ReviewOchsner journal2014
Tuberous sclerosis complex: perioperative considerations.
Review in Ochsner journal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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.
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.
Who cites it
6 citing papers in PubMed, 15 citations in OpenAlex.
- Managing Different Spectrums of Tuberous Sclerosis Facial Angiofibroma: A Report of Two Cases.Cureus · 2023Article
- A Case of Uterine Lymphangioleiomyomatosis Complicated by Tuberous Sclerosis Complex.Case reports in obstetrics and gynecology · 2022Article
- Early diagnosis of a newborn with tuberous sclerosis caused by a genetic mutation.The Journal of international medical research · 2021Article
- Familial genetic tuberous sclerosis complex associated with bilateral giant renal angiomyolipoma: A case report.Oncology letters · 2017Article
- Tuberous Sclerosis with Severe Cutaneous Manifestation and Multiples Facial Angiofibromas.Head and neck pathology · 2016Article
- Peripartum management of tuberous sclerosis complex complicated by massive angiomyolipomas.Anaesthesia reportsArticle
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundTuberous sclerosis complex (TSC), also known as Bourneville disease, is an inherited, progressive neurocutaneous disorder characterized by the potential for hamartoma formation throughout the body. TSC is an autosomal dominant genetic disorder, but more than two-thirds of cases are sporadic.
methodsClinical manifestations and treatment options are discussed. Both surgical and anesthetic perioperative considerations are described in this review.
resultsRoutine monitoring is appropriate for minor surgical procedures for patients with TSC who have mild disease manifestations. More extensive monitoring is indicated for major procedures that have the potential for significant blood loss and for patients with more severe pathology. Postoperatively, TSC patients should be admitted for monitoring and treatment after more extensive procedures or if significant organ dysfunction occurs. Postoperative complications, which may be related to either the surgery or the TSC pathology itself, may have origins in many different organs and may include seizures, severe hypertension, and bradyarrhythmias.
conclusionTSC is a rare disease with a highly variable clinical presentation and provides a multitude of challenges for the patient, the family, and the healthcare team.
Indexed as
Identifiers
24940133PMC4052590W1923989203What OpenQuestion holds
Registered trials
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.