •11.1.1.1 RPE Cells
- •11.2.1.2 Anterior Segment Manifestations
- •11.2.2 Grading
- •11.4.2.2 Retinotomy
- •11.4.2.3 Retinectomy
- •11.4.3 Radial Retinotomy
- •11.5 Summary
- •12.2.2 Anti-VEGF Intraocular Injection
- •12.2.3 Retinal Laser Photocoagulation
- •12.2.4 Vitreoretinal Surgery
- •12.3.1 Overview
- •12.5 Summary
- •13.8 Showcase Your Art Works
- •13.9 Summary
- •15: Combined Phaco/Vitrectomy
- •15.1 The Surgery
- •15.2 Main Surgical Steps
- •15.3.2 Phacoemulsification
- •15.3.10 Fluid Against Air Exchange
- •15.3.13 Tamponade
- •15.3.14.1 Postoperative Posture
- •15.3.14.2 Complications
- •15.3.14.5 Fractionized PFCL Injection
- •15.3.15 FAQ
- •16.1 Surgery
- •16.2 Main Surgical Steps
- •16.4 FAQ
- •17: Easy Diabetic Retinopathy
- •17.1 Introduction
- •17.3 Vitrectomy
- •17.3.1 The Surgery Step-by-Step
- •17.3.2 Complications
- •17.4 FAQ
- •19.1 Introduction
- •19.3 The Surgery Step-by-Step
- •19.4.1 Encircling Band (cerclage)
- •19.4.3 Pars Plana Vitrectomy
- •19.4.5 Vitreous Base Shaving
- •19.4.6 Membrane Dissection
- •19.4.9 Retinotomy
- •19.4.11 Laser Photocoagulation
- •19.4.13 Tamponade
- •20: Difficult Proliferative Diabetic Retinopathy
- •20.1 Introduction
- •20.2 General Introduction
- •20.3.5 Hemostasis
- •20.3.9 Intravitreal Avastin
- •20.3.10 Internal Postoperative Tamponade
- •20.4 Complications
- •20.5 FAQ
- •Bibliography

352
20 Dicult Proliferative Diabetic Retinopathy
ab
cd
ef
Fig. 20.4 (a, b) The rst important step of diabetic vitrectomy: The posterior hyaloid rhexis. (c,
d) Perform a rhexis of the detached posterior hyaloid on the height of the equator. (e, f) Then con-
tinue with the removal of the vitreous to the nasal and temporal arcades. The attached (nasal)
hyaloid cannot be removed in this stage (f)

ab
cd
ef
20.3 The Surgery Step-by-Step
353
Fig. 20.5 (a) Posterior hyaloid rhexis without subhyaloidal hemorrhage. (b) Be careful not to
damage the retina. (c) Perform a posterior hyaloid rhexis of the detached hyaloid. A rhexis of the
attached hyaloid is not possible. (d) An opening of the posterior hyaloid with presence of subhyaloidal hemorrhage. (e) Use the vitreous cutter with a low cutting frequency such as 1000 cuts/min.
(f) Open the posterior hyaloid as far as possible, i.e., try to perform a round rhexis as far as possible

354
20 Dicult Proliferative Diabetic Retinopathy
detachment is present. This means that the vitreous is still attached centrally but
partially detached in the mid-periphery. Try to nd where the peripheral vitreous is
detached. Create here an opening of the posterior hyaloid on the height of the equator. Then remove the vitreous along the posterior vitreous face (Figs.20.4 and 20.5)
on a constant level in a circular fashion (posterior hyaloid rhexis). Do not perform a
posterior hyaloid rhexis in the area where the posterior hyaloid is attached.
Then carefully vitrectomize further from the periphery toward the beginning of
the tractional membranes. Be careful that you do not exert any strain on the membranes. If the surgeon succeeds with the posterior hyaloid rhexis, he or she can
continue removing the tractional membranes bimanually.
20.3.3 Removal ofTractional Membranes
The brovascular membranes are usually located along the vascular arcades. The
membranes are removed together with the posterior hyaloid. The way to success is
bimanual delamination (Fig.20.6).
20.3.4 Instruments fortheRemoval ofProliferations
For lifting the membranes, both the 27G endgripping forceps and the backush
instrument are suitable. The forceps grasp the membrane and the ute needle elevates the membrane through aspiration force. For manipulation of the membrane,
use the vacuum cleaner, the 27G retrobulbar cannula (Atkinson, Beaver Visitec), the
curved scissors, and the vitreous cutter.
Fig. 20.6 The next and
most difcult step is the
bimanual removal of
brovascular membranes

20.3 The Surgery Step-by-Step
355
• Delamination of Membranes with 27G Atkinson Cannula and 27G Vacuum
Cleaner or 25G Knob Spatula
This instrument is suitable for opening of the posterior hyaloid or delamination
of at membranes. The membrane can be lifted up with the blunt cannula and then
removed with the microforceps (Figs.20.7, 20.8, and 20.9).
Grasp the peripheral portion of the membrane with the Eckardt forceps or a
backush instrument in one hand and delaminate the membrane with the knob spatula (Figs. 20.10, 20.11, and 20.12) or the vacuum cleaner in the other hand
(Figs.20.13, 20.14, 20.15, and 20.16).
• Dissection of Membranes with 27G Curved or 25G Straight Scissors
The membranes are partially attached by “tissue bridges” to the retina. These
bridges have to be identied by careful delamination and then be cut with the
straight or curved scissors (Fig.20.17). The vertical scissors can be used for horizontal tissue bridges. The tractional membranes are dissected and removed through
a constant change of instruments between delamination and cauterization. If a
bleeding occurs during this step, then perform a hemostasis.
Fig. 20.7 Create an
opening in the posterior
hyaloid with the 27G blunt
cannula (Atkinson, B&D)
Fig. 20.8 Enlarge the
opening in the posterior
hyaloid

356
Fig. 20.9 The blunt
cannula (25G and 27G) is
a very convenient
instrument for opening of
the posterior hyaloid and
for delamination of
membranes
Fig. 20.10 Delaminate
the membrane with a knob
spatula or a vacuum
cleaner
20 Dicult Proliferative Diabetic Retinopathy
• Removal of Dissected Membranes with Vitreous Cutter
Grasp the membrane with intravitreal forceps, and hold it in the middle of the
vitreous cavity. Then cut it with the vitreous cutter (1000–2000 cuts/min) (Figs.20.18
and 20.19).
Surgical Pearls No. 103
Peeling and choroidal hemorrhage: Do not pull a membrane forwards to the lens—
you may cause a choroidal hemorrhage. Pull the membrane parallel to the retina.

20.3 The Surgery Step-by-Step
Fig. 20.11 If necessary
stain the posterior hyaloid
with trypan blue, and
delaminate it from the
retina
Fig. 20.12 Use a knob
spatula or Charles ute
needle with silicone tip or
membrane pic for
delamination
357

358
Fig. 20.13 You can also
remove membranes with a
silicone tip ute needle and
a forceps
Fig. 20.14 Always pull
the membrane parallel to
the retina. Pulling
vertically may cause a
choroidal bleeding
20 Dicult Proliferative Diabetic Retinopathy

20.3 The Surgery Step-by-Step
Fig. 20.15 For
delamination of
membranes, the knob
spatula and the silicone tip
ute needle are superior to
the membrane pic
Fig. 20.16 The surgeon’s
right hand pulls the
membrane parallel to the
retina, and the left hand
cuts the tissue bridges with
the straight scissors
359
20.3.5 Hemostasis
There are different methods to stop intraoperative bleeding, depending on its
severity:
• Slight Bleeding
Increase the intraocular pressure to approximately 40mmHg.
Aspirate the blood with the left hand, and cauterize the bleeding source with
endodiathermy or the laser probe in the right hand. Inside the arcades, we cauterize
the bleeding sites with laser. Outside the arcades, we cauterize retinal bleeding sites
with endodiathermy (Figs.20.20 and 20.21). Start with relatively low energy, as too

360
Fig. 20.17 The 27G
curved microscissors
allows precise cutting of
vitreoretinal adhesions
Fig. 20.18 Hold the
membrane in the middle of
the vitreous cavity, and cut
the membrane
20 Dicult Proliferative Diabetic Retinopathy
vigorous endodiathermy may create breaks in ischemic retinal tissue. Avoid diathermy on the disk; this may cause destruction of nerve ber bundles. If the bleeding occurs within the temporal vascular arcades, then use a laser probe to cauterize
the bleeding instead. Often you have to work bimanually.
• Moderate Bleeding and Bleeding at the Optic Disc
In the case of a strong bleeding source, hold the knob spatula or the vitreous cutter for about 1minute onto the bleeding source (1minute is longer than most people think).

20.3 The Surgery Step-by-Step
Fig. 20.19 The membrane
is completely removed
Fig. 20.20 Perform a
meticulous hemostasis. We
use endodiathermy outside
the temporal arcades and
laser inside the temporal
arcades
361
Fig. 20.21 Also
hemostasis is performed
bimanually. The surgeon’s
left hand holds the Charles
ute needle and aspirates
the blood. The right hand
cauterizes the bleeding
source
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