How midwives manage rapid pre-loading of fluid in women prior to low dose epidurals: A retrospective chart review

2018 ◽  
Vol 74 (11) ◽  
pp. 2588-2595 ◽  
Author(s):  
Hannah Lindstrom ◽  
Lauren Kearney ◽  
Debbie Massey ◽  
Guy Godsall ◽  
Emma Hogan

2008 ◽  
Vol 13 (2) ◽  
pp. 80-87
Author(s):  
Bethany A. Lynch ◽  
Peter Gal ◽  
J. Laurence Ransom ◽  
Rita Q. Carlos ◽  
Mary Ann V.T. Dimaguila ◽  
...  

OBJECTIVE Aminophylline is a methylxanthine with multiple physiologic actions. At low doses, aminophylline can antagonize adenosine and improve renal function via increased glomerular filtration rate. Despite its clinical use, little data exists in neonates for this indication. Therefore, the objective of this report is to describe the impact of aminophylline on renal function indices in a series of neonates with acute renal failure. MATERIALS AND METHODS This was a retrospective chart review of 13 neonates with acute renal failure who received aminophylline during a 15-month study period. Aminophylline was administered at 1 mg/kg intravenously or orally every twelve hours. Forty-six percent (n = 6) of the patients received a 5 mg/kg loading dose before initiation of maintenance therapy. Most patients had already received other treatments for renal failure, including diuretics and dopamine. RESULTS Resolution of acute renal failure (with normalization of serum creatinine and blood urea nitrogen) was documented in 10 patients (77%). Four of the thirteen patients died from complications due to their prematurity. Failure of low-dose aminophylline was observed in 3 of the 4 patients who died. CONCLUSIONS Low-dose aminophylline in neonates with acute renal failure is associated with an improvement in renal function indices.





2021 ◽  
Vol 2021 ◽  
pp. 1-5
Author(s):  
James D. Phillips ◽  
Tyler Merrill ◽  
J. Reed Gardner ◽  
R. Thomas Collins ◽  
Jenika Sanchez ◽  
...  

Objective. Low-dose nonselective β blockade is an effective treatment for problematic infantile hemangioma (PIH). Screening electrocardiograms (ECG) are performed prior to the initiation of propranolol to minimize the risk of exacerbating undiagnosed heart block. How ECG results affect subsequent propranolol usage and patient management remains unclear. We examined the value of ECG prior to propranolol therapy in a quaternary pediatric hospital. Methods. A retrospective chart review was performed on all infants who received propranolol (2 mg/kg/day divided three times daily) to treat PIH at Arkansas Children’s Hospital from Sept. 2008 to Sept. 2015. All available demographic, historical, and clinical data were obtained. ECGs and echocardiographic data were reviewed and summarized. A pediatric cardiologist read all ECGs. Results. A total of 333 patients (75% female) received propranolol therapy. ECG information was available for 317 (95%). Abnormal findings were present on 44/317 (13.9%) of study ECGs. The most common abnormal finding was “voltage criteria for ventricular hypertrophy” ( n = 35 , 76.1%). Two patients had abnormal rhythms; one had first-degree atrioventricular (AV) block, and one had occasional premature atrial contractions. Of the 31 patients who underwent echocardiograms, 20 (35%) were abnormal. 2.9% of infants with PIH treated with propranolol required a follow-up with a cardiologist. No patient was precluded from taking propranolol due to the findings on screening ECG. Conclusions. Screening ECGs prior to propranolol therapy are abnormal in nearly 14% of patients with PIH but are unlikely to preclude therapy. In the absence of prior cardiac history, this cohort offers further evidence suggesting that screening ECGs may be of limited value in determining the safety of propranolol in otherwise healthy infants with PIH.





Blood ◽  
2013 ◽  
Vol 122 (21) ◽  
pp. 5386-5386
Author(s):  
Dominic Duquette ◽  
Vincent Laroche

Abstract Introduction   The use of bortezomib has evolved since the APEX study published in 2005. It remains, however, the only study providing a detailed account of the changes in hematological parameters in response to bortezomib-based chemotherapy. The APEX trial enrolled multiple myeloma patients in relapse.  In first-line transplant eligible multiple myeloma patients, we use bortezomib twice weekly with low-dose dexamethasone (VelDex) or bortezomib once weekly with dexamethasone and cyclophosphamide (CyBorD). For patients non-eligible to transplant, we use bortezomib once or twice weekly with melphalan and prednisone (VMP).  The goal of this study is to describe changes in platelet counts during these three types of bortezomib-based induction therapys. Methods.   We conducted a retrospective chart review to examine the complete blood count (CBC) results during treatment with VelDex, CyBorD or VMP. Neutrophil count, hemoglobin and platelet count were measured before every bortezomib infusion. Patients not receiving the anticipated protocol or less than 3 cycles of VelDex or CyBorD or 6 cycles of VMP were excluded from this review. Results   30 patients were included in this review (VelDex = 11, CyBorD =10, VMP = 9) Results are showed in the following graphs. The use of twice weekly bortezomib is associated with a more pronounced drop in platelets.  CyborD once weekly is associated with less severe drop in platelets. Conclusion   These findings show that once weekly bortezomib is associated with less severe thrombocytopenia.  This suggests that the blood monitoring could be less frequent than at each dose of bortezomib.  A biweekly monitoring of blood counts could reduce significantly blood tests and waiting time for patients. Disclosures: Duquette: Janssen: Consultancy, Honoraria. Off Label Use: CyborD is a widely accepted regimen but has not been accepted by the FDA.



2020 ◽  
Vol 41 (3) ◽  
pp. 447-456
Author(s):  
Mi-jung Yoon ◽  
Na-kyung Cho ◽  
Hong-sic Choi ◽  
Seung-mo Kim ◽  
Sang-chan Kim ◽  
...  


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