1.Estimation of Serum C-terminal Cross-linked Telopeptide Type II Collagen (CTX II) Level to Diagnose Early Knee Osteoarthritis
Malaysian Orthopaedic Journal 2025;19(No. 2):18-24
Introduction: This study aimed to study the usefulness of
CTX II levels to identify normal population with patients of
knee osteoarthritis, and its utility in identifying the severity
of disease in primary knee osteoarthritis (KOA).
Materials and methods: This research recruited 80 cases of
KOA and 80 healthy adults (160 subjects). Patients with
primary knee osteoarthritis were graded according to the KL
grading system, and serum CTX II (sCTX II) value were
analysed. The age, gender, and BMI of the subjects were
recorded.
Results: The sCTX-II value in cases (719.87 ± 256.1pg/ml)
was more than in controls (419.26 ± 208.18pg/ml, p<0.001).
The sCTX-II value in case group was significantly higher in
males (812.67 ± 289.24) than in females (680.11 ± 236.59,
p=0.03). In the control group, males (426.13 ± 221.06) and
females (398.66 ± 166.92) had similar values (p=0.60).
sCTX II level was higher with higher age, but this difference
is significant in the case group only (p=0.003). Multivariate
analysis revealed that the sCTX II level was only dependent
on the severity of the disease. Analysis of the ROC curve
reveals a cut-off value of sCTX II as 557.5pg/ml among
cases and controls, 407.5pg/ml between KL grade 0-I, as
528.5pg/ml between KL grade I-II, as 681.1pg/ml between
KL grade II-III, and as 866.4pg/ml between KL grade III-IV.
Conclusion: sCTX II values are dependent only on the
severity of the disease. sCTX II level estimation is an
excellent diagnostic tool for identifying the normal
population with knee osteoarthritis patients and has a clinical
significance in identifying KOA cases of KL grade I and II.
2.Infarcts Due to Large Vessel Occlusions Continue to Grow Despite Near-Complete Reperfusion After Endovascular Treatment
Johanna M. OSPEL ; Nathaniel REX ; Karim OUEIDAT ; Rosalie MCDONOUGH ; Leon RINKEL ; Grayson BAIRD ; Scott COLLINS ; Gaurav JINDAL ; Matthew D. ALVIN ; Jerrold BOXERMAN ; Phil BARBER ; Mahesh JAYARAMAN ; Wendy SMITH ; Amanda AMIRAULT-CAPUANO ; Michael D. HILL ; Mayank GOYAL ; Ryan MCTAGGART
Journal of Stroke 2024;26(2):260-268
Background:
and Purpose Infarcts in acute ischemic stroke (AIS) patients may continue to grow even after reperfusion, due to mechanisms such as microvascular obstruction and reperfusion injury. We investigated whether and how much infarcts grow in AIS patients after near-complete (expanded Thrombolysis in Cerebral Infarction [eTICI] 2c/3) reperfusion following endovascular treatment (EVT), and to assess the association of post-reperfusion infarct growth with clinical outcomes.
Methods:
Data are from a single-center retrospective observational cohort study that included AIS patients undergoing EVT with near-complete reperfusion who received diffusion-weighted magnetic resonance imaging (MRI) within 2 hours post-EVT and 24 hours after EVT. Association of infarct growth between 2 and 24 hours post-EVT and 24-hour National Institutes of Health Stroke Scale (NIHSS) as well as 90-day modified Rankin Scale score was assessed using multivariable logistic regression.
Results:
Ninety-four of 155 (60.6%) patients achieved eTICI 2c/3 and were included in the analysis. Eighty of these 94 (85.1%) patients showed infarct growth between 2 and 24 hours post-reperfusion. Infarct growth ≥5 mL was seen in 39/94 (41.5%) patients, and infarct growth ≥10 mL was seen in 20/94 (21.3%) patients. Median infarct growth between 2 and 24 hours post-reperfusion was 4.5 mL (interquartile range: 0.4–9.2 mL). Post-reperfusion infarct growth was associated with the 24-hour NIHSS in multivariable analysis (odds ratio: 1.16 [95% confidence interval 1.09–1.24], P<0.01).
Conclusion
Infarcts continue to grow after EVT, even if near-complete reperfusion is achieved. Investigating the underlying mechanisms may inform future therapeutic approaches for mitigating the process and help improve patient outcome.
3.Low-dose Perioperative Dexamethasone Improves 24-hour Post-Operative Pain after Anterior Cruciate Ligament Reconstruction
Khatri K ; Sidhu G ; Jindal S ; Bansal D ; Goyal D
Malaysian Orthopaedic Journal 2022;16(No.1):76-83
Introduction: Post-operative pain following anterior
cruciate ligament reconstruction remains an important
challenge. Steroids are used in various surgical procedures to
decrease post-operative nausea, vomiting and pain.
However, only a few studies have reported the effect of
systemic administration of steroids in controlling postoperative pain after anterior cruciate ligament surgery.
Materials and methods: We have conducted a prospective
randomised trial with 109 patients divided into two groups to
determine if administration of dexamethasone in the
perioperative period improves pain in the post-operative
period. The patients were divided into two groups: D,
treatment (dexamethasone) and P, control placebo (saline).
Patients in the D treatment group were given the first dose of
10mg of intravenous dexamethasone intravenously intraoperatively and the second dose on transferring of the patient
to the inpatient department. The patients in the placebo P
group, were administered normal saline in the perioperative
period in a similar manner.
Result: Post-operative pain was significantly less in the
dexamethasone group at rest and on walking (p<0.001) for
the first 24 hours after surgical procedure. Subsequently, the
VAS pain scores were almost similar in both groups at 48
and 72 hours. The administration of dexamethasone resulted
in less requirement of antiemetic and rescue analgesia
medication There was no difference in range of motion and
wound complications rate during the follow-up period at six
months. No adverse side effect, like osteonecrosis of the hip,
was detected.
Conclusion: The pain following anterior cruciate ligament
reconstruction is severe during the first 24 hours and
perioperative administration of dexamethasone can decrease
the post-operative pain substantially.
4.Male Oxidative Stress Infertility (MOSI): Proposed Terminology and Clinical Practice Guidelines for Management of Idiopathic Male Infertility
Ashok AGARWAL ; Neel PAREKH ; Manesh Kumar PANNER SELVAM ; Ralf HENKEL ; Rupin SHAH ; Sheryl T HOMA ; Ranjith RAMASAMY ; Edmund KO ; Kelton TREMELLEN ; Sandro ESTEVES ; Ahmad MAJZOUB ; Juan G ALVAREZ ; David K GARDNER ; Channa N JAYASENA ; Jonathan W RAMSAY ; Chak Lam CHO ; Ramadan SALEH ; Denny SAKKAS ; James M HOTALING ; Scott D LUNDY ; Sarah VIJ ; Joel MARMAR ; Jaime GOSALVEZ ; Edmund SABANEGH ; Hyun Jun PARK ; Armand ZINI ; Parviz KAVOUSSI ; Sava MICIC ; Ryan SMITH ; Gian Maria BUSETTO ; Mustafa Emre BAKIRCIOĞLU ; Gerhard HAIDL ; Giancarlo BALERCIA ; Nicolás Garrido PUCHALT ; Moncef BEN-KHALIFA ; Nicholas TADROS ; Jackson KIRKMAN-BROWNE ; Sergey MOSKOVTSEV ; Xuefeng HUANG ; Edson BORGES ; Daniel FRANKEN ; Natan BAR-CHAMA ; Yoshiharu MORIMOTO ; Kazuhisa TOMITA ; Vasan Satya SRINI ; Willem OMBELET ; Elisabetta BALDI ; Monica MURATORI ; Yasushi YUMURA ; Sandro LA VIGNERA ; Raghavender KOSGI ; Marlon P MARTINEZ ; Donald P EVENSON ; Daniel Suslik ZYLBERSZTEJN ; Matheus ROQUE ; Marcello COCUZZA ; Marcelo VIEIRA ; Assaf BEN-MEIR ; Raoul ORVIETO ; Eliahu LEVITAS ; Amir WISER ; Mohamed ARAFA ; Vineet MALHOTRA ; Sijo Joseph PAREKATTIL ; Haitham ELBARDISI ; Luiz CARVALHO ; Rima DADA ; Christophe SIFER ; Pankaj TALWAR ; Ahmet GUDELOGLU ; Ahmed M A MAHMOUD ; Khaled TERRAS ; Chadi YAZBECK ; Bojanic NEBOJSA ; Damayanthi DURAIRAJANAYAGAM ; Ajina MOUNIR ; Linda G KAHN ; Saradha BASKARAN ; Rishma Dhillon PAI ; Donatella PAOLI ; Kristian LEISEGANG ; Mohamed Reza MOEIN ; Sonia MALIK ; Onder YAMAN ; Luna SAMANTA ; Fouad BAYANE ; Sunil K JINDAL ; Muammer KENDIRCI ; Baris ALTAY ; Dragoljub PEROVIC ; Avi HARLEV
The World Journal of Men's Health 2019;37(3):296-312
Despite advances in the field of male reproductive health, idiopathic male infertility, in which a man has altered semen characteristics without an identifiable cause and there is no female factor infertility, remains a challenging condition to diagnose and manage. Increasing evidence suggests that oxidative stress (OS) plays an independent role in the etiology of male infertility, with 30% to 80% of infertile men having elevated seminal reactive oxygen species levels. OS can negatively affect fertility via a number of pathways, including interference with capacitation and possible damage to sperm membrane and DNA, which may impair the sperm's potential to fertilize an egg and develop into a healthy embryo. Adequate evaluation of male reproductive potential should therefore include an assessment of sperm OS. We propose the term Male Oxidative Stress Infertility, or MOSI, as a novel descriptor for infertile men with abnormal semen characteristics and OS, including many patients who were previously classified as having idiopathic male infertility. Oxidation-reduction potential (ORP) can be a useful clinical biomarker for the classification of MOSI, as it takes into account the levels of both oxidants and reductants (antioxidants). Current treatment protocols for OS, including the use of antioxidants, are not evidence-based and have the potential for complications and increased healthcare-related expenditures. Utilizing an easy, reproducible, and cost-effective test to measure ORP may provide a more targeted, reliable approach for administering antioxidant therapy while minimizing the risk of antioxidant overdose. With the increasing awareness and understanding of MOSI as a distinct male infertility diagnosis, future research endeavors can facilitate the development of evidence-based treatments that target its underlying cause.
Antioxidants
;
Classification
;
Clinical Protocols
;
Diagnosis
;
DNA
;
Embryonic Structures
;
Female
;
Fertility
;
Health Expenditures
;
Humans
;
Infertility
;
Infertility, Male
;
Male
;
Membranes
;
Ovum
;
Oxidants
;
Oxidation-Reduction
;
Oxidative Stress
;
Reactive Oxygen Species
;
Reducing Agents
;
Reproductive Health
;
Semen
;
Spermatozoa
;
Subject Headings


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