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Items: 1 to 20 of 96

1.

Differences in pain management between hematologists and hospitalists caring for patients with sickle cell disease hospitalized for vasoocclusive crisis.

Shah N, Rollins M, Landi D, Shah R, Bae J, De Castro LM.

Clin J Pain. 2014 Mar;30(3):266-8. doi: 10.1097/AJP.0b013e318295ec04.

2.

Hospitalist management of vaso-occlusive pain crisis in patients with sickle cell disease using a pathway of care.

Allen Liles E, Kirsch J, Gilchrist M, Adem M.

Hosp Pract (1995). 2014 Apr;42(2):70-6. doi: 10.3810/hp.2014.04.1105.

PMID:
24769786
3.

Comparison of Hospital Resource Use and Outcomes Among Hospitalists, Primary Care Physicians, and Other Generalists.

Stevens JP, Nyweide DJ, Maresh S, Hatfield LA, Howell MD, Landon BE.

JAMA Intern Med. 2017 Dec 1;177(12):1781-1787. doi: 10.1001/jamainternmed.2017.5824.

4.

Patient-controlled analgesia versus continuous infusion of morphine during vaso-occlusive crisis in sickle cell disease, a randomized controlled trial.

van Beers EJ, van Tuijn CF, Nieuwkerk PT, Friederich PW, Vranken JH, Biemond BJ.

Am J Hematol. 2007 Nov;82(11):955-60.

5.

A Mixed-Methods Study of Pain-related Quality of Life in Sickle Cell Vaso-Occlusive Crises.

Lin RJ, Evans AT, Wakeman K, Unterbrink M.

Hemoglobin. 2015;39(5):305-9. doi: 10.3109/03630269.2015.1055576. Epub 2015 Jun 26.

PMID:
26114739
6.

Comparison of processes and outcomes of pneumonia care between hospitalists and community-based primary care physicians.

Rifkin WD, Conner D, Silver A, Eichorn A.

Mayo Clin Proc. 2002 Oct;77(10):1053-8.

PMID:
12374249
7.

Outcomes of care by hospitalists, general internists, and family physicians.

Lindenauer PK, Rothberg MB, Pekow PS, Kenwood C, Benjamin EM, Auerbach AD.

N Engl J Med. 2007 Dec 20;357(25):2589-600.

8.

Impact of PCA strategies on pain intensity and functional assessment measures in adults with sickle cell disease during hospitalized vaso-occlusive episodes.

Dampier CD, Wager CG, Harrison R, Hsu LL, Minniti CP, Smith WR; Investigators of the Sickle Cell Disease Clinical Research Network (SCDCRN).

Am J Hematol. 2012 Oct;87(10):E71-4. doi: 10.1002/ajh.23302. Epub 2012 Aug 7. No abstract available.

9.

A Randomized Trial of Yoga for Children Hospitalized With Sickle Cell Vaso-Occlusive Crisis.

Moody K, Abrahams B, Baker R, Santizo R, Manwani D, Carullo V, Eugenio D, Carroll A.

J Pain Symptom Manage. 2017 Jun;53(6):1026-1034. doi: 10.1016/j.jpainsymman.2016.12.351. Epub 2017 Feb 10.

PMID:
28192225
10.

Variation in length of stay and outcomes among hospitalized patients attributable to hospitals and hospitalists.

Goodwin JS, Lin YL, Singh S, Kuo YF.

J Gen Intern Med. 2013 Mar;28(3):370-6. doi: 10.1007/s11606-012-2255-6. Epub 2012 Nov 6.

11.

Frequently asked questions by hospitalists managing pain in adults with sickle cell disease.

Smith WR, Jordan LB, Hassell KL.

J Hosp Med. 2011 May;6(5):297-303. doi: 10.1002/jhm.933. Review.

PMID:
21661104
12.

A comparison of two regimens of patient-controlled analgesia for children with sickle cell disease.

Trentadue NO, Kachoyeanos MK, Lea G.

J Pediatr Nurs. 1998 Feb;13(1):15-9.

PMID:
9503762
13.

Clinical and Geographic Characterization of 30-Day Readmissions in Pediatric Sickle Cell Crisis Patients.

McMillan JE, Meier ER, Winer JC, Coco M, Daymont M, Long S, Jacobs BR.

Hosp Pediatr. 2015 Aug;5(8):423-31. doi: 10.1542/hpeds.2014-0184.

14.

Risk Factors for 30-Day Readmission in Adults with Sickle Cell Disease.

Brodsky MA, Rodeghier M, Sanger M, Byrd J, McClain B, Covert B, Roberts DO, Wilkerson K, DeBaun MR, Kassim AA.

Am J Med. 2017 May;130(5):601.e9-601.e15. doi: 10.1016/j.amjmed.2016.12.010. Epub 2017 Jan 5.

PMID:
28065771
15.

Opioid selection during sickle cell pain crisis and its impact on the development of acute chest syndrome.

Buchanan ID, Woodward M, Reed GW.

Pediatr Blood Cancer. 2005 Oct 15;45(5):716-24.

PMID:
15926170
16.

Does e-pain plan improve management of sickle cell disease associated vaso-occlusive pain crisis? a mixed methods evaluation.

Kato-Lin YC, Krishnamurti L, Padman R, Seltman HJ.

Int J Med Inform. 2014 Nov;83(11):814-24. doi: 10.1016/j.ijmedinf.2014.08.003. Epub 2014 Aug 17.

PMID:
25179666
17.

Inpatient management of sickle cell pain: a 'snapshot' of current practice.

Miller ST, Kim HY, Weiner D, Wager CG, Gallagher D, Styles L, Dampier CD; Investigators of the Sickle Cell Disease Clinical Research Network (SCDCRN).

Am J Hematol. 2012 Mar;87(3):333-6. doi: 10.1002/ajh.22265. Epub 2012 Jan 9.

18.

Day hospital versus inpatient management of uncomplicated vaso-occlusive crises in children with sickle cell disease.

Raphael JL, Kamdar A, Wang T, Liu H, Mahoney DH, Mueller BU.

Pediatr Blood Cancer. 2008 Sep;51(3):398-401. doi: 10.1002/pbc.21537.

PMID:
18300322
19.

Pain Management for Sickle Cell Disease in the Pediatric Emergency Department: Medications and Hospitalization Trends.

Cacciotti C, Vaiselbuh S, Romanos-Sirakis E.

Clin Pediatr (Phila). 2017 Oct;56(12):1109-1114. doi: 10.1177/0009922816674521. Epub 2016 Oct 23.

PMID:
27798391
20.

Pain experience of children with sickle cell disease who had prolonged hospitalizations for acute painful episodes.

Jacob E, Mueller BU.

Pain Med. 2008 Jan-Feb;9(1):13-21. doi: 10.1111/j.1526-4637.2006.00252.x.

PMID:
18254762

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