Добавил:
kiopkiopkiop18@yandex.ru t.me/Prokururor I Вовсе не секретарь, но почту проверяю Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз: Предмет: Файл:

Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_3740_Библиотеки_им_академика_М_И_Перельмана

.pdf
Скачиваний:
0
Добавлен:
31.08.2026
Размер:
26 Мб
Скачать
16 Aortic Arch andAscending Aorta Replacement
https://t.me/medicina_free
121
vein over a guidewire is performed, or cannulation of the superior vena cava using a three-stage cannula achieves excellent venous drainage. The patient is cooled to 32°C, and the pericardial eld ooded with CO2. Cold blood car­dioplegia is delivered intermittently both ante- and retro-gradely.
The diseased aorta is excised taking great care not to dam­age the right pulmonary artery which is frequently adherent to the back of the aorta. In this eventuality, repair of a dam­aged pulmonary artery is best done using a pericardial patch rather than direct approximation. A suitably sized vascular graft is chosen and cut to an appropriate length. A 4/0 prolene suture is used to construct the proximal and distal anastomo­ses. The needle is mounted forehand, and suturing of the proximal anastomosis begins at 4 o’clock on the graft, pass­ing the needle from outside to inside. The suture length is equalised, and the distal end pinned to the drapes using a rubber-shod. Suturing continues with the needle mounted forehand, passing from native aorta to graft, until about 10 o’clock. The other needle is then used to complete the anas-
tomosis using a forehand suture technique throughout. The distal aortic suture line is constructed in a similar fashion, but starting with the needle passing outside to inside of the native aorta. As this distal anastomosis is coming to a conclusion, the left ventricular vent is switched off to allow passive lling of the heart. A ‘Y’-cannula is placed in the graft and used for venting and delivering a hotshot prior to clamp removal so the anastomotic patency can be conrmed. Any remedial sutures are placed if needed, and then after a thorough de-airing drill, the cross-clamp is removed.
Suggested Reading
Cooley DA. A brief history of aortic aneurysm surgery. Aorta
(Stamford). 2013;1(1):1–3.
Coselli JS. Evolution of aortic arch repair. Tex Heart Inst J.
2009;36(5):435–7.
Xydas S, Mihos CG, Williams RF, LaPietra A, Mawad M, Wittels SH,
et al. Hybrid repair of aortic arch aneurysms: a comprehensive review. J Thorac Dis. 2017;9(Suppl 7):S629–34.
Part VI
https://t.me/medicina_free
Surgery of the Failing Heart
Cardiopulmonary Transplantation:
https://t.me/medicina_free
AnOverview
MariusBerman
17
Heart Transplantation
The rst interhuman, orthotopic, heart transplant was per­formed by Dr. Christiaan Nethling Barnard at the Groote Schuur hospital in Cape Town 1967. The patient survived for 18days.
In the current era, there are approximately 5000 trans­plants performed worldwide each year. The outcomes are excellent.
The most signicant development in the past 10years is the advent of hearts that have become usable after circulatory (DCD) death. It requires utilisation of novel technologies, with in- or ex situ organ perfusion, to resuscitate and assess the quality of the heart. The outcome of heart transplantation with DCD hearts is equal to heart transplantation after brain death (DBD) [1].
The indication, contraindications [2], and outcomes are as follows.
Indications
Ambulatory
• Patients on optimal medical therapy with symptoms on
exertion
• More than 2 hospitalisation episodes/year
• Deterioration of renal function or inability to clear heart
failure congestion
• Worsening right ventricular function with rising pulmo-
nary artery pressure
• High natriuretic peptide
• Ventricular arrhythmias
• Anaemia, weight loss, hyponatremia, or liver dysfunction
attributable to heart failure
M. Berman (*) Royal Papworth Hospital NHS Foundation Trust, Cambridge, UK e-mail: Marius.berman@nhs.net
Urgent Inpatient Referral
The inability to wean inotropic support
• Mechanical circulatory support for cardiogenic shock
• Pulmonary oedema and ventilation
• Refractory ventricular arrhythmias
Contraindications
• Active infection
• Symptomatic cerebral or peripheral vascular disease
• Diabetes mellitus with end-organ damage
• Current or recent neoplasm
• Forced expiratory volume in 1 s (FEV1) or forced vital capacity (FVC) <50%
• Irreversible kidney or liver dysfunction (In selected cases, there is a potential option of combined organ transplantation)
• Recent pulmonary thromboembolism
• Pulmonary hypertension; systolic pulmonary pressure >60mmHg, transpulmonary gradient >15 mmHg and/or pulmonary vascular resistance >5 Wood units. Suitability is assessed with pharmacological management or bridg­ing with mechanical circulatory support.
• Psychological factors
• Obesity (BMI >35kg/m2)
Outcomes
The outcomes are largely dependent on donor and recipient factors—to name some—donor age, ischemic time, recipient pathology, previous surgery, institution volume, geographi­cal region, and many others (Figs.17.1 and 17.2). The full report is published on a yearly basis by the International Society of Heart and Lung Transplantation [3].
© The Author(s), under exclusive license to Springer Nature Switzerland AG 2023 F. C. Wells (ed.), Atlas of Cardiac Surgery, Springer Surgery Atlas Series, https://doi.org/10.1007/978-3-031-43195-1_17
125
126
ab
https://t.me/medicina_free
M. Berman
Fig. 17.1 Adult heart recipient survival by era (a) and by region (b). DCM dilated cardiomyopathy, ICM ischaemic cardiomyopathy, HCM hyper- trophic cardiomyopathy, RCM restrictive cardiomyopathy, CHD congenital heart disease. (From Perch etal. [3]; with permission)
(DCD). This potentially requires in situ or exvivo organ per­fusion and ventilation to assess its quality. The matching of donor and recipient is affected by multiple variables.
Indications
This is a multidisciplinary decision. Patients must meet the following criteria [4]:
• High (>50%) risk of death due to lung disease within 2years if lung transplantation is not performed.
• High (>80%) likelihood of surviving at least 90days after
Fig. 17.2 Adult heart transplant recipient survival by pathology. DCM dilated cardiomyopathy, ICM ischaemic cardiomyopathy, HCM hyper­trophic cardiomyopathy, RCM restrictive cardiomyopathy, CHD con­genital heart disease. (From Perch etal. [3]; with permission)
Lung Transplantation
Lung transplantation progressed signicantly in the past 10 years. Vast majority are performed without mechanical support, with some units using extracorporeal membrane oxygenation (ECMO) or cardiopulmonary bypass. The access is via thoracotomy, sternotomy, or clamshell with recently reports of robotic-assisted lung transplants. One of the major developments in lung transplantation is the increas­ing use of organs from donation after circulatory death
lung transplantation.
• High (>80%) likelihood of 5-year post transplant survival from a general medical perspective provided adequate graft function.
Contraindications
• A recent history of malignancy; 5-year disease free inter­val required
• Poorly controlled signicant dysfunction of another organ
• Coronary disease, non-amenable to revascularisation
• An uncorrectable bleeding disorder
• Poorly controlled infection
• Chest wall or spinal deformity which will affect graft function
17 Cardiopulmonary Transplantation: AnOverview
https://t.me/medicina_free
127
• BMI >35kg/m
2
• Noncompliance with medication
• Psychological factors
• Illicit substance abuse or dependence
Outcomes
Outcomes of Chronic Obstructive Pulmonary Disease (COPD) recipients are better than other pathologies (Fig.17.3). In addition, the prognosis of double lung trans­plantation is better compared to single lung transplantation (Fig.17.4). The report is published on a yearly basis by the International Society of Heart and Lung Transplantation.
Fig. 17.3 Adult lung transplant outcome by diagnosis. (From Perch etal. [3]; with permission)
Fig. 17.4 Adult lung transplant outcome of single versus double lung transplant. COPD chronic obstructive pulmonary disease, other— A1ATD alpha 1 antitrypsin deciency, CF cystic brosis, IPAH idio- pathic pulmonary hypertension, IPF interstitial pulmonary brosis, retransplantation. (From Perch etal. [3]; with permission)
Conclusion
Cardiopulmonary transplantation has become a fully accepted therapy with excellent results. Organ donation remains the rate limiting step but has been enhanced by recent changes in the law to an opting out system and the advent of the availability of DCD organs. Until genetically engineered xenotransplantation becomes a reality and/or mechanical replacement comes of age, human organ dona­tion will be the mainstay of treatment for cardiopulmonary failure.
References
1. Messer M, Cernic S, Page A, et al. A 5-year single-centre early experience of heart transplantation from donation after circulatory death donors. J Heart Lung Transplant. 2020;39(12):1463–75.
2. Bhagra S, Pettit S, Parameshwar J. Cardiac transplantation: indi­cations, eligibility and current outcomes. Heart. 2019;105:252–60.
3. Perch M, Hayes D, Cherikh WS, Zuckermann A, Harhay MO, Hsich E, International Society for Heart and Lung Transplantation, et al. The international thoracic organ transplant registry of the International Society for Heart and Lung Transplantation: thirty­ninth adult lung transplantation report-2022; focus on lung trans­plant recipients with chronic obstructive pulmonary disease. J Heart Lung Transplant. 2022;41(10):1335–47. https://doi.org/10.1016/j.
healun.2022.08.007.
4. Weill D.Lung transplantation: indications and contraindications. J Thorac Dis. 2018;10(7):4574–87.
Lung Transplantation
https://t.me/medicina_free
PradeepKaul, LuWang, andMohamedOsman
18
Procurement
Lungs are susceptible to damage and injury stemming from resuscitation, ventilator-associated infection, barotrauma, and brainstem death process. Therefore, lung allografts have the lowest utilisation rate for transplantation among all the solid organs. Due to the increasing disparity between waiting list and lung transplant activities and change in donor demo­graphics, the donor selection criteria have evolved over time. Table 18.1 summarises the ideal and extended criteria and contraindications for donor selection.
Once donor lungs are provisionally accepted by a transplant centre, donor operation proceeds at a time agreed by the retrieval teams and donor hospital. Donor operation is a continuous process of allograft optimisation and procurement.
Table 18.1 Main donor selection criteria for lung transplantation
Ideal donor Extended-criteria donor Contraindication Age 25–45years 45–75years >75years Cause of death No chest trauma
No aspiration Past medical history Non-diabetic Diabetes mellitus Severe lung pathology Social history No smoking history <20 pack years history of smoking >20 pack years history of smoking Ventilation <5days 5–7days Oxygenation Bronchoscopy • Clear bronchoscopy • Small amount of white secretion
Chest X-ray Clear chest X-ray Minimal opacity Severe opacity in large proportion of lung eld Ischaemic time <4h
a
PaO2/FiO2 ratio after at least 10min of ventilation with FiO2 100% and positive end-expiratory pressure (PEEP) of 5–10 cmH2O
a
>350mmHg 200–350mmHg <200mmHg
• Mild inammation in airway
The steps for procurement of a lung block are as follows:
1. Median sternotomy is the commonest incision for cardio­thoracic organ procurement. The pericardium is then opened with an inverted “T” shaped incision.
2. Two or three pericardial stay sutures are placed on each side of the opened pericardium. The stay sutures are secured with artery forceps for easy mobilisation of the pericardium to facilitate access to the bilateral pleural spaces. Both pleurae are opened, and the lungs are inspected for the nal component of allograft assessment. Table18.2 lists the main considerations of the intraopera­tive evaluation.
If the recipient centre formally accepts the lung allograft with the nal piece of information, the retrieval team can proceed to dissection in preparation for lung procurement.
Aspiration pneumonia
• Large amount of secretion or blood
• Secretion reaccumulating
• Gross contact bleeding from airway
• Abnormal bronchial tree anatomy
P. Kaul (*) Royal Papworth Hospital, Cambridge, UK e-mail: pradeep.kaul@nhs.net
L. Wang · M. Osman Transplant Surgery, Royal Papworth Hospital, Cambridge, UK e-mail: lu.wang@nhs.net; mohamed.osman2@nhs.net
© The Author(s), under exclusive license to Springer Nature Switzerland AG 2023 F. C. Wells (ed.), Atlas of Cardiac Surgery, Springer Surgery Atlas Series, https://doi.org/10.1007/978-3-031-43195-1_18
129
130
a
b
e
https://t.me/medicina_free
Table 18.2 Intraoperative ndings for donor lungs assessment
• Palpate to assess adhesions—Adhesion should be safely divided before lungs are mobilised for inspection to avoid parenchymal injury, which can compromise donor lung preservation and lead to prolonged air leak post-transplant.
• Inspect the colour of the lungs—Anthracotic pigment on the pleural surfaces is expected due to exposure to air pollution and smoking.
• Inspect for bullae, blebs and scarring—A few bullae or blebs in the apices are acceptable.
• Examine any parenchymal injury– Contusion or penetration injury can occur in trauma cases or donors who received aggressive cardiopulmonary resuscitation.
• Inate the lungs to recruit the atelectatic areas —If atelectasis recurs, repeat bronchoscopy to remove any secretion reaccumulated in the airway.
• Deate the lungs—Once lungs are fully recruited, ask the anaesthetist to deate the lungs at the point of full ination. A quick collapse of the lungs excludes any airway obstruction.
• Palpate for lung nodules—While the lungs are deated, palpate for any nodules or mass. If there is a positive nding, biopsy and frozen section should be performed immediately if possible. All the transplant centres receiving organs from this donor should be informed of this nding and the histopathology results.
• Perform differential blood gases—The lungs should then be ventilated with FiO2 100% and PEEP 5–10 cmH2O for at least 10min before blood samples are collected from each of four pulmonary veins and an arterial line for systemic gases.
P. Kaul et al.
b
3. Divide the aortopulmonary fold and use blunt dissection to separate the ascending aorta from the pulmonary artery (PA) trunk as well as the right PA.
4. Divide the pericardium on top of superior vena cava (SVC) and isolate it from the surrounding connective tis­sue and right PA. Place a black silk tie with snugger loosely around the SVC.
5. Lift the SVC gently and use blunt dissection to isolate azygos vein which drains into the posterior aspect of SVC. Place two black silk ties loosely around azygos vein.
6. Carefully divide the pericardial reection between infe­rior vena cava (IVC) and right inferior pulmonary vein.
7. Isolation and even division of innominate vein is optional, but this step helps provide better access to trachea later during the explant.
The cardiothoracic retrieval team must remain in theatre while waiting for the abdominal team to complete their dis­section in case the donor becomes haemodynamically unsta­ble. Once both the retrieval teams are ready and a cross-clamp time is agreed with the recipient centres, 300units/kg donor bodyweight of heparin is given via a central venous line.
8. While waiting for heparin to be circulated in the donor’s
cardiovascular system, insert a 4-0 proline purse-string suture at the PA bifurcation and the ascending aorta.
9. Place the respective perfusion catheters and secure them
with the purse-string sutures. The perfusion tubing is
c
Fig. 18.1 The surgical steps prior to organ explant. (a) separate ascending aorta from pulmonary artery trunk, (b) isolate superior vena cava, (c) dissect around inferior vena cava, (d) insert cardioplegia can­nula into ascending aorta, (e) secure perfusion catheter into pulmonary artery at the level of bifurcation (From Sundaresan et al. [1]; with permission)
handed out, primed with pulmonary ush solution and cardioplegia, and connected to the respective perfusion catheters (Fig.18.1) [1].
10. Use a pair of dissecting scissors to develop the Waterston’s groove between the left and right atria, about 1cm anterior and medial to the conuence of the right superior and inferior pulmonary veins.
Conrm with the abdominal team about the cross-clamp and venting strategies. It is preferable to cross-clamp the supradiaphragmatic descending aorta and vent the abdomi­nal organs below the diaphragm. If the abdominal team requests to cross-clamp the descending aorta above the dia­phragm, use blunt dissection to isolate the descending aorta at the level of diaphragm. If the abdominal team requests
c
18 Lung Transplantation
https://t.me/medicina_free
venting to be performed above the diaphragm, prepare another pool sucker to collect blood and abdominal organ ush solution returning from the IVC.
Once all the parties are ready for organ explant and the
donor is fully heparinised,
131
11. Tie the silk ligatures around the azygos vein and ask the central venous lines to be withdrawn out of the SVC.
12. Inject 250 mcg of Prostacyclin (PGE1) directly into the PA trunk to dilate the pulmonary vascular system and facilitate distribution of the pulmonary ush solution.
13. Tighten the snugger around the SVC to occlude the venous return from the upper body.
14. Place an angled DeBakey clamp on the IVC just above the diaphragm to occlude the venous return from the lower body.
15. Partially divide IVC and left atrial appendage to vent the heart.
16. Apply a cross-clamp at the distal ascending aorta just inferior to the innominate artery and deliver the pulmonary ush solution and cardioplegia through the perfusion catheters. Make sure the PA pressure does not exceed 15–20mmHg by placing the cold ush solution bags about 30–60cm above the donor. During lung per­fusion, the tidal volume should be set at 6–8mL/kg ideal bodyweight, FiO2 at 50% and ination pressure at 15–20 cmH2O.Cover both the heart and lungs with some cold saline to swiftly reduce the organ temperature and thus their metabolic rate (Fig.18.2) [1].
17. After the cardioplegia and antegrade pulmonary ush solution are delivered, the donor heart is retrieved rst. Make three stabbing incisions into the left atrium at the appropriate level, one in the middle of the developed Waterston’s groove, one in the middle of the left atrium base at 1.5 cm from the coronary sinus by lifting the ventricles up superiorly, and the last one at the base of the left atrial appendage.
18. Divide the IVC fully. Extend the stabbing incision in the Waterston’s groove superiorly towards the base of SVC and inferiorly to connect to the stabbing incision in the left atrial base. Continue excising the left atrium towards the third stabbing incision at the base of the left atrial appendage and complete the excision by dividing the left atrial roof.
19. Remove the perfusion catheters. Fully divide the ascend­ing aorta at the level just inferior to the cross-clamp. Open the pulmonary artery trunk by extending the inci­sion made for the perfusion catheter. Disconnect the PA trunk from the right and left PA at the level of the bifur­cation. Remove the snugger around the SVC and tran­sect the SVC just inferior to the innominate vein. Divide the azygos vein in between the two sutures. At this point, cardiectomy is completed (Fig.18.3) [1].
a
b
Fig. 18.2 The surgical steps at the initial stage of organ explant. (a) Inject Prostacyclin into pulmonary artery, (b) snug superior vena cava, (c) clamp and divide inferior vena cava, partially divide left atrial appendage, clamp distal ascending aorta, deliver cardioplegia, and pul­monary ush solution. (From Sundaresan etal. [1]; with permission)
Fig. 18.3 The nal steps for cardiectomy. Divide ascending aorta close to the cross-clamp, separate pulmonary artery trunk from right and left pulmonary arteries at the level of bifurcation, and divide supe­rior vena cava. Lower image shows pulmonary venous cuff. (From Sundaresan etal. [1]; with permission)
20. Deliver 250–500mL of the cold pulmonary ush solu­tion retrogradely into each of the pulmonary vein ori­ce. Make sure the balloon of the retrograde perfusion catheter seals the pulmonary vein ostium tightly to mini­mise the ush solution leakage. The retrograde perfu-
132
https://t.me/medicina_free
sion can be stopped once the perfusion solution returning from the respective pulmonary artery is clear without blood clots.
21. Remove the pericardium anterior to the phrenic nerves on both sides and inferior to the inferior pulmonary veins in the mediastinum. Lift the right lung out of the right pleural space. Complete the division of the right inferior pulmonary ligament up to the base of the right inferior pulmonary vein. Dissect the mediastinal pleura posterior to the right hilum and the connective tissues in the pre-oesophageal plane from the inferior end until the azygos vein is encountered. Use blunt dissection as much as possible to avoid damaging the oesophagus at this stage. Divide the azygos vein. Place the right lung back into the right pleural cavity. The same steps are performed on the left side, except the descending part of the aortic arch which is divided at this time.
22. During the retrograde perfusion and lung dissection pro­cess, the lungs should be continuously ventilated.
23. Pull the aortic arch down and divide it from the three neck arteries. Clear the tissues in the para-tracheal space bilater­ally to isolate the trachea circumferentially. Care shall be taken to prevent injury to membranous trachea. At this point, the lung block is only connected to the donor by the trachea. Ask the anaesthetist to partially retract the endo­bronchial tube to ensure there is adequate length of trachea on the lung block side. Place a TA stapler as superior as possible around the trachea (Fig.18.4). The lungs are venti­lated with a peak pressure of 20 cmH2O.When the lungs are inated, re the TA stapler. Place another stapler proximal to the rst one. Divide the trachea between the staple lines. Proximal prevent the spillage of secretion from the upper airway.
P. Kaul et al.
Fig. 18.5 Package of the lungs
24. Transfer the lung block from the chest cavity to the back bench. Make a nal inspection of the lungs for paren­chymal injury and residual atelectasis. It is possible to repeat ination or perfusion at this stage. Once the lungs are ready for package, place them in three sterile bags each lled with 2L of cold saline or pulmonary ush solution. Remove all the air from the bags before tying them with heavy strings (Fig.18.5). The lung block is then placed into an icebox together with the donor’s blood samples, lymph nodes, bronchoalveolar lavage sample, a piece of spleen, and documents. The icebox is then transported to the transplant centre without unnec­essary delays.
Fig. 18.4 Division of trachea and and the left atrial cuff after donor cardiectomy
Special Considerations if Heart Is Retrieved forTransplantation
If heart is also retrieved for transplant, use the angled DeBakey clamp to slightly push against the diaphragm before occluding the IVC to ensure that there is adequate IVC on the heart side. This helps avoid damage the coronary sinus when dividing the IVC. Pay special attention when separating the left atrium from the cuff around the pulmo­nary veins. Make sure that there is adequate left atrial cuff for anastomosis during the heart implantation.
Special Considerations intheDonation After Circulatory Death Donors
For the donation after circulatory death (DCD) donors, a futility of continued treatment statement is required to replace the certicate of brainstem death.
18 Lung Transplantation
https://t.me/medicina_free
133
1. After the retrieval teams are ready, the patient is trans­ferred to the operation theatre or the anaesthetic room of the theatre where withdrawal of life sustaining treatment takes place.
2. The patient is positioned with the head of the bed up at 30°. Once ventilation and inotrope support are with­drawn, the patient’s vital signs are closely monitored and recorded every 5minutes initially. Once the arterial pres­sure trace becomes a at line (mechanical asystole) and no respiratory effort is observed, a 5-minute stand-off period starts.
3. At the end of this stand-off period, circulatory death is conrmed by an anaesthetist and the donor is expedi­tiously prepared for organ donation. While the donor is being cleaned and draped, re-intubation and bronchoscopy are performed at the same time. After a rapid sternotomy and opening of the pericardium, 25,000 units/kg of heparin is injected into the PA. A purse-string suture and pulmonary ush perfusion cath­eter are placed on the main PA.
4. At 10minutes from the mechanical asystole, a single tidal breath is given.
5. The SVC, IVC, descending aorta, and ascending aorta are clamped in sequence. Once the aorta is clamped, ventila­tion can be re-started.
6. The left atrial appendage is amputated to facilitate vent­ing. The antegrade pulmonary ush perfusion is then delivered.
7. The donor lung assessment is performed after the ante­grade perfusion completes.
8. If the lungs are accepted for transplant, lung block explant and preservation are carried out in the same way as for the brainstem death donors.
Implantation
Some lung recipients’ clinical condition deteriorates since they are listed for transplantation. Therefore, patient reviews immediately before the operation is important.
Once the donor lungs are formally accepted after the additional information from the retrieval team’s assessment is gathered, the recipient can be sent to theatre for anaesthe­sia. A double lumen endotracheal tube, ideally a left sided one, is placed to facilitate single lung ventilation during the operation. In addition to the central venous catheter and arte­rial line, it is preferrable to have a pulmonary artery catheter inserted via recipient’s right internal jugular vein, trans­oesophageal echocardiography probe ready for cardiac func­tion assessment, and cerebral saturation monitoring set up to observe cerebral perfusion throughout the procedure.
The recipient is placed in a supine position, with arms either tucked in loosely or secured to the armrests in the
extended position away from the body, to facilitate surgical exposure to the mid-axillary lines. To improve surgical access during the operation, rolls or pneumatic bags can be placed under the chest to push the operative side up. In addi­tion, the operative table can be rotated, provided the recipient is securely strapped to the operating table.
The common incisions for lung transplantation are clam­shell or transverse thoraco-sternotomy, anterolateral thora­cotomy, and median sternotomy (Fig. 18.6). Individual transplant centres have described video-assisted thoraco­scopic surgery and robotic-assisted approaches with smaller incisions, such as mini-anterior thoracotomies.
The choice of incision depends on the indication for transplantation, requirement of mechanical circulatory sup­port, and surgeon’s personal experience and preference.
For clamshell incision,
1. Mark the second to sixth ribs on both sides.
2. Make a skin incision in the sub-mammary fold simulta-
neously on both sides and join them across the sternum at the level of fourth intercostal space.
3. Dissect into the retro-mammary plane and raise a ap.
4. Enter the pleural cavities through the fourth intercostal
space.
5. Identify and ligate the internal mammary arteries on
both sides as the dissection approaches towards the sternum.
6. Make a transverse sternotomy at the level of fourth inter-
costal space.
7. Divide the mediastinal pleura to the level of
pericardium.
8. Place a Finochietto retractor on each side and open them
simultaneously.
9. Divide the intercostal muscles at the top of the bottom
rib. In each opened space, this helps in avoiding rib frac­tures whilst opening the retractor for access.
10. The serratus muscle bres can be prized apart without
dividing.
11. Latissimus dorsi muscle is spared.
For anterior thoracotomy incision, the skin incision is also made in the sub-mammary fold and a ap is raised as the dissection proceeds in the retro-mammary plane. The pleural cavity is entered via the fourth or fth intercostal space. It is certainly preferred over the clamshell incision in the cases of single lung transplantation. In bilateral sequential lung trans­plantation, it does avoid the sternal related complications like malunion. It also allows better respiratory effort in the immediate post-operative period. However, the recipient’s groin areas need to be prepared to establish extra-corporeal membrane oxygenation via femoral cannulation in case mechanical circulatory support is required during the operation.