American Journal of Medicine and Medical Sciences

p-ISSN: 2165-901X    e-ISSN: 2165-9036

2018;  8(1): 312-317

doi:10.5923/j.ajmms.20180811.03

 

Surgical Treatment of Cardiac Echinococcosis

F. G. Nazirov, M. M. Zufarov, Kh. A. Abdumadjidov, M. M. Akbarov, Sh. N. Khudaybergenov, Kh. J. Buranov

«Republican Specialized Research Centre of Surgery named after academician V.Vakhidov» state unitary enterprise, Tashkent, Uzbekistan

Copyright © 2018 The Author(s). Published by Scientific & Academic Publishing.

This work is licensed under the Creative Commons Attribution International License (CC BY).
http://creativecommons.org/licenses/by/4.0/

Abstract

The results of diagnostic methods and surgical treatment of 56 patients with cardiac echinococcosis have been analyzed. The patients were divided into 2 groups subject to the nature of the lesion: the 1st group – 25 patients with isolated echinococcosis of heart/pericardium, the 2nd group – 31 patients with combined cardiac echinococcosis and the other target organs (lungs or liver). A basic diagnostic technique was echocardiogram and MRI. In 64.2% of cases the patients were performed surgery in the conditions of cardiopulmonary bypass; in 35.7% - without cardiopulmonary bypass. Postoperative lethality made up 8.9%. Spontaneous perforation and anaphylactic shock were observed in 3.5% of cases. Rhythm disturbance was mostly observed as a non-fatal complication.

Keywords: Cardiac echinococcosis, Cardiopulmonary bypass, Surgical treatment

Cite this paper: F. G. Nazirov, M. M. Zufarov, Kh. A. Abdumadjidov, M. M. Akbarov, Sh. N. Khudaybergenov, Kh. J. Buranov, Surgical Treatment of Cardiac Echinococcosis, American Journal of Medicine and Medical Sciences, Vol. 8 No. 1, 2018, pp. 312-317. doi: 10.5923/j.ajmms.20180811.03.

1. Introduction

Cardiac echinococcosis is a severe zooanthroponosious disease which is characterized by long-duration chronic course, severe organic and systemic pathology, leads to disability and often to the patient’s death [3, 4, 6, 7, 11]. Currently echinococcosis remains a serious social and medical issue in many countries, especially in the endemic regions [33]. It is necessary to point that there is a tendency of increasing patients quantity in the developed countries of Europe and in the USA. This fact, probably, is connected with the growth of emigrants quantity suffering from hydatid disease [33].
The Central Asia is the region where a morbidity frequency reaches high digits making up approximately 9 people to 100000 of population [33].
In spite of concrete progress of medicamental and surgical treatment of cardiac echinococcosis it still remains a serious medical-social issue. It should be mentioned that there are very few researches on cardiac echinococcosis surgery [6-18]. A small number of publications and clinical observations on diagnostics and surgical treatment testifies an insufficient information awareness of clinicians about diagnostic features and facilities of surgical treatment. There are no opinions agreement in the literature about surgical treatment tactics for cardiac echinococcosis and the issues of simultaneous surgeries in the combined hepatocardial and cardiopulmonary hydatid still remain open [26, 30, 33].

2. Goal

To analyze and to estimate surgical treatment results of the patients with cardiac echinococcosis.

3. Materials and Methods

56 patients were performed surgery associated with cardiac echinococcosis at the Republican Specialized Research Centre of Surgery named after academician V.Vakhidov between 1994 and 2017. All the patients were divided into 2 groups subject to the nature of parasitogenic lesion: the 1st group – 25(44.6%) patients with isolated cardiopericardiac echinococcosis; the 2nd group – 31(55.3%) patients with combined echinococcosis of heart/pericardium and target organs (liver, lungs, mediastinum).
The age of the patients ranged from 7 to 64 years (mean age 26.7 ± 2.7 years) There were 27(48.2%) males and 29 (51.7%) females. The diagnostics of heart parasitogenic lesion was performed by the following investigations: chest X-ray (Fig.3), transthoracal (TT) and trans-esophageal (TE) echocardiography (ECG) (Fig.1; Fig.2), multi-slice computer tomography (MSCT) and coronarography.
Figure 1. ECG of LV hydatid
Figure 2. ECG of interventricular septum hydatid
Figure 3. X-ray pattern of LV hydatid
Operative intervention in 36 (64.2%) cases was performed in the conditions of cardiopulmonary bypass (CPB) (75.0 ± 7.6 min) and cardioplegia (45.3 ±4.9 min) from sternal approach. In 20 (35.7%) cases of pericardium parasitogenic lesion or combined echinococcosis of pericardium and lungs the surgeries were performed without CPB.
The surgeries in the conditions of CPB included a standard connection to the pump oxygenator (aorta – cava scheme). The hydatid area was put round with gauze tampon after asystolia, then cystotomy and echinococcectomy (EE) were performed (Fig. 4; Fig.5). A residual cavity was processed with 30% solution of sodium chloride or 80-100% solution of glycerin. Cystotomy area was sutured by double-row suture with 2/0 etibond thread on the Teflon pads (Fig.6; Fig. 7). The hydatids from interventricular septum (IVS) were extracted through right atrium approach. After puncture and aspiration of the cyst’s content with external aspirator we opened the cyst cavity (cystotomy), the cavity was processed with anti-scleric agents. We remained the cavity widely open creating a common cavity with the right ventricle one for permanent irrigation of parasite’s cavity with blood.
Figure 4. Cystotomy
Figure 5. Removal of the chitin
Figure 6. Closure
Figure 7. Final view
In 4 (7.1%) observations cardiac echinococcosis was combined with parasitogenic lesion of liver. The postoperative period in those patients coursed comparatively well (Tab. 1).
In 5 (8.9%) cases we registered a combined echinococcosis of heart and lung (Tab.1). 20 (35.7%) cases were a combined lesion of pericardium and lungs. In all cases the patients were successfully operated from thoracotomic approach without CPB and they performed simultaneous EE from lung and pericardium with an excision of the last one.
In 2 (3.5%) cases we observed multi-focal lesion of the heart, pericardium, lungs and mediastinum. In spite of the process prevalence and possible danger of the cyst perforation and cardiac tamponade, the patients were operated due to the life indications (Tab.1). During sternotomy we observed the clinical presentation of anaphylactic shock which caused the lethal outcome.
Table 1. The nature of performed surgeries for cardiac echinococcosis
     
In the postoperative period we performed 3 courses of anthelminthic chemotherapy using Mebendazole or Albendazole (10-15 mg/kg/a day) with monthly intervals under the control of blood analysis [1, 2, 13, 15, 16].

4. Results

General postoperative lethality in the groups made up 5 (8.9%) patients. 2 patients from the group with isolated cardiopericardiac echinococcosis group died in the early postoperative group. In one of them we revealed a critical stenosis of anterior interventricular branch (AIVB). The patient was performed simultaneous surgery – EE from the left ventricle and coronary artery bypass grafting (CABG) of AIVB in the conditions of CPB and cardioplegia. The early postoperative period was complicated by hemorrhage: we performed resternotomy, sanation and hemostasis. The patient died due to multiple organ failure. In the second case the lethal outcome was caused by the rupture of the left ventricle wall after the removal of intramurally located cyst.
In the group with combined echinococcosis of heart/pericardium and target organs (liver, lungs, mediastinum) the lethality made up 3 (5.3%). In one case the reason of the lethal outcome was an injury of anterior interventricular artery during the removal of hydatid from interventricular septum. Perforations were the fatal complications which had occured in 2 (3.5%) patients during sternotomy. Those patients had perforation of stressed hydatid of the heart right parts to the right ventricle cavity with the development of severe anaphylactic shock which led to the fatal outcome.
There was no relapse of the disease during 5 years. Anthelminthic therapy was conducted according to the recommendations.
Among non-fatal complications we mostly observed ventricular rhythm disturbance which were registered in 7 (28%) patients with isolated cardiopericardiac echinococcosis and in 6 (19.3%) patients with combined echinococcosis of heart/pericardium and target organs. Heart failure in the patients with isolated cardiopericardiac echinococcosis (the 1st group) was observed in 4 (16%) cases, in the group with combined echinococcosis of heart/pericardium and target organs (the 2nd group) – in 5 (16,1%) patients (Table.2). In 2 (8%) patients of the 1st group we observed a clinical presentation of compressive exudative pericarditis and they were performed pericardium cavity drainage. 2 patients (1 in each group) had pneumopathy. There were no complications connected with abdominal and pleural cavities.
Table 2. Non-fatal complications
     
We did not reveal any changes of volumetric-functional parameters of the heart by echocardiography data (Table 3).
Table 3. Echocardiography rates in the early postoperative period
     
As it has been presented in the Table 3, the dynamics of linear and volumetric heart rates and their changes in the postoperative period were insignificant. But in the early postoperative period we pointed a tendency for the improvement of ejection fraction (EF) in all the patients. This fact testified the improvement of myocardium contractile capacity. In 36 (64,2%) patients among 56 operated ones we observed a residual cavity (up to 1.5cm) by ECG data. In other cases so called “forgotten” cysts or a residual cavity were not revealed. We did not reveal any changes in the volumetric-functional parameters of the heart.

5. Discussion

Cardiac echinococcosis is rare parasitogenic lesion and its occurrence frequency does not exceed 2% [1-26, 32-37]. Clinical presentation of cardiac echinococcosis is not specific and depends on the sizes and localization, their relations with neighbouring cardiac structures [1-6, 11-18]. There are some data in the literature about the patients with cardiac echinococcosis taken to the hospitals with clinical presentation of coronary blood flow disturbance [33]. We revealed 22.7% cases of myocardial ischemia by ECG in preoperational period and their signs disappeared after surgery. Only in one case we performed CABG due to the critical stenosis of anterior interventricular artery. In the other observations the ischemia was conditioned by the compression of neighbouring coronary vessels of the stressed hydatid and had a transient nature.
In our cohort of patients a combination of cardiac echinococcosis and target organs was observed in 55.3% of cases.
According to the literary data a spontaneous perforation of hydatid into pericardium cavity or to the cardial cavity with the development of embolic syndrome and anaphylactic shock is observed in 7-15% of cases [2, 5, 27, 29, 31, 32, 37, 38]. Some authors describe the cases of hydatids perforation during cardiopulmonary resuscitation. In our investigation 2 (3.5%) patients died due to the hydatids perforation in the cardial cavity.
A special place in the intravital diagnostics of cardiac echinococcosis belongs to echocardiography [19, 32, 36]. We perform echocardiography and MSCT in all patients – it allows not only to detect hydatids but to detail their topographic localization, size and relation with coronary vessels.
Surgical treatment is a method of choice for cardiac echinococcosis by the world literary data [6, 11, 15, 20, 35]. Some authors prefer “off-pump” surgeries from thoracotomic approach, especially for pericardium echinococcosis. This method is interfaced with a number of complications such as: dissemination of hydatid content, a probability of neighbouring coronary vessels accidental taking to the suture during cardiac cycle, hydatid perforation during parasite’s bed handling, the risk of aeroembolism and non-radical removal with a high risk of disease relapse.
Analyzing the literature it has been determined that each sixth patient dies due to the hemorrhage during the operative treatment, especially if it is performed “off-pump”. That is why some authors being concerned about the occurrence of complications (hemorrhage, myocardium rupture and etc.) consider performing EE in the conditions of CPB and cardioplegia (CP) as the most reasonable method [11, 21, 26, 33]. We also think that performing EE in the conditions of CPB and CP on immobilized heart is rational and reasonable surgical method. Unfortunately, there is no a unified point of view in the literature concerning surgical treatment tactics of combined cardiac echinococcosis and target organs. Kabbani S.S. et al. [20] in their 8 observations first performed EE from the heart and 3-6 months later – from the liver and the lungs.
The up-to-date level of cardio-anesthesiology and cardiac surgery allows to perform successful simultaneous operations in the heart and target organs at combined cardiac echinococcosis. In N.O.Travin’s [33] opinion, at the echinococcosis of pericardium and lungs the simultaneous surgeries are possible due to the hydatids location in the same anatomical cavity. Our investigation results testify the possibility of simultaneous surgeries even at the parasitic cyst’s location simultaneously in the different anatomical cavities (thoracic and abdominal).
R. Parvizi et al. [26] offers to undergo a simultaneous surgery at the combined echinococcosis of heart and liver – he used a subcostal approach for hepatic hydatid removal and longitudinal sternotomy – for cardiac hydatid. The lacks of this method are a high traumatism of subcostal approach (transection of all groups of anterior abdominal muscles), a high frequency of postoperative hernias development and deformation of the anterior abdominal wall.
A hospital lethality after surgical treatment has not been sufficiently presented in the literature because in the majority of observations they speak about single surgeries. According to the literary data the postoperative lethality made up 5-28% [11, 21, 26, 33]. The postoperative lethality in our cohort of patients made up 8.9%. In 2 patients during 5 years of observation we registered the relapse of the disease. Those patients were successfully re-operated.
There is still no unity of opinions for optimal strategy of cardiac echinococcosis medicamental treatment. There are some reports about positive results of conservative treatment with Albendazole [10]. The other authors reduce the area of chemotherapy use without surgical intervention only for the patients with inoperable variants or for the patients who refused from the surgery. The third ones perform cardiac surgery after chemotherapy and also recommend to conduct therapy after the surgery. The fourth ones consider that treatment with Albendazole is deadly dangerous and absolutely contraindicative due to the softening of parasite wall during the treatment and a multiple increasing of hydatid rupture. And at last, the fifth ones point a low efficiency of the chemotherapy even after the hydatids removal. We use the chemotherapy only in the postoperative period for the prevention of the disease relapse.

6. Conclusions

Transthoracal echocardiography is a screening method for the diagnostics of cardiac echinococcosis. In 55.3% of cases we observed a combination of cardiac echinococcosis and target organs (lungs and liver). It is reasonable to perform echinococcectomy in the conditions of cardiopulmonary bypass and cardioplegia. It is possible to perform a simultaneous surgery at hepatocardiac and cardiopulmonary combined echinococcosis.

References

[1]  Bouassida I, Pricopi C, Mangiameli G, Arame A, Auliac JB, Gorbatai B, Riquet M, Le Pimpec Barthes F. Cardiac compression of hydatid origin. Rev Pneumol Clin. 2018 May 17.
[2]  Ben Khalfallah A, Ben Slima H. Cardiac hydatid cyst. Which imaging modality for an accurate diagnosis? Ann Cardiol Angeiol (Paris). Epub 2017 Mar 23.
[3]  Streliaeva AV, Sagieva AT, Abdiev FT, Sadykov RV, Sadykov VM, Gabchenko AK, Murtazaev ZI, Akhmedov IuM, Zakirova NA, Baĭmuradov NS, Sabirova SÉ, Zakirova F.I. Cardiac involvement in adults with echinococcosis. Med Parazitol (Mosk). 2012 Oct-Dec;(4):40-2.
[4]  Kara SS, Gullu UU. A case of intracardiac echinococcosis. Cardiol Young. 2017 Sep; Epub 2017 Jun 20.
[5]  Seth HS, Mishra P, Khandekar JV, Raut C, Mohapatra CKR1, Ammannaya GKK. A Concomitant Intramyocardial and Pulmonary Hydatid Cyst: A Rare Case Report. Braz J Cardiovasc Surg. 2017 Mar-Apr;32(2):138-140.
[6]  Yaman M, Ates AH, Arslan U, Ozturk H, Aksakal A. A giant cardiac hydatid cyst presenting with chest pain and ventricular tachycardia in a pregnant woman undergoing cesarean section. Indian Heart J. 2016 Sep.Epub 2016 Apr 28.
[7]  Rossetti E, Boto A, González Cambaceres C, Ruvinsky S, Sagray E; Colaboradores. Acute arterial embolism as the clinical presentation of a disseminated hydatidosis: case report. Arch Argent Pediatr. 2018 Aug 1;116(4):e616-e620.
[8]  Gencheva DG, Menchev DN, Penchev DK, Tokmakova MP. An Incidental Finding of Heart Echinococcosis in a Patient with Infective Endocarditis: a Case Report. Folia Med (Plovdiv). 2017 Mar 1;59(1):110-113.
[9]  Sanaei Dashti A, Kadivar MR, Alborzi A, Sadeghi E, Pouladfar GR, Bagherian N, Honar N, Khalifeh M. Analysis of hospital records of children with hydatid cyst in south of Iran. J Parasit Dis. 2017 Dec;41(4):1044-1048.
[10]  Carmona P, Alonso J, Aparicio S, Zarragoikoetxea I, Ibañez F, Argente P. Cardiac Hydatid Disease: An Uncommon Cause of Cardiac Tumors. J Cardiothorac Vasc Anesth. 2017 Apr;31(2):675-677.
[11]  Nunes MC, Guimarães Júnior MH, Diamantino AC, Gelape CL, Ferrari TC. Cardiac manifestations of parasitic diseases. Heart. 2017 May;103(9):651-658.
[12]  Mezgar Z Khrouf M, Ben Soltane H, Mahjoub M, Ben Fredj S, Amara A, Jedidi M, Sandid SH, Zaouali S, Waz I, Saada A, Methamem M. Case of Massive Hydatid Pulmonary Embolism Incidentally Discovered in a 56-Year-Old Woman with Posttraumatic Abdominal Pain. Case Rep Pulmonol. 2018 May 13;2018:7831910.
[13]  Aala F, Badali H, Hashemi Fesharaki S, Boroumand M, Sotoudeh Anvari M, Davari H, Agha Kuchak Afshari S, Khodavaisy S. Coexistence of aspergilloma and pulmonary hydatid cyst in an immunocompetent individual. J Mycol Med. 2017 Sep;27(3):396-399.
[14]  Aldahmashi M, Alassal M, Kasb I, Elrakhawy H. Conservative Surgical Management for Pulmonary Hydatid Cyst: Analysis and Outcome of 148 Cases. Can Respir J. 2016;2016:8473070.
[15]  Prati G, Gatti G, Belgrano M, Pinamonti B, Rauber E, Gripshi F, Pappalardo A, Sinagra G. Disseminated echinococcosis: follow your heart. J Cardiovasc Med (Hagerstown). 2016 Dec;17 Suppl 2:e146-e148.
[16]  Travin N, Shevchenko Y. Heart echinococcosis: Current problems and surgical treatment. Multimed Man Cardiothorac Surg. 2017 Sep 26;2017.
[17]  Blanco M, Echevarría JR, Fernández-Gutiérrez M, Laguna G. Heart Failure for Superinfected Giant Pericardial Hydatid Cyst. Ann Thorac Surg. 2017 Feb;103(2):e197.
[18]  Tefera E, Knapp J, Teodori M. Hydatid cyst of the interventricular septum. J Tehran Heart Cent. 2017 Oct;12(4):192-193.
[19]  Zalaquett E, Menias C, Garrido F, Vargas M, Olivares JF, Campos D Pinochet N, Luna A, Dahiya N, Huete Á. Imaging of Hydatid Disease with a Focus on Extrahepatic Involvement. Glob Cardiol Sci Pract. 2017 Mar 31;2017(1):e201709.
[20]  Kastengren M, Liska J, Svenarud P, Dalén M. Intraventricular Septal Echinococcosis. Ann Thorac Surg. 2017 Jul;104(1):e89.
[21]  Díaz-Menéndez M, Pérez-Molina JA, Norman FF, Pérez-Ayala A, Monge-Maillo B, Fuertes PZ, López-Vélez R. Management and outcome of cardiac and endovascular cystic echinococcosis. PLoS Negl Trop Dis. 2012 Jan;6(1):e1437.
[22]  Abad-Torrent A, Sueiras-Gil A, Martínez-Vilalta M, Vallet-Fernández J, Guisasola-Rabés M. Monitoring of the intraoperative analgesia by pupillometry during laparoscopic splenectomy for splenic hydatid cyst. J Clin Anesth. 2017 Feb;36:94-97.
[23]  Nikmanesh B, Mirhendi H, Mahmoudi S, Rokni MB. Multilocus sequence analysis of Echinococcus granulosus strains isolated from humans and animals in Iran. Exp Parasitol. 2017 Dec;183:50-55.
[24]  Kohansal MH, Nourian A, Rahimi MT, Daryani A, Spotin A, Ahmadpour E. Natural products applied against hydatid cyst protoscolices: A review of past to present. Acta Trop. 2017 Dec;176:385-394.
[25]  Şahpaz A, İrez A, Gülbeyaz H, Şener MT, Kök AN. Non-thrombotic Pulmonary Embolism Due to Liver Hydatic Cyst: A Case Report. Balkan Med J. 2017 May 5;34(3):275-277.
[26]  Inzirillo F, Giorgetta C, Ravalli E. Pericardial echinococcosis: unusual presentation in a non-endemic region. Asian Cardiovasc Thorac Ann. 2014 Nov;22(9):1126-7.
[27]  Kocabay G, Yilmazer S, Korkmaz Y, Karadeniz A, Duran NE. Primary cardiac hydatid cyst presenting as noncompaction cardiomyopathy. Echocardiography. 2017 Jan;34(1): 141-142.
[28]  Padmanabhan TNC, Kumar KVK, Sadiq Azam M, Kumar Bilolikar A. Primary echinococcus infection of the heart: a rare type of cystic echinococcosis. Eur Heart J. 2017 Aug 1;38(29):2255.
[29]  Sadashiva N, Shukla D, Devi BI. Rupture of Intraventricular Hydatid Cyst: Camalote Sign. World Neurosurg. 2018 Feb;110:115-116.
[30]  Emam Hadi MA, Najari F, Soleimani L. Sudden Death due to Hydatid Cyst Emboli; a Case Report. Emerg (Tehran). 2018;6(1):e20. Epub 2018 Mar 19.
[31]  Wadhawa V, Shah J, Doshi C, Ramani J, Lakhia K, Rathod D, Tavar R, Kothari J. Surgical overview of cardiac echinococcosis: a rare entity. Interact Cardiovasc Thorac Surg. 2018 Aug 1;27(2):191-197.
[32]  Agnino A, Lanzone AM, Spira G, Anselmi A. Surgical treatment of left ventricular echinococcosis through the HeartPort technique. Interact Cardiovasc Thorac Surg. 2018 Feb 1;26(2):357-359.
[33]  Sabbagh A, Sonon P, Sadissou I, Mendes-Junior CT, Garcia A, Donadi EA, Courtin D. The role of HLA-G in parasitic diseases. HLA. 2018 Apr;91(4):255-270.
[34]  Mantini C, Capparuccia C, Cademartiri F, Messalli G, Mastrodicasa D, Cinalli S, Cotroneo AR, Caputo M. Uncommon Isolated Unilocular Myocardial Cyst in a Dog-Friendly Young Female Patient- Multimodality Imaging. Circ J. 2017 Jun 23;81(7):1056-1058.
[35]  Gurzu S, Beleaua MA, Egyed-Zsigmond E, Jung I. Unusual Location of Hydatid Cysts: Report of Two Cases in the Heart and Hip Joint of Romanian Patients. Korean J Parasitol. 2017 Aug;55(4):429-431.
[36]  Singh A, Sharma R, Garg A, Nanda NC, Elsayed M, Taher A, Bulur S. Usefulness of bubble study in echocardiographic diagnosis of contained rupture of hydatid cyst in the right ventricular outflow tract. Echocardiography. 2016 Sep;33(9):1402-8.
[37]  Atayi Z, Borji H, Moazeni M, Saboor Darbandi M, Heidarpour M. Zataria multiflora would attenuate the hepatotoxicity of long-term albendazole treatment in mice with cystic echinococcosis. Parasitol Int. 2018 Apr;67(2):184-187.
[38]  Kahlfuß S, Flieger RR, Roepke TK, et alDiagnosis and treatment of cardiac echinococcosis. Heart 2016;102:1348-1353.