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Inicio Annals of Hepatology A Latin American survey on demographic aspects of hospitalized, decompensated ci...
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Vol. 19. Issue 4.
Pages 396-403 (July - August 2020)
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2778
Vol. 19. Issue 4.
Pages 396-403 (July - August 2020)
Original article
Open Access
A Latin American survey on demographic aspects of hospitalized, decompensated cirrhotic patients and the resources for their management
Visits
2778
Julio D. Vorobioffa,
Corresponding author
vorodiez@fibertel.com.ar
jdvorobioff@hotmail.com

Corresponding author at: Gastroenterology Department & Liver Unit, University of Rosario Medical School, Morrison 8750, 2000 Rosario, Argentina.
, Fernando Contrerasb, Federico Tannoa, Lucía Hernándezc, Fernando Bessonea, Luis Colombatod, José Adie, Eduardo Fassiof, Mirta Felgueresg, Guillermo Fernándezh, Luis Gaitei, Diana Gibellij, Hernán Gómez Darrichonk, Matías Lafagel, Daniel Lombardom, Susana Lópezn, Alejandro Mateoo, Manuel Mendizábalp, Julieta Pecoraroq, Andrés Rufr..., Pablo Ruizs, Javier Severinit, Teodoro Stiebenu, Marcela Sixtov, Fabián Záratew, Sergio de la Barra Barrazax, Irene Donoso Sierray, Violeta Rivas Pachecoz, Juan P. Robleroaa, Juan O. Rojasbb, Patricio Ruiz Gonzálezcc, Diego San Martín Rodríguezdd, Armando Sierraltaee, Alvaro Urzúa Manchegoff, Eliana Valdesgg, Pamela Yaquichhh, Rodrigo Wolffii, Flor Beltran Valdiviajj, Roxana C. Gallegoskk, Rocío Gallosoll, Julio S. Marcelomm, Pedro Montesnn, Laura Tenoriooo, Isabel Veramendipp, Elizabeth Alavaqq, Ximena Armijosrr, Gonzalo Benalcazarss, Enrique Carreratt, Galo F. Pazmiñouu, Eduardo Marriott Díazvv, Miguel Garassiniww, Rosalía P. Marreroxx, Mirta Infanteyy, Dayron Páez Suárezzz, José C. Gutiérrezaaa, Carmen M. Villadoniga Reyesbbb, Yoel M. Serranoccc, Rivardo Hernández Hernándezddd, Orelvis Martínez Martínezeee, Teresita Pérez Gonzálezfff, María T. Andaraggg, Marco Sánchez Hernándezhhh, Solange Geronaiii, Iván Garcíajjj, Fátima de la Tijerakkk, Edmundo Pessoa Lópezlll, Kenia Torresmmm, Martín GarzónnnnVer más
a Gastroenterology Department & Liver Unit, Hospital Provincial del Centenario, Rosario, Argentina
b Gastroenterology Department, Hospital Luis E. Aybar, Santo Domingo, Dominican Republic
c Facultad de Ciencias Económicas y Estadística, Universidad de Rosario, Argentina
d Gastroenterology Department, & Liver Unit, Hospital Británico, CABA, Argentina
e Gastroenterology Department, Hospital Lagomaggiore, Mendoza, Argentina
f Gastroenterology Department & Liver Unit, Hospital Alejandro Posadas, El Palomar, Argentina
g Hospital El Carmen, Godoy Cruz, Argentina
h Hospital Teodoro Shestakow, San Rafael, Argentina
i Gastroenterology Department, Hospital Cullen, Santa Fe, Argentina
j Gastroenterology Department, Hospital San Roque, Córdoba, Argentina
k Internal Medicine Department, Hospital San José, Diamante, Argentina
l Gastroenterology Department, Instituto Lanari, CABA, Argentina
m Gastroenterology Department, Hospital Angel Padilla, Tucumán, Argentina
n Gastroenterology Department, Hospital Juan Garraham, CABA, Argentina
o Gastroenterology Department, Hospital Eva Perón, Granadero Baigorria, Argentina
p Liver Unit, Hospital Universitario Austral, Pilar, Argentina
q Liver Unit, Sanatorio Parque, Rosario, Argentina
r Liver Unit, Hospital Privado, Rosario, Argentina
s Internal Medicine Department, Hospital Regional, Río Gallegos, Argentina
t Internal Medicine Department, Hospital Alberdi, Rosario, Argentina
u Gastroenterology Department, Hospital San Martín, Paraná, Argentina
v Gastroenterology Department, Hospital Jaime Ferré, Rafaela, Argentina
w Gastroenterology Department, Hospital Córdoba, Córdoba, Argentina
x Gastroenterology Department, Complejo Hospitalario San José, Santiago, Chile
y Hospital San Pablo, Coquimbo, Chile
z Hospital Clínico UC Christus, Santiago, Chile
aa Gastroenterology Department, Hospital San Borja Arriaran, Santiago, Chile
bb Gastroenterology Department, Hospital Dr. Sotero del Río, Santiago, Chile
cc Gastroenterology Department, Hospital Barros Luco, Santiago, Chile
dd Gastroenterology Department, Hospital Las Higueras, Talcahuano, Chile
ee Gastroenterology Department, Hospital Aravena, Temuco, Chile
ff Gastroenterology & Liver Unit, Hospital Clínico Universidad de Chile, Santiago, Chile
gg Gastroenterology Department, Hospital Regional de Talca, Talca, Chile
hh Gastroenterology Department, Hospital San Juan de Dios, Santiago, Chile
ii Gastroenterology Department & Liver Unit, Hospital Clínico, Universidad Católica de Chile, Santiago, Chile
jj Gastroenterology Department, Hospital Central de Policía, Lima, Peru
kk Gastroenterology Department, Hospital María Auxiliadora, Lima, Peru
ll Gastroenterology Department, Hospital San José, Callao, Peru
mm Gastroenterology Department, Hospital Villa El Salvador, Lima, Peru
nn Gastroenterology Department, Hospital Nacional Daniel A. Carrión, Callao, Peru
oo Gastroenterology Department & Liver Unit, Hospital Edgardo Rebagliati, Lima, Peru
pp Gastroenterology Department, Hospital Hipólito Unanue, Lima, Peru
qq Department of Internal Medicine, Hospital Verdi Ceballos, Portoviejo, Ecuador
rr Gastroenterology Department & Liver Unit, Hospital Andrade Marín, Quito, Ecuador
ss Gastroenterology Department & Liver Unit, Hospital Luis Vernaza, Guayaquil, Ecuador
tt Gastroenterology Department, Hospital Eugenio Espejo, Quito, Ecuador
uu Gastroenterology Department, Hospital de Especialidades FFAA, Quito, Ecuador
vv Gastroenterology Department, Hospital Teodoro M. Carbo, Guayaquil, Ecuador
ww Gastroenterology Department, Centro Médico La Trinidad, Caracas, Venezuela
xx Gastroenterology Department, Hospital Pérez Carreño, Caracas, Venezuela
yy Sociedad Cubana de Gastroenterología, La Habana, Cuba
zz Gastroenterology Department, Hospital Hermanos Ameijeiras, La Habana, Cuba
aaa Hospital Abel Santamaría, Pinar del Río, Cuba
bbb Hospital Celia Sánchez Manduley, Manzanillo, Cuba
ccc Hospital Carlos M. De Céspedes, Bayamo, Cuba
dddHospital Faustino Pérez, Matanzas, Cuba
eee Hospital Manuel Fajardo, La Habana, Cuba
fff Hospital Ivan Portuondo, Artemisa, Cuba
ggg Instituto Hondureño de la Seguridad Social, Tegucigalpa, Honduras
hhhGastroenterology Department, Hospital Universitario, Tegucigalpa, Honduras
iii Liver Unit, Hospital de Fuerzas Armadas, Montevideo, Uruguay
jjj Gastroenterology Department, Hospital Rooselvet, Guatemala, Guatemala
kkk Gastroenterology Department & Liver Unit, Hospital General de Mexico Dr. E. Liceaga, Ciudad de Mexico, Mexico
lll Gastroenterology Department & Liver Unit, Hospital das Clinicas, Recife, Brazil
mmm Santo Domingo, Dominican Republic
nnn Gastroenterology Department, Hospital de la Samaritana, Bogotá, Colombia
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Tables (8)
Table 1. Centers and patient distribution according to participating countries.
Table 2. Demographic characteristics of included patients.
Table 3. Main admission causes.
Table 4. Clinical characteristics of included patients.
Table 5. Etiology distribution in participating countries.
Table 6. Management of variceal bleeding.
Table 7. Management of ascites, SBP, HRS and infections.
Table 8. Major differences according to hospital complexity.
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Abstract
Introduction & objectives

Liver cirrhosis is a major cause of mortality worldwide. Adequate diagnosis and treatment of decompensating events requires of both medical skills and updated technical resources. The objectives of this study were to search the demographic profile of hospitalized cirrhotic patients in a group of Latin American hospitals and the availability of expertise/facilities for the diagnosis and therapy of decompensation episodes.

Methods

A cross sectional, multicenter survey of hospitalized cirrhotic patients.

Results

377 patients, (62% males; 58±11 years) (BMI>25, 57%; diabetes 32%) were hospitalized at 65 centers (63 urbans; 57 academically affiliated) in 13 countries on the survey date. Main admission causes were ascites, gastrointestinal bleeding, hepatic encephalopathy and spontaneous bacterial peritonitis/other infections. Most prevalent etiologies were alcohol-related (AR) (40%); non-alcoholic-steatohepatitis (NASH) (23%), hepatitis C virus infection (HCV) (7%) and autoimmune hepatitis (AIH) (6%). The most frequent concurrent etiologies were AR+NASH. Expertise and resources in every analyzed issue were highly available among participating centers, mostly accomplishing valid guidelines. However, availability of these facilities was significantly higher at institutions located in areas with population>500,000 (n=45) and in those having a higher complexity level (Gastrointestinal, Liver and Internal Medicine Departments at the same hospital (n=22).

Conclusions

The epidemiological etiologic profile in hospitalized, decompensated cirrhotic patients in Latin America is similar to main contemporary emergent agents worldwide. Medical and technical resources are highly available, mostly at great population urban areas and high complexity medical centers. Main diagnostic and therapeutic approaches accomplish current guidelines recommendations.

Keywords:
Survey
Cirrhosis
Decompensation
Ascites
Full Text
1Introduction

Cirrhosis is the end-stage of different etiology-related chronic liver diseases, being alcohol-related (AR), hepatitis C virus infection (HCV) and non-alcoholic steatohepatitis (NASH) the most commonly involved [1,2].

Along its natural history the disease undergoes different progressive stages, either considered as compensated or decompensated [3,4]. The compensated state, usually the longest, is almost devoid of symptoms and therefore, liver disease related hospital admissions are uncommon. On the other hand, almost every event characterizing the decompensated stage requires admission, in order to be properly diagnosed and treated.

Main decompensating events are: esophageal variceal bleeding (EVB), ascites, hepatic encephalopathy (HE) and jaundice. Closely related, either as the cause or as a consequence, infections and hepatorenal syndrome (HRS) are frequently present in decompensated patients [4–7]. Alone or combined, all these complications represent a threatening condition in cirrhotic patients, decreasing their life expectancy [4,8,9]. Moreover, the growing incidence of primary liver cancer, mostly hepatocellular carcinoma (HCC), is another determinant of frequent nosocomial admissions [10].

For each of these complications, diagnostic and therapeutic algorithms have been proposed and translated into different valid guidelines [11–16]. The challenging consequence of these recommendations is a permanent requirement of both adequate medical and technical resources at the institutions where these patients are treated. In fact, decompensated cirrhotic patients are mainly admitted to Gastroenterology or Int Med Depts, as Liver Units are usually restricted to specific referral centers, mostly located at great urban areas. Given the diversity of institutions involved, a potential lack of homogeneity may translate into uneven quality in medical care provided for those decompensating events [17–19].

Therefore, the present study was designed in order to search: (a) the demographic and clinical–epidemiological characteristics of cirrhotic patients hospitalized on certain date at different medical centers of Central and South America and (b) the availability of resources and expertise for diagnosis and treatment of the most frequent complications of liver cirrhosis.

2Methods

A cross-sectional, multicenter, observational study, performed on March 21st, 2018. Every national society affiliated to the Latin American Association for the Study of the Liver (ALEH) and all regional associations subsidiaries of the Argentine Federation of Gastroenterology (FAGE) were invited to partipate. Those accepting provided a list of medical institutions where cirrhotic patients are frequently admitted. Invitations including detailed objectives and design of the study were mailed. Those centers accepting completed the questionaire with data corresponding to the aforementioned date.

The whole survey contained 52 questions, divided in 3 sections: (1) data related to the participating medical center and its location (10 questions), (2) a clinical/demographic profile of every cirrhotic patient remaining hospitalized on March 21st/2018 (13 questions) and (3) an inquiry regarding usual therapeutic attitudes and corresponding available resources for the management of (a) EVB; (b) ascites, spontaneous bacterial peritonitis (SBP), HRS and non-SBP infections; (c) HE; (d) liver transplantation (LT) and (e) HCC (29 questions).

The investigation was approved by the Human Investigation Committees of participating institutions.

All data were centralized at one center (Gastroenterology and Liver Dept, University of Rosario Medical School, Rosario, Argentina) and assembled and processed by JV, LH and FT.

2.1Statistical analysis

Continuous variables are shown as Mean±SD or Median and Range. Categorical variables are shown as relative and absolute frequencies. Associations between categorical variables were analyzed by the Chi-Square test or Fisher's Exact test. Results were considered significant at p values of<0.05 [20,21].

3Results3.1Participating centers

One hundred and seventy five centers from 16 countries were invited to participate. Sixty five (37%) of them, corresponding to 13 countries, completed the survey (Table 1). Sixty three (97%) were located at urban areas, 45 (71%) with populations>500,000 (Table 2). Fifty seven (88%) centers, either public (47) or private (10), were University affiliated. Within 63 institutions, Int Med & Gastroenterology Depts were present at 33 (52%); Int Med, Gastroenterology & Liver Depts at 22 (35%) and only an Int Med Dept at 8 (13%). LT units were available at 16 centers (Supplementary Table 1).

Table 1.

Centers and patient distribution according to participating countries.

Country  Centers n (%)  Patients n (%) 
Argentina  23 (35)  71 (19) 
Chile  12 (19)  104 (28) 
Cuba  7 (11)  38 (10) 
Peru  7 (11)  45 (12) 
Ecuador  6 (9)  40 (10) 
Venezuela  2 (3)  3 (1) 
Honduras  2 (3)  11 (3) 
Brasil  1 (1.5)  1 (0.4) 
Colombia  1 (1.5)  5 (1) 
Guatemala  1 (1.5)  34 (9) 
México  1 (1.5)  18 (5) 
R. Dominicana  1 (1.5)  1 (0.4) 
Uruguay  1 (1.5)  6 (1) 
Total  65  377 
Table 2.

Demographic characteristics of included patients.

  n (%) 
Sex (n=373)
Males  231 (62%) 
Females  142 (38%) 
Age (years)
<20  13 (3%) 
21–40  36 (10%) 
41–60  167 (44%) 
61–80  149 (40%) 
>80  12 (3%) 
Body weight (kg) (M±SD) (range)  70±18 (5.6–164) 
BMI
<18.5  19 (5%) 
18.5–24.9  144 (38%) 
25–29.9  127 (34%) 
>30  87 (23%) 
Diabetes  122 (32%) 

BMI: body mass index.

Patients: Three hundred and seventy seven cirrhotic patients were hospitalized on the date of the survey. Gender data was available in 373, of whom 231 (62%) were males. Those between 41 and 80 years accounted for 84% (316) of the population (41–60 and 61–80, 44% (167) and 40% (149); respectively) (NS). Mean body weight of 377 patients was 70±18kg (5.6–164) and the body mass index (BMI) was>25 in 214 (57%). Diabetes was present in 122 (32%) patients (Table 2). Sex distribution among different age ranges was not significantly different (Supplementary Table 2).

Main identifiable admission causes were: ascites (n=134; 36%), gastrointestinal beeding (GIB) (n=104; 27%), HE (n=94; 24%), SBP/other infections (n=84; 22%) and HRS (n=38; 10%) (Table 3). Within 367 patients, 151 CP class B and 149 CP class C comprised 82% of them. MELD was available in 328 patients, of whom 182 (55%) scored within 10 to 19 and 100 (30%) from 20 to 38 (Table 4).

Table 3.

Main admission causes.

  n (%) 
Ascites  134 (86%) 
GI bleeding  104 (28%) 
Hematemesis  47 (45%) 
Hematochezia  9 (9%) 
Melena  48 (46%) 
HE  94 (25%) 
SBP  20 (5%) 
Other infections  64 (17%) 
HRS  38 (10%) 
Pre-LT evaluation  30 (8%) 
HCC  17 (5%) 
Staging  15 (88%) 
Complications  2 (12%) 

GI: gastrointestinal; HE: hepatic encephalopathy; SBP: spontaneous bacterial peritonitis; HRS: hepatorenal syndrome; LT: liver transplantation; HCC; hepatocellular carcinoma.

Table 4.

Clinical characteristics of included patients.

  n (%) 
Etiology (n=376)
AR  149 (40%) 
NASH  86 (23%) 
HCV  25 (7%) 
AI  21 (6%) 
PBC  13 (3%) 
AR+NASH  12 (3%) 
HBV  6 (2%) 
AR+HCV  5 (1%) 
Hemocromatosis  4 (1%) 
PSC  4 (1%) 
Wilson's disease  3 (1%) 
Co-infections  4 (1%) 
Other  16 (4%) 
Not registered  28 (7%) 
Child–Pugh class (n=367)
67 (18%) 
151 (41%) 
149 (41%) 
MELD (n=328)
<10  44 (13%) 
10–19  182 (55%) 
20–29  75 (23%) 
30–39  25 (8%) 
>39  2 (1%) 
Vaccinations
Hepatitis B  83 (22%) 
Hepatitis A  27 (7%) 
Pneumococcus  51 (14%) 
Influenza  97 (26%) 

AR: alcohol related; NASH: non-alcoholic steatohepatitis; HCV: hepatitis C virus; AI: autoimmune hepatitis; PBC; primary biliary cholangitis; HBV: hepatitis B virus; PSC; primary sclerosing cholangitis; CP class: Child–Pugh class; MELD: Model for End-Stage Liver Disease.

AR (40%); NASH (23%), HCV infection (7%) and autoimmune hepatitis (AIH) (6%) were the most prevalent etiologies being AR+NASH the most common concurrent etiology (Table 4). Liver disease etiology, according to gender distribution, showed significant differences, being NASH, HCV, AIH and PBC more prevalent in females and AR among men (Supplementary Table 3). No significant difference related to etiology was observed when comparing countries recruiting more than 30 patients versus all others. However, NASH resulted highly prevalent within patients enrolled in the Pacific coast (Chile, Perú and Ecuador) (Table 5).

Table 5.

Etiology distribution in participating countries.

Etiologya  Argentina (n=59)  Chile (n=96)  Cuba (n=38)  Ecuador (n=33)  Guatemala (n=33)  Peru (n=44)  Others (n=41) 
AR  31 (53%)  35 (37%)  23 (61%)  10 (30%)  21 (64%)  14 (32%)  15 (37%) 
NASH  5 (9%)  29 (30%)  4 (11%)  17 (52%)  6 (18%)  16 (36%)  9 (22%) 
HCV  6 (10%)  4 (4%)  7 (18%)  –  3 (9%)  3 (7%)  2 (5%) 
AIH  5 (8%)  10 (10%)  –  –  1 (3%)  1 (2%)  4 (10%) 
PBC  –  4 (4%)  2 (5%)  –  (6%)  2 (5%)  3 (7%) 
AR/NASH  –  5 (5%)  –  2 (6%)  –  2 (5%)  3 (7%) 
Others  12 (20%)  9 (9%)  2 (5%)  4 (12%)  –  6 (13%)  5 (12%) 

AR: alcohol-related; NASH: non-alcoholic steatohepatitis; HCV: hepatitis C virus; AIH: autoimmune hepatitis; PBC: primary biliary cholangitis; AR/NASH; alcohol-related/non-alcoholic steatohepatitis.

a

NS.

3.2Management of variceal bleeding

Bleeders are always admitted to the ICU at 10 (17%) centers while most others (50; 83%) consider ICU indication on an individual basis. Endoscopy is available on a 24h/7 days basis in 32/56 (57%) centers and studies are performed within 12h after admission in 41/56 (73%). Banding is the preferred therapeutic choice. Among 50 institutions, Octreotide and Terlipressin are the most utilized vasoactive drugs and are always administered before the endoscopic study in 36 (72%) of them (Table 6). ATB are administered since admission in 52 (80%) centers, being ceftriaxone the most utilized. Regarding the SBT 39 (60%) centers use it only when all other therapeutic measures fail. The tube is not available at 21 (32%) institutions while it is the only available therapeutic tool at 5 (8%). Eight centers (12%) can offer TIPS in the emergency setting while self-expandable metal stents are available at 11 (17%) institutions (Supplementary Table 4).

Table 6.

Management of variceal bleeding.

  n (%) 
Admission to ICU (n=60)a
Always  10 (17%) 
According to each case  50 (83%) 
Own resources for endoscopic studies (n=56)a
Available 24h/7 days  32 (57%) 
Only on a scheduled basis  24 (43%) 
Endoscopic study after admission (n=64)a
Within 6–826 (41%) 
Within 1215 (23%) 
Within 2419 (30%) 
After 244 (6%) 
Endoscopic therapeutic procedures (n=65)a
Banding  51 (78%) 
Sclerotherapy  5 (8%) 
Unavailable  9 (14%) 
Available vasoactive drugs
Octreotide  31 (62%) 
Terlipressin  19 (38%) 
Somatostatin 
Unavailable  15 
Early administration of vasoactive drugs (before the endoscopic study)
Always  36 (72%) 
Occasionally  14 (28%) 
a

(n=answering centers).

Management of ascites, SBP, HRS and infections: Diagnostic paracentesis is mandatory in 46 (71%) centers while in other 19 (29%) is performed only when SBP is suspected. The basic therapeutic approach includes spironolactone (100–150mg/day) plus furosemide (40mg/day) plus low Na diet or only spironolactone (100–150mg/day) plus low Na diet in 45 (69%) and 20 (31%) institutions, respectively. Intractable/refractory ascites is treated with paracentesis plus serum albumin in 63 (97%) institutions and is considered a criterion for LT evaluation in 44 (68%) centers. HRS is treated with terlipressin plus serum albumin in 32 (55%) centers while 8 (14%) others utilize octreotide plus serum albumin (p<0.01) (Table 7). Among 59 responders, SBP is routinely treated with cephalosporins while in nosocomial or health care-associated infections another ATB scheme is utilized. Bacterial rescue in ascitic fluid is low: <20% in 38 (59%) centers. Secondary prophylaxis of SBP is managed with quinolones in most centers. Urinary and respiratory are the most prevalent non-SBP infections (Table 7).

Table 7.

Management of ascites, SBP, HRS and infections.

  n (%) 
Diagnostic paracentesis (n=65)a
All patients with clinically detectable ascites  46 (71%) 
Only if SBP is suspected  19 (29%) 
Basic therapeutic scheme for ascites (n=65)a
Spironolactone (100–150mg/day)+Furosemide (40mg/day)+low Na diet  45 (69%) 
Spironolactone (100–150mg/day)+low Na diet  20 (31%) 
Therapy for refractory/intractable ascites (n=65)a
Therapeutic paracentesis+Serum albumin  63 (97%) 
Therapeutic paracentesis+Other expanders  2 (3%) 
Evaluation for LT  44 (68%) 
TIPS a an available option  16 (25%) 
Treatment of HRS (n=58)a
Terlipressin+Albumin  32 (55%) 
Octreotide+Albumin  8 (14%) 
No treatment available  18 (31%) 
Treatment of SBP (n=59)a
Cephalosporins  59 (100%) 
Nosocomial or Health Care-Associated Infections (n=59)a
Other ATB scheme  44 (75%) 
Bacterial rescue in ascitic fluid (n=65)a
Low (<20% of the cases)  38 (59%) 
Moderate (20–50% of the cases)  25 (38%) 
High (>50% of the cases)  2 (3%) 
Secondary prophylaxis of SBP (n=64)a
Quinolones  56 (87%) 
Rifaximin  7 (11%) 
Not performed  1 (2%) 
Most prevalent non-SBP infections (n=64)a
Urinary  36 (56%) 
Respiratory  26 (41%) 
Skin  2 (3%) 

ATB: antibiotics; SBP: spontaneous bacterial peritonitis; LT: liver transplantation; TIPS: transjugular intrahepatic porto-systemic shunt; HRS: hepatorenal syndrome.

a

(n=answering centers).

3.3Management of HE

HE was focused on 2 different scenarios: a) prevention during the acute bleeding episode, which is performed at 58 (89%) institutions, 33 (51%) of which utilize Lactulose and b) chronic HE, which is mostly treated with Lactulose plus Rifaximine, also at 33 (51%) centers (Supplementary Table 5).

3.4Liver transplantation

LT is available at 21 (32%) institutions, 8 of them performing more than 20 transplants per year. Within 20 of these centers, the most prevalent etiologies in transplanted patients are NASH in 9 (45%), AR in 6 (30%) and HCV in 5 (25%) (Supplementary Table 6).

3.5Screening and management of HCC

An US plus alpha-pheto protein or an US (every 6 months in both cases) are the standard screening methods in 43 (69%) and 18 (29%) centers; respectively. The most available therapeutic modalities are surgery and transarterial chemoembolization (23 institutions) (Suplementary Table 7).

Resources and therapeutic modalities according to center affiliation, complexity and location:

Several differences related to therapeutic attitudes and resources were observed among centers, related to hospital complexity (Int Med & Liver & Gastroenterology Depts., Int Med & Gastroenterology Depts. or only an Int Med Dept) and population at its location (< or >500,000). Among university affiliated/non-affiliated centers the only significant difference was related to the treatment of intractable/refractory ascites for which therapeutic paracentesis plus serum albumin is more frequently used in affiliated ones (p<0.01). Differences according to institution complexity and area population are depited in Table 8 and Supplementary Tables 8 and 9; respectively.

Table 8.

Major differences according to hospital complexity.

  Gastroenterology Liver & Int Med n (%)  Gastroenterology & Int Med n (%)  Int Med n (%)  p 
EVB
Endoscopic study
Within 6–8h post-admission  14 (64%)  11 (34%)  1 (13%)  0.01
Within 12h post-admission  5 (23%)  8 (25%)  1 (13%) 
Within 24h post-admission  3 (13%)  12 (38%)  3 (37%) 
>24h post-admission  0 (0%)  1 (3%)  3 (37%) 
Endoscopic therapy
Banding  21 (95%)  25 (76%)  4 (50%)  0.05
Sclerotherapy  0 (0%)  3 (9%)  1 (13%) 
Unavailable  1 (5%)  5 (15%)  3 (37%) 
ATB since admission
Always  20 (91%)  26 (79%)  4 (50%)  0.05
Occasionally  2 (9%)  7 (21%)  3 (37%) 
Never  0 (0%)  0 (0%)  1 (13%) 
Balloon tamponade
Only at the ICU  9 (41%)  8 (24%)  4 (50%)  0.02 
TIPS
Available for the emergency  7 (32%)  1 (3%)  0 (0%)  0.01 
Ascites, SBP, HRS and infections
Refractory ascites/OLT evaluation  19 (86%)  19(58%)  6 (75%)  0.053 
TIPS for refractory ascites  10 (45%)  4 (12%)  2 (25%)  0.02 
Non-SBP infections
Urinary tract  17 (77%)  17 (53%)  1 (13%)  0.01
Respiratory tract  5 (23%)  13 (41%)  7 (87%) 
Dermatologic  0 (0%)  2 (6%)  0 (0%) 
HCC
Systematic screening  22 (100%)  32 (100%)  6 (75%)  0.02 
Therapeutic modalities
Surgery  18 (82%)  15 (47%)  4 (50%)  0.05 
Chemoembolization  19 (86%)  7 (22%)  3 (38%)  0.001 
Liver transplantation  14 (64%)  2 (6%)  1 (13%)  0.001 
Thermal ablation  11 (50%)  6 (19%)  2 (25%)  0.05 
None  3 (14%)  16 (50%)  4 (50%)  0.02 

EVB: esophageal variceal bleeding; ATB: antibiotics; TIPS: transjugular intrahepatic porto-systemic shunt; SBP: spontaneous bacterial peritonitis; HRS: hepatorenal syndrome; HCC: hepatocellular carcinoma.

4Discussion

Cirrhosis is a major cause of morbidity and mortality worldwide [1,2,22–24]. Regardless of successful preventive measures and specific therapies for certain etiologies [25–27], the growing incidence of other agents as main determinants of chronic liver injury sustains its prevalence [2,28]. Advanced cirrhotic patients face the risk of decompensation that, once present, requires frequent hospital admissions [5–7,29–32]. In order to diagnose and treat them adequately, they should take place at centers where both medical know-how and updated technical resources are available. However, this is not always feasible, and patients may be admitted at institutions lacking expertise for their management [17–19].

The present survey, the first of its kind performed in Latin America, analyses data obtained from a group of mostly urban located centers, sharing a high degree of academic affiliation. The existence of Gastroenterology Depts at most of them, frequently associated to Liver Units, explain the significant presence of decompensated cirrhotic patients at these institutions.

The final data includes 13 (81%) of 16 originally invited countries, with a global answer rate of 37%. The contribution was quite heterogeneous, showing, in some specific cases, a disproportion between country population and the number of participating centers. Therefore, 53% of the countries recruited 85% of the centers providing 93% of included patients. Given this limited territorial projection, representative value of these data may be questioned. However, as mentioned before, no significant difference was observed between those patients recruited at major contributing countries (>30 pts) versus those included at less contributors.

AR was the global leading cause. However, as previously mentioned, NASH resulted highly prevalent within patients enrolled in the Pacific coast (Chile, Perú and Ecuador). In spite of this, BMI categories and diabetes incidence did not differ between these 3 countries and the others (not shown in Results). Reasons for this distinctive feature remain unknown as neither etnicity nor dietary habits were part of the inquiry.

Male predominance, a treshold age of 40 years for the majority and both CP/MELD scores reflecting advanced disease characterized this population. Interestingly, a BMI>25 and diabetes were present in 57% (n=214) and 32% (n=122) of them, respectively. AR and NASH were the most prevalent etiologies, both accounting for 63% (n=235) of the population while HCV, the third related cause, represented 7% (n=25) of the cases. This profile is coincident with reports showing a shift toward AR and NASH as the main contemporary emergent agents of chronic liver disease [1,2,23,24,28,33,34]. Interestingly, HCV infection was higher in females, as has been previously reported in specific Latin American geographic areas [35] (Supplementary Table 3).

Remarkably, a low vaccination rate was observed in these patients, far away from recommended schedules for cirrhotic patients [36].

Sign and symptom overlap (i.e. GIB/HE, infections/HRS) is frequent in decompensated cirrhotics, making identification of a single admission cause occasionally difficult. Therefore, given the high frequency of such combinations, admission cause was defined as the prevailing feature at presentation (“main admission cause”). Accordingly, ascites, GIB, HE and infections were the main identifiable admission causes, as reported elsewhere [7,32,37,38].

Regarding EVB, recommended steps are adequately followed at most institutions [11]. Nevertheless, some disparities deserve comment. Bleeders are “always” admitted to ICUs at only 20% of these institutions. According to the Baveno VI consensus meeting “patients with acute variceal hemorrhage should be considered for ICU or other well-monitored units” [11]. Although desirable, wether most centers not admitting bleeders to ICUs are doing it at “other well-monitored units” is difficult to assume. Vasoactive drugs and ATB administration associated to diagnostic/therapeutic endoscopic procedures performance was homogeneously qualified among all centers. A remarkable point is the unavailability of a SBT at 32% (n=21) of the places while, on the other hand, SBT is the only available therapeutic tool at 5 of them. May this implie its under or over usage is hipothetical. However, given the limited availability of both emergency TIPS (8 centers; 12%) and self-expandable metal stents (11 centers; 17%), possession of a SBT must be strongly encouraged.

Ascites therapy is a well standardized issue [13,19], however, care of these patients may be suboptimal [18]. The fact that in the present survey diagnostic paracentesis is performed “only” when SBP is suspected in almost 30% of the centers is worrisome, as SBP may be absolutely asymptomatic. Moreover, its suspicion is not the only indication to perform a diagnostic paracentesis [13,39,40]. This criterion must be necessarily reconsidered. Both standard medical treatment of ascites and therapy at its refractory status were homogeneously satisfactory, endorsing guidelines recommendations [13,40,41]. On the other hand, 1 every 3 centers lacks an adequate treatment for HRS. Finally, regarding SBP, a delicate problem is the low bacterial rescue in ascitic fluid in almost 60% of the institutions, well below reported standard results [41,42]. Inadequate sample collection and/or lack of updated culture technology may explain these dissapointing results.

Prevention of HE either during the acute bleeding episode or as therapy of its chronic stage is accomplished in most centers [15]. Regarding LT, it is available at 32% (n=21) of participating hospitals endorsing the assertion that referral centers were highly represented at this survey. Moreover, liver disease etiology of transplanted patients shows the same changing trend actually observed in the United States [43–45].

Remarkably, HCC screening is performed at 95% (n=62) of the institutions. This elevated screening index is also mirroring a group of mostly liver disease devoted institutions, overcoming suboptimal surveillance observed in non-liver disease oriented centers [46,47]. Nevertheless, a mix of different treatment proposals is only available at 33 of the centers. Finally, medical skills, updated technology and a higher level of adherence to guidelines recommendations prevailed in centers located at the most populated areas (>500,000) as well as in those having simultaneous Gastroenterolgy, Liver and Int Med Depts.

A weakness of this study may be its representative value. Nevertheless, in this group of mainly urban located centers, patient characteristics were homogeneous, regardless number included and countries considered. Therefore, we believe the results are confident enough to accomplish the survey objectives. It may also be argued that Acute on Chronic Liver Disease (ACLF) was not considered among admission causes. In fact, proposal of ACLF as a late decompensation event appeared on a subsequent date of this survey development [4]. Additionally, the survey may be qualified as biased, not acknowledging the “real world”. In fact it is so. As mentioned, medical care of decompensated cirrhotic patients requires a degree of complexity not available anywhere, but at referral centers, to which this survey was intentionally addressed.

In conclusion, this study updates the current status of capacities aimed at the medical care of decompensated cirrhotic patients in a group of Latin American medical centers. Notwithstanding its limited representation, it shows a high degree of resources availability, mostly according with current guidelines recommendations. Several facilities are available, mainly at referral centers, thereby providing the coordinated and multidisciplinary interventions required for the adequate treatment of these patients [18,19,48].AbbreviationsAIH

autoimmune hepatitis

AR

alcohol-related

ATB

antibiotics

BMI

body mass index

Dpts

departments

CP

Child–Pugh

EVB

esophageal variceal bleeding

GIB

gastro-intestinal bleeding

HCC

hepatocellular carcinoma

HCV

hepatitis C virus

HE

hepatic encephalopathy

HRS

hepatorenal syndrome

ICU

Intensive Care Unit

Int Med

internal medicine

LT

liver transplant

MELD

Model for End-stage Liver Disease

NASH

non-alcoholic steatohepatitis

PBC

primary biliary cholangitis

SBP

spontaneous bacterial peritonitis

SBT

Sengstaken-Blakemore tube

TIPS

transjugular intrahepatic porto-systemic shunt

US

ultrasound

Funding information

No financial support specific for this study was received.

Conflict of interest

The authors have no conflicts of interest that pertain to this work.

Acknowledgements

A special recognition to ALEH and FAGE for their institutional and administrative support. The authors are indebted to Professor Roberto Groszmann, M.D. for his generous assistance.

References
[1]
S. Scaglione, S. Kliethermes, G. Cao, D. Shoham, R. Durazo, A. Luke, et al.
The epidemiology of cirrhosis in the United States. A population-based study.
J Clin Gastroenterol, 49 (2015), pp. 690-696
[2]
S.K. Asrani, H. Devarbhavi, J. Eaton, P.S. Kamath.
Burden of liver diseases in the world.
J Hepatol, 70 (2019), pp. 151-171
[3]
G. Garcia-Tsao, S. Friedman, J. Iredale, M. Pinzani.
Now there are many (stages) where before there was one: In search of a pathophysiological classification of cirrhosis.
Hepatology, 51 (2010), pp. 1445-1449
[4]
G. D’Amico, A. Morabito, M. D’Amico, L. Pasta, G. Malizia, P. Rebora, et al.
New concepts on the clinical course and stratification of compensated and decompensated cirrhosis.
Hepatol Int, 12 (2018), pp. S34-S43
[5]
J.S. Bajaj, K.R. Reddy, P. Tandon, F. Wong, P.S. Kamath, G. Garcia-Tsao, et al.
The 3-month readmission rate remains unacceptably high in a large North American cohort of patients with cirrhosis.
Hepatology, 64 (2016), pp. 200-208
[6]
F. Kanwal, S.M. Asch, J.R. Kramer, Y. Cao, S. Asrani, H.B. El-Serag.
Early outpatient follow-up and 30-day outcomes in patients hospitalized with cirrhosis.
Hepatology, 64 (2016), pp. 569-581
[7]
S. Chirapongsathorn, C. Krittanawong, F.T. Enders, R. Pendegraft, K.C. Mara, B.J. Borah, et al.
Incidence and cost analysis of hospital admission and 30-day readmission among patients with cirrhosis.
Hepatol Commun, 2 (2018), pp. 188-198
[8]
G. D’Amico, G. Garcia-Tsao, L. Pagliaro.
Natural history and prognostic indicators of survival in cirrhosis: a systematic review of 118 studies.
J Hepatol, 44 (2006), pp. 217-231
[9]
A. Zipprich, G. Garcia-Tsao, S. Rogowski, W.E. Fleig, T. Seufferlein, M.M. Dollinger.
Prognostic indicators of survival in patients with compensated and decompensated cirrhosis.
Liver Int, 32 (2012), pp. 1407-1414
[10]
M. Sayiner, P. Golabi, Z.M. Younossi.
Disease burden of hepatocellular carcinoma: a global perspective.
Dig Dis Sci, 64 (2019), pp. 910-917
[11]
P. Tandon, I.M. Gralnek, G. Lo, L. Aabakken, F. Nevens, J.C. García-Pagan.
Management of acute variceal bleeding in patients with cirrhosis: General management, drug therapy, and endoscopic treatment.
Portal hypertension VI. Proceedings of the sixth Baveno consensus workshop: stratifying risk and individualizing care, pp. 241-260
[12]
F. Wong, M.K. Nadim, J.A. Kellum, F. Salerno, R. Bellomo, A. Gerbes, et al.
Working party proposal for a revised classification system of renal dysfunction in patients with cirrhosis.
[13]
The European Association for the Study of the Liver.
EASL Practice Clinical Guidelines for the management of patients with decompensated cirrhosis.
J Hepatol, 69 (2018), pp. 406-460
[14]
R. Jalan, J. Fernandez, R. Wiest, B. Schnabl, R. Moreau, P. Angeli, et al.
Bacterial infections in cirrhosis: a position statement based on the EASL Special Conference 2013.
J Hepatol, 60 (2014), pp. 1310-1324
[15]
H. Vilstrup, P. Amodio, J. Bajaj, J. Cordoba, P. Ferenci, K.D. Mullen, et al.
Hepatic encephalopathy in chronic liver disease: 2014 Practice Guideline by the American Association for the Study of Liver Diseases and the European Association for the Study of the Liver.
Hepatology, 60 (2014), pp. 715-735
[16]
J.K. Heimbach, L.M. Kulik, R.S. Finn, C.B. Sirlin, M.M. Abecassis, L.R. Roberts, et al.
AASLD guidelines for the treatment of hepatocellular carcinoma.
Hepatology, 67 (2018), pp. 358-380
[17]
F. Kanwal, J.R. Kramer, P. Buchanan, S.M. Asch, Y. Assioun, B.R. Bacon, et al.
The quality of care provided to patients with cirrhosis and ascites in the Department of Veterans Affairs.
Gastroenterology, 143 (2012), pp. 70-77
[18]
J.L. Mellinger, M.L. Volk.
Multidisciplinary management of patients with cirrhosis: a need for care coordination.
Clin Gastroenterol Hepatol, 11 (2013), pp. 217-223
[19]
M.K. Nadim, F. Durand, J.A. Kellum, J. Levitsky, J.G. O’Leary, C.J. Karvellas, et al.
Management of the critically ill patient with cirrhosis: a multidisciplinary perspective.
J Hepatol, 64 (2016), pp. 717-735
[20]
M. Szklo, F.J. Nieto.
Epidemiology: beyond the basis.
Jones and Bartlett, (2000),
[21]
Handbook of epidemiology,
[22]
E.B. Tapper, N.D. Parikh.
Mortality due to cirrhosis and liver cancer in the United States, 1999–2016: observational study.
BMJ, 362 (2018),
[23]
L. Pimpin, H. Cortez-Pinto, F. Negro, E. Corbould, J.V. Lazarus, L. Webber, et al.
Burden of liver disease in Europe: epidemiology and analysis of risk factors to identify prevention policies.
J Hepatol, 69 (2018), pp. 718-735
[24]
J.A. Baki, E.B. Tapper.
Contemporary epidemiology of cirrhosis.
Curr Treat Options Gastro, (2019),
[25]
D.S. Chen.
Hepatitis B vaccination: the key towards elimination and eradication of hepatitis B.
J Hepatol, 50 (2009), pp. 805-816
[26]
P. Nahon, V. Bourcier, R. Layese, E. Audureau, C. Cagnot, P. Marcellin, et al.
Eradication of hepatitis C virus infection in patients with cirrhosis reduces risk of liver and non-liver complications.
Gastroenterology, 152 (2017), pp. 142-156
[27]
F. Carrat, H. Fontaine, C. Dorival, M. Simony, A. Diallo, C. Hezode, et al.
Clinical outcomes in patients with chronic hepatitis C after direct-acting antiviral treatment: a prospective cohort study.
Lancet, 393 (2019), pp. 1453-1464
[28]
D. Kim, A.A. Li, B.J. Perumpail, C. Gadiparthi, W. Kim, G. Cholankeril, et al.
Changing trends in etiology- and ethnicity-based annual mortality rates of cirrhosis and hepatocellular carcinoma in the United States.
Hepatology, 69 (2019), pp. 1064-1074
[29]
M.L. Volk, R.S. Tocco, J. Bazick, M.O. Rakoski, A.S. Lock.
Hospital readmissions among patients with decompensated cirrhosis.
Am J Gastroenterol, 107 (2012), pp. 247-252
[30]
A. Tansel, J. Kramer, H. Feng, H.B. El Serag, F. Kanwal.
Risk trajectories for readmission and death after cirrhosis related hospitalization.
Dig Dis Sci, 64 (2019), pp. 1470-1477
[31]
G. D’Amico, A. Morabito, L. Pagliaro, E. Marubini, The Liver Study Group of “V Cervello” Hospital.
Survival and prognostic indicators in compensated and decompensated cirrhosis.
Dis Sci, 31 (1986), pp. 468-475
[32]
J. Cordoba, M. Ventura-Cots, M. Simón-Talero, A. Amorós, M. Pavesi, H. Vilstrup, et al.
Characteristics, risk factors, and mortality of cirrhotic patients hospitalized for hepatic encephalopathy with and without acute-on-chronic liver failure (ACLF) Consortium.
J Hepatol, 60 (2014), pp. 275-281
[33]
A. Poonwala, S.P. Nair, P.J. Thuluvath.
Prevalence of obesity and diabetes in patients with cryptogenic cirrhosis: a case–control study.
Hepatology, 32 (2000), pp. 689-692
[34]
A. Berzigotti, J.G. Abraldes.
Impact of obesity and insulin-resistance on cirrhosis and portal hypertension.
Gastroenterol Hepatol, 36 (2013), pp. 527-533
[35]
N. Méndez-Sánchez, Y. Gutiérrez-Grobe, R.A. Kobashi-Margáin.
Epidemiology of HCV infection in Latin America.
Ann Hepatol, 9 (2010), pp. S27-S29
[36]
M.D. Leise, J.A. Talwalkar.
Immunizations in chronic liver disease: what should be done and what is the evidence.
Curr Gastroenterol Rep, 15 (2013), pp. 300
[37]
P. Gines, E. Quintero, V. Arroyo, J. Teres, M. Bruguera, A. Rimola, et al.
Compensated cirrhosis: natural history and prognostic factors.
Hepatology, 7 (1987), pp. 122-128
[38]
A.S. Barritt 4th, Y. Jiang, M. Schmidt, P.H. Hayashi, R. Bataller.
Charges for alcoholic cirrhosis exceed all other etiologies of cirrhosis combined: a national and state inpatient survey analysis.
Dig Dis Sci, 64 (2019), pp. 1460-1469
[39]
L.T. Evans, W.R. Kim, J.J. Poterucha, P.S. Kamath.
Spontaneous bacterial peritonitis in asymptomatic outpatients with cirrhotic ascites.
Hepatology, 37 (2003), pp. 897-901
[40]
G. Garcia-Tsao.
Current management of the complications of cirrhosis and portal hypertension: variceal hemorrhage, ascites, and spontaneous bacterial peritonitis.
Gastroenterology, 120 (2001), pp. 726-748
[41]
European Association for the Study of the Liver.
EASL clinical practice guidelines on the management of ascites, spontaneous bacterial peritonitis, and hepatorenal syndrome in cirrhosis.
J Hepatol, 53 (2010), pp. 397-417
[42]
S. Piano, S. Fasolato, F. Salinas, A. Romano, M. Tonon, F. Morando, et al.
The empirical antibiotic treatment of nosocomial spontaneous bacterial peritonitis: results of a randomized, controlled clinical trial.
Hepatology, 63 (2016), pp. 1299-1309
[43]
R.J. Wong, M. Aguilar, R. Cheung, R.B. Perumpail, S.A. Harrison, Z.M. Younossi, et al.
Nonalcoholic steatohepatitis is the second leading etiology of liver disease among adults awaiting liver transplantation in the United States.
Gastroenterology, 148 (2015), pp. 547-555
[44]
D. Goldberg, I.C. Ditah, K. Saeian, M. Lalehzari, A. Aronsohn, E.C. Gorospe, et al.
Changes in the prevalence of hepatitis C virus infection, nonalcoholic steatohepatitis, and alcoholic liver disease among patients with cirrhosis or liver failure on the waitlist for liver transplantation.
Gastroenterology, 152 (2017), pp. 1090-1099
[45]
G. Cholankeril, A. Ahmed.
Alcoholic liver disease replaces hepatitis C virus infection as the leading indication for liver transplantation in the United States.
Clin Gastroenterol Hepatol, 16 (2018), pp. 1356-1358
[46]
A.G. Singal, X. Li, J. Tiro, P. Kandunoori, B.M.S. Adams-Huet, M.S. Nehra, et al.
Racial, social, and clinical determinants of hepatocellular carcinoma surveillance.
Am J Med, 128 (2015), pp. 90.e1-90.e7
[47]
D.S. Goldberg, T.H. Taddei, M. Serper, R. Mehta, E. Dieperink, A. Aytaman, et al.
Identifying barriers to hepatocellular carcinoma surveillance in a national sample of patients with cirrhosis.
Hepatology, 65 (2017), pp. 864-874
[48]
E.B. Tapper, S. Hao, M. Lin, J.N. Mafi, H. McCurdy, N.D. Parikh, et al.
The quality and outcomes of care provided to patients with cirrhosis by advanced practice providers.
Hepatology, 71 (2020), pp. 225-234
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