Point-of-Care Pregnancy Testing

Author(s):  
Patrick M. Sluss
2019 ◽  
Vol 37 (27_suppl) ◽  
pp. 246-246
Author(s):  
Christian Eastlake ◽  
Kate Jeffers

246 Background: Many cancer therapies currently available are teratogenic in nature. Several patients cared for within our community ambulatory oncology infusion center are women of childbearing potential (WOCP). Pregnancy testing of these women within our oncology infusion center was sporadic at best. There currently are no standardized guidelines related to pregnancy testing of these women. Methods: A retrospective chart analysis of WOCP receiving chemotherapy was done to determine baseline pregnancy screening rates. Subsequently a protocol was developed in which WOCP was defined as women under 50 years of age, without a history of hysterectomy or tubal ligation. The nurse-driven protocol allowed the infusion nursing staff to order a pregnancy screen to be done within the infusion center if testing had not already taken place within 48 hours of initiation of treatment. Following protocol implementation a retrospective chart analysis was performed to re-examine screening rates. Results: Utilizing patients with an active treatment plan within a one month time period, retrospective analysis of pregnancy screening prior to initiation of chemotherapy was performed. Baseline pregnancy screening rate was 21%. Point of care pregnancy equipment was obtained and nursing staff was educated on the protocol to include a medical delegation. Post-implementation chart analysis of WOCP initiating chemotherapy within a six-week timeframe resulted in improved pregnancy screening to 57% compliance. Continued education and clarification of the protocol was provided to the nurses in an effort to further improve compliance. Conclusions: Lack of standard guidelines regarding pregnancy screening of WOCP led to the development and implementation of a protocol for pregnancy screening for this at-risk population. Medical delegation allowed nursing to initiate the screening for these patients allowing for improvements in the safety and quality of patient care provided.


2013 ◽  
Vol 10 (7) ◽  
pp. 533-537 ◽  
Author(s):  
Keith Herr ◽  
Courtney Coursey Moreno ◽  
Corinne Fantz ◽  
Pardeep K. Mittal ◽  
William C. Small ◽  
...  

2016 ◽  
Vol 17 (4) ◽  
pp. 449-453 ◽  
Author(s):  
Michael Gottlieb ◽  
Kristopher Wnek ◽  
Jordan Moskoff ◽  
Errick Christian ◽  
John Bailitz

2015 ◽  
Vol 66 (4) ◽  
pp. S23
Author(s):  
M. Gottlieb ◽  
K. Wnek ◽  
E. Christian ◽  
J. Moskoff ◽  
J. Bailitz

2013 ◽  
Vol 44 (1) ◽  
pp. 155-160 ◽  
Author(s):  
Richard T. Griffey ◽  
Caleb J. Trent ◽  
Rebecca A. Bavolek ◽  
Jacob B. Keeperman ◽  
Christopher Sampson ◽  
...  

VASA ◽  
2011 ◽  
Vol 40 (6) ◽  
pp. 429-438 ◽  
Author(s):  
Berent ◽  
Sinzinger

Based upon various platelet function tests and the fact that patients experience vascular events despite taking acetylsalicylic acid (ASA or aspirin), it has been suggested that patients may become resistant to the action of this pharmacological compound. However, the term “aspirin resistance” was created almost two decades ago but is still not defined. Platelet function tests are not standardized, providing conflicting information and cut-off values are arbitrarily set. Intertest comparison reveals low agreement. Even point of care tests have been introduced before appropriate validation. Inflammation may activate platelets, co-medication(s) may interfere significantly with aspirin action on platelets. Platelet function and Cox-inhibition are only some of the effects of aspirin on haemostatic regulation. One single test is not reliable to identify an altered response. Therefore, it may be more appropriate to speak about “treatment failure” to aspirin therapy than using the term “aspirin resistance”. There is no evidence based justification from either the laboratory or the clinical point of view for platelet function testing in patients taking aspirin as well as from an economic standpoint. Until evidence based data from controlled studies will be available the term “aspirin resistance” should not be further used. A more robust monitoring of factors resulting in cardiovascular events such as inflammation is recommended.


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