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1.
Afr Health Sci ; 24(1): 145-150, 2024 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-38962350

RESUMEN

Background: Antenatal corticosteroids (ACS) are given to pregnant women at risk of preterm delivery to hasten the maturation of the lungs, lowering the risk of newborn respiratory distress syndrome (RDS) and perinatal mortality. Objective: The aim of this study was to determine whether exposure to ACS was associated with lower rates of perinatal mortality and RDS in preterm infants delivered by women with preterm labour. Methods: This is a secondary analysis of data from four hospitals in Mwanza, Tanzania. All singletons and twins born to women who were in preterm labour between July 2019 and February 2020 and delivered in-hospital between 24 and 34 weeks of gestation were included. Data were recorded from participants' medical records and analysed using STATA Version 14. Results: Over an eight-month period, 588 preterm infants were delivered to 527 women. One hundred and ninety (36.1%) women were given ACS. Infants who were exposed to ACS in utero had a lower rate of perinatal mortality (6.8% vs 19.1%) and RDS (12.3% vs 25.9%) compared to those not exposed to ACS. In adjusted multivariable models, ACS exposure was related to a lower risk of perinatal mortality, aRR 0.23 (95% CI 0.13 - 0.39), and RDS, aRR 0.45 (95% CI 0.30 - 0.68). Conclusion: ACS significantly reduced the risk of perinatal mortality and RDS among preterm infants exposed to ACS in utero and delivered by women in preterm labour. The use of ACS should be encouraged in low-resource settings where preterm birth is prevalent to improve perinatal outcomes.


Asunto(s)
Corticoesteroides , Trabajo de Parto Prematuro , Mortalidad Perinatal , Atención Prenatal , Síndrome de Dificultad Respiratoria del Recién Nacido , Humanos , Femenino , Embarazo , Tanzanía/epidemiología , Trabajo de Parto Prematuro/prevención & control , Recién Nacido , Síndrome de Dificultad Respiratoria del Recién Nacido/prevención & control , Síndrome de Dificultad Respiratoria del Recién Nacido/epidemiología , Adulto , Corticoesteroides/administración & dosificación , Corticoesteroides/uso terapéutico , Atención Prenatal/métodos , Recien Nacido Prematuro , Edad Gestacional , Nacimiento Prematuro/prevención & control , Nacimiento Prematuro/epidemiología , Adulto Joven
2.
Afr Health Sci ; 24(1): 220-227, 2024 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-38962356

RESUMEN

Background: The implementation of surfactant for respiratory syndrome approbates the therapy as a revolutionary method in intensive neonatal therapy and respiratory resuscitation. It is important to investigate the costs of this treatment. Objective: The aim of the study is to analyze the data by the application of the surfactant Curosurf to preterm babies with respiratory complications and describe the treatment costs, healthcare resource utilization and evaluate economic benefits of surfactant use in the treatment of neonates with respiratory distress syndrome (RDS) and hyaline-membrane disease (HDM). Methods: A retrospective survey was performed covering 167 babies based on respiratory complications due to preterm birth and the necessity to apply a surfactant therapy. A documentary method was implemented and for each patient, an individual research protocol was filled out - a questionnaire created specifically for the purposes of the study. Results and discussion: An analysis of the data from the application of CUROSURF was made and the obtained therapeutic results were compared to expenditures for the therapy, short-term therapeutic effect, benefits and consequences of the therapy of preterm newborns with respiratory complications. The application of CUROSURF to babies with RDS resulted in the realization of net savings due to the elimination of the necessity of conducting several diagnostic and therapeutic procedures as well as their duration reduction of hospital stay, thus defining its health-economic benefits. Conclusions: The models of evaluation of cost effectiveness reveal that the medicinal product is expensive but effective from the aspect of short-term therapeutic results.


Asunto(s)
Análisis Costo-Beneficio , Recien Nacido Prematuro , Surfactantes Pulmonares , Síndrome de Dificultad Respiratoria del Recién Nacido , Humanos , Recién Nacido , Síndrome de Dificultad Respiratoria del Recién Nacido/tratamiento farmacológico , Síndrome de Dificultad Respiratoria del Recién Nacido/economía , Estudios Retrospectivos , Surfactantes Pulmonares/administración & dosificación , Femenino , Masculino , Enfermedad de la Membrana Hialina/tratamiento farmacológico , Fosfolípidos/administración & dosificación , Productos Biológicos
3.
Afr Health Sci ; 24(1): 91-93, 2024 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-38962355

RESUMEN

This case report describes a pregnant patient with recent diagnosis of Human Immuno-Deficiency Virus (HIV) infection initiated on Anti-Retroviral Therapy (ART) in the second trimester, as well as high dose acyclovir high for large infected genital warts. She had no other HIV related opportunistic infections, and no prior anti tuberculosis treatment or preventive medication. Despite little response to acyclovir, patient was continuing on acyclovir for over 4 months. She subsequently developed recurrent anemia requiring frequent transfusion (14 units in total) over a 6-week period. On stopping acyclovir, the anemia subsided, a few weeks later she had a normal delivery, followed by surgical removal of the warts. At a follow-up 8 months later, she was well, with a healthy baby, and reported no other episodes of blood transfusion.


Asunto(s)
Aciclovir , Anemia , Antivirales , Infecciones por VIH , Complicaciones Infecciosas del Embarazo , Recurrencia , Humanos , Femenino , Embarazo , Aciclovir/uso terapéutico , Aciclovir/efectos adversos , Aciclovir/administración & dosificación , Infecciones por VIH/tratamiento farmacológico , Infecciones por VIH/complicaciones , Complicaciones Infecciosas del Embarazo/tratamiento farmacológico , Antivirales/efectos adversos , Antivirales/uso terapéutico , Adulto , Uganda , Resultado del Tratamiento , Herpes Genital/tratamiento farmacológico , Transfusión Sanguínea
4.
Nagoya J Med Sci ; 86(2): 304-313, 2024 May.
Artículo en Inglés | MEDLINE | ID: mdl-38962412

RESUMEN

Radiotherapy combined with temozolomide (TMZ+RT) is the primary treatment for high-grade glioma. TMZ is classified as a moderate emetic risk agent and, thus, supportive care for nausea and vomiting is important. In Nagoya University Hospital, all patients are treated with a 5-hydroxy-tryptamine 3 receptor antagonist (5-HT3RA) for the first 3 days. The daily administration of 5-HT3RA is resumed after the 4th day based on the condition of patients during TMZ+RT. Therefore, the present study investigated risk factors for nausea and vomiting in patients requiring the daily administration of 5-HT3RA. Patients with high-grade glioma who received TMZ+RT between January 2014 and December 2019 at our hospital were included. Patients were divided into two groups: a control group (patients who did not resume 5-HT3RA) and resuming 5-HT3RA group (patients who resumed 5-HT3RA after the 4th day), and both groups were compared to identify risk factors for nausea and vomiting during TMZ+RT. There were 78 patients in the control group (68%) and 36 in the resuming 5-HT3RA group (32%). A multivariate analysis of patient backgrounds in the two groups identified age <18 years, PS 2 or more, and occipital lobe tumors as risk factors for nausea and vomiting. Nausea and vomiting were attenuated in 30 patients (83%) in the resuming 5-HT3RA group following the resumption of 5-HT3RA. The results obtained highlight the importance of extracting patients with these risk factors before the initiation of therapy and the early resumption or daily administration of 5-HT3RA according to the condition of each patient.


Asunto(s)
Glioma , Náusea , Antagonistas del Receptor de Serotonina 5-HT3 , Temozolomida , Vómitos , Humanos , Temozolomida/uso terapéutico , Temozolomida/administración & dosificación , Temozolomida/efectos adversos , Masculino , Antagonistas del Receptor de Serotonina 5-HT3/uso terapéutico , Antagonistas del Receptor de Serotonina 5-HT3/administración & dosificación , Femenino , Vómitos/inducido químicamente , Vómitos/tratamiento farmacológico , Persona de Mediana Edad , Glioma/tratamiento farmacológico , Glioma/radioterapia , Factores de Riesgo , Anciano , Neoplasias Encefálicas/tratamiento farmacológico , Neoplasias Encefálicas/radioterapia , Adulto , Antineoplásicos Alquilantes/uso terapéutico , Antineoplásicos Alquilantes/efectos adversos , Antineoplásicos Alquilantes/administración & dosificación , Quimioradioterapia/efectos adversos , Quimioradioterapia/métodos
5.
Nagoya J Med Sci ; 86(2): 345-350, 2024 May.
Artículo en Inglés | MEDLINE | ID: mdl-38962415

RESUMEN

Exercise induced anaphylaxis (EIA) is a rare and potentially life-threatening syndrome characterized by anaphylaxis provoked by exercise. Although vaginal delivery with labor pain is a physical strain for women and a possible trigger for EIA, no consensus exists on the management strategy of delivery in patients with EIA. A 28-year-old primigravida was referred to our hospital because of history of EIA, associated with pruritus, urticaria, and respiratory distress, exacerbated during physical activity. To avoid physical stress, we chose scheduled labor induction with epidural anesthesia, and administered prophylactic intravenous hydrocortisone. She delivered vaginally with no symptoms suggestive of EIA during labor. Since it is quite possible for patients with EIA to develop anaphylaxis during vaginal delivery with labor pain, epidural anesthesia and prophylactic steroid administration may be the most rational approaches for delivery in pregnant women with EIA.


Asunto(s)
Anafilaxia , Anestesia Epidural , Parto Obstétrico , Ejercicio Físico , Humanos , Femenino , Anafilaxia/etiología , Embarazo , Adulto , Anestesia Epidural/efectos adversos , Ejercicio Físico/fisiología , Hidrocortisona/administración & dosificación , Hidrocortisona/uso terapéutico , Alergias Inducidas por el Ejercicio
6.
Nagoya J Med Sci ; 86(2): 252-261, 2024 May.
Artículo en Inglés | MEDLINE | ID: mdl-38962419

RESUMEN

Until recently, the Thai national program of seasonal influenza vaccination for high-risk people has been using a walk-in service system. However, in 2020, an online registration system was introduced in Bangkok to improve vaccine coverage. This study aimed to compare the coverage of influenza vaccination between the walk-in service and online registration systems. The study participants included 374,710 Thai individuals who obtained an influenza vaccination from the national program in the Bangkok health region in 2018 (n = 162,214) and in 2020 (n = 212,496). The registration systems that were examined were the walk-in service system in 2018 and the online registration system in 2020. The characteristics of vaccine recipients and the vaccine coverage in each risk group and health facility level were compared between the two systems. Coverage comparison in Bangkok between the years 2018 and 2020 showed an increase in coverage, particularly among individuals who had an influenza vaccination at health facilities of the primary level and in the elderly and obesity groups. The coverage among children was lowest among all high-risk groups. To improve coverage in Thailand, the online registration system should be introduced in all regions. Additionally, information about influenza vaccination for children should be disseminated to parents using handbooks or by word-of-mouth from healthcare workers.


Asunto(s)
Vacunas contra la Influenza , Gripe Humana , Cobertura de Vacunación , Humanos , Tailandia , Vacunas contra la Influenza/uso terapéutico , Vacunas contra la Influenza/administración & dosificación , Masculino , Persona de Mediana Edad , Adulto , Femenino , Gripe Humana/prevención & control , Cobertura de Vacunación/estadística & datos numéricos , Niño , Anciano , Adolescente , Adulto Joven , Preescolar , Lactante , Vacunación/estadística & datos numéricos , Sistemas en Línea
7.
Nagoya J Med Sci ; 86(2): 333-340, 2024 May.
Artículo en Inglés | MEDLINE | ID: mdl-38962420

RESUMEN

To the best of our knowledge, this is the first case of pregnancy with a healthy baby after treatment with an oral gonadotropin-releasing hormone (GnRH) antagonist in women with premature ovarian insufficiency. A 36-year-old female presented at our hospital after being diagnosed with premature ovarian insufficiency by a previous doctor. We administered clomiphene, human menopausal gonadotropin (hMG), and GnRH antagonist (injection) together with estrogen replacement for 11 cycles (27 months), but no follicular development was observed. When the oral GnRH antagonist (relugolix), which has recently become available, was used in the 12th cycle, follicular growth of 13 mm was confirmed on the 14th day of stimulation. After stimulation, the use of hMG and GnRH antagonist (injection) was continued, and a maturation trigger, human chorionic gonadotropin 10000 IU, was administered. Oocyte retrieval was performed successfully, intracytoplasmic sperm injection and frozen embryo transfer were performed, and fetal heartbeat was confirmed. The patient was admitted to the perinatal management facility. She delivered a healthy baby of 3,732 g via cesarean section at 41 weeks +2. This case shows the possibility of using an oral GnRH antagonist as an option for infertility treatment.


Asunto(s)
Hormona Liberadora de Gonadotropina , Insuficiencia Ovárica Primaria , Humanos , Femenino , Hormona Liberadora de Gonadotropina/antagonistas & inhibidores , Insuficiencia Ovárica Primaria/tratamiento farmacológico , Adulto , Embarazo , Administración Oral , Antagonistas de Hormonas/uso terapéutico , Antagonistas de Hormonas/administración & dosificación , Inducción de la Ovulación/métodos
8.
Digit J Ophthalmol ; 30(2): 33-37, 2024.
Artículo en Inglés | MEDLINE | ID: mdl-38962669

RESUMEN

Central retinal artery occlusion (CRAO), a type of acute retinal arterial ischemia, analogous to an ocular stroke, is a medical emergency that warrants immediate diagnosis and treatment. CRAO usually presents with sudden, painless, monocular vision loss. Ipsilateral carotid artery disease is an important associated finding in these patients. The primary limitation to effective treatment of CRAO is that patients are rarely seen in the acute stage. Moreover, there are no guidelines for effective treatment. We report a patient with right CRAO whose treatment with intravenous thrombolysis with tenecteplase and anterior chamber paracentesis with ocular massage resulted in a good clinical outcome.


Asunto(s)
Fibrinolíticos , Oclusión de la Arteria Retiniana , Tenecteplasa , Terapia Trombolítica , Humanos , Tenecteplasa/uso terapéutico , Tenecteplasa/administración & dosificación , Fibrinolíticos/uso terapéutico , Oclusión de la Arteria Retiniana/diagnóstico , Oclusión de la Arteria Retiniana/tratamiento farmacológico , Terapia Trombolítica/métodos , Enfermedad Aguda , Masculino , Activador de Tejido Plasminógeno/uso terapéutico , Activador de Tejido Plasminógeno/administración & dosificación , Isquemia/diagnóstico , Isquemia/tratamiento farmacológico , Persona de Mediana Edad , Angiografía con Fluoresceína/métodos , Femenino , Anciano
9.
Acta Chir Orthop Traumatol Cech ; 91(3): 151-155, 2024.
Artículo en Inglés | MEDLINE | ID: mdl-38963893

RESUMEN

PURPOSE OF THE STUDY: Our aim was to compare the effects of intraarticular and intravenous (IV) tranexemic acid (TXA) application on bleeding and complication rates in patients who underwent total knee arthroplasty (TKA). MATERIAL AND METHODS: Between 2017 and 2021, 406 patients who underwent TKA with 2 g of IV TXA and retrograde 1.5 g of TXA applied through the drain were included in the study. Of the patients, 206 were in the IV TXA group. Preoperative and postoperative hemoglobin levels, drain output, BMI, ASA score, blood loss, and the number of transfused patients were recorded. Complications such as symptomatic venous thromboembolism were also recorded. RESULTS: There was no significant difference between the two groups in terms of age, sex, American Society of Anesthesiologists (ASA) score, or BMI (p = 0.68, 0.54, 0.28, 0.45). Total drain output and blood loss were significantly higher in the IV TXA group than in the intraarticular TXA group (p < 0.0001, p < 0.0001). Eighteen patients in the IV TXA group and 1 patient in the intraarticular TXA group received a blood transfusion (p < 0.0001). There was no difference between the two groups in terms of preoperative hemoglobin or platelet count (p = 0.24). However, postoperative hemoglobin level was higher in the patients who received intraarticular TXA (p=0.0005). More thromboembolism events were seen in the IV TXA group (p < 0.0001). CONCLUSIONS: Intraarticular TXA application reduces blood loss more than IV application, reduces the blood transfusion rate, and causes fewer complications. KEY WORDS: tranexemic acid, total knee arthroplasty, intraarticular injection, blood loss, blood transfusion.


Asunto(s)
Antifibrinolíticos , Artroplastia de Reemplazo de Rodilla , Pérdida de Sangre Quirúrgica , Ácido Tranexámico , Humanos , Artroplastia de Reemplazo de Rodilla/métodos , Artroplastia de Reemplazo de Rodilla/efectos adversos , Femenino , Masculino , Ácido Tranexámico/administración & dosificación , Pérdida de Sangre Quirúrgica/prevención & control , Anciano , Inyecciones Intraarticulares , Antifibrinolíticos/administración & dosificación , Persona de Mediana Edad , Transfusión Sanguínea/estadística & datos numéricos , Administración Intravenosa , Hemorragia Posoperatoria/prevención & control , Hemorragia Posoperatoria/etiología , Constricción , Estudios Retrospectivos
10.
Acta Chir Orthop Traumatol Cech ; 91(3): 182-187, 2024.
Artículo en Inglés | MEDLINE | ID: mdl-38963898

RESUMEN

BACKGROUND: Adequate postoperative pain treatment is important for quality of life, patient satisfaction, rehabilitation, function, and total opioid consumption, and might lower both the risk of chronic postoperative pain and the costs for society. Prolonged opioid consumption is a well-known risk factor for addiction. Previous studies in upper extremity surgery have shown that total opioid consumption is a third of the amount prescribed, which can be explained by package size. The aim of this study was to examine whether implementation of prepacked takehome analgesia bags reduced the quantity of prescribed and dispensed opioids. MATERIAL AND METHODS: We introduced prepacked take-home analgesia bags for postoperative pain treatment in outpatient surgery. The bags came in two sizes, each containing paracetamol, etoricoxib, and oxycodone. The first 147 patients who received the prepacked analgesia bags were included in the study, and received a questionnaire one month after surgery covering self-assessed pain (visual analog scale of 0-10) and satisfaction (0-5), as well as opioid consumption. Prescription data after introducing the analgesia bags were compared with data before the bags were introduced. RESULTS: Of the 147 patients included in the study, 58 responded. Compared to standard prescription (small bag group: 14 oxycodone immediate release capsules (5 mg), large bag group: additional 28 oxycodone extended release tablets (5 mg), based on the smallest available package), the patients in the small analgesia bag group received 50% less oxycodone and 67% less for the large bag group. Patients with small bags consumed a median of 0.0 mg oxycodone and those with large bags consumed a median of 25.0 mg oxycodone. The median satisfaction was 5.0 (range: 2-5) and the median pain score was acceptable at the first postoperative day. Prescription data showed a significant reduction of 60.0% in the total amount of prescribed opioids after the introduction of prepacked analgesia bags. CONCLUSIONS: The introduction of prepacked analgesia bags dramatically reduced the quantity of opioids prescribed after outpatient hand surgery. Patient satisfaction was high and the postoperative pain level was acceptable. KEY WORDS: analgesia, hand surgery, opioids, outpatint surgery, wrist surgery.


Asunto(s)
Procedimientos Quirúrgicos Ambulatorios , Analgésicos Opioides , Dolor Postoperatorio , Humanos , Dolor Postoperatorio/prevención & control , Dolor Postoperatorio/tratamiento farmacológico , Analgésicos Opioides/administración & dosificación , Procedimientos Quirúrgicos Ambulatorios/métodos , Femenino , Masculino , Mano/cirugía , Dimensión del Dolor , Persona de Mediana Edad , Satisfacción del Paciente , Oxicodona/administración & dosificación , Adulto , Manejo del Dolor/métodos , Acetaminofén/administración & dosificación , Acetaminofén/uso terapéutico
11.
Skin Therapy Lett ; 29(4): 1-4, 2024 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-38963911

RESUMEN

Acne vulgaris is a common, often chronic inflammatory disease that can affect all ages and skin tones. Beyond acute lesions, the sequelae of acne - specifically scarring and dyspigmentation - can be long-lasting, challenging to treat and have substantial psychosocial impact on affected individuals. For acne scarring, treatment modalities include topical, physical, and laser and light therapies, with combination approaches typically yielding optimal outcomes. Trifarotene is a novel fourth generation retinoid with targeted action towards retinoid acid receptor gamma (RAR-γ), the most common isotype found in the epidermis, that has previously been approved for the management of moderate-to-severe facial and truncal acne in individuals over the age of 12 years. Recently, data on trifarotene supports its application in acne scarring. Herein, we provide a succinct review on various treatments for acne scarring and explore how trifarotene and its mechanism of action present an additional topical approach to target atrophic acne scarring.


Asunto(s)
Acné Vulgar , Cicatriz , Retinoides , Humanos , Acné Vulgar/complicaciones , Acné Vulgar/tratamiento farmacológico , Cicatriz/tratamiento farmacológico , Cicatriz/etiología , Retinoides/uso terapéutico , Fármacos Dermatológicos/uso terapéutico , Fármacos Dermatológicos/administración & dosificación , Atrofia , Administración Cutánea
13.
BMJ Case Rep ; 17(7)2024 Jul 04.
Artículo en Inglés | MEDLINE | ID: mdl-38964873

RESUMEN

Multisystem inflammatory syndrome in children (MIS-C) is a known complication of COVID-19. There is still limited knowledge about this condition. Here, we report the case of a previously healthy toddler boy, who presented with acute liver failure and duodenal lesions resulting in severe haematemesis and haemorrhagic shock, requiring intensive care unit care. The patient had persistent transaminitis, a deranged coagulation profile, inflammatory markers were elevated, and laboratory tests were negative for common infectious hepatitis aetiologies as well as COVID-19 Reverse transcription polymerase chain reaction. His COVID-19 antibody was reactive. Upper gastrointestinal endoscopy revealed a Forrest grade III duodenal ulcer. Looking into the constellation of symptoms and laboratory findings a confirmed diagnosis of acute viral hepatitis caused by MIS-C was made. Hence, he was given intravenous methylprednisolone along with intravenous immunoglobulins, after which he improved clinically and transaminitis resolved. The patient was discharged on clinical improvement and was doing fine on follow-up up to 6 months.


Asunto(s)
COVID-19 , Hemorragia Gastrointestinal , Fallo Hepático Agudo , Metilprednisolona , Síndrome de Respuesta Inflamatoria Sistémica , Humanos , Masculino , Síndrome de Respuesta Inflamatoria Sistémica/diagnóstico , Síndrome de Respuesta Inflamatoria Sistémica/complicaciones , COVID-19/complicaciones , Fallo Hepático Agudo/diagnóstico , Fallo Hepático Agudo/etiología , Fallo Hepático Agudo/complicaciones , Hemorragia Gastrointestinal/etiología , Hemorragia Gastrointestinal/diagnóstico , Metilprednisolona/uso terapéutico , Metilprednisolona/administración & dosificación , Inmunoglobulinas Intravenosas/uso terapéutico , Hematemesis/etiología , Úlcera Duodenal/complicaciones , Úlcera Duodenal/diagnóstico , SARS-CoV-2 , Preescolar
14.
Zhonghua Gan Zang Bing Za Zhi ; 32(6): 497-503, 2024 Jun 20.
Artículo en Chino | MEDLINE | ID: mdl-38964891

RESUMEN

In order to achieve the early goal of "eliminating viral hepatitis as a public health threat by 2030" as proposed by the World Health Organization, the relevant issues that have not yet reached consensus on the aspects of hepatitis B prevention and treatment, including population-wide screening, adult hepatitis B vaccination, the evaluation of quantitative values of hepatitis B virus DNA, the alanine aminotransferase threshold for initiating antiviral therapy, the treatment of patients in the "indeterminate phase," the treatment of patients with co-infections and comorbidities, and others. Thus, experts have formulated recommendations to further expand hepatitis B prevention and treatment, with the aim of accelerating the elimination of hepatitis B virus infection.


Asunto(s)
Hepatitis B , Humanos , Hepatitis B/prevención & control , Hepatitis B/epidemiología , Virus de la Hepatitis B , Vacunas contra Hepatitis B/administración & dosificación , Antivirales/uso terapéutico , Organización Mundial de la Salud
15.
Zhonghua Xue Ye Xue Za Zhi ; 45(5): 468-474, 2024 May 14.
Artículo en Chino | MEDLINE | ID: mdl-38964921

RESUMEN

Objective: To investigate the efficacy and safety of protein A immunoadsorption (PAIA) combined with rituximab (RTX) in highly sensitized patients who underwent haplo-hematopoietic stem cell transplantation (haplo-HSCT) . Methods: The clinical data of 56 highly sensitized patients treated with PAIA and RTX before haplo-HSCT at the First Affiliated Hospital of Soochow University and Soochow Hopes Hematonosis Hospital between March 2021 and June 2023 were retrospectively analyzed. The number of human leukocyte antigen (HLA) antibody types and the mean fluorescence intensity (MFI), humoral immunity, adverse reactions during adsorption, and survival within 100 days before and after adsorption were measured. Results: After receiving the PAIA treatment, the median MFI of patients containing only HLA Ⅰ antibodies decreased from 7 859 (3 209-12 444) to 3 719 (0-8 275) (P<0.001), and the median MFI of HLA Ⅰ+Ⅱ antibodies decreased from 5 476 (1 977-12 382) to 3 714 (0-11 074) (P=0.035). The median MFI of patients with positive anti-donor-specific antibodies decreased from 8 779 (2 697-18 659) to 4 524 (0-15 989) (P<0.001). The number of HLA-A, B, C, DR, and DQ antibodies in all patients decreased after the PAIA treatment, and the differences were statistically significant (A, B, C, DR: P<0.001, DQ: P<0.01). The humoral immune monitoring before and after the PAIA treatment showed a significant decrease in the number of IgG and complement C3 (P<0.001 and P=0.002, respectively). Forty-four patients underwent HLA antibody monitoring after transplantation, and the overall MFI and number of antibody types decreased. However, five patients developed new antibodies with low MFI, and nine patients continued to have high MFI. The overall survival, disease-free survival, non-recurrent mortality, and cumulative recurrence rates at 100 days post-transplantation were 83.8%, 80.2%, 16.1%, and 4.5%, respectively. Conclusions: The combination of PAIA and RTX has a certain therapeutic effect and good safety in the desensitization treatment of highly sensitive patients before haplo-HSCT.


Asunto(s)
Trasplante de Células Madre Hematopoyéticas , Rituximab , Proteína Estafilocócica A , Humanos , Rituximab/uso terapéutico , Rituximab/administración & dosificación , Trasplante de Células Madre Hematopoyéticas/métodos , Estudios Retrospectivos , Antígenos HLA/inmunología , Masculino , Femenino , Inmunidad Humoral
16.
Zhonghua Xue Ye Xue Za Zhi ; 45(5): 505-508, 2024 May 14.
Artículo en Chino | MEDLINE | ID: mdl-38964927

RESUMEN

Systemic mastocytosis (SM) with RUNX1-RUNX1T1 positive acute myeloid leukemia (AML) is a rare myeloid tumor with no standard treatment. Two cases of SM patients with RUNX1-RUNX1T1 positive AML treated with sequential avapritinib after allogeneic hematopoietic stem cell transplantation (allo-HSCT) were reported in Henan Cancer Hospital. Mast cell in bone marrow disappeared, C-KIT mutation and RUNX1-RUNX1T1 fusion gene remained negative. Allo-HSCT sequential avapritinib is an effective treatment for SM patients with RUNX1-RUNX1T1 positive AML.


Asunto(s)
Subunidad alfa 2 del Factor de Unión al Sitio Principal , Trasplante de Células Madre Hematopoyéticas , Leucemia Mieloide Aguda , Mastocitosis Sistémica , Humanos , Leucemia Mieloide Aguda/terapia , Leucemia Mieloide Aguda/genética , Mastocitosis Sistémica/genética , Mastocitosis Sistémica/terapia , Subunidad alfa 2 del Factor de Unión al Sitio Principal/genética , Masculino , Femenino , Adulto , Proteína 1 Compañera de Translocación de RUNX1/genética , Proteínas de Fusión Oncogénica/genética , Persona de Mediana Edad , Trasplante Homólogo , Pirazinas/administración & dosificación , Pirazoles , Pirroles , Triazinas
17.
Zhonghua Xue Ye Xue Za Zhi ; 45(5): 488-494, 2024 May 14.
Artículo en Chino | MEDLINE | ID: mdl-38964924

RESUMEN

Objective: To explore the efficacy and safety of cryopreservation-free integrated autologous hematopoietic stem cell transplantation (HSCT) model for patients with multiple myeloma. Methods: A total of 96 patients with newly diagnosed multiple myeloma (NDMM) between July 31, 2020, and December 31, 2022, were retrospectively analyzed, of which 41 patients in the observation group received integrated non-cryopreserved transplantation mode. After hematopoietic stem cells were mobilized and collected, melphalan was started immediately for pre-transplant conditioning, and non-cryopreserved grafts from the medical blood transfusion refrigerator were directly injected intravenously into the patient within 24-48 h after the melphalan conditioning. The control group consisted of 55 patients who received traditional transplantation mode. After hematopoietic stem cells were collected, stem cell cryopreservation was performed in liquid nitrogen, and then the transplant plans were started at the right time. All patients received mobilization of autologous hematopoietic stem cells using the G-CSF combined with the plerixafor. Results: ① A total of 34 patients (82.9% ) with VGPR plus CR in the observation group were significantly higher than 33 patients (60.0% ) in the control group (P=0.016). ②Compared with the control group, the incidence of grade 1 oral mucosal inflammation was higher in the observation group (P<0.001) ; however, the incidence of grades 2 and 3 oral mucosal inflammation was lower (P=0.004, P=0.048), and neither group experienced grade 4 or above oral mucosal inflammation. The incidence of grade 1 diarrhea was higher in the observation group (P=0.002), whereas the incidence of grade 3 diarrhea was lower (P=0.007). No statistically significant difference was observed in the incidence of grade 4 diarrhea (P=0.506), and neither group experienced grade 5 diarrhea. ③ The incidence of bacterial infection in the observation group was lower than that in the control group (34.1% vs 65.5%, P=0.002), whereas no statistically significant difference was observed in the incidence of fungal infection (29.3% vs 31.4%, P=0.863) and viral infection (4.88% vs 3.64%, P=0.831). ④No statistically significant difference was observed in the implantation time of granulocytes and platelets between the observation and control groups [10 (8-20) days vs 11 (8-17) days, P=0.501; 13 (10-21) days vs 15 (10-20) days, P=0.245]. ⑤ All patients did not receive lenalidomide treatment 100 days post-transplantation. At 30 days post-transplantation, the CTL, NK, and Th cell counts in the observation group were lower than those in the control group (P<0.001, P=0.002, P=0.049), and the NKT cell counts were higher than those in the control group (P=0.024). At 100 days post-transplantation, the CTL, NKT, and Th cell counts in the observation group were higher than those in the control group (P=0.025, P=0.011, P=0.007), and no statistically significant difference in NK cell counts was observed between the two groups (P=0.396). ⑥ The median follow-up was 18 (4-33) months. The overall 2-year survival rates of the observation and control groups post-transplantation were 91.5% and 78.2%, respectively (P=0.337). The recurrence-free survival rates were 85.3% and 77.6%, respectively (P=0.386), and the cumulative recurrence rates were 9.8% and 16.9%, respectively (P=0.373) . Conclusion: In NDMM, the cryopreservation-free integrated autologous HSCT model can achieve similar therapeutic effects as traditional transplantation models, with lower rates of severe mucosal inflammation and infection compared with traditional transplantation models.


Asunto(s)
Trasplante de Células Madre Hematopoyéticas , Mieloma Múltiple , Trasplante Autólogo , Humanos , Mieloma Múltiple/terapia , Trasplante de Células Madre Hematopoyéticas/métodos , Estudios Retrospectivos , Criopreservación , Movilización de Célula Madre Hematopoyética/métodos , Factor Estimulante de Colonias de Granulocitos/administración & dosificación , Masculino , Femenino , Persona de Mediana Edad
18.
Lasers Med Sci ; 39(1): 172, 2024 Jul 05.
Artículo en Inglés | MEDLINE | ID: mdl-38965092

RESUMEN

The study utilized 5-ALA-PDT to treat patients with CIN or VaIN and assessed their clinical response, HPV clearance, and influencing factors after photodynamic therapy (PDT). This study involved 56 patients who received 5-ALA-PDT in a single center from May 2020 to March 2022, including 12 patients with CIN, 30 patients with VaIN, and 14 patients with both CIN and VaIN. Follow-up were conducted within 6 and 12 months after treatment to evaluate the clinical effectiveness of PDT. The assessment criteria included histological response (ER, elimination rate, RR, regression rate) and HPV clearance. Additionally, factors that could potentially influence the outcomes were analyzed. After PDT, the histological response showed an ER of 48.2% (27/56) and a RR of 80.4% (45/56) within 6 months of follow-up. The elimination rate increased to 69.6% (39/56) within 12 months, along with a regression rate of 82.1% (46/56). The rates of HPV clearance were observed to be 37.5% (21/56) and 44.6% (25/56) within 6 and 12 months, respectively. The study also revealed that HPV clearance significantly influenced histologic elimination within 6 months (p < 0.001) and histologic regression within 12 months (p < 0.01). Furthermore, premenopausal women exhibited a higher HPV clearance rate compared to postmenopausal women (61.5% vs. 30.0%, p = 0.036). 5-ALA PDT can be considered as an available option for the treatment of lower genital squamous intraepithelial lesions. The efficacy of its histologic response depends on HPV clearance. Additionally, it has been found that premenopausal women may benefit more from this treatment.


Asunto(s)
Ácido Aminolevulínico , Fotoquimioterapia , Fármacos Fotosensibilizantes , Humanos , Femenino , Fotoquimioterapia/métodos , Ácido Aminolevulínico/uso terapéutico , Ácido Aminolevulínico/administración & dosificación , Adulto , Fármacos Fotosensibilizantes/uso terapéutico , Fármacos Fotosensibilizantes/administración & dosificación , Persona de Mediana Edad , Resultado del Tratamiento , Displasia del Cuello del Útero/tratamiento farmacológico , Displasia del Cuello del Útero/virología , Displasia del Cuello del Útero/patología , Infecciones por Papillomavirus/tratamiento farmacológico , Infecciones por Papillomavirus/virología , Neoplasias del Cuello Uterino/tratamiento farmacológico , Neoplasias del Cuello Uterino/virología , Neoplasias del Cuello Uterino/patología , Adulto Joven , Anciano
19.
Asia Pac J Clin Nutr ; 33(3): 405-412, 2024 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-38965728

RESUMEN

BACKGROUND AND OBJECTIVES: If the proportion of calcium intake over a whole day is related to the risk of cognitive impairment in adults is still largely unknown. This research aimed to examine the relation of dietary calcium intake at dinner versus breakfast with the risk of cognitive impairment by using data from the China Health and Nutrition Survey (CHNS). METHODS AND STUDY DESIGN: A total of 2,099 participants (including 668 cognitive impairment) in the CHNS (1997-2006) were included. The participants were categorized into 5 groups in accordance with the ratio of dietary calcium intake at dinner and breakfast (Δ = dinner/breakfast). After adjustment was conducted for a series of confounding factors, Cox hazard regression modelling was performed to discuss the relation of Δ with cognitive impairment. Dietary substitution models were used to explore the changes in cognitive impairment risk when a 5% dietary calcium intake at dinner was replaced with dietary calcium intake at breakfast. RESULTS: Participants in the highest distribution of Δ showed a greater susceptibility to cognitive impairment than those in the lowest quintile, with an adjusted hazard ratio of cognitive impairment of 1.38 (95% CI: 1.08-1.76). When maintaining total calcium intake, substituting 5% of dietary calcium intake at dinner with calcium intake at breakfast was related to an 8% decrease in the risk of cognitive impairment. CONCLUSIONS: Higher dietary calcium intake at dinner was associated with an increased risk of cognitive impairment, emphasizing the importance of appropriately distributing dietary calcium intake between breakfast and dinner.


Asunto(s)
Desayuno , Calcio de la Dieta , Disfunción Cognitiva , Humanos , Calcio de la Dieta/administración & dosificación , Masculino , Femenino , China/epidemiología , Persona de Mediana Edad , Disfunción Cognitiva/epidemiología , Estudios de Cohortes , Adulto , Comidas , Encuestas Nutricionales , Anciano , Factores de Riesgo , Pueblos del Este de Asia
20.
Asia Pac J Clin Nutr ; 33(3): 413-423, 2024 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-38965729

RESUMEN

BACKGROUND AND OBJECTIVES: Non-alcoholic fatty liver disease (NAFLD) has become a worldwide public health problem. Current evidence on the association between dietary iron intake and the risk of NAFLD is limited. The present study aimed to investigate the associations of animal-derived dietary iron (ADDI) intake, plant-derived dietary iron (PDDI) intake, and the ratio of PDDI:ADDI with NAFLD risk among U.S. adult population. METHODS AND STUDY DESIGN: This was a repeated cross-sectional study. Data were collected from the National Health and Nutrition Examination Survey (NHANES) 2007-2018. NAFLD was defined as a United States Fatty Lives Index ≥30, and dietary iron intake was assessed through two 24-h dietary recall in-terviews. Logistic regression and restricted cubic spline models were applied to examine the associations between dietary iron intake from different sources and NAFLD risk. RESULTS: A total of 9478 participants aged ≥20 years were enrolled in the present study. After adjustment for multiple confounding factors, relative to the lowest quartile, the odds ratio (OR) and 95% confidence interval (CI) of NAFLD for the highest quartile was 1.01(95% CI, 0.82-1.24) for ADDI intake, 0.82 (95% CI, 0.64-0.99) for PDDI intake, and 1.00 (95% CI, 0.81-1.24) for the PDDI: ADDI intake ratio. In stratified analysis by sex and age, the significantly negative associations of PDDI intake with NAFLD was observed in women and participants older than 45 years. Dose-response analyses indicated that NAFLD was negatively associated with PDDI intake in a non-linear manner. CONCLUSIONS: PDDI intake was negatively associated with NAFLD in U.S. adults.


Asunto(s)
Hierro de la Dieta , Enfermedad del Hígado Graso no Alcohólico , Encuestas Nutricionales , Humanos , Enfermedad del Hígado Graso no Alcohólico/epidemiología , Masculino , Femenino , Adulto , Estudios Transversales , Hierro de la Dieta/administración & dosificación , Persona de Mediana Edad , Dieta/métodos , Dieta/estadística & datos numéricos , Adulto Joven , Estados Unidos/epidemiología
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