MD667Z - Method for treatment of infectious mononucleosis in children - Google Patents
Method for treatment of infectious mononucleosis in childrenInfo
- Publication number
- MD667Z MD667Z MDS20130054A MDS20130054A MD667Z MD 667 Z MD667 Z MD 667Z MD S20130054 A MDS20130054 A MD S20130054A MD S20130054 A MDS20130054 A MD S20130054A MD 667 Z MD667 Z MD 667Z
- Authority
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- Moldova
- Prior art keywords
- group
- treatment
- children
- patients
- therapy
- Prior art date
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Abstract
Description
Invenţia se referă la medicină, în special la bolile infecţioase şi poate fi utilizată pentru tratamentul mononucleozei infecţioase la copii. The invention relates to medicine, especially to infectious diseases and can be used for the treatment of infectious mononucleosis in children.
Este cunoscută metoda de tratament al mononucleozei infecţioase la copii, care include repausul la pat, evitarea eforturilor fizice pe perioada persistării splenomegaliei şi a modificărilor electrocardiogramei, dieta nr.5 după Pevzner, care menajează ficatul. Tratamentul patogenetic şi simptomatic se face cu antipiretice (paracetamol, ibuprofen etc.), antihistaminice (suprastin, taveghil etc.), acid ursodeoxicolic şi hepatoprotectoare în caz de afectare a ficatului, diuretice, vitamine (C, B1, B6, B12), la fel este cunoscută utilizarea aciclovirului sau a remediilor antivirale [1]. The method of treating infectious mononucleosis in children is known, which includes bed rest, avoiding physical exertion during the persistence of splenomegaly and changes in the electrocardiogram, diet No. 5 according to Pevzner, which takes care of the liver. The pathogenetic and symptomatic treatment is done with antipyretics (paracetamol, ibuprofen, etc.), antihistamines (suprastin, taveghil, etc.), ursodeoxycholic acid and hepatoprotectors in case of liver damage, diuretics, vitamins (C, B1, B6, B12), at the use of aciclovir or antiviral remedies is also known [1].
Dezavantajele acestei metode constau în eficacitatea joasă a preparatelor antivirale care nu permit de a obţine rezultatele scontate, totodată ele provoacă dezvoltarea reacţiilor adverse, ceea ce limitează aplicarea metodei cunoscute în practică pentru majoritatea pacienţilor, mai ales a celor de vârstă mică. The disadvantages of this method consist in the low effectiveness of antiviral preparations that do not allow to obtain the expected results, at the same time they cause the development of adverse reactions, which limits the application of the known method in practice for most patients, especially those of young age.
Problema pe care o rezolvă invenţia constă în elaborarea unei metode de tratament al mononucleozei infecţioase cu sindrom hepatic la copii, prin administrarea preparatului autohton - Pacovirină, care reduce semnificativ frecvenţa manifestărilor sindromului toxic general, poliadenopatiei, dereglărilor digestive şi hepatomegaliei, normalizează indicii ALAT, ASAT şi γGT, contribuind respectiv la micşorarea duratei de spitalizare a pacienţilor. The problem that the invention solves consists in the development of a method of treatment of infectious mononucleosis with liver syndrome in children, by administering the native preparation - Pacovirine, which significantly reduces the frequency of manifestations of the general toxic syndrome, polyadenopathy, digestive disorders and hepatomegaly, normalizes ALAT, AST indices and γGT, respectively contributing to the reduction of the length of hospitalization of patients.
Conform invenţiei, metoda revendicată constă în aceea că se administrează antibioticoterapia, vitaminoterapia, terapia hepatoprotectoare, de dezintoxicare şi simptomatică, iar suplimentar se administrează zilnic, per os, cu 30 min înainte de masă 5α-furostan-3β,22,26-triol-3-[O-β-D-glucopiranozil(1→2)-β-D-glucopiranozil(1→4)-β-D-galactopiranozil]-26-O-β-D-glucopiranozid, câte 50 mg, de 2 ori pe zi, timp de 30 zile. According to the invention, the claimed method consists in the fact that antibiotic therapy, vitamin therapy, hepatoprotective, detoxification and symptomatic therapy are administered, and in addition, 5α-furostan-3β,22,26-triol- 3-[O-β-D-glucopyranosyl(1→2)-β-D-glucopyranosyl(1→4)-β-D-galactopyranosyl]-26-O-β-D-glucopyranoside, 50 mg each, of 2 times a day for 30 days.
Rezultatul obţinut constă în crearea unei metode de tratament al mononucleozei infecţioase la copii bazată pe administrarea, concomitent cu terapia de bază, a Pacovirinei, cu efect imunomodulator, antioxidant, interferonogen şi antiviral. The result obtained consists in the creation of a method of treatment of infectious mononucleosis in children based on the administration, simultaneously with the basic therapy, of Pacovirine, with an immunomodulatory, antioxidant, interferonogenic and antiviral effect.
Pentru aprobarea metodei revendicate de tratament al mononucleozei infecţioase cu sindrom hepatic la copii la Spitalul Clinic Municipal de Boli Infecţioase pentru Copii (IMSP SCMBCC) au fost efectuate următoarele investigaţii: For the approval of the claimed method of treatment of infectious mononucleosis with liver syndrome in children at the Municipal Clinical Hospital for Infectious Diseases for Children (IMSP SCMBCC) the following investigations were carried out:
1) clinice; 1) clinics;
2) paraclinice (hemoleucograma cu determinarea nivelului leucocitozei, prezenţa limfocitozei cu monocitoză şi a limfocitelor atipice; examenul biochimic cu aprecierea nivelului aminotransferazelor (ALAT, ASAT), fosfatazei alcaline, bilirubinei serice şi fracţiilor ei, la fel se determină β-lipoproteidele, gamma-glutamiltansferaza, lactatdehidrogenaza şi proba cu timol; 2) paraclinical (hemoleukogram with the determination of the level of leukocytosis, the presence of lymphocytosis with monocytosis and atypical lymphocytes; the biochemical examination with the assessment of the level of aminotransferases (ALT, AST), alkaline phosphatase, serum bilirubin and its fractions, as well as β-lipoproteins, gamma- glutamyl transferase, lactate dehydrogenase and thymol test;
3) examenele imunologice (metoda imunoenzimatică (ELISA) pentru determinarea markerilor serologici ai infecţiei cu virusul Epstein-Barr (VCA IgM, VCA IgG, EA IgG, EBNA IgG) ai hepatitelor virale (AgHBs, anti-HBcor IgM şi anti-HBcor sum, anti-HCV, anti-HCV IgM, anti-HDV sumar şi anti-HDV IgM); 3) immunological examinations (immunoenzymatic method (ELISA) for the determination of serological markers of Epstein-Barr virus infection (VCA IgM, VCA IgG, EA IgG, EBNA IgG) of viral hepatitis (HBsAg, anti-HBcor IgM and anti-HBcor sum, anti-HCV, anti-HCV IgM, anti-HDV summary and anti-HDV IgM);
4) examenul ultrasonografic al organelor abdominale (la necesitate). 4) ultrasound examination of the abdominal organs (if necessary).
Drept obiect al studiului au servit 175 pacienţi (84 pacienţi - grupul experimental şi 91 - grupul martor) şi fişele lor de observaţie (forma 003/e), cu diagnostic clinic de mononucleoză infecţioasă cu virusul Epstein-Barr cu sindrom hepatic, internaţi în IMSP Spitalul Clinic Municipal de Boli Contagioase de Copii, pe perioada anilor 2009…2012. The object of the study were 175 patients (84 patients - the experimental group and 91 - the control group) and their observation sheets (form 003/e), with a clinical diagnosis of infectious mononucleosis with the Epstein-Barr virus with liver syndrome, hospitalized in IMSP The Municipal Clinical Hospital for Children's Contagious Diseases, during the years 2009...2012.
Toţi bolnavii din studiu au primit tratament patogenic şi simptomatic, care a inclus regim igieno-dietetic (regim de salon, dieta nr. 5 după Pevzner), antibiotice (în cazul amigdalitelor purulente), hepatoprotectoare (silimarină, fosfolipide esenţiale, acid ursodezoxiholic), terapia de dezintoxicare la prezenţa sindromului de intoxicare generală (administrarea i/v a soluţiilor fiziologice, de glucoză etc.) şi vitamine. Pacienţilor din lotul experimental (n-84) li s-a administrat suplimentar Pacovirină (forma medicamentoasă - capsule). Durata curei a fost de o lună, în doza corespunzătoare vârstei (de 2 ori pe zi). All the patients in the study received pathogenic and symptomatic treatment, which included a hygienic-dietary regimen (salon regimen, diet no. 5 according to Pevzner), antibiotics (in the case of purulent tonsillitis), hepatoprotectors (silymarin, essential phospholipids, ursodeoxyholic acid), detoxification therapy in the presence of general intoxication syndrome (i/v administration of physiological solutions, glucose, etc.) and vitamins. The patients in the experimental group (n-84) were additionally administered Pacovirine (medicinal form - capsules). The duration of the cure was one month, in the dose corresponding to the age (2 times a day).
Rezultatele metodei de tratament al copiilor cu mononucleoză infecţioasă cu virusul Epstein-Barr cu sindrom hepatic au fost analizate la finele tratamentului în staţionar şi la o lună de catamneză. The results of the method of treatment of children with infectious mononucleosis with the Epstein-Barr virus with liver syndrome were analyzed at the end of the inpatient treatment and after one month of catamnesis.
Rezultatele obţinute. The results obtained.
În ambele grupuri din studiu ponderea cea mai mare au avut-o băieţii: I grup - 47 (55)%), al II-lea grup - 57 (62,6%), şi mai puţin fetele: I grup - 37 (44,1%), al II-lea grup - 34 (37,4%). In both groups in the study, boys had the highest share: 1st group - 47 (55%), 2nd group - 57 (62.6%), and less girls: 1st group - 37 (44 .1%), the 2nd group - 34 (37.4%).
Circa 2/3 din pacienţii I grup de studiu (experimental) au fost copii cu vârsta până la 7 ani - 66 (78,6%), inclusiv cu vârsta până la 3 ani - 34 (40,5%) şi cu vârsta între 3…7 ani - 32 (38,1%), iar cu vârsta între 7…14 şi 14…18 ani - 14 (16,7%) şi 4 (4,7%), corespunzător. Grupul II (martor) de asemenea preponderent a fost alcătuit din preşcolari (copii cu vârsta până la 7 ani) - 71 (78,0%), iar cu vârsta între 7…14 ani - 18 (19,8%) şi între 14…18 ani - 2 (2,2%), toate aceste date sunt prezentate în figură, care reprezintă repartizarea bolnavilor cu mononucleoză infecţioasă cu sindrom hepatic, în dependenţă de vârstă. About 2/3 of the patients in the 1st study group (experimental) were children up to 7 years old - 66 (78.6%), including up to 3 years old - 34 (40.5%) and aged between 3...7 years - 32 (38.1%), and aged between 7...14 and 14...18 years - 14 (16.7%) and 4 (4.7%), respectively. Group II (control) also mainly consisted of preschoolers (children up to 7 years old) - 71 (78.0%), and between 7...14 years old - 18 (19.8%) and between 14 ...18 years - 2 (2.2%), all these data are presented in the figure, which represents the distribution of patients with infectious mononucleosis with liver syndrome, depending on age.
Aproximativ 1⁄2 (43…51,2%) din copiii primului grup frecventau colectivităţi (grădiniţe, şcoli, licee etc.), iar în cazul grupului doi, frecvenţa celor prezenţi în colectivităţi era mai joasă (45 - 43,4%). Approximately 1⁄2 (43...51.2%) of the children of the first group attended collectives (kindergartens, schools, high schools, etc.), and in the case of the second group, the frequency of those present in collectives was lower (45 - 43.4%) .
Debutul maladiei a fost acut la majoritatea pacienţilor: în I grup - la 80 (95,2%) copii, în al II-lea grup - la 87 (95,6%). După criteriile de severitate a bolii (semne de intoxicaţie generală, nivelul febrei, intensitatea poliadenopatiei, hepatosplenomegaliei etc.) la secţia de internare starea generală gravă a fost apreciată la 30 (23,8%) şi de gravitate medie la 64 (76,2%) copii din I grup. La copiii grupului II, starea generală gravă s-a stabilit la 14…15,4%, iar de gravitate medie la 77…84,6%. The onset of the disease was acute in most patients: in the 1st group - 80 (95.2%) children, in the 2nd group - 87 (95.6%). According to the criteria of the severity of the disease (signs of general intoxication, the level of fever, the intensity of polyadenopathy, hepatosplenomegaly, etc.) at the hospitalization department, the general condition was assessed as serious at 30 (23.8%) and of medium severity at 64 (76.2 %) children from the 1st group. In the children of group II, the general serious condition was established at 14...15.4%, and of medium severity at 77...84.6%.
La domiciliu, de către medicul de familie sau alţi specialişti, au fost consultaţi 35 (41,7%) şi 40 (43,9%) copii din I şi al II-lea grup. Majoritatea (I grup - 32 (38,0%), al II-lea grup - 33 (36,3%)) din ei au iniţiat tratament cu antibiotice ambulatoriu, care nu a dus la ameliorarea stării generale. Cel mai frecvent antibiotic administrat în grupul I a fost din gr. cefalosporinelor (la 19 pacienţi). De menţionat că la 8 copii s-a prescris augmentin sau amoxicilină. At home, by the family doctor or other specialists, 35 (41.7%) and 40 (43.9%) children from the 1st and 2nd groups were consulted. The majority (I group - 32 (38.0%), II group - 33 (36.3%)) of them started outpatient antibiotic treatment, which did not improve the general condition. The most frequent antibiotic administered in group I was from gr. cephalosporins (in 19 patients). It should be mentioned that 8 children were prescribed augmentin or amoxicillin.
La iniţierea tratamentului toţi pacienţii, atât din grupul experimental, cât şi din cel martor prezentau simptome specifice (febră, respiraţie nazală dificilă, angină cu sau fără depuneri purulente, poliadenopatie, hepatomegalie, splenomegalie şi semne hematologice specifice) caracteristice infecţiei cu virusul Epstein-Barr (mononucleoză infecţioasă) cu sindrom hepatic. At the start of treatment, all patients, both in the experimental group and in the control group, presented specific symptoms (fever, difficult nasal breathing, angina with or without purulent deposits, polyadenopathy, hepatomegaly, splenomegaly and specific hematological signs) characteristic of Epstein-Barr virus infection (infectious mononucleosis) with liver syndrome.
Febra s-a apreciat la 78 (92,8%) bolnavi din grupul I, cu apariţia în primele trei zile de la debutul bolii la 29 (34,5%). Valorile maximale ale febrei, stabilite între 38…39°C, au fost înregistrate la 34 pacienţi (40,4%) şi peste 39°C - la 44 (52,4%) pacienţi. Durata medie a febrei a fost de 7 zile, inclusiv între 4…7 zile - la 35 şi între 8…14 zile - la 34, iar la 9 copii a persistat peste 14 zile. Fever was assessed in 78 (92.8%) patients from group I, with the appearance in the first three days from the onset of the disease in 29 (34.5%). The maximum values of the fever, established between 38...39°C, were recorded in 34 patients (40.4%) and above 39°C - in 44 (52.4%) patients. The average duration of the fever was 7 days, including between 4...7 days - in 35 and between 8...14 days - in 34, and in 9 children it persisted for more than 14 days.
La peste 2/3 (62…73,8%) din pacienţii grupului I şi la 66 (72,5%) din grupul II s-a observat respiraţie nazală dificilă, nas înfundat, voce nazală. Păstozitatea feţei cu edem palpebral, în unele cazuri cu edem periganglionar a fost observată în 28 (33,3%) de cazuri, faringite în 67 (79,8%) de cazuri, dureri abdominale în 11 (13,1%). In more than 2/3 (62...73.8%) of the patients in group I and in 66 (72.5%) in group II, difficult nasal breathing, stuffy nose, nasal voice were observed. Facial puffiness with eyelid edema, in some cases with periganglionic edema was observed in 28 (33.3%) cases, pharyngitis in 67 (79.8%) cases, abdominal pain in 11 (13.1%).
Amigdalita purulentă, la momentul internării în staţionar, s-a depistat la majoritatea pacienţilor atât din grupul I (72…85,7%), cât şi din grupul II (80…87,9%). Purulent tonsillitis, at the time of hospitalization, was detected in the majority of patients from both group I (72...85.7%) and group II (80...87.9%).
Poliadenopatia cu mărirea ganglionilor limfatici cervicali anteriori şi posteriori, submandibulari, axilari, inghinali, cubitali a fost prezentă la toţi (100%) pacienţii. Polyadenopathy with enlargement of anterior and posterior cervical, submandibular, axillary, inguinal, ulnar lymph nodes was present in all (100%) patients.
Hepatomegalia, în grupul I, a fost determinată la 82 (97,6%) pacienţi, în grupul II la 89 (97,8%). La majoritatea copiilor din grupul I, ficatul depăşea rebordul costal drept cu 4 cm, inclusiv cu 2…3 cm la 39 (46,4%) şi cu 3…4 cm la 19 (22,6%). Hepatomegalie pronunţată, unde ficatul depăşea cu 4…5 cm rebordul costal, s-a depistat la 14 (16,7%) şi peste 5 cm la 10 (11,9%) bolnavi. Hepatomegaly, in group I, was determined in 82 (97.6%) patients, in group II in 89 (97.8%). In most of the children in group I, the liver exceeded the right costal edge by 4 cm, including by 2...3 cm in 39 (46.4%) and by 3...4 cm in 19 (22.6%). Pronounced hepatomegaly, where the liver exceeded the costal edge by 4...5 cm, was detected in 14 (16.7%) and over 5 cm in 10 (11.9%) patients.
Splenomegalia a fost observată la 63 (75,0%) bolnavi din I grup, cu 1 cm sub rebordul costal stâng la 16 (19,0%), cu 1…2 cm la 14 (16,7%) şi cu 2…3 cm la 15 (17,8%) bolnavi. Splenomegalia evidentă a fost observată la 18 pacienţi (cu 3…4 cm sub rebordul costal la 11 (13,1%), cu 4…5 cm la 4 (4,8%) şi peste 5 cm la 3 (3,6%) bolnavi. Splenomegaly was observed in 63 (75.0%) patients from the 1st group, with 1 cm below the left costal edge in 16 (19.0%), with 1...2 cm in 14 (16.7%) and with 2... 3 cm in 15 (17.8%) patients. Obvious splenomegaly was observed in 18 patients (with 3...4 cm below the costal edge in 11 (13.1%), with 4...5 cm in 4 (4.8%) and over 5 cm in 3 (3.6% ) sick.
Semnele clinice caracteristice au fost prezente în egală măsură şi în cazul copiilor din grupul II (tab.1). The characteristic clinical signs were equally present in the case of children from group II (tab. 1).
Tabelul 1 Table 1
Semnele clinice prezente la pacienţii cu MI cu EBV din studiu Clinical signs present in MI patients with EBV in the study
Semne clinice Grupul experimental Grupul martor Abs. % Abs. % Febră 78 92,8 85 93,4 Odinofagie 67 79,8 64 70,3 Dureri abdominale 11 13,1 16 17,6 Respiraţie nazală dificilă 62 73,8 66 72,5 Faringoamigdalită 72 85,7 80 87,9 Limfadenopatie generalizată 84 100,0 91 100,0 Hepatomegalie 82 97,6 89 97,8 Splenomegalie 63 75,0 70 76,9 Clinical signs Experimental group Control group Abs. % Abs. % Fever 78 92.8 85 93.4 Odynophagia 67 79.8 64 70.3 Abdominal pain 11 13.1 16 17.6 Difficult nasal breathing 62 73.8 66 72.5 Pharyngoatonsillitis 72 85.7 80 87.9 Lymphadenopathy generalized 84 100.0 91 100.0 Hepatomegaly 82 97.6 89 97.8 Splenomegaly 63 75.0 70 76.9
La momentul spitalizării hemoleucogramele se caracterizau prin prezenţa anemiei, cu o frecvenţă mai mare la copiii din grupul experimental (34…40,5%) decât la copiii din grupul martor (28…30,8%). At the time of hospitalization, the blood counts were characterized by the presence of anemia, with a higher frequency in children from the experimental group (34...40.5%) than in children from the control group (28...30.8%).
Leucocitoza a fost prezentă în ambele grupuri de studiu cu aceeaşi frecvenţă (în grupul I la 58,3%, în grupul II la 50,0%). Limfocitoza şi monocitoza la prima investigaţie a fost depistată cu aceeaşi legitate ca şi leucocitoza: la copiii grupului I în 58,3% din cazuri, la copii grupului II în 50,5%. Limfocite atipice s-au vizualizat la 61,9% la copiii din I grup de studiu şi la 59,2% din grupul II. Nivelul limfocitelor atipice în majoritatea cazurilor la copiii grupului I a fost de 30…50% (41,6%), comparativ cu copiii grupului II (26,6%). Viteza de sedimentare a hematiilor accelerată în ambele grupuri s-a înregistrat la acelaşi nivel (grupul I la 76,2%, grupul II la 73,6% copii). Leukocytosis was present in both study groups with the same frequency (in group I at 58.3%, in group II at 50.0%). Lymphocytosis and monocytosis at the first investigation was detected with the same legitimacy as leukocytosis: in group I children in 58.3% of cases, in group II children in 50.5%. Atypical lymphocytes were visualized in 61.9% of the children in the first study group and in 59.2% of the second group. The level of atypical lymphocytes in most cases in group I children was 30...50% (41.6%), compared to group II children (26.6%). Accelerated erythrocyte sedimentation rate in both groups was recorded at the same level (group I at 76.2%, group II at 73.6% children).
Hipertransaminazemie, ca semn de citoliză hepatică, cu nivelul crescut de ALAT a fost determinată la 100% din copiii ambelor grupuri şi de ASAT - la 83,3% din I grup şi la 83,5% din grupul II. Valorile ALAT între 49…100 UI/oră au fost determinate la 56 (66,7%) bolnavi din grupul experimental, între 101…150 UI/oră - la 14 (16,7%), între 151…250 UI/oră - la 9 (10,7%), peste 250 UI/oră - la 5 (5,9%) copii. Nivelul bilirubinei a fost în limitele normei în toate cazurile. Hypertransaminasemia, as a sign of liver cytolysis, with the increased level of ALT was determined in 100% of the children of both groups and of AST - in 83.3% of the I group and in 83.5% of the II group. ALAT values between 49...100 IU/hour were determined in 56 (66.7%) patients from the experimental group, between 101...150 IU/hour - in 14 (16.7%), between 151...250 IU/hour - in 9 (10.7%), over 250 IU/hour - in 5 (5.9%) children. The bilirubin level was within the normal range in all cases.
Toţi copii incluşi în studiu (atât din grupul experimental, cât şi din grupul martor) au beneficiat de tratament patogenetic şi simptomatic, iar după necesitate li s-a administrat antibiotice şi tratament de detoxificare. În faza acută a bolii au fost indicate: repaus la pat, dieta nr. 5. All children included in the study (both from the experimental group and from the control group) benefited from pathogenetic and symptomatic treatment, and if necessary, they were given antibiotics and detoxification treatment. In the acute phase of the disease, the following were indicated: bed rest, diet no. 5.
Toţi pacienţii au fost monitorizaţi, zilnic pe perioada spitalizării şi la o lună de catamneză, de către medicul curant, cu aprecierea tuturor parametrilor clinici caracteristici mononucleozei infecţioase şi a posibilelor reacţii adverse la administrarea preparatului. Evoluţia bolii la toţi pacienţii a fost benignă. La momentul externării din staţionar, hepatomegalia s-a păstrat în grupul experimental la 50 (59,5%) copii şi în grupul martor la 55 (60,4%). Splenomegalia spre momentul externării s-a observat la 32 (38,0%) copii din I grup şi la 33 (36,3%) din grupul II. All patients were monitored, daily during the hospitalization and one month after diagnosis, by the attending physician, with the assessment of all the clinical parameters characteristic of infectious mononucleosis and possible adverse reactions to the administration of the preparation. The evolution of the disease in all patients was benign. At the time of discharge from the hospital, hepatomegaly was preserved in the experimental group in 50 (59.5%) children and in the control group in 55 (60.4%). Splenomegaly at the time of discharge was observed in 32 (38.0%) children from group I and 33 (36.3%) from group II.
Evoluţia comparativă a semnelor clinice de bază la copiii cu mononucleoză infecţioasă cu virusul Epstein-Barr cu sindrom hepatic care au primit tratament cu Pacovirină şi cei care au primit tratament patogenetic este prezentată în tab. 2. The comparative evolution of basic clinical signs in children with infectious mononucleosis with the Epstein-Barr virus with liver syndrome who received treatment with Pacovirine and those who received pathogenetic treatment is presented in tab. 2.
Tabelul 2 Table 2
Evoluţia comparativă a principalelor semne clinice la bolnavii cu hepatită cu EBV (grupul experimental care au primit tratament cu Pacovirină şi martor care au primit tratament The comparative evolution of the main clinical signs in patients with EBV hepatitis (the experimental group that received treatment with Pacovirine and the control group that received treatment
de bază) până şi la o lună după tratament baseline) up to one month after treatment
Nr Parametrii clinici/nr. de pacienţi Grupul I (experimental) (n=84) P Grupul II (martor) (n=91) P Până la tratament După tratament (1 lună catamneză) Până la tratament După tratament (1 lună catamneză) Abs. M±m (%) Abs. M±m (%) Abs. M±m (%) Abs. M±m (%) 1 Debut acut (cu febră, respiraţiea nazală dificilă etc.) 80 95,2 ±2,4 0 0 P<0,001 87 95,6± 2,2 0 0 P<0,001 2 Amigdalită purulentă 72 85,7±4,1 0 0 P<0,001 80 87,9± 3,6 0 0 P<0,001 3 Poliadenopatie generalizată 84 100 67 79,8± 4,9 P<0,001 91 100 83 91,2± 3,1 P<0,001 4 Hepatomegalie 82 97,6±1,7 8 9,5±1 0,3 P<0,001 89 97,8± 2,2 29 31,9± 8,6 P<0,001 5 Splenomegalie 63 75,0±5,4 4 4,8±1 0,7 P<0,001 70 76,9± 5,0 14 15,4± 9,6 P<0,001 No. Clinical parameters/no. of patients Group I (experimental) (n=84) P Group II (control) (n=91) P Before treatment After treatment (1 month follow-up) Before treatment After treatment (1 month follow-up) Abs. M±m (%) Abs. M±m (%) Abs. M±m (%) Abs. M±m (%) 1 Acute onset (with fever, difficult nasal breathing, etc.) 80 95.2 ±2.4 0 0 P<0.001 87 95.6± 2.2 0 0 P<0.001 2 Purulent tonsillitis 72 85 .7±4.1 0 0 P<0.001 80 87.9± 3.6 0 0 P<0.001 3 Generalized polyadenopathy 84 100 67 79.8± 4.9 P<0.001 91 100 83 91.2± 3.1 P<0.001 4 Hepatomegaly 82 97.6±1.7 8 9.5±1 0.3 P<0.001 89 97.8± 2.2 29 31.9± 8.6 P<0.001 5 Splenomegaly 63 75.0 ±5.4 4 4.8±1 0.7 P<0.001 70 76.9± 5.0 14 15.4± 9.6 P<0.001
La bolnavii din grupul experimental s-a redus semnificativ hepatomegalia şi splenomegalia la o lună din momentul externării din staţionar, faţă de cei din lotul martor. Dinamica sindromului toxic general, manifestat prin febră şi semne toxice generale (inapetenţă, somnolenţă, slăbiciuni generale), pe parcursul perioadei de supraveghere nu s-a deosebit esenţial la pacienţii din grupul I şi II. In patients from the experimental group, hepatomegaly and splenomegaly were significantly reduced one month after discharge from the hospital, compared to those in the control group. The dynamics of the general toxic syndrome, manifested by fever and general toxic signs (lack of appetite, drowsiness, general weakness), during the surveillance period did not differ significantly in patients from groups I and II.
Datele obţinute în grupul martor sunt mai modeste, totuşi s-a depistat o diferenţă statistică semnificativă conform criteriilor clinice monitorizate în catamneză. Hepatomegalia (la o lună după externare) era prezentă la 8 (9,5%) pacienţi din I grup, comparativ cu grupul II - la 29 (31,9%). Prezenţa splenomegaliei a fost determinată la 4 (4,8%) copii din grupul I şi la 14 (15,4%) din grupul II. The data obtained in the control group are more modest, however, a significant statistical difference was detected according to the clinical criteria monitored in the catamnesis. Hepatomegaly (one month after discharge) was present in 8 (9.5%) patients in group I, compared to group II - in 29 (31.9%). The presence of splenomegaly was determined in 4 (4.8%) children from group I and 14 (15.4%) from group II.
O dinamică pozitivă mai rapidă s-a observat în descreşterea nivelului ALAT-ului şi ASAT-ului în ser (tab.3). Valorile ALAT-ului la finele tratamentului a fost în limitele normei la 56 (66,7%) pacienţi din grupul experimental, comparativ cu 43 (47,2%) din grupul martor. Nivelul ASAT-ului normal la momentul externării a fost apreciat la 68 (80,9%) copii din grupul I şi la 56 (61,5%) din grupul II. Hiperbilirubinemia nu a fost determinată nici la un copil din grupul de studiu. A faster positive dynamic was observed in the decrease of the level of ALT and AST in the serum (tab.3). ALAT values at the end of treatment were within the normal range in 56 (66.7%) patients from the experimental group, compared to 43 (47.2%) from the control group. The normal ASAT level at the time of discharge was assessed in 68 (80.9%) children from group I and 56 (61.5%) from group II. Hyperbilirubinemia was not determined in any child in the study group.
Tabelul 3 Table 3
Caracteristica indicilor biochimici la pacienţii cu mononucleoză infecţioasă cu sindrom hepatic (grupul experimental care au primit tratament cu Pacovirină şi martor care au primit tratament de bază) până şi după tratament Characteristics of biochemical indices in patients with infectious mononucleosis with liver syndrome (experimental group who received treatment with Pacovirine and control who received basic treatment) before and after treatment
Parametrul biochimic/termenul testării/numărul de pacienţi Grupul I (pacienţi, care au beneficiat de tratament cu Pacovirină) n=84 Grupul II (pacienţi, care au beneficiat de tratament de bază) n=91 norma > norma norma > norma abs. % abs. % abs. % abs. % ALAT boln. (indicele) 0…49 mmol/l Până la tratament 0 0 84 100 0 0 91 100 După tratament 56 66,7 28 33,3 43 47,2 48 52,8 P P<0,001 P<0,001 P<0,001 P<0,001 ASAT boln. (indicele) 0…46 mmol/l Până la tratament 14 16,7 70 83,3 15 16,5 76 83,5 După tratament 68 80,9 16 19,1 56 61,5 35 38,5 P P<0,001 P<0,001 P<0,001 P<0,001 Creşterea nivelului γGTP (indicele) 35…100 Până la tratament 78 92,8 6 7,2 89 97,8 2 2,2 După tratament 84 100 0 0 91 100 0 0 P P>0,05 P>0,05 P>0,05 P>0,05 Biochemical parameter/term of testing/number of patients Group I (patients, who benefited from treatment with Pacovirine) n=84 Group II (patients, who benefited from basic treatment) n=91 norm > norm norm > norm abs. % abs. % abs. % abs. % ALAT ill. (index) 0...49 mmol/l Before treatment 0 0 84 100 0 0 91 100 After treatment 56 66.7 28 33.3 43 47.2 48 52.8 P P<0.001 P<0.001 P<0.001 P<0.001 SO sick. (index) 0...46 mmol/l Before treatment 14 16.7 70 83.3 15 16.5 76 83.5 After treatment 68 80.9 16 19.1 56 61.5 35 38.5 P P<0.001 P <0.001 P<0.001 P<0.001 Increase in γGTP level (index) 35…100 Before treatment 78 92.8 6 7.2 89 97.8 2 2.2 After treatment 84 100 0 0 91 100 0 0 P P>0, 05 P>0.05 P>0.05 P>0.05
Toţi pacienţii la momentul iniţierii şi finisării tratamentului cu Pacovirină au fost supuşi investigaţiilor serologice cu determinarea markerilor specifici anti-EBV. Seroconversia markerilor infecţiei cu EBV în catamneză a fost depistată mai frecvent (56…66,7%) la copiii care au beneficiat de tratament cu Pacovirină, comparativ cu cei care au primit tratament de bază (39…42,8%). All patients at the time of initiation and completion of Pacovirine treatment were subjected to serological investigations with the determination of specific anti-EBV markers. Seroconversion of markers of EBV infection in catamnesis was detected more frequently (56...66.7%) in children who benefited from Pacovirine treatment, compared to those who received basic treatment (39...42.8%).
Astfel, rezultatele studiului clinic pe un lot de 84 bolnavi ne permite să afirmăm că administrarea preparatului Pacovirină a avut o acţiune pozitivă asupra manifestării principalelor semne clinice ale sindromului toxic general, poliadenopatiei, dereglărilor digestive care au dispărut la un număr semnificativ de bolnavi. La majoritatea bolnavilor din grupul experimental s-a observat micşorarea dimensiunilor ficatului şi splinei apreciate palpator, spre finele curei de tratament cu Pacovirină. În lotul experimental dinamica pozitivă a indicilor paraclinici (nivelul ALAT, ASAT şi γGTP) a fost mai evidentă. Thus, the results of the clinical study on a group of 84 patients allow us to state that the administration of the Pacovirine preparation had a positive effect on the manifestation of the main clinical signs of the general toxic syndrome, polyadenopathy, digestive disorders that disappeared in a significant number of patients. In the majority of the patients in the experimental group, the reduction of the size of the liver and spleen assessed by palpation was observed towards the end of the Pacovirine treatment course. In the experimental group, the positive dynamics of the paraclinical indices (ALAT, AST and γGTP level) was more obvious.
Administrarea preparatului Pacovirină în calitate de remediu medicamentos suplimentar la tratamentul de bază, în conformitate cu metoda revendicată, a dus la o normalizare mai rapidă şi mai intensivă a indicilor clinici şi paraclinici, favorizând o evoluţie mai favorabilă a procesului patologic cu recuperarea mai rapidă a bolnavilor, o normalizare mai intensivă a indicilor biochimici cu reducerea semnificativă a duratei de manifestare a principalelor semne clinice în lotul experimental, comparativ cu grupul martor. The administration of the Pacovirine preparation as an additional medicinal remedy to the basic treatment, in accordance with the claimed method, led to a faster and more intensive normalization of the clinical and paraclinical indices, favoring a more favorable evolution of the pathological process with a faster recovery of the patients , a more intensive normalization of biochemical indices with a significant reduction in the duration of manifestation of the main clinical signs in the experimental group, compared to the control group.
Metoda revendicată se realizează în felul următor: se administrează antibioticoterapia, vitaminoterapia, terapia hepatoprotectoare, de dezintoxicare şi simptomatică, iar suplimentar se administrează zilnic, per os, cu 30 min înainte de masă 5α-furostan-3β,22,26-triol-3-[O-β-D-glucopiranozil(1→2)-β-D-glucopiranozil(1→4)-β-D-galactopiranozil]-26-O-β-D-glucopiranozid, câte 50 mg, de 2 ori pe zi, timp de 30 zile. The claimed method is carried out in the following way: antibiotic therapy, vitamin therapy, hepatoprotective, detoxification and symptomatic therapy are administered, and in addition 5α-furostan-3β,22,26-triol-3 is administered daily, orally, 30 min before meals -[O-β-D-glucopyranosyl(1→2)-β-D-glucopyranosyl(1→4)-β-D-galactopyranosyl]-26-O-β-D-glucopyranoside, 50 mg each, 2 times per day for 30 days.
Exemplul 1 Example 1
Pacientul Ş., 2 ani, a fost internat la a 9-a zi de la debutul bolii în IMSP Spitalul Clinic Municipal de Boli Contagioase la Copii (IMSP SCMBCC) pe perioada 26.10.2012 - 06.11.2012 cu diagnosticul clinic de: mononucleoză infecţioasă provocată de virusul Epstein-Barr (primoinfecţie), gravitate medie. Hepatită mononucleozică. Bronhopneumonie bazală pe dreapta S7…S10, perioada de convalescenţă. Patient Ş., 2 years old, was hospitalized on the 9th day after the onset of the disease in the IMSP Municipal Clinical Hospital for Contagious Diseases for Children (IMSP SCMBCC) during the period 26.10.2012 - 06.11.2012 with the clinical diagnosis of: infectious mononucleosis caused by the Epstein-Barr virus (primary infection), medium severity. Hepatitis mononucleosis. Basal bronchopneumonia on the right S7...S10, the convalescence period.
La secţia de internare prezenta acuze la: febră până la 39°C, odinofagie, respiraţie nazală dificilă, forăit, tumefierea tuturor ganglionilor limfatici, hiporexie, slăbiciune generală, fatigabilitate. At the hospitalization department, he presented complaints of: fever up to 39°C, odynophagia, difficult nasal breathing, wheezing, swelling of all lymph nodes, hyporexia, general weakness, fatigue.
Conform anamnesticului, s-a îmbolnăvit cu o săptămână în urmă (pe 18.10.2012) cu debut acut (febră, tusă uscată rară, slăbiciune generală, fatigabilitate). Este consultat de medicul de familie care iniţiază tratamentul cu amoxicilină. Pe 21.10.2012 după un consult repetat, în lipsa eficacităţii, se schimbă antibioticul (pe cefatoxim). Pe fonul terapiei administrate starea generală nu se ameliorează, apare respiraţia nazală dificilă cu forăit în timpul somnului, poliadenopatia, dureri în abdomen. Pe 23.10.2012 se internează în Spitalul Clinic Municipal de Copii nr.1, unde se stabileşte diagnosticul de bronhopneumonie bazală pe dreapta S7…S10, perioada de reconvalescenţă şi se administrează augmentin concomitent cu metronidazol, endovenos. Persistenţa febrei şi a altor semne clinice caracteristice impun transferul pacientului pe 26.10.2012 la IMSP SCMBCC. According to the medical history, he fell ill a week ago (on 18.10.2012) with an acute onset (fever, rare dry cough, general weakness, fatigue). He is consulted by the family doctor who initiates the treatment with amoxicillin. On 21.10.2012, after a repeated consultation, in the absence of efficacy, the antibiotic was changed (to cefatoxime). Against the background of the administered therapy, the general condition does not improve, difficult nasal breathing with snoring occurs during sleep, polyadenopathy, pain in the abdomen. On 23.10.2012, he was admitted to the Municipal Clinical Hospital for Children no. 1, where the diagnosis of basal bronchopneumonia was established on the right S7...S10, the convalescence period and augmentin was administered simultaneously with metronidazole, intravenously. The persistence of fever and other characteristic clinical signs require the transfer of the patient on 26.10.2012 to IMSP SCMBCC.
La internare starea generală a copilului este apreciată ca fiind de gravitate medie. Examenul clinic constată: istm faringian hiperemiat difuz cu amigdalele palatine hipertrofiate de gr. II şi depuneri purulente în lacune bilateral; ganglionii limfatici submandibulari până la 1,8…2,5 cm, cervicali anteriori până la 1,5 cm, cervicali posteriori până la 1,0 cm, axilari până la 0,8 cm, inghinali până la 0,8 cm, indolori. Ficatul fiind apreciat cu +2,5; +3,0; +4,0 cm sub rebordul costal, elastic, indolor, iar splina cu +1,0 cm sub rebordul costal. At admission, the general condition of the child is assessed as being of medium severity. The clinical examination reveals: diffusely hyperemic pharyngeal isthmus with hypertrophied palatine tonsils of gr. II and purulent deposits in bilateral gaps; submandibular lymph nodes up to 1.8...2.5 cm, anterior cervical up to 1.5 cm, posterior cervical up to 1.0 cm, axillary up to 0.8 cm, inguinal up to 0.8 cm, painless. The liver being appreciated with +2.5; +3.0; +4.0 cm below the costal border, elastic, painless, and the spleen +1.0 cm below the costal border.
Pe parcursul spitalizării s-au efectuat următoarele investigaţii: During the hospitalization, the following investigations were carried out:
1) Hemoleucograma 1) Blood count
Data/valorile obţinute 27.10.2012 05.11.2012 Unităţi de măsură Hemoglobină 118 114 g/l Eritrocite 4,1 3,9 *1012/l Indice de culoare 0,86 0,88 Trombocite 241 313 *109/l Leucocite 17,5 9,4 *109/l Nesegmentate 0 0 % Segmentate 23 15 % Eozinofile 1 0 % Bazofile 0 0 % Limfocite 64 78 % Monocite 12 7 % Mononucleare atipice 11 0 VSH 25 10 mm/oră Date/values obtained 27.10.2012 05.11.2012 Units of measurement Hemoglobin 118 114 g/l Erythrocytes 4.1 3.9 *1012/l Color index 0.86 0.88 Platelets 241 313 *109/l Leukocytes 17.5 9.4 *109/l Unsegmented 0 0 % Segmented 23 15 % Eosinophils 1 0 % Basophils 0 0 % Lymphocytes 64 78 % Monocytes 12 7 % Atypical mononuclear cells 11 0 ESR 25 10 mm/hour
2) Urograma - în normă. 2) Urogram - normal.
3) Analiza maselor fecale la: ouă de helminţi - negativ, protozoare - negativ. 3) Analysis of faecal masses for: helminth eggs - negative, protozoa - negative.
4) Analiza biochimică a sângelui 4) Biochemical blood analysis
Data/valorile obţinute 27.10.2012 05.11.2012 Unităţi de măsură Ureea 2,9 - mmol/l Createnina 68,9 - mmol/l ALT 66,4 18,6 U/l AST 62,5 36,3 U/l Bilirubina totală 9,9 10,8 mcmol/l Bilirubina conjugată 0 0 mcmol/l Bilirubina liberă 9,9 10,8 mcmol/l Proba cu timol 3,1 - Un Glucoza 4,3 - mmol/l Amilaza 34,7 - U/l Fosfataza alcalină 639,3 373,5 U/l Date/values obtained 27.10.2012 05.11.2012 Units of measurement Urea 2.9 - mmol/l Creatine 68.9 - mmol/l ALT 66.4 18.6 U/l AST 62.5 36.3 U/l Bilirubin total 9.9 10.8 mcmol/l Conjugated bilirubin 0 0 mcmol/l Free bilirubin 9.9 10.8 mcmol/l Thymol sample 3.1 - Un Glucose 4.3 - mmol/l Amylase 34.7 - U /l Alkaline phosphatase 639.3 373.5 U/l
5) Examenul serologic la markeri cu EBV (27.12.2012) anti EBV VCA IgM - pozitiv, EA IgG - negativ, EBNA IgG - negativ. 5) Serological examination for EBV markers (27.12.2012) anti EBV VCA IgM - positive, EA IgG - negative, EBNA IgG - negative.
6) Picătura groasă la malarie (27.23.2012) - negativ. 6) Thick drop in malaria (27.23.2012) - negative.
7) Hemocultura (25.12.2012) N 232 - negativ. 7) Blood culture (25.12.2012) N 232 - negative.
8) Urocultura (27.12.2012) N 637 - negativ. 8) Uroculture (27.12.2012) N 637 - negative.
9) ECG (25.12.2012) Ritmul sinuzal regulat. Axa electrică verticală. Semne de modificări de repolarizare a ventriculului stâng. 9) ECG (25.12.2012) Regular sinus rhythm. Vertical electrical axis. Signs of left ventricular repolarization changes.
10) Ecografia abdomenului a determinat hepatosplenomegalie moderată cu modificări difuze în parenchim. 10) Ultrasound of the abdomen determined moderate hepatosplenomegaly with diffuse changes in the parenchyma.
Ca rezultat al tratamentului starea generală a devenit satisfăcătoare. Febra a persistat 10 zile. Ganglionii limfatici submandibulari fiind apreciaţi măriţi la externare, cu dimensiuni până la 0,8 cm, cervicali anteriori până la 0,7 cm, cervicali posteriori până la 0,7 cm, axilari până la 0,5 cm, inghinali până la 0,5 cm, indolori. Ficatul proemină cu +2; +2,5; +2,5 cm sub rebordul costal, elastic, indolor. Splina nu se palpează. Pe parcursul spitalizării pacientul a primit: tratament de bază, inclusiv regimul igieno-dietetic, terapia cu antibiotice (ceftriaxon 600 mg de 2 ori pe zi, timp de 7 zile, i/m) şi hepatoprotectoare (ursofalc 150 mg per os, timp de 10 zile). I s-a administrat Pacovirină per os 50 mg x 2 ori pe zi, cu continuarea tratamentului în condiţii de ambulator, timp de 1 lună sub supravegherea medicului de familie şi a infecţionistului. Peste o lună de la iniţierea tratamentului cu Pacovirină nivelul leucocitelor (5,6*109/l) şi al limfocitelor (în 45%) au revenit la normă. Valorile aminotransferazelor se menţineau în normă: ALAT - 23,2 U/l; ASAT - 31,3 U/l. Dimensiunile ficatului, spre finele tratamentului, depăşeau rebordul costal cu 1,0; +1,5; +1,5 cm. Pe parcursul tratamentului reacţii adverse la Pacovirină nu s-au constatat. As a result of the treatment the general condition became satisfactory. The fever persisted for 10 days. The submandibular lymph nodes were estimated to be enlarged at discharge, with sizes up to 0.8 cm, anterior cervical up to 0.7 cm, posterior cervical up to 0.7 cm, axillary up to 0.5 cm, inguinal up to 0.5 cm, painful. Liver protrudes +2; +2.5; +2.5 cm below the costal edge, elastic, painless. The spleen is not palpable. During the hospitalization, the patient received: basic treatment, including the hygienic-dietary regimen, antibiotic therapy (ceftriaxone 600 mg 2 times a day, for 7 days, i/m) and hepatoprotective (ursofalc 150 mg per bone, for 10 days). He was administered Pacovirine per os 50 mg x 2 times a day, with the continuation of the treatment in outpatient conditions, for 1 month under the supervision of the family doctor and the infectious disease specialist. More than a month after starting treatment with Pacovirine, the level of leukocytes (5.6*109/l) and lymphocytes (in 45%) returned to normal. Aminotransferase values remained normal: ALAT - 23.2 U/l; SAT - 31.3 U/l. The dimensions of the liver, towards the end of the treatment, exceeded the costal border by 1.0; +1.5; +1.5 cm. No adverse reactions to Pacovirine were observed during the treatment.
Exemplul 2 Example 2
Pacienta C., 3 ani, a fost internată la a 3-a zi de la debutul bolii în IMSP SCMBCC secţia nr. 4 pe perioada 26.10.2012…06.11.2012 cu diagnosticul clinic de: mononucleoză infecţioasă provocată de virusul Epstein-Barr (primoinfecţie), gravitate medie. Hepatită mononucleozică. Pielonefrită bilaterală acută. Cardiopatie toxiinfecţioasă. Patient C., 3 years old, was hospitalized on the 3rd day after the onset of the disease in IMSP SCMBCC ward no. 4 during the period 26.10.2012…06.11.2012 with the clinical diagnosis of: infectious mononucleosis caused by the Epstein-Barr virus (primary infection), medium severity. Hepatitis mononucleosis. Acute bilateral pyelonephritis. Toxic infectious cardiopathy.
La secţia de internare prezenta acuze la: febră până la 38,2°C, odinofagie, respiraţie nazală dificilă, forăit, tumefierea tuturor ganglionilor limfatici, hiporexie, slăbiciune generală, fatigabilitate. At the hospitalization department, he presented complaints of: fever up to 38.2°C, odynophagia, difficult nasal breathing, wheezing, swelling of all lymph nodes, hyporexia, general weakness, fatigue.
Pacientul s-a îmbolnăvit pe 24.10.2012 cu febră, odinofagie. După consultaţia medicului de familie s-a iniţiat terapia cu zimax, dar starea generală nu se ameliora, febra persista. Pe 26.10.2012, după consultaţia chirurgului maxilo-facial, care a exclus limfadenita cervicală purulentă, se spitalizează în IMSP SCMBCC. The patient fell ill on 24.10.2012 with fever, odynophagia. After consultation with the family doctor, Zimax therapy was initiated, but the general condition did not improve, the fever persisted. On 26.10.2012, after consultation with the maxillofacial surgeon, who ruled out purulent cervical lymphadenitis, he was hospitalized in IMSP SCMBCC.
La internare starea generală a copilului este apreciată de gravitate medie. Examenul clinic denotă hiperemia istmului farigian cu amigdalele palantine hipertrofiate de gr. III şi depuneri purulente în lacune bilateral; ganglionii limfatici submandibulari până la 2,5…2,8 cm, cervicali anteriori până la 1,9 cm, cervicali posteriori până la 1,5 cm, axilari până la 0,8 cm, inghinali până la 0,8 cm, în lanţ, indolori. Ficatul fiind apreciat cu +4,0+4,5+4,5 cm sub rebordul costal, elastic, indolor, iar splina cu +4,0 cm sub rebordul costal. At admission, the general condition of the child is rated as medium serious. The clinical examination shows hyperemia of the pharyngeal isthmus with hypertrophied palantine tonsils of gr. III and purulent deposits in bilateral gaps; submandibular lymph nodes up to 2.5...2.8 cm, anterior cervical up to 1.9 cm, posterior cervical up to 1.5 cm, axillary up to 0.8 cm, inguinal up to 0.8 cm, in a chain , painful. The liver being appreciated +4.0+4.5+4.5 cm below the costal border, elastic, painless, and the spleen +4.0 cm below the costal border.
Pe parcursul spitalizării s-au efectuat următoarele investigaţii During the hospitalization, the following investigations were carried out
1) Hemoleucograma 1) Blood count
Data/valorile obţinute 27.10.2012 05.1.2012 Unităţi de măsură Hemoglobină 110 116 g/l Eritrocite 3,9 4,1 *1012/L Indice de culoare 0,85 0,85 Trombocite 158 194 *109/l Leucocite 15,6 13,5 *109/l Nesegmentate 0 0 % Segmentate 31 26 % Eozinofile 0 0 % Bazofile 0 0 % Limfocite 51 64 % Monocite 18 10 % Mononucleare atipice 15 0 VSH 37 18 mm/oră Date/values obtained 27.10.2012 05.1.2012 Units of measurement Hemoglobin 110 116 g/l Erythrocytes 3.9 4.1 *1012/L Color index 0.85 0.85 Platelets 158 194 *109/l Leukocytes 15.6 13.5 *109/l Unsegmented 0 0 % Segmented 31 26 % Eosinophils 0 0 % Basophils 0 0 % Lymphocytes 51 64 % Monocytes 18 10 % Atypical mononuclear cells 15 0 ESR 37 18 mm/hour
2) Urograma 2) Urogram
Data Densit. Reacţ. Trans. Prot. Acet. Epit. Leuc. Erit. Cilin. Muc. Săr. 27.10 1010 Alcal Tran 0 0 1-3 6-8 0 0 0 0 Date Dense. React. Trans. Prot. This. Epit. Leuc. Erith. Cylin. Mucus. I jump. 27.10 1010 Alcal Tran 0 0 1-3 6-8 0 0 0 0
3) Urina după Neciporenco 3) Urine after Neciporenco
Data/valorile obţinute 29.10.2012 Unităţi de măsură Leucocite 800 mm3 Eritrocite 1000 mm3 Cilin. 0 mm3 Date/values obtained 29.10.2012 Units of measurement Leukocytes 800 mm3 Erythrocytes 1000 mm3 Cylin. 0 mm3
4) Analiza maselor fecale la: ouă de helminţi - negativ, protozoare - negativ. 4) Analysis of faecal masses for: helminth eggs - negative, protozoa - negative.
5) Analiza biochimică a sângelui: 5) Biochemical blood analysis:
Data/valorile obţinute 27.10.2012 05.11.2012 Unităţi de măsură Ureea 3,8 - mmol/l Createnina 88,2 - mmol/l ALAT 87,1 39,7 U/l ASAT 96,4 36,5 U/l Bilirubina totală 9,6 7,2 mcmol/l Bilirubina conjugată 0 0 mcmol/l Bilirubina liberă 9,6 7,2 mcmol/l Proba cu timol 3,0 - Un Glucoza 10,2 3,18 mmol/l γGTP 28,9 15,5 U/l β lipoproteina 41,0 - Un Fosfataza alcalină 620,7 460,8 U/l Date/values obtained 27.10.2012 05.11.2012 Units of measurement Urea 3.8 - mmol/l Creatine 88.2 - mmol/l ALAT 87.1 39.7 U/l SAT 96.4 36.5 U/l Bilirubin total 9.6 7.2 mcmol/l Conjugated bilirubin 0 0 mcmol/l Free bilirubin 9.6 7.2 mcmol/l Thymol sample 3.0 - One Glucose 10.2 3.18 mmol/l γGTP 28.9 15.5 U/l β lipoprotein 41.0 - Un Alkaline phosphatase 620.7 460.8 U/l
6) Examenul serologic la markeri cu EBV (27.23.2012) anti EBV VCA IgM - pozitiv, EA IgG - negativ, EBNA IgG - pozitiv. 6) Serological examination for EBV markers (27.23.2012) anti EBV VCA IgM - positive, EA IgG - negative, EBNA IgG - positive.
7) ECG (25.12.2012) Ritmul sinuzal neregulat. Axa electrică verticală. Suprasolicitarea miocardului ventriculului. Semne de modificări de repolarizare a ventriculului stâng. 7) ECG (25.12.2012) Irregular sinus rhythm. Vertical electrical axis. Overstrain of the myocardium of the ventricle. Signs of left ventricular repolarization changes.
8) USG abdominală (01.11.2012) Hepatomegalie. Pancreatită reactivă. Suspecţie la pielonefrită bilaterală S>D. 8) Abdominal USG (01.11.2012) Hepatomegaly. Reactive pancreatitis. Suspicion of bilateral pyelonephritis S>D.
Se externează în stare satisfăcătoare. Dimensiunile ganglionilor limfatici submandibulari până la 1,1 cm, cervicali anteriori până la 0,9 cm, cervicali posteriori până la 0,7 cm, axilari până la 0,5 cm, inghinali până la 0,5 cm, indolori. Ficatul se palpa cu +3,0; +3,5; +3,5 cm sub rebordul costal, elastic, indolor, iar splina cu +2,5 cm, elastică, indoloră. He is discharged in satisfactory condition. The sizes of submandibular lymph nodes up to 1.1 cm, anterior cervical up to 0.9 cm, posterior cervical up to 0.7 cm, axillary up to 0.5 cm, inguinal up to 0.5 cm, painless. The liver is palpated with +3.0; +3.5; +3.5 cm below the rib cage, elastic, painless, and the spleen +2.5 cm, elastic, painless.
Tratamentul în staţionar a inclus: regim de salon pe toată perioada, regim dietetic, antibiotice (cefotaxim 500 mg de 2 ori pe zi timp de 7 zile, i/m), hormoni (sol. Dexametazon 4 mg/zi, timp de 2 zile, i/m), hepatoprotectoare (ursofalc 150 mg, per os, timp de 10 zile). Pacovirina s-a indicat per os câte 50 mg x 2 ori pe zi, tratamentul fiind prelungit ambulator timp de 1 lună sub supravegherea medicului de familie şi a infecţionistului. La o lună după iniţierea tratamentului cu Pacovirină valorile leucocitelor (7,9٭109/l) se normalizează, iar nivelul limfocitelor a constituit 47%, ceea ce corespunde normei fiziologice conform vârstei. Nivelul de ALAT (18,6 U/l) şi ASAT (21,5 U/l) fiind în limitele normei. Ficatul în catamneză se apreciază cu 1,0; +1,0; +1,5 cm sub rebordul costal. Splina nu se palpează. Pe parcursul tratamentului reacţii adverse la Pacovirină nu au fost constatate. Inpatient treatment included: salon regimen throughout the period, dietary regimen, antibiotics (cefotaxime 500 mg 2 times a day for 7 days, i/m), hormones (sol. Dexamethasone 4 mg/day, for 2 days , i/m), hepatoprotective (ursofalc 150 mg, per os, for 10 days). Pacovirin was indicated per os 50 mg x 2 times a day, the treatment being extended on an outpatient basis for 1 month under the supervision of the family doctor and the infectious disease specialist. One month after starting treatment with Pacovirine, the leukocyte values (7.9٭109/l) normalized, and the lymphocyte level was 47%, which corresponds to the physiological norm according to age. The level of ALT (18.6 U/l) and AST (21.5 U/l) being within the norm. The liver in catamanesis is appreciated with 1.0; +1.0; +1.5 cm below the costal edge. The spleen is not palpable. No adverse reactions to Pacovirine were observed during the treatment.
1. Rusu Galina, Galeţchi Axenia, Popovici Parascovia. Boli infecţioase la copii. Chişinău, 2012, p. 131-138 1. Rusu Galina, Galetchi Axenia, Popovici Parascovia. Infectious diseases in children. Chisinau, 2012, p. 131-138
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| MD1875G2 (en) * | 1999-11-01 | 2002-09-30 | Национальный Научно-Практический Центр Превентивной Медицины Министерства Здравоохранения Республики Молдова | Method of treatment of the acute viral hepatitis B |
| MD2068G2 (en) * | 2001-07-10 | 2003-06-30 | Национальный Научно-Практический Центр Превентивной Медицины Министерства Здравоохранения Республики Молдова | Method of treatment of the Herpes simplex infection |
| MD2549G2 (en) * | 2003-07-18 | 2005-08-31 | Национальный Научно-Практический Центр Превентивной Медицины Министерства Здравоохранения Республики Молдова | Method of treatment of the chronic viral hepatitis C |
| MD596Y (en) * | 2012-10-09 | 2013-02-28 | Ct Nat De Sanatate Publica Al Ministerului Sanatatii Al Republicii Moldova | Method for treating the chronic viral hepatitis C |
| MD4177C1 (en) * | 2011-01-14 | 2013-02-28 | Национальный Центр Общественного Здоровья Министерства Здравоохранения Республики Молдова | Method for vaccination against hepatitis B of persons with immunodeficiency |
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| MD1875G2 (en) * | 1999-11-01 | 2002-09-30 | Национальный Научно-Практический Центр Превентивной Медицины Министерства Здравоохранения Республики Молдова | Method of treatment of the acute viral hepatitis B |
| MD2068G2 (en) * | 2001-07-10 | 2003-06-30 | Национальный Научно-Практический Центр Превентивной Медицины Министерства Здравоохранения Республики Молдова | Method of treatment of the Herpes simplex infection |
| MD2549G2 (en) * | 2003-07-18 | 2005-08-31 | Национальный Научно-Практический Центр Превентивной Медицины Министерства Здравоохранения Республики Молдова | Method of treatment of the chronic viral hepatitis C |
| MD4177C1 (en) * | 2011-01-14 | 2013-02-28 | Национальный Центр Общественного Здоровья Министерства Здравоохранения Республики Молдова | Method for vaccination against hepatitis B of persons with immunodeficiency |
| MD596Y (en) * | 2012-10-09 | 2013-02-28 | Ct Nat De Sanatate Publica Al Ministerului Sanatatii Al Republicii Moldova | Method for treating the chronic viral hepatitis C |
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