Evidence map›Paper›PMID 37664395›Full record

ReviewCureus2023

Oral Therapeutics Post Menopausal Osteoporosis.

Ryan J Schroeder, Julia Staszkiewicz, Collyn O'Quin, Brandon Carroll, Nicolette Doan, Sagar Patel, Shahab Ahmadzadeh, Anusha Kallurkar, Omar Viswanath, Giustino Varrassi and 2 more

Open access · diamondAbstract readReview
In one paragraph

Review in Cureus, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Molecular and Cellular Mechanisms of Osteoporosis.International journal of molecular sciences · 2023
    Review
  10. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 2 countries.

Ryan J SchroederMedicine, Louisiana State University Health Sciences Center New Orleans, New Orleans, USA.
Julia StaszkiewiczAnesthesiology, Louisiana State University Health Sciences Center, Shreveport, USA.
Collyn O'QuinSchool of Medicine, Louisiana State University Health Sciences Center, Shreveport, USA.
Brandon CarrollMedicine, Louisiana State University Health Sciences Center New Orleans, New Orleans, USA.
Nicolette DoanAnesthesiology, Louisiana State University Health Sciences Center, Shreveport, USA.
Sagar PatelAnaesthesiology, Louisiana State University Health Sciences Center, Shreveport, USA.
Shahab AhmadzadehAnesthesiology, Louisiana State University Health Sciences Center, Shreveport, USA.
Anusha KallurkarAnaesthesiology, Louisiana State University Health Sciences Center, Shreveport, USA.
Omar ViswanathPain Management, Valley Pain Consultants - Envision Physician Services, Phoenix, USA.
Giustino VarrassiPain Medicine, Paolo Procacci Foundation, Rome, ITA.
Sahar ShekoohiAnesthesiology, Louisiana State University Health Sciences Center, Shreveport, USA.
Alan D KayeAnesthesiology, Louisiana State University Health Sciences Center, Shreveport, USA.
Fondazione Roma · ITLouisiana State University Health Sciences Center New Orleans · USLouisiana State University Health Sciences Center Shreveport · USPain Management Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoporosis affects a significant number of postmenopausal women in the United States. Screening is performed using clinical assessments and bone mineral density scans via dual x-ray absorptiometry. Oral therapy is indicated to prevent pathologic fractures in those deemed at increased risk following screening. Bisphosphonates including alendronate, ibandronate, and risedronate are currently first-line oral therapeutics in fracture prevention following the diagnosis of osteoporosis. Hormonal therapies include estrogen-containing therapies, selective estrogen receptor modulators, and other compounds that mimic the effects of estrogen such as tibolone. Lifestyle modifications such as supplementation and physical activity may also contribute to the prevention of osteoporosis and are used as adjuncts to therapy following diagnosis. These therapeutics are limited primarily by their adverse effects. Treatment regimens should be tailored based on significant risk factors demonstrated by patients, adverse effects, and clinical response to treatment. The most severe risk factors relevant to pharmacological selection involve hormone replacement therapies, where concern for venous thrombosis, coronary artery disease, breast, and uterine cancer exist. Bisphosphonates are most commonly associated with gastrointestinal discomfort which may be mitigated with proper administration. Although adverse effects exist, these medications have proven to be efficacious in the prevention of vertebral and non-vertebral fractures in post-menopausal women. Fracture risk should be weighed against the risk of adverse events associated with each of the regimens, with clinical judgment dictating the treatment approach centered around patient goals and experiences.

Indexed as

bisphosphonatesfracture riskhormonal therapyoral therapeuticsosteoporosispost-menopausalselective estrogen receptor modulators

Identifiers

PMID37664395
PMCPMC10474253
OpenAlexW4385551085

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.