SGLT2 inhibitors linked to lower glaucoma risk, reveals research

A study published in the American Journal of Ophthalmology suggests that the use of SGLT2 inhibitors in diabetes is linked to a lower risk of glaucoma.

Pleiotropic cardiovascular benefits of sodium glucose co-transporter 2 inhibitors (SGLT2i) have been demonstrated in patients with type 2 diabetes mellitus due to vascular remodeling effects. It is unclear whether a similar benefit may be seen for glaucoma. The purpose of this study is to assess the effect of SGLT2i on the risk of glaucoma in patients with type 2 diabetes. Adults with type 2 diabetes in the United States who newly initiated treatment with SGLT2i, dipeptidyl peptidase 4 inhibitors (DPP4i), or glucagon-like peptide-1 receptor agonists (GLP1RA) between 2013 and 2023. After propensity score matching, 722,446 patients were included in the SGLT2i arm and the DPP4i arm, respectively. Participants were matched based on age at index, race and sex, comorbidities, and concomitant use of medications. Results: Patients on SGLT2i compared to those on DPP4 had a lower risk of glaucoma (HR: 0.815, 95% confidence interval [CI]: 0.794, 0.837), including open-angle glaucoma (HR: 0.755, 95%CI: 0.729, 0.781) and primary angle-closure glaucoma (HR: 0.592, 95%CI: 0.540, 0.650). Among all SGLT2i, ertugliflozin (HR: 0.668, 95%CI: 0.512, 0.871) was associated with the lowest risk of glaucoma, followed by empagliflozin (HR: 0.727, 95%CI: 0.696, 0.759), then dapagliflozin (HR: 0.814, 95%CI: 0.774, 0.855). The protective effect of SGLT2i on glaucoma was validated when compared with GLP1RA (HR: 0.932, 95%CI: 0.906, 0.959). Patients on SGLT2i, especially ertugliflozin and empagliflozin, had a significantly lower risk of incident glaucoma compared to those on DPP4i, an association that was less robust but significant in a sensitivity analysis using GLP1RA as the active comparator. SGLT2i had a protective effect for both open-angle glaucoma and angle-closure glaucoma.

Reference:

Sodium-glucose cotransporter 2 inhibitors and glaucoma in patients with type 2 diabetes

Kathleen Eng1 ∙ Nazlee Zebardast2 ∙ Michael V. Boland2,3 ∙ Jui-En Lo4 ∙ Swarup S. Swaminathan5 ∙ David S. Friedman, Kevin Sheng-Kai Ma6. American Journal of Ophthalmology

Keywords:

Use, SGLT2, inhibitors, Diabetes, linked, lower risk, glaucoma, study, American Journal of Ophthalmology, Glaucoma, type 2 diabetes mellitus. SGLT2 inhibitors, DPP4 inhibitors, GLP1 receptor agonists, Target trial emulation study

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Unexplained changes in cholesterol may help identify older adults at risk for dementia, claims research

When older adults have significant year-to-year fluctuations in their cholesterol levels without changes in medication, it could indicate an increased risk of developing dementia or cognitive decline, according to a preliminary study to be presented at the American Heart Association’s Scientific Sessions 2024.

The meeting, Nov. 16-18, 2024, in Chicago, is a premier global exchange of scientific advancements, research and evidence-based clinical practice updates in cardiovascular science.

“Older people with fluctuating cholesterol levels unrelated to whether they were taking lipid-lowering medications – particularly those experiencing big year-to-year variations — may warrant closer monitoring and proactive preventive interventions,” said lead author Zhen Zhou, Ph.D., a postdoctoral research fellow in the School of Public Health and Preventive Medicine at Monash University in Melbourne, Australia.

The current project used the in-trial and post-trial data of participants enrolled in a randomized clinical trial called ASPirin in Reducing Events in the Elderly (ASPREE) that determined low-dose aspirin was not effective for reducing heart disease risk in Australian and American adults. While one-third were taking cholesterol-lowering medication, none of the almost 10,000 participants started, stopped or changed lipid-lowering medication during the follow-up period.

All participants were relatively healthy adults without dementia who had been having their cholesterol levels monitored annually. The first three cholesterol measurements taken in the ASPREE study were used to determine how much each person’s lipid levels varied from year to year.

During almost six years of follow-up after the yearly assessments, 509 participants developed dementia and another 1,760 developed cognitive decline without dementia.

Compared with those who had the most stable cholesterol levels, the study found:

High fluctuations (in the top 25%) in total cholesterol were associated with a 60% increase in dementia and a 23% increase in cognitive decline.

Low-density lipoprotein cholesterol (LDL cholesterol or “bad” cholesterol) and total cholesterol fluctuations were associated with significantly faster declines in overall cognitive health test scores and tests involving memory and reaction speed.

High fluctuations in high-density lipoproteins (HDL “good” cholesterol) or triglycerides were not associated with dementia or cognitive decline. Triglycerides are the most common type of fat in the body, storing excess energy from food.

“We need future studies to help us understand the relationship between cholesterol variability and dementia risk,” Zhou said. “Are cholesterol variability levels a real risk factor, a precursor or a biomarker of dementia risk? One possible explanation is that significant fluctuations in total and LDL cholesterol levels may destabilize atherosclerotic plaques, which are mostly composed of LDL cholesterol. This destabilization can raise the risk of plaque growth, rupture and subsequent obstruction of blood flow in the brain, which may therefore impact brain function.”

The study had some limitations, including that cholesterol readings can vary for many reasons, and the connection between cholesterol variability and dementia risk may be affected by these unanalyzed factors. In addition, the study participants were mostly white adults (96%), so, the findings may not apply to people in other population groups. As an observational study, it cannot prove a cause-and-effect relationship between cholesterol fluctuations and dementia risk.

“If future research confirms a cause-and-effect relationship, reducing cholesterol variability could potentially be a promising therapeutic target for dementia,” Zhou said. “Importantly, our results should not be misinterpreted as suggesting that lowering cholesterol through lifestyle modification or lipid-lowering medications is harmful for brain health.”

Based on data from 2017 to 2020, 63.1 million or 25.5%, of U.S. adults had high “bad” cholesterol levels (130 mg/dL or higher). Globally, in 2021, 3.72 million deaths were attributed to excessive “bad” cholesterol levels, according to the American Heart Association’s Heart Disease and Stroke Statistics 2024 Update.

“In the past, studies have focused on the connection between individual vascular risk factors and cognitive decline. However, there is evidence that an increase in the variability of certain functions in the body, such as blood pressure or blood sugar levels, can be harmful to both the heart and the brain,” said American Heart Association volunteer expert, Fernando D. Testai M.D., Ph.D., FAHA, a professor of neurology and rehabilitation at the University of Illinois Chicago, who also served as chair for the Association’s recent “Cardiac Contributions to Brain Health” scientific statement. “This study adds an important piece to the puzzle of preserving brain health by providing evidence that increasing variability in cholesterol levels is associated with cognitive decline. The study did not include people who started or stopped taking lipid-lowering medications during the study period. So, the results cannot be explained by the effect of statins. From a practical standpoint, not sticking to strategies that improve the lipid profile, such as following a healthy diet and exercising, can worsen the negative impact of harmful lipids on the brain.”

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Annual DXA Screening in Lung Transplant Patients in First Two Years may help prevent osteoporosis: Study

USA: A recent study recommends that lung transplant patients undergo annual screening with dual-energy X-ray absorptiometry (DXA) for the first two years following their surgery to monitor bone health. The study, published in the Journal of Heart and Lung Transplantation, highlights the increased risk of bone mineral density (BMD) loss in lung transplant recipients, which can elevate the likelihood of osteoporosis and fractures.

The researchers found that many lung transplant patients experience a significant decline in BMD after surgery. This loss can result in weakened bones, making them more prone to fractures. “Early detection of low BMD can facilitate timely intervention and treatment before fractures develop,” the study authors wrote.

Each year, around 2,700 lung transplants are performed in the United States. These patients face an elevated risk of developing low bone mineral density (osteopenia/osteoporosis), which can lead to fractures associated with osteoporosis. Dual-energy X-ray absorptiometry is the gold standard for assessing bone mineral density. It provides a reliable measure of bone health and is widely used in clinical practice to diagnose osteoporosis and monitor changes in bone density over time. However, the ideal frequency for monitoring low BMD with DXA remains unclear.

To fill this knowledge gap, the stud authors Ronnie Sebro and Mahmoud Elmahdy from the Department of Radiology, Mayo Clinic, Jacksonville, FL, and colleagues assessed changes in BMD at the femoral neck, total femur, and lumbar spine (L1, L2, L3, and L4) following lung transplant. This retrospective cohort included 259 patients (69.9% male) who were monitored with serial DXA scans over a median follow-up period of 725 days (interquartile range (IQR): 361–1116 days) post-transplant.

Generalized linear mixed-effects models were employed to analyze the rate of change in bone mineral density (BMD) at each site, incorporating random intercepts and slopes. These models were adjusted for variables including sex, time, time-squared, baseline osteopenia/osteoporosis, active rejection, and their interaction terms. The final multivariable models for BMD measurements at the femoral neck, L1, and L4 included random slopes and intercepts, while models for the total hip, L2, and L3 BMD measurements included random slopes.

The key findings of the study were as follows:

  • 65% of lung transplant patients had osteopenia or osteoporosis before their transplant.
  • Men had higher baseline bone mineral density levels than women at all measurement sites.
  • After the transplant, the greatest rate of BMD decrease occurred at the femoral neck.
  • Patients with low BMD (osteopenia/osteoporosis) had significantly lower baseline BMD compared to those with normal BMD, however, they experienced a slower rate of BMD decline at all sites compared to those with normal BMD at baseline.
  • All patients in the study received corticosteroids.
  • 25% of patients had a history of active rejection.
  • Patients with low BMD at baseline had significantly higher odds of receiving bisphosphonate therapy (Odds Ratio = 3.95).
  • A significant change in femoral neck BMD was estimated to occur within 409 days and again at 867 days post-transplant.

“On average, lung transplant patients should undergo annual DXA screening for the first two years post-transplant, in line with the current guidelines from the International Society for Heart and Lung Transplantation (ISHLT),” the researchers concluded.

Reference:

Sebro, R., & Elmahdy, M. (2024). Optimized surveillance frequency for low bone mineral density (BMD) screening using dual energy X-ray absorptiometry (DXA) in patients after lung transplant. The Journal of Heart and Lung Transplantation. https://doi.org/10.1016/j.healun.2024.10.028

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Increased Risk of Aortic Events During Pregnancy may adverse Impact Maternal and Neonatal health: Study

Taiwan: A recent study published in the European Heart Journal confirmed the link between pregnancy and an increased risk of aortic events. The study revealed that pregnant women face an increased risk of aortic events from the onset of pregnancy through the first year postpartum.

The researchers found that maternal mortality was notably higher in pregnancies complicated by aortic events compared to those without. Additionally, neonatal outcomes were worse, with increased late mortality and a higher incidence of complications in infants born to mothers who experienced aortic events.

Aortic events during pregnancy are relatively rare but carry high morbidity and mortality rates. Considering this, Shao-Wei Chen, Center for Big Data Analytics and Statistics, Chang Gung Memorial Hospital, Linkou Medical Center, Taoyuan City, Taiwan, and colleagues aimed to examine the relationship between pregnancy and aortic complications and assess the associated maternal and neonatal outcomes.

For this purpose, the researchers retrieved records of pregnancies and neonatal deliveries from the Taiwan National Health Insurance Research Database from 2000 to 2020. The incidence rate ratio (IRR) was calculated to assess the risk factors associated with aortic events. Additionally, survival analysis was performed to compare maternal and neonatal mortality rates in cases with and without aortic events.

The study led to the following findings:

  • 4,785,266 pregnancies were identified among 2,833,271 childbearing women, with 2,852,449 neonatal deliveries.
  • In the vulnerable period (pregnancy), 57 aortic events occurred, and in the control period (non-pregnant), 20 aortic events were recorded.
  • The incidence rates of aortic events were 1.19 per 100,000 pregnancies in the vulnerable period and 0.42 per 100,000 pregnancies in the control period.
  • Pregnancy was identified as a significant risk factor for aortic events, with an incidence rate ratio (IRR) of 2.86.
  • The 1-year maternal mortality rate was significantly higher in pregnancies with aortic events (19.3%) compared to those without (0.05%).
  • Neonates born to mothers who experienced aortic events had a higher late mortality rate (6.3%) compared to those whose mothers did not experience such events (0.6%).

The findings from the large observational study suggest that pregnancy is associated with an increased risk of aortic events, particularly in women with coexisting connective tissue diseases or hypertensive disorders of pregnancy. The study also revealed that the 1-year maternal mortality rate was significantly higher in pregnancies complicated by aortic events compared to those without such events. Additionally, neonates born to mothers who experienced aortic events had a higher late mortality rate.

“Therefore, early identification of pregnant women at risk for aortic events—particularly those with concurrent hypertensive disorders, relevant family histories, or aortopathy—is essential for effective management and prevention,” the researchers concluded.

Reference:

Chen, S., Chang, F., Chen, C., Cheng, Y., Hsiao, F., Tung, Y., Lin, C., Wu, V. C., Chu, P., & Chou, A. Pregnancy, aortic events, and neonatal and maternal outcomes. European Heart Journal. https://doi.org/10.1093/eurheartj/ehae757

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About ten percent of women may develop PTSD at two months after cesarean delivery: Study

Researchers have found that cesarean deliveries may affect maternal mental health to a great extent, as almost 1 in 11 women may show symptoms of posttraumatic stress disorder (PTSD) two months after giving birth. A recent study was published in the American Journal of Obstetrics and Gynecology conducted by Alizee F. and colleagues.

The TRAAP2 study was a prospective ancillary cohort research study which aimed to inform the way cesarean delivery relates to PTSD symptoms and actual diagnoses. The study was conducted from 2018 to 2020 in 27 French hospitals on women scheduled for cesarean delivery at or beyond 34 weeks of gestation. The prevalence of PTSD two months postpartum was evaluated using the Self-reported Impact of Event Scale – Revised (IES-R) and Traumatic Event Scale (TES) questionnaires. Nonresponse was addressed by using inverse probability weighting for increased precision.

The study involved 4431 women who were to be delivered via cesarean section either pre-planned or in labor. Analysis of responses was conducted from 2785 participants who responded to the IES-R and 2792 participants who responded to the TES. The study only analyzed participants who did not have risk factors and whose data was not missing. Logistic and linear regression models were applied to find possible associations between cesarean delivery experiences and risk for PTSD.

  • Of the participants who completed the IES-R, 9% exhibited symptoms of PTSD as measured by their scores.

  • Moreover, 1.7% fulfilled provisional criteria as given by the diagnostic algorithm in terms of achieving a diagnosis of PTSD.

  • There were several prepregnancy risk factors identified in this study. These included younger age, higher BMI, and an African-born migrant.

  • There was a strong association among these factors and PTSD presence following a cesarean delivery.

There were some cesarean delivery risk factors that increased the risk for PTSD:

  • Women who received a cesarean after an induction of labour had an increased risk of 1.81 times the presence of PTSD (95% CI, 1.14–2.87).

  • Participants who experienced severe bleeding at the time of delivery were found to have 1.61-fold risk in the development of PTSD, compared with controls (95% CI, 1.04–2.46).

  • Women with significant pain during the postpartum period had 1.90 times higher risk of developing PTSD (95% CI, 1.17–3.11).

  • Immediate skin-to-skin contact with newborns showed a protective effect, reducing PTSD risk (OR, 0.66; 95% CI, 0.46–0.98).

  • Negative memories of the delivery experience by day two postpartum increased PTSD risk significantly (OR, 3.20; 95% CI, 1.97–5.12).

Women who deliver via cesarean may develop symptoms of PTSD postpartum, and enhanced support and mental health interventions during postpartum care could reduce some risks associated with childbirth trauma. This study shows the importance of considering maternal mental health in recovery from childbirth, especially for those pregnant women who underwent cesarean delivery under emotionally challenging conditions.

Reference:

Froeliger, A., Deneux-Tharaux, C., Loussert, L., Madar, H., Sentilhes, L., Sentilhes, L., Senat, M. V., Le Lous, M., Winer, N., Rozenberg, P., Kayem, G., Verspyck, E., Fuchs, F., Azria, E., Gallot, D., Korb, D., Desbrière, R., Le Ray, C., Chauleur, C., … Deneux-Tharaux, C. (2024). Posttraumatic stress disorder 2 months after cesarean delivery: a multicenter prospective study. American Journal of Obstetrics and Gynecology, 231(5), 543.e1-543.e36. https://doi.org/10.1016/j.ajog.2024.03.011

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Long-acting Mesalamine may effectively reduce symptoms in Postinfectious Irritable Bowel Syndrome: Study

A new study revealed that Mesalamine, an anti-inflammatory drug, can effectively treat postinfectious irritable bowel syndrome (PI-IBS) symptoms and improve the quality of life. The study results were published in the journal Neurogastroenterology & Motility. 

Irritable bowel syndrome (IBS) is a common gastrointestinal disorder characterized by abdominal pain and alteration in bowel frequency or consistency in the absence of a gross structural or biochemical abnormality. Postinfectious irritable bowel syndrome ((PI-IBS) is a condition associated with low-grade intestinal inflammation. It develops in a subset of patients after gastroenteritis. Previous studies showed that long-acting Mesalamine can be used to treat IBS. Hence, researchers conducted a study to investigate the efficacy of long-acting Mesalamine in individuals with PI-IBS particularly those with diarrhea-predominant IBS (IBS-D) following gastroenteritis, as PI-IBS is linked to low-grade intestinal inflammation.

A Randomized double-blind placebo-controlled study was carried out on a total of 61 patients who developed IBS-D after gastroenteritis. Individuals were randomly assigned to receive either 2.4 g of long-acting mesalamine or a placebo daily for 8 weeks. The study assessed symptoms including abdominal pain, bloating, stool frequency, stool consistency, severity of diarrhea and constipation, satisfaction with bowel habits, and how much IBS affected or interfered with life. Quality of life (QOL) was measured using the IBS-QOL questionnaire. The primary outcome was the overall bowel symptom score (BSS) after 8 weeks of treatment. Effect sizes were quantified using standardized mean differences (Cohen’s d).

Findings:

  • Of the 61 participants, 54 completed the 8-week study with 28 in the mesalamine group and 26 in the placebo group.
  • The majority of participants (91%) were male, with an age range of 23–71 years (mean ± SD: 43 ± 13 years).
  • Mesalamine showed greater efficacy than placebo in reducing overall BSS, with a medium effect size (Cohen’s d = 0.57, p = 0.042).
  • A significant improvement in the secondary outcomes was noticed on how IBS affects daily life (d = 0.72, p = 0.01).
  • For the individual IBS symptoms, all seven symptoms assessed showed trends favoring mesalamine, and eight of nine IBS-QOL subscales also showed trends indicating mesalamine’s superiority.

In patients with PI-IBS, long-acting mesalamine was effective in reducing IBS symptoms and improving quality of life suggesting that mesalamine could be a promising treatment option for managing PI-IBS.

Take-home Points:

  • This placebo-controlled randomized trial assessed the efficacy of 2.4 g of long-acting mesalamine for the treatment of postinfectious diarrhea-predominant IBS.
  • Among 54 patients who underwent 8-week treatment, mesalamine resulted in greater improvements on the Bowel Symptoms Score (change, −13 vs −4; P = .042); however, the difference between mesalamine and placebo was no longer significant when the constipation subscore was removed.
  • Apart from the Bowel Symptoms Score, mesalamine largely failed to demonstrate superiority to placebo for other measures of symptom severity and QoL measures.
  • Mesalamine may have some role in improving overall symptom severity in postinfectious IBS; however, additional larger studies are needed.

Further reading: Tuteja, Ashok K et al. “Randomized double-blind placebo-controlled study to evaluate the effect of long-acting mesalamine on postinfectious irritable bowel syndrome with diarrhea.” Neurogastroenterology and motility, e14889. 5 Aug. 2024, doi:10.1111/nmo.14889

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High levels of omega-3, omega-6 may protect against cancer: Study

In addition to lowering your cholesterol, keeping your brain healthy and improving mental health, new research from the University of Georgia suggests omega-3 and omega-6 fatty acids may help ward off a variety of cancers.

The study relied on data from more than 250,000 people and found that higher levels of omega-3 and omega-6 fatty acids were associated with a lower risk of developing cancer.

“Higher omega-3 and omega-6 levels were associated with lower rates of cancer,” said Yuchen Zhang, lead author of the study and a doctoral student in UGA’s College of Public Health. “These findings suggest that the average person should focus on getting more of these fatty acids in their diets.”

Participants with higher levels of omega-3s had lower rates of colon, stomach and lung cancer, in addition to lower rates of other digestive tract cancers.

High omega-6 levels led to lower rates of 14 different cancers, including brain, malignant melanoma, bladder and more.

Healthy fats reduce risk of developing 19 types of cancer

The study relied on data from a United Kingdom-based study of over 250,000 people who were followed for more than a decade. Of those participants, almost 30,000 developed some form of cancer during the study period.

Some earlier research drew connections between levels of fatty acids and risk of developing cancer. However, no studies could conclusively determine whether omega-3 and omega-6 fatty acids reduced cancer rates or increased the likelihood of surviving a cancer diagnosis.

Importantly, the benefits of high levels of fatty acids were not dependent on other risk factors like BMI, alcohol use or physical activity.

Fish oil supplements come with a variety of health benefits

Known as “healthy fats,” omega-3 and omega-6 fatty acids are essential for human health. They’re present in fatty fish, nuts and even some plant oils such as canola oil.

But most Americans probably aren’t eating enough of these foods to reach the recommended amounts.

That’s why many individuals turn to fish oil supplements. They’re one of the most popular dietary pills on the market and for good reason.

Previous studies suggest omega-3 supplements can reduce the risk of developing high cholesterol and lower the risk of heart disease.

Benefits of fish oil may not be one-size-fits-all

But the decision to take the popular fish oil pills isn’t one-size-fits-all.

In the present study, for example, the researchers found that high omega-3 levels could be associated with a slightly higher risk of prostate cancer.

“For women, it’s an easy decision: Eat more omega-3,” said Kaixiong Ye, corresponding author of the study and an associate professor in UGA’s Franklin College of Arts and Sciences.

The researchers also saw a stronger beneficial effect of omega-6 in younger participants, particularly women.

Reference:

Yuchen Zhang, Yitang Sun, Suhang Song, Nikhil K. Khankari, J. Thomas Brenna, Ye Shen, Kaixiong Ye, Associations of plasma omega-6 and omega-3 fatty acids with overall and 19 site-specific cancers: A population-based cohort study in UK Biobank, International Journal of Cancer, https://doi.org/10.1002/ijc.35226

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EOI block useful component of multimodal analgesia regimens for upper abdominal surgeries, suggests study

Upper abdominal surgical incisions result in significant pain during and after surgery. While neuraxial techniques are the standard for managing pain, they can be linked to complications. There’s a recognition of interfascial plane block techniques as a component of multimodal pain relief for upper abdominal surgeries with subcostal incisions, such as the TAP block, QL block, and ESP block. Recent study compared the effectiveness of the external oblique intercostal (EOI) block versus the subcostal transversus abdominis plane (TAP) block for postoperative pain management in patients undergoing upper abdominal surgeries.

The study involved 50 patients who were randomly assigned to receive either the EOI block or the subcostal TAP block. The primary outcome was the time to activation of patient-controlled analgesia (PCA) after the surgery. The researchers also assessed secondary outcomes such as 24-hour opioid consumption, pain scores, patient satisfaction, and block-related complications. The results showed that patients who received the EOI block had a significantly longer time to activation of the PCA compared to the subcostal TAP block group (610 minutes vs. 410 minutes, p=0.001). The 24-hour postoperative opioid (fentanyl) consumption was also lower in the EOI block group (102 μg vs. 123 μg, p=0.019). Patients in the EOI block group had better pain scores at 30 minutes and 6 hours, as well as higher patient satisfaction scores.

Conclusion

The researchers conclude that the EOI block provides more effective postoperative analgesia compared to the subcostal TAP block in patients undergoing upper abdominal surgeries. The EOI block was able to prolong the duration of PCA activation and reduce opioid consumption, leading to better pain control and higher patient satisfaction. No significant block-related complications were observed in either group.

Future Implications

The authors suggest that the EOI block may be a useful component of multimodal analgesia regimens for upper abdominal surgeries, as it can effectively target the lateral and anterior cutaneous branches of the intercostal nerves. Further studies comparing the EOI block to other regional anesthesia techniques, such as erector spinae or paravertebral blocks, may provide additional insights into the optimal pain management strategies for this patient population.

Key Points

1. The study compared the effectiveness of the external oblique intercostal (EOI) block versus the subcostal transversus abdominis plane (TAP) block for postoperative pain management in patients undergoing upper abdominal surgeries.

2. The primary outcome was the time to activation of patient-controlled analgesia (PCA) after the surgery, and the researchers also assessed secondary outcomes such as 24-hour opioid consumption, pain scores, patient satisfaction, and block-related complications.

3. Patients who received the EOI block had a significantly longer time to activation of the PCA compared to the subcostal TAP block group, and their 24-hour postoperative opioid consumption was also lower.

4. Patients in the EOI block group had better pain scores at 30 minutes and 6 hours, as well as higher patient satisfaction scores.

5. The researchers concluded that the EOI block provides more effective postoperative analgesia compared to the subcostal TAP block in patients undergoing upper abdominal surgeries.

6. The authors suggest that the EOI block may be a useful component of multimodal analgesia regimens for upper abdominal surgeries, and further studies comparing the EOI block to other regional anesthesia techniques may provide additional insights.

Reference –

Shrey S, Sinha C, Kumar A, Kumar A, Kumar A, Nambiar S. Comparison of analgesic efficacy of ultrasound‑guided external oblique intercostal plane block and subcostal transverses abdominis plane block in patients undergoing upper abdominal surgery: A randomised clinical study. Indian J Anaesth 2024;68:965‑70

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Clinical Outcome of Vernal Keratoconjunctivitis in Childhood: Long-Term Observation

Vernal keratoconjunctivitis (VKC) is an ocular disorder
characterized by severe inflammation affecting both the cornea and conjunctiva
that mainly affects boys in the first decade of life. Although the symptoms of
VKC usually persist despite treatment, with seasonal deterioration, the
condition generally resolves spontaneously with the onset of puberty. Some
cases of VKC result in refractory atopic keratoconjunctivitis (AKC) in
adulthood. Those cases complicated by atopic dermatitis (AD) may require
therapeutic measures beyond this age into adulthood to control the disease, and
permanent changes to the ocular surface and visual impairment may occur. Long-term
follow-up has been rarely reported for VKC because of the need for long-term
clinical evaluation. Authors investigated the long-term clinical outcome of VKC
treated and controlled in their hospital, which might reflect the recent
changes in clinical features of VKC especially derived by the introduction of
immunosuppressive eye drops. The most relevant clinical features that emerged
from this evaluation were analyzed for their prognostic value based on longterm
follow-up. The aim of the present study was also to evaluate the relationship
between the cure/non-cure groups and clinical findings derived from long-term
observation of VKC cases

In total, 45 consecutive patients clinically diagnosed with
VKC aged 4 to 12 years at onset at the Department of Ophthalmology of Fukuoka
University Hospital were included. Patients were treated with immunosuppressive
eye drops without simultaneous corticosteroid eye drops, except for the
occurrence of exacerbations. Collated variables were gender, age at onset,
clinical score of ocular lesions (conjunctival giant papillae, limbal edema and
corneal epithelial lesions) at the first visit, and clinical score of atopic
dermatitis (AD) at baseline.

The observation period ranged from 24 to 188 months, with
median of 70 months. Among the 45 cases enrolled, all noncured cases (14 cases)
observed clinically were complicated by AD. Cumulative cure rate was 74.5% and
84.9% at eight- and ten-year follow-up, respectively. Ten-year cumulative cure
rates of cases with and without AD were 50.5% and 100%, respectively, and a
significant difference was found between these cumulative cure curves. Binomial
regression analysis revealed that AD and gender were significantly related to
worse outcome, and this binomial regression model had high sensitivity and
specificity.

In conclusion, several novel findings have been gained from
this observational case series. In this chronological survey, the ten-year
cumulative cure rate of VKC was 84.9%, and 15.1% of cases remained uncured after
10 years of observation in the cure curve. There was a significant difference
in the long-term outcome between VKC cases with and without AD. Binomial
regression analysis showed that AD and male gender were significantly related
to a worse outcome. The binomial regression model had high sensitivity and
specificity. The clinical outcome in VKC might be predicted by several factors
that can be evaluated in the early clinical phase.

Source: Shimokawa et al; Clinical Ophthalmology 2024:18
2339–2347

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Ten point preoperative checklist for selecting patients for outpatient joint replacement surgery, enumerates study

With advancements in perioperative care, joint replacement (JR) surgery is undergoing a transition from opacified in-patient institutions to nimble out-patient Ambulatory Surgical Centers (ASC). The goal of JR in ASC setting is safe patient discharge with subsequent rehabilitation without readmission. Multi-modal preoperative rehabilitation (MMPR) is a novel field of perioperative care, encompassing comprehensive parameters to ensure smooth transition from fitness for surgery to JR in outpatient setting. At present, there are no open-access schemes for selecting patients qualified for JR in the ASC setting.

In the article, Madhav Chowdhry & Edward J. McPherson proposed an evidence-based, 10-point systematic evaluation of patients with target endpoints for MMPR to qualify patients for JR as an outpatient procedure. It has been published in ‘Arthroplasty’ journal

This checklist is a non-proprietary scheme serving as an initial framework for surgeons exploring surgery in the ASC setting.

The authors introduced factors for a prehabilitation scheme, called Checklist Outpatient-Joint Replacement (CO-JR) to qualify patients for outpatient JR surgery.

These factors have been developed based on an extensive literature review and the significant experience of authors to incorporate variables that drive a successful outpatient JR procedure.

The factors include patient education, psychiatric & cognitive ability, medical fitness, musculoskeletal capability, financial ability, transportation access, patient motivation, information technology (IT) capabilities, along with ability to recover independently at home postoperatively.

The CO-JR scheme is under the process of validation at multiple institutions.

The authors commented – “Our goal is to develop a non-proprietary, open access 10-point CO-JR scheme, developed by the collaborative effort of surgeons across the world, serving as a framework for successfully selecting patients for JR surgery in the ASC setting. We acknowledge that the needs of global populations vary, and the available medical resources are not alike. In the future, we envision a Modified CO-JR for various countries requiring different needs suiting their local ethnic and demographic variances, e.g., Modified CO-JR India, Modified CO-JR Nigeria, Modified CO-JR New Zealand, Modified CO-JR USA etc. The proposed scheme is aimed to serve as a benchmark and is currently under the process of validation. With this initial proposal, we encourage concomitant input and validation to create a common, global platform for JR in the ASC setting. In the future, we would encourage an in-person consensus meeting to further expand this grading system.”

Further reading:

A 10‑point preoperative checklist: selecting patients for outpatient joint replacement surgery.

Chowdhry and McPherson

Arthroplasty (2024) 6:52

https://doi.org/10.1186/s42836-024-00270-2

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