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1.
BJOG ; 126(6): 804-813, 2019 May.
Article in English | MEDLINE | ID: mdl-30548529

ABSTRACT

OBJECTIVE: To evaluate if immediate catheter removal (ICR) after laparoscopic hysterectomy is associated with similar retention outcomes compared with delayed removal (DCR). STUDY DESIGN: Non-inferiority randomised controlled trial. POPULATION: Women undergoing laparoscopic hysterectomy in six hospitals in the Netherlands. METHODS: Women were randomised to ICR or DCR (between 18 and 24 hours after surgery). PRIMARY OUTCOME: The inability to void within 6 hours after catheter removal. RESULTS: One hundred and fifty-five women were randomised to ICR (n = 74) and DCR (n = 81). The intention-to-treat and per-protocol analysis could not demonstrate the non-inferiority of ICR: ten women with ICR could not urinate spontaneously within 6 hours compared with none in the delayed group (risk difference 13.5%, 5.6-24.8, P = 0.88). However, seven of these women could void spontaneously within 9 hours without additional intervention. Regarding the secondary outcomes, eight women from the delayed group requested earlier catheter removal because of complaints (9.9%). Three women with ICR (4.1%) had a urinary tract infection postoperatively versus eight with DCR (9.9%, risk difference -5.8%, -15.1 to 3.5, P = 0.215). Women with ICR mobilised significantly earlier (5.7 hours, 0.8-23.3 versus 21.0 hours, 1.4-29.9; P ≤ 0.001). CONCLUSION: The non-inferiority of ICR could not be demonstrated in terms of urinary retention 6 hours after procedure. However, 70% of the women with voiding difficulties could void spontaneously within 9 hours after laparoscopic hysterectomy. It is therefore questionable if all observed urinary retention cases were clinically relevant. As a result, the clinical advantages of ICR may still outweigh the risk of bladder retention and it should therefore be considered after uncomplicated laparoscopic hysterectomy. TWEETABLE ABSTRACT: The advantages of immediate catheter removal after laparoscopic hysterectomy seem to outweigh the risk of bladder retention.


Subject(s)
Device Removal/methods , Hysterectomy/adverse effects , Laparoscopy/adverse effects , Postoperative Care , Urinary Catheterization/methods , Urinary Retention , Adult , Female , Humans , Hysterectomy/methods , Laparoscopy/methods , Middle Aged , Outcome Assessment, Health Care , Postoperative Care/adverse effects , Postoperative Care/instrumentation , Postoperative Care/methods , Postoperative Complications/diagnosis , Postoperative Complications/etiology , Postoperative Complications/physiopathology , Postoperative Complications/therapy , Time Factors , Urinary Catheters , Urinary Retention/diagnosis , Urinary Retention/etiology , Urinary Retention/physiopathology , Urinary Retention/therapy , Urination/physiology
2.
Ned Tijdschr Geneeskd ; 161: D1672, 2017.
Article in Dutch | MEDLINE | ID: mdl-29098970

ABSTRACT

In the last decennia, the length of hospital stay of admitted patients has significantly decreased in all medical fields. As a result, postoperative recovery mainly takes place at home, inherently leading to new challenges. Here, two patients are being discussed for whom the postoperative period was substandard. To guarantee optimal quality of care in the home situation, the medical specialist and the general practitioner need to make the necessary arrangements. We would first of all recommend providing each discharged patient with specific, structured and individualised advices regarding postoperative recovery but also regarding alarm symptoms and logistics (e.g. who to call in case of emergency). Finally, we believe that, as (serious) complications are rare, it should be agreed on the fact that the responsible medical specialist is the coordinator of the postoperative period and the first contact point for postoperative patients.


Subject(s)
Length of Stay , Patient Discharge , Aged , Family Practice , Female , Hospital Costs , Humans , Middle Aged , Netherlands , Postoperative Period
3.
BJOG ; 123(13): 2183-2187, 2016 12.
Article in English | MEDLINE | ID: mdl-27533508

ABSTRACT

OBJECTIVE: Uncontained morcellation of leiomyomas during laparoscopic surgery has recently been discouraged, as undetected malignant tumours, namely leiomyosarcomas, could be fragmented which may result in upstaged disease. However, enucleating leiomyomas per se may be inappropriate from an oncological perspective because complete, radical resection of malignant tumours to prevent further tumour growth or recurrence is not achieved. Thus, the aim of this study was to determine whether spillage of leiomyoma cells occurs during laparotomic myomectomy. DESIGN: Observational study. SETTING: Tertiary academic centre in the Netherlands. POPULATION: Women undergoing laparotomic myomectomy were included in the study. METHODS: Peritoneal abdominal washings were obtained on two occasions during the myomectomy procedure; the first one immediately after opening the abdomen and the second one after resection of the leiomyoma(s). Cytological evaluation of the fluids was performed. MAIN OUTCOME MEASURES: The presence of leiomyoma cells in any of the washings. RESULTS: Five patients were included in this pilot study. All first washings were negative for leiomyoma cells. However, cytology positive for the presence of leiomyoma cells was found in three of the five second, post-myomectomy washings. CONCLUSION: Tissue spillage from leiomyoma(s) occurs during conventional open myomectomy. The clinical relevance of tissue dissemination after myomectomy is unclear but it cannot be excluded that this may negatively affect the patient's outcome if there is malignant change within the enucleated leiomyoma(s). Therefore, it is questionable whether morcellation in specially designed containment bags after laparoscopic myomectomy, guarantees any additional oncological safety. TWEETABLE ABSTRACT: Even during conventional myomectomy, tissue spillage occurs during resection of leiomyoma(s).


Subject(s)
Leiomyoma/pathology , Leiomyoma/surgery , Neoplasm Seeding , Neoplastic Cells, Circulating , Uterine Myomectomy/adverse effects , Uterine Neoplasms/pathology , Uterine Neoplasms/surgery , Adult , Female , Humans , Laparoscopy , Uterine Myomectomy/methods
4.
J Minim Invasive Gynecol ; 22(6S): S207, 2015.
Article in English | MEDLINE | ID: mdl-27679052
6.
Oncogene ; 31(50): 5144-52, 2012 Dec 13.
Article in English | MEDLINE | ID: mdl-22330140

ABSTRACT

Brain-specific angiogenesis inhibitor 1 (BAI1), an orphan G protein-coupled receptor-type seven transmembrane protein, was recently found mutated or silenced in multiple human cancers and can interfere with tumor growth when overexpressed. Yet, little is known about its regulation and the molecular mechanisms through which this novel tumor suppressor exerts its anti-cancer effects. Here, we demonstrate that the N terminus of BAI1 is cleaved extracellularly to generate a truncated receptor and a 40-kDa fragment (Vasculostatin-40) that inhibits angiogenesis. We demonstrate that this novel proteolytic processing event depends on a two-step cascade of protease activation: proprotein convertases, primarily furin, activate latent matrix metalloproteinase-14, which then directly cleaves BAI1 to release the bioactive fragment. These findings significantly augment our knowledge of BAI1 by showing a novel post-translational mechanism regulating BAI1 activity through cancer-associated proteases, have important implications for BAI1 function and regulation, and present novel opportunities for therapy of cancer and other vascular diseases.


Subject(s)
Angiogenesis Inhibitors/metabolism , Angiogenic Proteins/metabolism , Brain Neoplasms/metabolism , Matrix Metalloproteinase 14/metabolism , Proprotein Convertases/metabolism , Angiogenic Proteins/genetics , Brain Neoplasms/blood supply , Brain Neoplasms/genetics , Cell Line, Tumor , Furin/metabolism , Genes, Tumor Suppressor , Human Umbilical Vein Endothelial Cells/cytology , Humans , Neovascularization, Pathologic/metabolism , Peptide Hydrolases/metabolism , Protein Processing, Post-Translational , Proteolysis , Receptors, G-Protein-Coupled
7.
Toxicol Pathol ; 20(2): 146-54, 1992.
Article in English | MEDLINE | ID: mdl-1475576

ABSTRACT

Weanling Fischer 344/N (F344) rats and the first filial hybrid of C57BL/6 x C3H (B6C3F1) mice and retired breeders from the parental stocks of these strains were monitored over a 5-yr-period by examining the histopathology of selected organs and comparing those results to viral and mycoplasmal serology and the intestinal tract bacterial flora of each animal on an individual basis. Serology gave no evidence of viral infection, but Mycoplasma arthriditis antibodies were detected. Reactivity of serum of adult C57BL/6 female mice with control cells or media (tissue culture, TC) was seen in a significant number of mice. TC reactivity correlated positively with lymphoid perivascular infiltrates, predominantly of the lungs, suggesting an allergic response in development of the lesions. Other lesions of note consisted of Harderian gland inflammation of rats, focal necrotizing lesions of the liver of both species, and thickening of the pleura and adjacent pulmonary interstitium of weanling rats. Embolization of bacteria from the gastrointestinal tract to the liver was considered a possible cause of the liver necrosis in both species. Although lesions of the lung and Harderian gland of the rats are similar to those caused by known viral agents, the cause of the latter could not be determined as these animals were negative for viral antibodies and the former was considered to be related to incomplete pulmonary development in the young rat. Features differentiating the lesions observed in animals of this survey from those caused by viral infection are discussed.


Subject(s)
Mice, Inbred C3H/anatomy & histology , Mice, Inbred C57BL/anatomy & histology , Mice, Inbred Strains/anatomy & histology , Rats, Inbred F344/anatomy & histology , Aging/pathology , Animals , Antibodies/blood , Digestive System/microbiology , Female , Lymphatic System/microbiology , Lymphatic System/pathology , Male , Mice , Mice, Inbred C3H/blood , Mice, Inbred C3H/microbiology , Mice, Inbred C57BL/blood , Mice, Inbred C57BL/microbiology , Mice, Inbred Strains/blood , Mice, Inbred Strains/microbiology , Rats , Rats, Inbred F344/blood , Rats, Inbred F344/microbiology , Reference Standards
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