metricas
covid
Buscar en
Annals of Hepatology
Toda la web
Inicio Annals of Hepatology Infected hepatic echinococcosis. Clinical, therapeutic, and prognostic aspects. ...
Información de la revista
Vol. 22.
(mayo - junio 2021)
Compartir
Compartir
Descargar PDF
Más opciones de artículo
Visitas
2956
Vol. 22.
(mayo - junio 2021)
Concise reviews
Open Access
Infected hepatic echinococcosis. Clinical, therapeutic, and prognostic aspects. A systematic review
Visitas
2956
Sergio Castilloa,b, Carlos Manterolaa,c,d,
Autor para correspondencia
carlos.manterola@ufrontera.cl

Corresponding author.
, Luis Grandee,f, Claudio Rojasa
a PhD Program in Medical Sciences, Universidad de La Frontera, Chile
b Clínica Red Salud Mayor Temuco, Temuco, Chile
c Department of Surgery, Universidad de La Frontera, Chile
d Center of Morphologic and Surgical Studies (CEMyQ), Universidad de La Frontera, Chile
e Department of Surgery, Institut Hospital del Mar d’Investigacions Mèdiques (IMIM), Barcelona, Spain
f Department of Surgery, Universidad Autónoma de Barcelona, Spain
Este artículo ha recibido

Under a Creative Commons license
Información del artículo
Resumen
Texto completo
Bibliografía
Descargar PDF
Estadísticas
Figuras (2)
Tablas (7)
Table 1. Search strategies for information source and results achieved. (N = 960).
Table 2. Distribution of analyzed studies by year of publication.
Table 3. Country origin of analyzed patients.
Table 4. Bacterial species reported in 250 patients.
Table 5. Surgical techniques, pom and mortality associated reported.
Table 6. Morbidity reported in 121 patients.
Table 7. Antibiotics used reported in 182 patients.
Mostrar másMostrar menos
Abstract

Infected hepatic echinococcosis (IHE), defined as a cystic infection, and the development of a liver abscess may be a complication in the natural history of hepatic echinococcosis. The aim of this study was to review the evidence available related to clinical, therapeutic, and prognostic aspects of IHE.

We conducted a systematic review. Trip Database, BIREME-BVS, SciELO, LILACS, IBECS, PAHO-WHO; WoS, EMBASE, SCOPUS and PubMed were consulted. Studies related to IHE in humans, without language restriction, published between 1966 and 2020 were considered. Variables studied were publication year, geographical origin of the samples, number of patients, therapeutic and prognosis aspects, and methodological quality (MQ) for each article. Descriptive statistics was applied. Subsequently, weighted averages (WA) of the MQ of each article were calculated for each variable of interest. 960 related articles were identified; 47 fulfilled selection criteria, including 486 patients with a median age of 48 years, 51.6% being male. The largest proportion of articles were from Spain, India, and Greece (36.1%). Mean cyst diameter was 14.1 cm, and main location was right liver lobe (74.0%). WA for morbidity, mortality, hospital stay, and follow-up were 28.5%, 7.4%, 8.5 days and 14.8 months, respectively. The most common causative microorganisms of superinfection isolated were Enterobacteriaceae. An association with cholangitis was reported in 13.4% of cases. Mean MQ of the 47 articles included was 7.6 points.

We can conclude that the information related to IHE is scarce and scattered throughout articles of small casuistry and poor quality, and consequently does not provide strong evidence.

Keywords:
Echinococcosis, hepatic
Echinococcosis, hepatic/complications
Liver abscess
Liver abscess, pyogenic
Systematic review
Abbreviations:
CE
IHE
SR
MQ
WA
POM
Texto completo
1Introduction

Cystic echinococcosis (CE) is characterized by cystic lesions, most commonly in the liver and lungs, which can be fatal if left untreated. CE can be found worldwide, and the World Health Organization considers it as one of the 17 neglected tropical diseases [1,2].

Different complications may occur during the natural history of CE, of which cystic superinfection is of note. This condition is recognized as infected hepatic echinococcosis (IHE) and includes diagnoses such as hepatic hydatid abscess, liver abscess of hepatic origin or superinfection of liver hydatid cysts. Superinfection may occur as a complication of bacteremia by any cause, but in most cases it develops when the integrity of the cyst membrane has been lost and communication is established between the cyst and the bile ducts [3,4]. In fact, as early as 1891 there is evidence that infection of hydatid cysts could lead to subsequent rupture [5]. Thus, it is estimated that superinfection may complicate ruptured hepatic echinococcosis in up to 25% of cases, leading to the development of a liver abscess [6].

In contrast to the usual clinical course of a liver abscess, IHE usually appears with nonspecific clinical manifestations. These manifestations may be due to the presence of a pericystic membrane, that is, an inflammatory reaction of the host against the Echinococcus which generates a nonspecific defense mechanism in the host. Hence, it is possible that clinical features and abnormal lab results may not derive from IHE (which explains the difficulty in achieving an adequate diagnosis). Early diagnosis is important since it reduces high postoperative morbidity (POM) and mortality which have been estimated at 24.4% and 2.0%, respectively [6–8].

The general objective of this review was to summarize the evidence available related to the clinical, therapeutic, and prognostic aspects of IHE. The specific objectives were to describe the different treatments used, POM and mortality associated, reported in the primary articles. To determine results of emergency treatment adopted versus elective surgery. To describe other therapeutic resources reported in the primary articles.

2Material and methods

This manuscript was written following the guidelines of the PRISMA statement (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) [9], and AMSTAR (Assessing the methodological quality of systematic reviews) Guidelines.

2.1Protocol and registration

Systematic review registration number PROSPERO CRD42020143171.

2.2Design

Systematic Review (SR).

2.3Eligibility criteria

Studies related to IHE in an adult human population published between 1966 and 2020 were included. No language or design type restriction was applied. Articles contaminated with other types of liver abscesses; echinococcosis alveolaris, multilocularis and vogeli were excluded. Narrative reviews, consensus documents and discussion papers were also not considered.

2.4Information sources

The following Meta search engines, libraries and databases were reviewed: Trip Database, BIREME-BVS, SciELO, LILACS, IBECS, PAHO-WHO; Web of Science, EMBASE, SCOPUS and PubMed. The closing date for article search and recruitment was March 30, 2020.

2.5Search

The search was carried out according to PECO components (population study [P], exposure [E], comparator [C], and outcome [O]). Studies were searched for subjects with hepatic echinococcosis [P], complicated with a secondary infection [E], without comparing [C], clinical features [O]. Sensitive searches were performed using MeSH terms, free words, truncated terms and Boolean connectors (AND and OR); with strategies adapted to each database (Table 1). A systematic and sensitive literature search was performed. Therefore, search strategies were developed, using MeSH terms, free words, truncated terms and Boolean connectors (AND, OR and NOT); using strategies adapted to each source of information consulted. In addition, a manual cross-reference search, and a directed search in infectious disease and parasitology journals was performed.

Table 1.

Search strategies for information source and results achieved. (N = 960).

Information sources  Search strategies 
Trip Database (n = 9)  ("Echinococcosis, Hepatic" OR “hepatic hydatid cyst” OR “hepatic hydatidosis” OR “liver echinococcosis” OR “liver hydatid cyst” OR “liver hydatidosis” OR "Echinococcosis, Hepatic/complications") AND ("Liver Abscess" OR "Liver Abscess, Pyogenic") 
BIREME-BVS (n = 38)  (mh:("Equinococosis Hepática/CO" OR "Equinococosis Hepática/DI" OR "Equinococosis Hepática/MO" OR "Equinococosis Hepática/SU") AND mj:("Absceso Hepático")) 
SciELO (n = 49)  ((hepatic echinococcosis) OR (liver hydatidosis) OR (hepatic hydatidosis) OR (liver hydatid cyst) OR (hepatic hydatid cyst)) AND (liver abscess) 
LILACS (n = 6)  Hepatic echinococcosis [Words] or Liver hydatid cyst [Words] and Liver abscess [Words] 
IBECS (n = 0)  "Hepatic echinococcosis" [Palabras] and "Liver hydatid cyst" [Palabras] and "Liver Abscess" [Palabras] 
PAHO- MA WHO (n = 94)  “Cystic echinococcosis” NOT alveolar NOT multilocularis 
Web of Science (n = 6)  #1 (Ti=(Hepatic Echinococcosis) OR Ti=(liver hydatid cyst) OR Ti=(Echinococcosis, Hepatic) OR Ti=(Hepatic hydatidosis)) 
  #2 (Ti=(Liver Abscess) OR Ti=(Liver Abscess, Pyogenic)) 
  #3 (#1 AND #2) 
EMBASE (n = 204)  ('liver hydatid cyst'/exp OR 'liver hydatid cyst' OR 'liver echinococcosis'/exp OR 'liver echinococcosis' OR 'hepatic echinococcosis'/exp OR 'hepatic echinococcosis') AND 'liver abscess'/exp AND [1967−2020]/py 
SCOPUS (n = 335)  ("Hepatic Echinococcosis" OR "liver hydatid cyst" OR "Hepatic hydatidosis") AND "Liver Abscess" AND (LIMIT-TO (DOCTYPE, "ar")) AND (LIMIT-TO (SRCTYPE, "j")) 
PubMed (n = 219)  ("Hepatic echinococcosis" OR "Echinococcosis, Hepatic" OR “hepatic hydatid cyst” OR “hepatic hydatidosis” OR “liver echinococcosis” OR “liver hydatid cyst” OR “liver hydatidosis” OR "Echinococcosis, Hepatic/complications") AND ("Liver Abscess" OR "Liver Abscess, Pyogenic" OR “Hepatic Abscess”) 

BIREME: Latinamerican and Caribbean Center on Health Science Information; BVS: Virtual Health Library; SciELO: Scientific Electronic Library Online, IBECS: Spanish Bibliographic Index of the Health Sciences.

2.6Study selection

Articles identified in each source of information, were filtered by duplication between databases. Three review authors (CM, SC, CR) independently screened the titles and abstracts of all the reports identified as a result of each search. Then, full-text study reports were retrieved, and two review authors (CM, SC) independently screened the full text, identified studies for inclusion, and identified and recorded reasons for exclusion of the ineligible studies. Disagreements were resolved by consensus or if required, a third review author (LG) was consulted. Duplicate articles identified were excluded.

2.7Data collection process

A critical review by 3 researchers (SC, CM and LG) of each selected article was applied. The selected data were extracted by three authors (SC, CM and CR), and then collected in an Excel spreadsheet (Mac Excel, version 15.24; 2016 Microsoft Corporation®). All studies meeting the inclusion criteria underwent analysis of methodological quality (MQ) according to an ad-hoc designed scale [10]. This scale with content and construct validity is composed of 3 domains: design, sample size and methodological aspects; and its final score is the sum of the 3 domains; the score may range between 6 and 36 points, with a cut-off point of MQ of 18 points.

2.8Data items

The following variables were considered: year of publication, geographic origin of the article, number of cases, main clinical manifestation, therapeutics, and prognosis (POM and mortality).

2.9Risk of bias in individual studies

Two review authors (CM, LG) independently assessed the risk of bias for each study applying a MQ scale [10].

2.10Summary measures

Descriptive statistics were applied, with calculation of percentages and averages.

2.11Synthesis of results

Weighted averages (WA) of each variable were determined by the sum of the product of the study variable by the MQ score of where the article came from, divided by the sum of MQ scores of all the study articles. For this purpose, the following formula was applied (WA=ΣXi*eiΣei), in which WA is weighted average; Xi, the value achieved for the outcome in the study i (for all outcomes); ei, represents the MQ score obtained in study I; and Σei, correspond to the sum of the scores obtained in all the studies [11].

2.12Ethics

In order to reduce possible biases in selection and analysis, masking of authors and study centers was implemented.

3Results3.1Study selection

A total of 960 studies were retrieved from the search (Table 1). Of these, 99 were excluded for duplication of information sources and 670 were discarded as being considered “irrelevant” after reading titles and abstracts. In-depth analysis of the 191 remaining articles allowed the exclusion of 156 studies that did not meet the selection criteria. Furthermore, 11 studies collected by cross-reference search and 1 collected by directed search in specialized journals (n = 12) were added. Finally, 47 studies were included in the study sample of this review (Fig. 1).

Fig. 1.

Flowchart of the participating studies (PRISMA).

(0.25MB).
3.2Study characteristics

All the studies analyzed were case reports or series including 486 patients [median age of 48 years (WA of 45.9 years), 51.6% males]. The largest series were those of Prousalidis (n = 77) [12] and Symeonidis (n = 75) [13]. The remainder were reports that included between 1 and 65 cases [14–58].

3.3Synthesis of results

The highest percentage (29.8%) of articles was published during the period 2010–2020 (Table 2). The countries with the highest number of publications were Spain, India, and Greece [14.9%, 12.8% and 8.4%, respectively (Table 3 and Fig. 2)].

Table 2.

Distribution of analyzed studies by year of publication.

Periods  Nº studies 
1958−1969  6.4 
1970−1979  8.5 
1980−1989  11  23.4 
1990−1999  8.5 
2000−2009  11  23.4 
2010−2020  14  29.8 
Total  47  100 
Table 3.

Country origin of analyzed patients.

Countries  Nº studies 
Spain  14.9 
India  12.8 
Greece  8.4 
Italy  6.4 
Turkey  6.4 
USA  6.4 
Germany  4.2 
Chile  4.2 
UK  4.2 
Algeria  2.1 
Bulgaria  2.1 
Cyprus  2.1 
Iraq  2.1 
Iran  2.1 
Kenya  2.1 
Lebanon  2.1 
Malaysia  2.1 
Morocco  2.1 
Romania  2.1 
Russia  2.1 
Saudi Arabia  2.1 
Sweden  2.1 
Taiwan  2.1 
Tunisia  2.1 
Total  47  100 
Fig. 2.

Geographic distribution of cases reported in the primary articles.

(0.48MB).

Mean cyst diameter reported in primary articles was 14.1 cm (WA of 12.5 cm). Regarding the location of IHE, 54.5% were found in the right liver lobe, 11.7% in the left liver lobe and in 7.4% were detected in both liver lobes. This data was not available in 128 cases.

Samples for microbiology were only reported in 250 out of 486 cases (49.3%). In 56 cases (11.6%) the cultures were negative. In positive cases, enterobacterias were the microorganisms most frequently isolated (Table 4).

Table 4.

Bacterial species reported in 250 patients.

Bacterial species  Nº patients 
Escherichia coli  111  44.4 
Pseudomonas aeruginosa  15  6.0 
Enterobacter sp.  14  5.6 
Klebsiella pneumoniae  2.4 
Salmonella typhi  2.4 
Haemophillus influenzae  1.6 
Proteus rettgeri  1.6 
Streptococcus viridans  1.6 
Staphylococus aureus  1.2 
Enterococcus sp.  1.2 
Klebsiella oxytoca  1.2 
Yersinia enterocolitica  0.8 
Mycobacterium sp.  0.8 
Bacterial polyphlora  2.4 
No bacterial development  56  22.4 
Other*  11  4.4 
Total  250  100 

Other*: Acinetobacter baumannii, Aeromonas hydrophila, Citrobacter, Haemophilus parainfluenzae, M. Gordonae, M. morganii, Salmonella paratyphi B, Staphylococcus epidermidis, Streptococcus bovis, Streptocuccus Milleri, and Streptococcus salivarius (one of each).

All cases were surgically treated. The surgical procedure most frequently used was cysto-pericystectomy, total or partial (56.1%). Techniques, POM and associated mortality are summarized in Table 5.

Table 5.

Surgical techniques, pom and mortality associated reported.

Techniques  Nº patients  (%)  POM (%)  Mortality (%) 
Cysto-pericystectomy  213  43.8  19.2  4.7 
Cystostomya  68  14.0  57.4  10.3 
Partial cysto-pericystectomy  60  12.3  24.2  12.1 
Semi-closed hydatidectomy  51  10.5  27.5  9.8 
Unroofing + drainage  45  9.3  26.6  8.9 
Percutaneous drainageb  27  5.6  14.8  14.8 
Endoscopic drainage  1.9  0.0  11.1 
Hepatectomyc  1.2  16.7  0.0 
Laparoscopic drainage  0.6  0.0  0.0 
Marsupialization  0.6  33.3  33.3 
PAIR and cystostomy  0.2  100  0.0 
Total  486  100     

POM: Postoperative morbidity.

a

Cystostomy: Open drainage.

b

Percutaneous drainage: Using radiological interventional approach.

c

Hepatectomy: Right (n = 2) and left hepatectomy (n = 4).

The WA for POM and mortality for all the articles were 28.5% and 7.4%, respectively. A description of POM causes was only available in 121 patients (Table 6), highlighting surgical site infection (30/121 cases, 24.8%) The causes of mortality were sepsis (19/36 cases; 52.8%), respiratory infections (7/36 cases; 19.4%), pulmonary thromboembolism (4/36 cases; 11.1%), myocardial infarction and cardiac arrhythmia (4/36 cases; 11.1%) and cerebral stroke (2/36 cases; 5.6%). The WA for hospital stay and follow-up were 8.5 days and 14.8 months, respectively.

Table 6.

Morbidity reported in 121 patients.

Etiology of morbidity  Nº patients 
Surgical site infection  30  24.8 
Biliary fistula  14  11.6 
Atelectasis  11  9.1 
Respiratory infection*  6.6 
Residual abscess  5.0 
Acute respiratory insufficiency  4.1 
Intra-abdominal abscess  3.3 
Upper digestive hemorrhage  2.5 
Pleural effusion  2.5 
Residual cavity  2.5 
Sepsis  3.3 
Incisional hernia  1.6 
Intraperitoneal hemorrhage  1.6 
Other*  3.3 
No morbidity  22  18.2 
Total  121  100 

Respiratory infection*: Pneumonia and pneumonitis.

Other*: Cardiac arrhythmia, pericarditis, pulmonary thromboembolism, and subphrenic abscess (one of each).

The use of an antibiotic scheme was described in 37.4% of cases (n = 182), and the regimens used were heterogeneous (Table 7). An association with cholangitis secondary to cholangiohydatidosis was described in 65 cases (13.4%).

Table 7.

Antibiotics used reported in 182 patients.

Antibiotics  Nº patients 
Antibioticsa  143  78.6 
Amoxycillin + clavulanic acid  3.9 
Ampicillin + Gentamicin  2.7 
Amikacin  2.2 
Ceftriaxone + metronidazole  2.2 
Chloramphenicol  1.6 
Rifampicin + isoniazid + ethambutol  1.6 
Erythromycin + Cephalexin + metronidazole  1.1 
Otherb  11  6.1 
Total  182  100 
a

Antibiotics: Primary articles reported only “use of antibiotics”, without specifying.

b

Other: Includes single drug cefotaxime, ceftazidime, ciprofloxacin, gentamicin (one case of each). And schemes: Cefazolin + gentamicin, cefazolin + metronidazole, cefuroxime + metronidazole, mefoxin + tetracycline, penicillin + streptomycin + tetracycline, piperacillin + tazobactam + imipenem, Imipenem + tobramycin + metronidazole (one case of each).

3.4Risk of bias within studies

All the articles selected were at high risk of bias. All had less than 15 points in the MQ scale used (average of 7.6 points, median of 6.0 points; minimum 6 points and maximum 14 points).

3.5Potential biases in the review process

We requested additional information from several authors to expand and/or verify some study data, unfortunately, with no response. Thus, missing data may introduce bias to this review.

3.6Risk of bias across studies

There may be a publication bias, given the scarcity of studies from certain geographic areas and countries, which could represent variants not verified in this review.

4Discussion4.1Summary of evidence

This SR is based on the evidence available regarding IHE. The information was retrieved from systematic searches of 10 sources of information over the last 60 years and represents a compilation of 47 primary articles (all are case series and case reports) including 486 patients diagnosed and treated worldwide. There are no other SR related to this topic.

Regarding the results obtained, it was of note that over 27% of the articles were published in the last decade. These percentages may be associated with the increase in diagnostic suspicion and better access to diagnostic technology. The origin of the studies may be associated with publication bias because cystic echinococcosis is endemic in many areas throughout the world, some of which are not represented in this review.

Concerning the clinical features of IHE, a large diameter of the infected cysts and a higher frequency in the right lobe of the liver are verified. It was verified that infected cysts have a large diameter and are more frequent in the right lobe of the liver. Surgical treatment was universal, with significant POM and mortality rates, being surgical site infection and organ dysfunction and sepsis the most common causes, respectively. Consequently, a long hospital stay was reported. These data justify not only timely treatment of liver hydatid cysts but also strict monitoring of patients awaiting surgery and those who refuse treatment.

Microbiological sampling policies and the antibiotic schemes administered were very heterogeneous and did not allow conclusions to be drawn. The microorganisms most frequently isolated were Enterobacteriaceae (E. coli, Pseudomonas, Enterobacter and Klebsiella). Additionally, in some cases a cholangitis secondary to cholangiohydatidosis was diagnosed (13.4%). Since infection of the surgical site is the most common cause of POM and sepsis/organ failure, the most common cause of death in the postoperative period, it seems that common sense would dictate the administration of a prophylactic antibiotic regimen against Gram-negative bacteria in patients who are to be operated for liver hydatidosis, and even continue this regimen as treatment for a short period of time following surgery [59].

Unfortunately, the MQ of the primary studies was low and had a high risk of bias. In this context, it should be noted that the scale used to assess MQ (MInCir-therapy) has been validated in inter- and intra-observer reliability [60,61] and content and criterion validity studies [10,61,62]; and has been used to measure MQ in different scenarios. Therefore, the results reported should be considered with caution.

4.2Answer to the specific objetives

  • 1

    The different treatments used, the postoperative morbidity and associated mortality reported in the primary articles, was informed in detail in the Table 5.

  • 2

    There was no comparison in the primary articles between emergency and elective treatments.

  • 3

    Other applied therapeutic resources, reported in the primary articles (percutaneous, endoscopic, and laparoscopic drainage, etc.), was infomed in Table 5.

4.3Limitations

The evidence available regarding IHE is limited, because it was obtained from level 4 studies (report and retrospective case series of reduced casuistry).

5Conclusions

The evidence of IHE available at present is scarce and is dispersed among articles of reduced casuistry, poor methodological quality and low level of evidence; making it difficult to sustain facts supported by an adequate grade of recommendation. Furthermore, new studies with appropriate internal validity and adequate number of patients are required to clarify the uncertainty.

Funding

Funded by projects DI19-0030, Universidad de La Frontera (Chile) and CONICYT-MEC 80190026 (Chile).

Conflict of interest

The authors have no conflicts of interest to declare

References
[1]
C.M. Budke, H. Carabin, P.C. Ndimubanzi, H. Nguyen, E. Rainwater, M. Dickey, et al.
A systematic review of the literature on cystic echinococcosis frequency worldwide and its associated clinical manifestations.
Am J Trop Med Hyg, 88 (2013), pp. 1011-1027
[2]
N.I. Agudelo Higuita, E. Brunetti, C. McCloskey.
Cystic echinococcosis.
J Clin Microbiol, 54 (2016), pp. 518-523
[3]
C. Manterola, A. Sanhueza, M. Vial, J. Moraga.
Liver abscess of hydatid origin as a risk factor for postoperative complications in hydatidosis.
Rev Chil Cir, 61 (2009), pp. 333-338
[4]
S. Castillo, C. Manterola.
Morphological characteristics of liver abscesses according its etiology.
Int J Morphol, 38 (2020), pp. 406-414
[5]
H. Herbsman, A.M. Tanaka, J.H. Stuckey.
The first case report of an echinococcus liver cyst infected with Salmonella saint paul.
[6]
C. Manterola, S. Urrutia.
Post surgery morbidity in patients with complicated hepatic hydatidosis.
Rev Chilena Infectol, 32 (2015), pp. 43-49
[7]
C. Manterola, T. Otzen, G. Muñoz, M. Alanis, E. Kruuse, G. Figueroa.
Surgery for hepatic hidatidosis. Risk factors and variables associated with postoperative morbidity. Overview of the existing evidence.
[8]
A. Parlakgumus, A. Ezer, K. Calhshan, T. Colakoglu, S. Belli, J. Karakaya, S. Yildirim.
Effects of a preoperative and perioperative multidisciplinary approach for complicated liver hydatid cyst on postoperative outcomes.
Hepatogastroenterology, 57 (2010), pp. 1493-1498
[9]
D. Moher, A. Liberati, J. Tetzlaff, D.G. Altman, PRISMA Group.
Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement.
BMJ, 339 (2009), pp. b2535
[10]
C. Manterola, R. Cartes-Velasquez, T. Otzen.
Instructions for the use of MInCir scale to assess methodological quality in therapy studies.
Int J Morphol, 33 (2015), pp. 1463-1467
[11]
C. Manterola, M. Vial, P. Pineda, A. Sanhueza.
Systematic review of literature with different type of designs.
Int J Morphol, 27 (2009), pp. 1179-1186
[12]
J. Prousalidis, C. Kosmidis, G. Anthimidis, E. Fachantidis, N. Harlaftis, H. Aletras.
Forty-four years’ experience (1963–2006) in the management of primarily infected hydatid cyst of the liver.
HPB (Oxford), 10 (2008), pp. 18-24
[13]
N. Symeonidis, T. Pavlidis, M. Baltatzis, K. Ballas, K. Psarras, G. Marakis, et al.
Complicated liver echinococcosis: 30 years of experience from an endemic area.
Scand J Surg, 102 (2013), pp. 171-177
[14]
R. Agarwal, A. Ayyagari, V.B. Yadav, K.N. Prasad, V.A. Saraswat.
Infection of hepatic hydatid cyst with Yersinia enterocolitica.
Trans R Soc Trop Med Hyg, 94 (2000), pp. 404
[15]
K. Alestig, C. Holm, G. Nyström, T. Scherstén.
Biliobronchial fistula secondary to echinococcal abscess of the liver.
Acta Chir Scand, 138 (1972), pp. 90-94
[16]
G.A. Androulakis.
Surgical management of complicated hydatid cysts of the liver.
Eur Surg Res, 18 (1986), pp. 145-150
[17]
T. Berri.
Infected hydatid cyst of the liver presenting as retroperitoneal abscess.
Hellenic J Surg, 87 (2015), pp. 188-191
[18]
J.I. Blenkharn, I.S. Benjamin, L.H. Blumgart.
Bacterial infection of hepatic hydatid cysts with Haemophilus influenzae.
J Infect, 15 (1987), pp. 169-171
[19]
A. Caniggia.
Recurrent cholangitis caused by an abscessed echinococcal cyst of the liver: compression of the inferior vena cava.
Minerva Med, 69 (1978), pp. 4355-4358
[20]
G. Cicero, A. Blandino, G. Ascenti, T. D’Angelo, L. Frosina, C. Visalli, et al.
Superinfection of a dead hepatic echinococcal cyst with a cutaneous fistulization.
Case Rep Radiol, 2017 (2017),
[21]
L. Castagnari, S. Delia.
A case of hydatid cyst of the liver infected with Salmonella typhi.
G Mal Infett Parassit, 23 (1971), pp. 229-232
[22]
J.V. Catto.
Multiple liver abscesses in hydatid disease.
Br J Radiol, 34 (1964), pp. 859-860
[23]
Y.C. Chen, T.S. Yeh, J.H. Tseng, S.F. Huang, D.Y. Lin.
Hepatic hydatid cysts with superinfection in a non-endemic area in Taiwan.
Am J Trop Med Hyg, 67 (2002), pp. 524-527
[24]
B. Durdu, I.N. Hakyemez, S. Bolukçu, G. Okay, T. Aslan.
A rare cause of liver abscess secondary to hydatid cyst: Pseudomonas stutzeri.
Cukurova Med J, 41 (2016), pp. 17-19
[25]
M.E. Ellis, W. Sinner, M. Asraf Ali, S.M. Qadri.
Echinococcal disease and mycobacterial infection.
Ann Trop Med Parasitol, 85 (1991), pp. 243-251
[26]
S. Ergüney, O. Tortum, A.H. Taspinar, M. Ertem, E. Gazioğlu.
Complicated hydatid cysts of the liver.
Ann Chir, 45 (1991), pp. 584-589
[27]
M. Ferrán, M. Buti, A. González, R. Boqué, R. Esteban, J. Guardia.
Pyogenic liver abscess by haemophilus influenzae complicating hydatid cysts.
Infection, 14 (1986), pp. 197
[28]
M.B. García, J.P. Lledías, I.G. Pérez, V.V. Tirado, L.F. Pardo, L.M. Bellvís, et al.
Primary super-infection of hydatid cyst—clinical setting and microbiology in 37 cases.
Am J Trop Med Hyg, 82 (2010), pp. 376-378
[29]
E. García Vicente, C. Hernández de Diego, M. Gobernado Serrano.
Quiste hidatídico hepático complicado.
REMI, C18 (2007),
[30]
U. Gottschalk, T. Zinner, M. Stoehr.
Liver abscess due to hydatid cyst.
Endo heute, 25 (2012), pp. 247-249
[31]
I.N. Hakyemez, M. Sit, G. Aktas, T. Tas, F.Z. Mengeloglu, A. Kucukbayrak.
A case of giant hepatic hydatid cyst infected with Morganella morganii and the literature review.
Case Rep Gastrointest Med, 2012 (2012),
[32]
H. Herbsman, A.M. Tanaka, J.H. Stuckey.
The first case report of an echinococcus liver cyst infected with Salmonella saint Paul.
[33]
H. Jerraya, W. Bouchaala, D. Chadli.
Hepatology: Images of hydatid cyst of the liver mimicking an hepatic abscess.
J Gastroenterol Hepatol, 29 (2014), pp. 1662
[34]
D. Karavias, C. Panagopoulos, C. Vagianos, C. Vagenas, S. Rathosis, J. Androulakis.
Infected echinococcal cyst. A common cause of pyogenic hepatic abscess.
Ups J Med Sci, 93 (1988), pp. 289-296
[35]
B. Lainez, V. Ruiz, J. Berjón, R. Lezaun.
Purulent pericarditis complicated by cardiac tamponade secondary to a hydatid cyst-associated hepatic abscess.
Rev Esp Cardiol, 62 (2009), pp. 948-949
[36]
J.J. Leichtling.
Unusual problems in surgery: case no. 7. Hydatid cyst of liver with abscess, rupture, empyema and broncho-hepatico-cystic fistula.
J Mt Sinai Hosp N Y, 34 (1967), pp. 496-507
[37]
A.J. Lopez-Marcano, J.M. Ramia, V. Arteaga, R. De la Plaza, J.D. Gonzales, A. Medina.
Percutaneous drainage as a first therapeutic step prior to surgery in liver hydatid cyst abscess: is it worth it?.
World J Hepatol, 9 (2017), pp. 114-118
[38]
A.A. Malik, S.U. Bari, R. Amin, M. Jan.
Surgical management of complicated hydatid cysts of the liver.
World J Gastrointest Surg, 2 (2010), pp. 78-84
[39]
C. Manterola, S. Urrutia, MINCIR GROUP.
Infected hepatic echinococcosis: results of surgical treatment of a consecutive series of patients.
Surg Infect (Larchmt), 16 (2015), pp. 553-557
[40]
C. Manterola, M. Barroso, M. Vial, L. Bustos, S. Muñoz, H. Losada, et al.
Liver abscess of hydatid origin: clinical features and results of aggressive treatment.
ANZ J Surg, 73 (2003), pp. 220-224
[41]
R.G. Masterton, C. Bridger, M. Ashton, R. Bury.
Subdiaphragmatic gas in hepatic hydatid disease.
Eur J Clin Microbiol Infect Dis, 8 (1989), pp. 576-577
[42]
R.G. Masterton, M.J. O’Doherty, S.J. Eykyn.
Streptococcus milleri infection of a hepatopulmonary hydatid cyst.
Eur J Clin Microbiol, 6 (1987), pp. 414-415
[43]
R.M. Matossian, F. Najjar.
Suppurative salmonellosis in human hepatic hydatid cysts.
Ann Trop Med Parasitol, 62 (1968), pp. 143-146
[44]
M.A. Medrano, V. Cuervas-Mons, T. Cantón, A. Albillos, J. Montes, R. Barbadillo.
Hepatic abscess caused by hydatid cyst. Analysis of 35 cases.
Rev Clin Esp, 177 (1985), pp. 318-320
[45]
S.O. Ordabekov.
Suppurative echinococcal cysts in the abdominal cavity.
Vestn Khir Im I I Grek, 135 (1985), pp. 58-62
[46]
M.M. Rahman, S.B. Safar.
Intrabiliary rupture of hepatic hydatid cyst.
Int Surg, 67 (1982), pp. 459-460
[47]
D. Sadhu, B.V. Moses, R. John, M.K. Lalitha.
Hydatid disease of the liver complicated by salmonellosis.
Trans R Soc Trop Med Hyg, 87 (1993), pp. 674-675
[48]
J.C. Salinas, J. Torcal, R. Lozano, R. Sousa, A. Morandeira, R. Cabezali.
Intracystic infection of liver hidatidosis.
Hepatogastroenterology, 47 (2000), pp. 1052-1055
[49]
G. Sgourakis, K. Gemos, G. Dedemadi, N. Spetzouris, H. Gyftakis, P. Salapa.
Laparoscopic drainage of infected hydatid liver cysts.
Minerva Chir, 56 (2001), pp. 169-173
[50]
B.C. Sharma, N. Agarwal, S. Garg, R. Kumar, S.K. Sarin.
Endoscopic management of liver abscesses and cysts that communicate with intrahepatic bile ducts.
Endoscopy, 38 (2006), pp. 249-253
[51]
V. Sitaram, M.K. Lalitha, G. Mathew.
S. typhi infection of hydatid cyst.
Indian J Pathol Microbiol, 33 (1990), pp. 74-75
[52]
C. Soussi, A. Alaoui, B. Naceur.
Liver hydatid cyst secondarily infected with Eberth bacillus.
Maroc Med, 535 (1970), pp. 318-319
[53]
G. Stoyanov, K.H. Derezhian.
Diagnosis and treatment of suppurative echinococcal cysts of the liver.
Khirurgiia (Sofiia), 34 (1981), pp. 530-535
[54]
E. Târcoveanu, A. Vasilescu, R. Moldovanu, N. Vlad, V. Rusu, C. Stanciu.
Unusual forms of liver abscesses.
Rev Med Chir Soc Med Nat Iasi, 112 (2008), pp. 688-697
[55]
J. Vahedian-Ardakani.
Hydatid cyst of the liver presenting as cutaneous abscesses.
Ann Saudi Med, 17 (1997), pp. 235-236
[56]
A.L. Viteri, P.H. Howard, J.L. May, G.S. Ramesh, J.W. Roberts.
Hepatic abscess due to Yersinia enterocolitica without bacteremia.
Gastroenterology, 81 (1981), pp. 592-593
[57]
G.D. Wagholikar, S.S. Sikora, A. Kumar, R. Saxena, V.K. Kapoor.
Surgical management of complicated hydatid cysts of the liver.
Trop Gastroenterol, 23 (2002), pp. 35-37
[58]
K.M. Wasunna, J.B. Were, T. Romig, P.H. Rees, J.A. Sherwood.
Bacterial infection of hydatid cyst following albendazole treatment.
Ann Trop Med Parasitol, 85 (1991), pp. 369-370
[59]
M. Sakoda, S. Iino, Y. Mataki, Y. Kawasaki, H. Kurahara, K. Maemura, et al.
Influence of a shorter duration of post-operative antibiotic prophylaxis on infectious complications in patients undergoing elective liver resection.
Surg Infect (Larchmt), 18 (2017), pp. 149-156
[60]
R.A. Cartes-Velásquez, C. Manterola, P. Aravena, J. Moraga.
Reliability and validity of MINCIR scale for methodological quality in dental therapy research.
Braz Oral Res (São Paulo), 28 (2014), pp. 1-5
[61]
J. Moraga, M.E. Burgos, C. Manterola, A. Sanhueza, R. Cartes-Velásquez, S. Urrutia.
Validation of a scale for assessing methodological quality of therapy studies. Pilot study.
Rev Chil Cir, 65 (2013), pp. 222-227
[62]
C. Manterola, V. Pineda, M. Vial, H. Losada.
What is the methodologic quality of human therapy studies in ISI surgical publications?.
Copyright © 2020. Fundación Clínica Médica Sur, A.C.
Descargar PDF
Opciones de artículo
es en pt

¿Es usted profesional sanitario apto para prescribir o dispensar medicamentos?

Are you a health professional able to prescribe or dispense drugs?

Você é um profissional de saúde habilitado a prescrever ou dispensar medicamentos