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Biomaterials forInguinal Hernia Repair
RolfUlrichHartung
5

5.1 Introduction

Biomaterial has been used for hernia repair since the beginning of hernia treatment. The idea to implant a material with high biocompatibility was already in the mind of surgeons since Billroth: “If we could articially produce tissues of the density and toughness of the fascia and tendon, the secret of radical cure of hernia can be discovered”. Injection of gold particles and trans­plantation of autografts such as the lata fascia and dura patches have been used to deal with the defect in the abdominal wall. Pre-fabricated pros­thetics made from tantalum gauze and silver­coated wire meshes were abandoned due to high complication rates. Francis Usher implanted the rst synthetic mesh made of polypropylene and published his rst experimental series of hernia repairs with Marlex mesh in 1959 [1]. Since then the development of meshes has exploded and resulted in biophysical and clinical research in order to nd the ideal mesh. Today more than 500 different meshes are on the market offering meshes of different material, size, composition, coating, density and weight, pore-size, structure, exibility, tensile strength and durability, pre­formed anatomical shape, self-xing surface and visibility in imaging techniques. The tremendous
R. U. Hartung (*) Medical Director, Mediclinic City Hospital—Dubai Healthcare City, Dubai, UAE
choices challenge surgeons and patients on which mesh to choose for the repair of an individual hernia. Detailed knowledge of available biomate­rials became therefore a necessary requirement for every hernia surgeon.
5.2 Biomaterial
andBiocompatibility ofMeshes forHernia Repair
A biomaterial is either a natural or a synthetic or a combined material that is suitable for introduc­tion into living tissue especially as a part of a medical device that treats, augments, or replaces any tissue, organ, or function of the body; espe­cially, material suitable for use in prostheses that will be in contact with living tissue [2]. Synthetic material might be any material including mesh, patch, sutures, staples, glue, plastic and metal. Transplanted material can be an autograft, allograft or xenograft. Modern medical devices and prostheses are often made of more than one material alone. Although biomaterials have been used for hernia repair since the beginning of sur­gery, the science of biomaterials is less than 60years old. The commonly used biomaterial for inguinal hernia repair is a mesh. The material and characteristics of the prosthetic mesh used deter­mine integration, durability, functionality, incor­poration and comfort.
© Springer Nature India Private Limited 2020 P. Chowbey, D. Lomanto (eds.), Techniques of Abdominal Wall Hernia Repair,
https://doi.org/10.1007/978-81-322-3944-4_5
77
78
R. U. Hartung
Biocompatibility is related to the behavior of
biomaterials in various contexts. The term refers
to the ability of a material to perform with an appropriate host response in a specic situation [3]. As modern medical devices and prostheses are often made of more than one material it might not always be sufcient to talk about the biocom­patibility of one specic material alone. The bio­compatibility of a long-term implantable medical device (non-absorbable mesh) refers to the ability of the device to perform its intended function, with the desired degree of incorporation in the host, without eliciting any undesirable local or systemic effects in that host. The biocompatibil­ity of a scaffold or matrix for a tissue-engineering product (biologic mesh) refers to the ability to perform as a substrate that will support the appro­priate cellular activity, including the facilitation of molecular and mechanical signaling systems, in order to optimize tissue regeneration, without eliciting any undesirable effects in those cells, or inducing any undesirable local or systemic responses in the eventual host.

5.3 Foreign Body Reaction

Any biomaterial will trigger a foreign body reac­tion starting at the very moment of its introduc­tion into the host [4]. Proteins will adhere to the prosthetic material only seconds after its implan­tation, followed by the invasion of platelets releasing a variety of cytokines that will attract white blood cells, macrophages and broblasts [5, 6]. Within hours the implant will be covered by an inammatory inltrate and broblasts, leading to the formation of a brotic capsule around each and every lament or part of the prosthetic implant. New vessels will invade 7–14 days after the onset of the reaction thus forming a foreign body granuloma. Different bio­materials have more or less accentuated foreign body reactions. Thicker the granuloma grows over each lament more likely it will cause excessive scar formation and the risk of bridging from one lament to the next thus transforming the exible mesh into a stiff scar and nally a solid plate. The functionality and biophysical
outcome of the prosthetic implant depend in major parts on the degree of this foreign reaction. Excessive scar formation and shrinkage of the prosthetic implant are the main reasons for a poor outcome after surgery possibly causing recur­rence, discomfort and pain.

5.4 The Material

Different biomaterials have been developed for the construction of meshes; synthetic non­absorbable material such as polypropylene being the most commonly used substance. Polyvinylidene uoride (PVDF), polyester (PET), polyamide (nylon) and polytetrauoro­ethylene (PTFE) are further synthetics used as either patches or knitted laments for the produc­tion of non-absorbable meshes [79]. Polyglactin 910 and polyglycolic acid are commonly used for absorbable implants (Table 5.1). Composite meshes are fabricated out of different materials most commonly with a permanent and an absorb­able component. Biologic implants have been developed for the production of scaffolds made from human, porcine or bovine origin with the aim to address the problem of chronic inamma­tion and foreign body reaction. The donor tissue is processed to acellular, porous matrix scaffolds of collagen and elastin. The porous structure allows cells to enter the mesh and to adhere. A process of degradation of the biologic mesh and regeneration of the collagen scaffold will lead to a replacement of the mesh by host tissue (Table 5.2). Surgeons hoped that there will be less risk of bacterial invasion of the implant lead­ing to the nal necessity of explantation of the biomaterial as the scaffold will disappear by time.
Once the mesh is knitted or woven it can be coated to avoid adhesions, minimize the risk of infection or reduce the foreign body reaction. Different materials will shrink more or less once implanted, polypropylene having the highest shrinkage rate [7]. The material is either hydro­phobic (polypropylene) or hydrophilic (polyester), the latter being less durable as hydrolysis can cause degradation of the laments. PTFE is com-
5 Biomaterials forInguinal Hernia Repair
79
Bard Polypropylene Monolament Small Heavy No
Brand name Company Material Structure Pore size Weight Absorbable
3DMax Bard Polypropylene Monolament/3D Small Heavy No
3D Max Light Bard Polypropylene Monolament/3D Large Light No
Dexon Syneture Polyglycolic acid Multilament Medium Medium Yes, entirely 60–90days
Dynamesh Endolap 3D FEG PVDF Monolament/3D Large Light No
Goretex Dualmesh Gore ePTFE Composite Small Heavy No
Table 5.1 Examples of synthetic meshes used for inguinal hernia repair including absorbable meshes
Marlex
Medtronic/Covidien Polyester Multilament Large Light No
(historic)
Optilene B.Braun Polypropylene Monolament Large Light No
Parietex
Hydrophilic
Parietex Lightweight Medtronic/Covidien Polyester Monolament Large Light No
ProGrip Medtronic/Covidien PET/PLA microgrips Monolament Large Light Partially, PLA 18months
Prolene Ethicon J&J Polypropylene Monolament Medium Heavy No
Ultrapro Advanced Ethicon J&J Polypropylene/polyglecapron Monolament Large Light Partially
Versatex Medtronic/Covidien Polyester Monolament Large Light No
Vicryl Ethicon J&J Polyglactin 910 Monolament Small Medium Yes, entirely 60–90days
80
Table 5.2 List of biologic meshes
Brand name Company Type Origin Cross-linked Sterilized Alloderm LifeCell Dermis Human No No Allomax CR Bard Dermis Human No Ye s Collamend CR Bard Dermis Porcine Ye s Yes Flex HD MTF Dermis Human No No Periguard Synovis Pericardium Bovine Yes Yes Permacol Covidien Dermis Porcine Ye s Yes Strattice LifeCell Dermis Porcine No Ye s Surgimend TEI Dermis Bovine No Yes Surgisis Cook Intestine Porcine No Yes Tutopatch Tutogen Pericardium Bovine No Yes Veritas Synovis Pericardium Bovine No Ye s XenMatrix CR Bard Dermis Porcine No Ye s BioA WL Gore Synthetic absorbable Synthetic N/A Yes TIGR Novus Scientic Synthetic absorbable Synthetic N/A Yes
R. U. Hartung
pletely inert and will be rather incapsulated than integrated. Not only the material itself matters when it comes to durability and risk of infection but also the characteristics of the mesh, how it is knitted or woven, whether mono- or polylaments are used. Accordingly some meshes can be cut into shape while others cannot be. Last but not least, the production of the raw material itself matters. Not every polypropylene mesh has the same char­acteristics in density, weight and porosity thus inuencing the biocompatibility and performance in the individual host. The mechanical strength and density of meshes have been thoroughly inves­tigated in experimental studies to determine weight and strength of reduced material, the ideal pore size and consequently the exibility and shrinkage rate [10]. Light-weight meshes have a weight of around 30 g/m
2
while heavy meshes weigh up to 100g/m2. The effective difference for a 10×15cm mesh is 1g (heavy weight 1.5g ver­sus light weight 0.5g). Large pores measure more than 1 mm (1–3 mm). Pores less than 75 μm in size will not allow macrophages to enter and hereby signicantly decrease the resistance to infection (PTFE). Even the lightest meshes avail­able on the market withstand twice the maximum intra-abdominal pressure peeks of 170mmHg dur­ing coughing and jumping. Different coatings shall not only minimize the tendency of adhesions but also prevent infection and possibly make meshes visible by imaging such as ultrasound and MRI investigations. Experimental and clinical
studies with iron nanoparticle coating have resulted in information about displacement and long-term shrinkage rates of different mesh types. 3D meshes aim to preform the anatomical shape of the inguinal region and might allow future onsite production of a precisely tting 3D printed mesh for an individual patient.
5.5 The Choice ofMesh
Ideally a mesh should be chemically inert, non­toxic, non-allergenic and non-carcinogenic, ster­ilizable, easy to be fabricated and formed, and easy to be handled and implanted. There should be no or very little foreign body reaction and no risk of adhesions. It should resist infection and seroma formation, have a sufcient mechanical strength and durability, and enough exibility to allow normal body movements. The mesh should be incorporated such as autologous tissue and guarantee a lifelong repair of the hernia without recurrence and pain.
However the success and long-term outcome of an inguinal hernia repair are not only dependent on the mesh itself but also on the condition of the indi­vidual patient, the size of the defect, the presence of infection or contamination. Large defects will need to be covered by larger and stronger meshes in order to avoid mesh migration and herniation into the defect. The discussion whether to implant a syn­thetic or a biologic mesh or no mesh at all in pres-
5 Biomaterials forInguinal Hernia Repair
81
ence of contamination and infection is still ongoing. Human acellular dermal matrix (HADM) and ani­mal skin and intestine from pigs (porcine) and cows (bovine) are commonly used biologic materials for hernia repair with own risks and side effects [11]. Cultural, religious and personal factors inuence the decision on the choice of biologic meshes. All biologic implants are considered to be temporary scaffolds, absorbable implants aiming to improve patients own repair mechanisms by forming durable scars. However the knowledge about decient col­lagen in acquired hernias limits the expectations of this ideal appearing concept. Furthermore the three­fold higher costs of biologic meshes are not in favour of the routine use of those implants.
When it comes to the decision about the choice of mesh for hernia repair, the surgeon will consider the ease of handling and xation of the implant. Introduction and deployment have to be guaranteed without damaging the structure or surface of the mesh. Self-xing meshes might apparently have less risk of displacement; however, the intracorpo­ral handling requires more advanced skills and pre­cision of the surgeon. Once the mesh is correctly placed, many surgeons prefer to x the mesh at least in one or two areas of reference, in inguinal hernia repair typically at Cooper’s ligament. All the available xation devices are equally made of bio­material, permanent or absorbable, whether sutures, tacks or glue are used. Every single com­ponent of the entire biomaterials used during ingui­nal hernia repair will inuence the outcome and possible side effects of the procedure. As in all dif­ferent open and laparoscopic surgical techniques of inguinal hernia repair the mesh will be placed in the pre- or extraperitoneal space, the mesh will not need to have an anti-adhesive coating. When it comes to the size of the mesh 10×15cm meshes are recommended for laparoscopic inguinal hernia repair and larger meshes are available to ensure a sufcient preferably 5cm overlap to all sides. Plugs placed inside the opening are not favoured any­more. For most cases of inguinal hernia repair a monolament synthetic mesh (polypropylene, polyester, PVDF) with large pores and low density will be the right choice [12, 13].

5.6 Clinical Outcome

Since the development of meshes for inguinal hernia repair the direct suture repair techniques have decreased signicantly. Only in pediatric hernias the suture repair is still the method of choice. Whether open Lichtenstein procedure is performed or laparoscopic techniques such as TEP and TAPP in all cases a mesh will be implanted. Long-term studies and analysis of hernia registries have shown that the tension free repair with mesh resulted in lower recur­rence rates and less pain after surgery in com­parison to direct suture repair techniques such as Shouldice and Bassini repair representing less than 10% of all inguinal hernia repairs today. All international guidelines have there­fore recommended the use of mesh for inguinal hernia repair over the direct suture repair based on level 1A evidence that mesh repair results in less recurrences when compared to techniques without the use of mesh. With level 1B evidence material-reduced meshes with large pores are favoured for the open inguinal hernia repair due to less long-term discomfort and foreign body sensation [14].

5.7 Summary

Nowadays the commonly used biomaterial for inguinal hernia repair is a mesh. Ninety percent of all inguinal hernia repairs are performed by implantation of synthetic meshes. The advantage of a tension-free repair over the suture repair with tension has resulted in lower recurrence rates and less pain. All international guidelines recom­mend the use of synthetic non-absorbable or composite mesh with a non-absorbable compo­nent based on Level 1A evidence. The develop­ment of material-reduced lightweight meshes with large pores has contributed to better long­term results with less discomfort for the patient. The implantation of biological meshes has not resulted in better outcomes but contributed to higher costs only.
82
R. U. Hartung

References

1. Skandalakis JE, Colborn GL, Skandalakis LJ,
McClusky DA.Historic aspects of groin hernia repair. In: Fitzgibbons RJ, Greenburg AG, editors. Nyhus and Condon’s hernia. 5th ed. Philadelphia: Lippincott, Williams & Wilkins; 2002. p.39.
2. Williams DF, editor. Denitions in biomateri-
als, Proceedings of a Consensus Conference of the European Society for Biomaterials. Amsterdam: Elsevier; 2004.
3. Williams DF.On the mechanisms of biocompatibility.
Biomaterials. 2008;29(20):2941–53.
4. Klosterhalfen B, Hermanns B, Rosch R. Biological
response to mesh. Eur Surg. 2003;35:16–20.
5. Pereira-Lucena CG, Artigiani-Neto R, Lopes-Filho
GJ, Frazao CV, Goldenberg A, Matos D, et al. Experimental study comparing meshes made of polypropylene, polypropylene + polyglactin and polypropylene + titanium: inammatory cytokines, histological changes and morphometric analysis of collagen. Hernia. 2010;14:299–304.
6. Klosterhalfen B, Junge K, Klinge U.The lightweight
and large porous mesh concept for hernia repair. Expert Rev Med Devices. 2005;2:103–17.
7. Klosterhalfen B, Klinge U, Schumpelick V.Polymers
in hernia repair-common polyester vs. polypropylene surgical meshes. J Mat Sci. 2000;35:4769–76.
8. Deeken CR, Abdo MS, Frisella MM, Matthews BD. Physicomechanical evaluation of polypropylene, polyester, and polytetrauoroethylene meshes for ingui­nal hernia repair. J Am Coll Surg. 2011;212:68–79.
9. Gonzalez R, Ramshaw BJ. Comparison of tissue integration between polyester and polypropylene prostheses in the preperitoneal space. Am Surg. 2003;69:471–6, discussion 476–7.
10. Agarwal BB, Agarwal KA, Mahajan KC.Prospective double-blind randomized controlled study comparing heavy- and lightweight polypropylene mesh in totally extraperitoneal repair of inguinal hernia: early results. Surg Endosc. 2009;23:242–7.
11. Harth KC, Rosen MJ. Major complications asso­ciated with xenograft biologic mesh implanta­tion in abdominal wall reconstruction. Surg Innov. 2009;16(4):324–9.
12. Bilsel Y, Abci I. The search for ideal hernia repair; mesh, materials and types. Int J Surg. 2012;10(6):317–21.
13. Brown CN, Finch JG.Which mesh for hernia repair. Ann R Coll Surg Engl. 2010;92(4):272–8.
14. Simons MP, Aufenacker T, Bay-Nielsen M, Bouillot JL, Campanelli G, Conze J, De Lange D, Fortelny R, Heikkinen T, Kingsnorth A, Kukleta J, Morales-Conde S, Nordin P, Schumpelick V, Smedberg S, Smietanski M, Weber G, Miserez M. European Hernia Society guidelines on the treatment of inguinal hernia in adult patients. Hernia. 2009;13(4):343–403.
Anaesthesia forLaparoscopic Abdominal Wall Hernia Repair
AparnaSinha andLakshmiJayaraman
6

6.1 Anaesthesia for Laparoscopic Abdominal Wall Hernia Repair

Abdominal wall hernia is a very common surgical problem. In the last two decades laparoscopic/ endoscopic approach has become the preferred surgical option for management of the same. Laparoscopic techniques have become popular due to the major advantages they offer. These include minimal incision size, minimal postopera­tive discomfort, earlier discharge readiness, lesser postoperative pain, enhanced recovery and lesser incidence of postoperative wound infections. These factors further contribute to lesser hospital stay and minimal perioperative morbidity.
The advancements in the surgical techniques of endohernia repair have led to innovations and renement in the anaesthetic management of the same. The repair endohernia is one of the most commonly performed surgeries today.
The endoscopic hernia repair includes man­agement of myriad of conditions including, totally extra-peritoneal (TEP), transabdominal preperitoneal (TAPP) repair of inguinal hernia and intraperitoneal onlay mesh (IPOM) repair of
A. Sinha (*) · L. Jayaraman Institute of Minimal Access, Metabolic and Bariatric Surgery, Max Super Speciality Hospital, New Delhi, India
ventral hernia. Laparoscopy allows identication of contralateral hernia and its safe repair by avoiding cord structures and regional nerves.
• Totally extra-peritoneal repair (TEP): In this technique there is the placement of mesh into the preperitoneal space.
• Trans-abdominal (TAPP): Placement of mesh over peritoneal defects in the abdominal wall.
• Laparoscopic intraperitoneal onlay mesh (IPOM).
The TEP is preferred in simple unilateral,
bilateral or recurrent hernia, whereas TAPP allows the surgeon to approach large scrotal, incarcerated and complex recurrent hernias, with greater ease. This also allows a concomitant diag­nostic laparoscopy. However, laparoscopy is not without its associated problems and complica­tions. Moreover, based on the type of hernia the repair may involve placing the patient in extremes of position, which brings its own challenges. Athorough understanding of anesthetic implica­tions of endoscopic hernia repair is mandatory for safe execution of anaesthesia.
Thorough preoperative evaluation, prepara-
tion, protocols to troubleshoot consequences of raised intra-abdominal pressure (IAP) and effec­tive pain management are keys to safe anaesthe­sia practice.
© Springer Nature India Private Limited 2020 P. Chowbey, D. Lomanto (eds.), Techniques of Abdominal Wall Hernia Repair,
https://doi.org/10.1007/978-81-322-3944-4_6
83
84
A. Sinha and L. Jayaraman
6.1.1 Pathophysiological Changes During Endoscopic Hernia Repair
Though laparoscopy offers advantages to both patients and surgeons, it can impose signicant alteration in respiratory and cardiovascular homeostasis and should never be regarded as another minor intervention. During laparoscopic procedures, the major barriers to normal homeo­stasis are patient positioning, introduction of sev­eral liters of gas (CO2) into the extraperitoneal space (TEP) or abdominal cavity (as in TAPP and IPOM) to produce carboperitoneum and the raised intra-abdominal pressure (IAP) that ensues from it. All these produce several pathophysio­logical changes, some of which are unique to laparoscopy (Tables 6.1 and 6.2).
6.1.2 Positioning andAssociated Pathophysiologic Problems
Initial introduction of the Verees needle may require the patient to be placed in the Trendelenburg position (15°–20°) for most her-
Table 6.1 Hemodynamic effects of carboperitoneum
• Hypertension, tachycardia: Increased myocardial oxygen demand
• Increased noradrenaline levels: Increased SVR (and decreased Q)
• Hypercarbia and acidosis
• Reduced urine output and increased plasma renin activity (PRA)
– Increased intra-abdominal pressure (IAP) – Local compression of renal vessels
• Intra-abdominal distension: Decrease in pulmonary dynamic compliance
• Low compliance plus increased minute volume of ventilation: Raised peak airway pressures
Table 6.2 Respiratory effects in endo-hernia repair
• Carboperitoneum ventilatory and respiratory changes
• Thoracopulmonary compliance (30–50%)
• PaCO
• PEtCO
• Increase PEtCO
15–20% (CO2 absorption from peritoneal
2
cavity)
plateaus in 30min
2
subcutaneous emphysema
>25% in<30min suggestive of
2
nia repairs to allow introduction of carbon dioxide.
This displaces the abdominal viscera and thus prevents visceral injury during trocar insertion. It increases venous return (VR), right atrial pres­sure (RAP), central blood volume and cardiac output [1, 2]. Respiratory mechanics are also affected, due to cephalad displacement of dia­phragm [13].
This augments development of atelectasis especially in obese, elderly and debilitated patients. In ASA I and II patients no major changes are seen [4].
The same IPOM procedure’s reverse Trendelenburg position (20°–30°) is adopted, this improves diaphragmatic functions and is more favourable for respiration; however, com­promises on the central blood volume and car­diac output [5]. The pathophysiological changes may vary in extra-peritoneal repairs (Fig.6.1).
The steepness of the tilt and duration of sur­gery ultimately decide the magnitude of these changes. Deleterious effects can occur in patients with cardiovascular dysfunction [4]. The reduced pressures due to Trendelenburg position reduce blood loss from the pelvic viscera, but increase the risk of gas embolism [4, 6].
Nerve injuries have been potential complica­tions of head low position. Caution must be exer­cised to prevent them particularly the brachial plexus injuries. This can be prevented by placing the arms of the patient by the side and applying shoulder supports (Figs.6.2 and 6.3).
6.1.3 Insuation ofExogenous Gas
Choice of an optimal insufating gas to create pneumoperitoneum remains a signicant issue in laparoscopy. Various gasses have been used for creating pneumo-peritonium in laparoscopy including oxygen, air, nitrous oxide (N2O), nitro­gen (N2), carbon di oxide (CO2), Argon and Helium. Carbon dioxide (CO2) has remained the insufation gas of choice. It is relatively inert, readily absorbed, and does not support combustion and hence permits the use of electro­cautery [7].
6 Anaesthesia forLaparoscopic Abdominal Wall Hernia Repair
85
Fig. 6.1 Effects of
position and carboperitoneum
Circulation:
Stroke Volume
Circulation–
Venous Return
CO
insufflation (intraperitoneal/extraperitoneal)
2
Contractility, dysrhythmias,
Venous gas embolism
(cephalad displacement of diaphragm)
Increased intra-abdominal pressure (IAP)
Systemic Vascular Resistance
Reverse Trendelenburg Position
Circulation–
Ø Venous Return Ø Afterload
Trendelenburg Position
Respiration:
Mean Arterial Blood Presssure Ø Cardiac Output
Respiration–
Ø Lung Volumes,Work of Breathing
Respiration–Hypercarbia
Lung volumes improve Ø Work of breathing
Fig. 6.2 Shows position of OT table, monitors and sur-
geons during TEP
Fig. 6.3 Patient in Trendelenburg position, both arms by
the side and shoulder supports in place to prevent sliding of patient during extremes of position
86
A. Sinha and L. Jayaraman
It is very highly soluble in blood (solubility coefcient=0.49) at 37°C and has a linear and steep dissociation curve. If PaCO2 ranges between 45 and 50mmHg, the absorption of CO2 during carboperitoneum has minimal impact on hemo­dynamics. Whereas, if the PaCO2 ranges between 51 and 60mmHg, it causes sympathetic response and alters the cardiovascular response. The eleva­tion in catecholamines and the pathophysiologi­cal changes of laparoscopy have been largely attributed to the increase in IAP rather than rise inCO2.
In healthy patients (ASA I and II), the rise in pCO2 and the resulting acidemia is clinically insignicant because of the buffering systems and rapid elimination by lungs. The rise in CO2 elimination is not due to hyper metabolism, as suggested by increase in CO2 elimination but unchanged O2 consumption. The initial rise in intracranial pressure is due to mechanical effects of raised IAP, whereas the delayed rise seen in prolonged surgeries is due to vasodilatation induced by hypercapnia. Caution needs to be exercised in patients of chronic obstructive pul­monary disease, who have elevated baseline PaCO2. These patients may show signs and symptoms of raised CSF pressure in the form of headache, blurring of vision and papilledema.
Central pipeline or cylinders may be used to supply carbon dioxide.
N2O is not a part of acid-base buffer system and has only weak hemodynamic effects. This is not a preferred agent due to its property to sup­port combustion. Nitrous oxide (N
O) is better as
2
an insufating gas when the procedure is to be conducted under regional anaesthesia, since it produces minimal irritation of the peritoneal cav­ity [8]. However; caution needs to be exercised with use of cautery.
Helium insufation is a reasonable alternative in patients at risk for CO2 retention or has signi­cant cardiopulmonary compromise [9]. Its low water and plasma solubility makes it unsuitable in the event of gas embolism.
Argon is yet another alternative, which is odorless, colorless gas, with no effect on acid­base status. It has poor solubility in blood makes it dangerous in case embolism happens.
Table 6.3 Properties of an ideal insufating gas
• Readily available
• Nontoxic and colorless
• Relatively inert
• Non-combustible
• Inexpensive
• High Ostwald blood/gas partition coefcient (0.48) (readily soluble and easily ventilated through lungs)
Carbon dioxide possesses most of the desirable characteristics hence the term carbo­peritoneum is used synonymously with pneumo­peritoneum [810] (Table6.3).
6.1.3.1 Carboperitoneum
andIncreased Intra-abdominal Pressure
With the rise in IAP, the perfusion of viscera par­ticularly that of the renal and hepatic perfusion is signicantly compromised and is a major con­cern in patients with existing disease. Duration of carboperitoneum can have signicant implica­tions on the outcomes.
The renal effects of carboperitoneum are rec­ognized as independent cause of acute kidney injury. The mechanism for this is secondary to the combined effect of reduced renal afferent ow due to impaired cardiac output and reduced efferent ow in view of raised renal venous pressure.
Increase in the intra-abdominal pressure con­tributes to circulatory instability during laparos­copy [11]. Since TEP is performed without establishing carboperitoneum, the adverse effects of a raised IAP are not seen, unlike in TAPP and IPOM, which necessitate the establishment of carboperitoneum [12].
Since the resorptive surface area is much larger in extra-peritoneal repairs, the rise in EtCO
is much greater [10, 13, 14]. The absorp-
2
tion of CO2 steadily increases in TEP repair, while it tends to reach a plateau in TAPP [15]. Disruption of the microvascular and lymphatic channels in TEP, facilitates direct intravascular uptake of CO2 [16].
The absorption of gases from the peritoneum is less at the commonly used pressure of 14–18 mmHg (for TAPP, IPOM repair) and