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1.
BMC Pregnancy Childbirth ; 17(1): 355, 2017 Oct 16.
Article in English | MEDLINE | ID: mdl-29037181

ABSTRACT

BACKGROUND: Previous studies have shown that complaints after episiotomy repair depend on the method and material used for repair. The objective of our study was to determine which of two frequently used suture materials, Monocryl® (poliglecaprone 25) and Vicryl Rapide™ (polyglactin 910), is superior for intracutaneous closure of the skin in mediolateral episiotomies. METHODS: In a randomized controlled trial performed in a teaching hospital in the Netherlands between 2010 and 2013 250 primiparous women with uncomplicated mediolateral episiotomies were randomly allocated to intracutaneous skin closure with either Monocryl® or Vicryl Rapide™. All other layers were sutured with Vicryl 2-0 and Vicryl 0 in both groups. Pain scores and complications were documented using questionnaires during the first three months post partum. The primary outcome was pain 10 days after delivery in sitting position established by Visual Analogous Scale (VAS). Secondary outcomes were pain scores at different time points and reported complications such as infections, dehiscence and dyspareunia one day, 10 days, six weeks and three months after delivery. RESULTS: Of 250 allocated women 54% returned questionnaires. No statistical difference was found between both groups for the primary outcome (VAS 2,8 (95% CI 2,18-3,44) vs. VAS 2,5 (95% CI 2,00-2,98), p = 0,43). With regard to secondary outcomes only self-reported dehiscence was significantly different, favouring Monocryl® (10% vs. 25%, p = 0.016). CONCLUSIONS: Use of Monocryl® 3-0 and Vicryl Rapide™ 3-0 for intracutaneous closure of the skin after mediolateral episiotomy leads to equal pain scores ten days after delivery and therefore both materials may be considered for this use. Monocryl® 3-0 might be favourable over Vicryl Rapide™ 3-0 due to less self-reported dehiscence after intracutaneous closure of the skin in mediolateral episiotomies. TRIAL REGISTRATION: The trial was retrospectively registered under trial nr. ISRCTN29869308 on 20-04-2016.


Subject(s)
Dioxanes/administration & dosage , Episiotomy/methods , Polyesters/administration & dosage , Polyglactin 910/administration & dosage , Suture Techniques , Sutures , Adult , Dyspareunia/etiology , Episiotomy/adverse effects , Female , Humans , Netherlands , Perineum/surgery , Postoperative Complications/etiology , Pregnancy , Surgical Wound Dehiscence/etiology , Surgical Wound Infection/etiology , Treatment Outcome , Wound Healing/drug effects
2.
J Pediatr Hematol Oncol ; 31(11): 816-9, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19801949

ABSTRACT

We report 3 cases of accidental intrathecal vincristine administration. All 3 patients died between 8 and 18 days after the incident because of decerebration. In the literature, we found 41 cases of accidental intrathecal injection of vincristine. These reports represent only a fraction of the existing problem. New in our report is the fact that the first 2 cases were attributed to viral infection, only after the detection of high levels of vincristine in the cerebrospinal fluid was the real cause of death ascertained. The third case occurred during the implementation of rules by the Dutch Childhood Oncology Group on how to handle intrathecal triple therapy; and despite sequential safety measures, the accident still occurred. In the Netherlands no more accidents of this nature have occurred in children after the introduction of a quadruple syringe system 8 years ago. In our opinion the best fail-safe solution would be the development of a unique connection that is incompatible with a standard Luer syringe.


Subject(s)
Accidents , Antineoplastic Agents, Phytogenic/adverse effects , Injections, Spinal/adverse effects , Vincristine/adverse effects , Antineoplastic Agents, Phytogenic/administration & dosage , Child , Child, Preschool , Fatal Outcome , Female , Humans , Male , Vincristine/administration & dosage
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