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  1. Article ; Online: Pediatric Acute-on-Chronic Liver Failure.

    Alam, Seema / Lal, Bikrant Bihari

    Indian journal of pediatrics

    2023  Volume 91, Issue 4, Page(s) 374–382

    Abstract: Acute-on-chronic liver failure (ACLF) is characterized by an acute hepatic insult happening in a patient with underlying cirrhosis with compromised hepatic reserve leading to development of systemic inflammation, sepsis, and organ failure resulting in ... ...

    Abstract Acute-on-chronic liver failure (ACLF) is characterized by an acute hepatic insult happening in a patient with underlying cirrhosis with compromised hepatic reserve leading to development of systemic inflammation, sepsis, and organ failure resulting in poor outcome in majority. While Asia Pacific Association for Study of Liver Diseases (APASL) emphasizes on early diagnosis before development of organ failure, European Association for Study of Liver Diseases (EASL) mandates the presence of organ failures to define ACLF. There is a lack of consensus definition of pediatric ACLF although recent APASL guidelines have tried to address the issue. While Wilson disease (WD) and autoimmune hepatitis (AIH) are the most common cause of underlying cirrhosis in children, acute viral hepatitis and flares of WD and AIH are the commonest acute precipitating events. Poor outcomes [death and liver transplantation (LT)] ranging from 19 to 59% have been reported. Prognosis in pediatric ACLF is usually better than that in adults due to greater proportion of treatable etiologies, lesser organ failures, comorbidities and better hepatic reserves. APASL ACLF Research Consortium (AARC) score more than or equal to 11 is predictive of poor 28-90 d mortality. Treatment of pediatric ACLF relies mainly on prompt diagnosis and medical management of a potentially treatable etiology of underlying cirrhosis. Bridging therapies, especially high volume plasma exchange can be initiated early as a bridge to LT or native liver recovery. Those with no improvement in 4-7 d should undergo LT before development of sepsis or multi-organ failure.
    MeSH term(s) Adult ; Humans ; Child ; Acute-On-Chronic Liver Failure/diagnosis ; Acute-On-Chronic Liver Failure/etiology ; Liver Cirrhosis/complications ; Liver Transplantation/adverse effects ; Liver Transplantation/methods ; Multiple Organ Failure ; Prognosis ; Sepsis
    Language English
    Publishing date 2023-06-22
    Publishing country India
    Document type Journal Article ; Review
    ZDB-ID 218231-2
    ISSN 0973-7693 ; 0019-5456
    ISSN (online) 0973-7693
    ISSN 0019-5456
    DOI 10.1007/s12098-023-04717-3
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Change in antibiotic regimen for emerging multidrug resistance in nosocomial ascitic fluid infection.

    Alam, Seema

    Hepatology international

    2019  Volume 14, Issue 1, Page(s) 1–4

    MeSH term(s) Anti-Bacterial Agents/therapeutic use ; Ascitic Fluid/microbiology ; Bacterial Infections/diagnosis ; Bacterial Infections/drug therapy ; Bacterial Infections/microbiology ; Cross Infection/diagnosis ; Cross Infection/drug therapy ; Cross Infection/microbiology ; Drug Resistance, Multiple, Bacterial ; Humans ; Peritonitis/diagnosis ; Peritonitis/drug therapy ; Peritonitis/microbiology
    Chemical Substances Anti-Bacterial Agents
    Keywords covid19
    Language English
    Publishing date 2019-11-21
    Publishing country United States
    Document type Editorial
    ZDB-ID 2270316-0
    ISSN 1936-0541 ; 1936-0533
    ISSN (online) 1936-0541
    ISSN 1936-0533
    DOI 10.1007/s12072-019-10000-5
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Longitudinal Extensive Transverse Myelitis in a Four-Year-Old Boy Liver Transplant Recipient.

    Koul, Roshan / Thapar, Shalini / Khanna, Rajeev / Alam, Seema

    Sultan Qaboos University medical journal

    2023  Volume 23, Issue 3, Page(s) 421–422

    MeSH term(s) Male ; Humans ; Child, Preschool ; Liver Transplantation ; Myelitis, Transverse/diagnosis ; Myelitis, Transverse/etiology
    Language English
    Publishing date 2023-08-28
    Publishing country Oman
    Document type Case Reports ; Journal Article
    ZDB-ID 2650196-X
    ISSN 2075-0528 ; 2075-0528
    ISSN (online) 2075-0528
    ISSN 2075-0528
    DOI 10.18295/squmj.5.2023.023
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Iodoxybenzoic Acid (IBX) in Organic Synthesis: A Septennial Review.

    Varala, Ravi / Seema, Vittal / Alam, Mohammed Mujahid / Dubasi, Narsimhaswamy / Vummadi, Rama Devi

    Current organic synthesis

    2023  

    Abstract: This study reviews the oxidative applications of 2-iodoxybenzoic acid (IBX) in organic synthesis, focusing on C-H functionalization, hetero-hetero bond formations, ring cleavage reactions, dehydrogenation, heterocyclic ring formations, and some ... ...

    Abstract This study reviews the oxidative applications of 2-iodoxybenzoic acid (IBX) in organic synthesis, focusing on C-H functionalization, hetero-hetero bond formations, ring cleavage reactions, dehydrogenation, heterocyclic ring formations, and some miscellaneous reactions in a comprehensive and critical way. It compiles the literature starting from mid-2015 to date.
    Language English
    Publishing date 2023-10-12
    Publishing country United Arab Emirates
    Document type Journal Article
    ISSN 1570-1794
    ISSN 1570-1794
    DOI 10.2174/0115701794263252230924074035
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Change in antibiotic regimen for emerging multidrug resistance in nosocomial ascitic fluid infection

    Alam, Seema

    Hepatology international

    Abstract: The Liver Transplant Society of India (LTSI) has come up with guidelines for transplant centres across the country to deal with liver transplantation during this evolving pandemic of COVID-19 infection The guidelines are applicable to both deceased donor ...

    Abstract The Liver Transplant Society of India (LTSI) has come up with guidelines for transplant centres across the country to deal with liver transplantation during this evolving pandemic of COVID-19 infection The guidelines are applicable to both deceased donor as well as living donor liver transplants In view of the rapidly changing situation of COVID-19 infection in India and worldwide, these guidelines will need to be updated according to the emerging data
    Keywords covid19
    Publisher WHO
    Document type Article
    Note WHO #Covidence: #820190
    Database COVID19

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  6. Article ; Online: Prognostication in Pediatric Acute Liver Failure Using CHALF Score-"Perspective From the Opposite Shore".

    Yadav, Deepika / Lal, Bikrant Bihari / Sood, Vikrant / Khanna, Rajeev / Alam, Seema

    Transplantation

    2024  Volume 108, Issue 4, Page(s) e64–e65

    MeSH term(s) Child ; Humans ; Liver Failure, Acute/diagnosis
    Language English
    Publishing date 2024-03-23
    Publishing country United States
    Document type Letter
    ZDB-ID 208424-7
    ISSN 1534-6080 ; 0041-1337
    ISSN (online) 1534-6080
    ISSN 0041-1337
    DOI 10.1097/TP.0000000000004935
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Recent updates on progressive familial intrahepatic cholestasis types 1, 2 and 3: Outcome and therapeutic strategies.

    Alam, Seema / Lal, Bikrant Bihari

    World journal of hepatology

    2021  Volume 14, Issue 1, Page(s) 98–118

    Abstract: Recent evidence points towards the role of genotype to understand the phenotype, predict the natural course and long term outcome of patients with progressive familial intrahepatic cholestasis (PFIC). Expanded role of the heterozygous transporter defects ...

    Abstract Recent evidence points towards the role of genotype to understand the phenotype, predict the natural course and long term outcome of patients with progressive familial intrahepatic cholestasis (PFIC). Expanded role of the heterozygous transporter defects presenting late needs to be suspected and identified. Treatment of pruritus, nutritional rehabilitation, prevention of fibrosis progression and liver transplantation (LT) in those with end stage liver disease form the crux of the treatment. LT in PFIC has its own unique issues like high rates of intractable diarrhoea, growth failure; steatohepatitis and graft failure in PFIC1 and antibody-mediated bile salt export pump deficiency in PFIC2. Drugs inhibiting apical sodium-dependent bile transporter and adenovirus-associated vector mediated gene therapy hold promise for future.
    Language English
    Publishing date 2021-12-15
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2573703-X
    ISSN 1948-5182
    ISSN 1948-5182
    DOI 10.4254/wjh.v14.i1.98
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Relapse following withdrawal of D-penicillamine from combination (D-penicillamine + zinc) therapy in hepatic Wilson disease.

    Panda, Kalpana / Lal, Bikrant B / Sood, Vikrant / Khanna, Rajeev / Alam, Seema

    Journal of pediatric gastroenterology and nutrition

    2024  Volume 78, Issue 5, Page(s) 1017–1026

    Abstract: Objectives: Long-term D-penicillamine (D-pen) therapy in Wilson disease (WD) has numerous adverse effects which advocates its withdrawal, but with an inherent risk of relapse. This prospective observational study was conducted with the objective of ... ...

    Abstract Objectives: Long-term D-penicillamine (D-pen) therapy in Wilson disease (WD) has numerous adverse effects which advocates its withdrawal, but with an inherent risk of relapse. This prospective observational study was conducted with the objective of evaluating incidence of relapse following withdrawal of D-pen from combination (D-pen + zinc) therapy in maintenance phase of previously symptomatic hepatic WD.
    Methods: Hepatic WD patients <18 years of age and on combination therapy for >2 years with 6 months of biochemical remission were included. Biochemical remission was defined as achievement of (i) aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤1.5 times upper limit of normal (ULN), (ii) serum albumin >3.5 g/dL, international normalized ratio (INR) <1.5 and (iii) 24-h urinary copper excretion (UCE) <500 mcg/day, nonceruloplasmin-bound-copper (NCC) <15 mcg/dL. After D-pen withdrawal, monthly liver function test (LFT) and INR and 3 monthly UCE and NCC were done till 1 year or relapse (elevation of AST/ALT/both >2 times ULN or total bilirubin >2 mg/dL), whichever occurred earlier.
    Results: Forty-five patients enrolled with median combination therapy duration of 36 months. Sixty percent of them had their index presentation as decompensated cirrhosis. Fourteen patients (31.8%) relapsed (cumulative incidence: 4 at 3 months, 11 at 6 months, and 14 at 12 months after D-pen discontinuation). All relapsers had index presentation as decompensated cirrhosis. On Cox-regression, ALT at D-pen withdrawal was an independent predictor of relapse (hazard ratio [HR]: 1.077, 95% confidence interval [CI]: 1.014-1.145, p = 0.017) with area under the receiver operating characteristic (AUROC) of 0.860. ALT ≥40 U/L predicted risk of relapse with 85.7% sensitivity, 70.9% specificity.
    Conclusion: Incidence of relapse after withdrawal of D-pen from combination therapy is 31.8% in hepatic WD. ALT ≥40 U/L, at the time of D-pen stoppage, predicts future relapse.
    MeSH term(s) Humans ; Hepatolenticular Degeneration/drug therapy ; Penicillamine/therapeutic use ; Penicillamine/administration & dosage ; Female ; Male ; Recurrence ; Prospective Studies ; Adolescent ; Child ; Drug Therapy, Combination ; Chelating Agents/therapeutic use ; Chelating Agents/administration & dosage ; Alanine Transaminase/blood ; Aspartate Aminotransferases/blood ; Zinc/administration & dosage ; Zinc/therapeutic use ; Liver Function Tests/methods ; Copper/blood ; Withholding Treatment
    Chemical Substances Penicillamine (GNN1DV99GX) ; Chelating Agents ; Alanine Transaminase (EC 2.6.1.2) ; Aspartate Aminotransferases (EC 2.6.1.1) ; Zinc (J41CSQ7QDS) ; Copper (789U1901C5)
    Language English
    Publishing date 2024-01-23
    Publishing country United States
    Document type Journal Article ; Observational Study
    ZDB-ID 603201-1
    ISSN 1536-4801 ; 0277-2116
    ISSN (online) 1536-4801
    ISSN 0277-2116
    DOI 10.1002/jpn3.12128
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Rare case of corneal keloid following radial keratotomy for myopia.

    Gupta, Noopur / Khan, Tanveer Alam / Jhajharia, Hemant / Kashyap, Seema

    BMJ case reports

    2023  Volume 16, Issue 7

    Abstract: An adult male in his 50s presented with complaints of glare and gradual, painless, progressive diminution of vision in the right eye (RE). Visual acuity in RE was noted to be 2/60, and slit lamp biomicroscopy revealed a pearly grey-white elevated corneal ...

    Abstract An adult male in his 50s presented with complaints of glare and gradual, painless, progressive diminution of vision in the right eye (RE). Visual acuity in RE was noted to be 2/60, and slit lamp biomicroscopy revealed a pearly grey-white elevated corneal opacity measuring 4 mm × 3 mm, obscuring the visual axis. There was no history of ocular trauma or infection. The patient had undergone bilateral radial keratotomy for myopia correction 25 years ago. Anterior segment optical coherence tomography imaging demonstrated increased corneal thickness of 1080 µm at the site of lesion and the height of the epicorneal mass was noted to be 493 µm. The patient underwent fibrin glue-aided anterior lamellar keratoplasty. Histopathological examination of the excised host tissue confirmed the diagnosis of corneal keloid.
    MeSH term(s) Adult ; Humans ; Male ; Keratotomy, Radial/adverse effects ; Keloid/etiology ; Keloid/surgery ; Keloid/diagnosis ; Corneal Diseases/pathology ; Eye Injuries/surgery ; Myopia/surgery ; Vision Disorders/surgery ; Connective Tissue Diseases
    Language English
    Publishing date 2023-07-18
    Publishing country England
    Document type Case Reports ; Journal Article
    ISSN 1757-790X
    ISSN (online) 1757-790X
    DOI 10.1136/bcr-2022-252776
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Alert: Not All Acute Hepatitis with Raised INR is Acute Liver Failure!

    Kaur, Prabhsaran / Lal, Bikrant Bihari / Sood, Vikrant / Khanna, Rajeev / Alam, Seema

    Indian journal of pediatrics

    2023  Volume 90, Issue 7, Page(s) 732

    MeSH term(s) Humans ; International Normalized Ratio ; Hepatitis ; Liver Failure, Acute ; Acute Disease
    Language English
    Publishing date 2023-04-19
    Publishing country India
    Document type Letter
    ZDB-ID 218231-2
    ISSN 0973-7693 ; 0019-5456
    ISSN (online) 0973-7693
    ISSN 0019-5456
    DOI 10.1007/s12098-023-04602-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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